Professor Grant Montgomery

NHMRC Leadership Fellow

Institute for Molecular Bioscience

Affiliate Professor

School of Public Health
Faculty of Medicine

Affiliate Professorial Research Fe

Queensland Brain Institute

Affiliate Professorial Research Fel

Office of the Pro-Vice-Chancellor (Research Infrastructure)
g.montgomery1@uq.edu.au
+61 7 334 62612

Overview

Professor Grant Montgomery FAHMS FSRB Hon FRSNZ

Professor Montgomery was born in New Zealand, completed PhD studies in Animal Science at Massey University and post-doctoral research in France. In 1987, he co-founded the New Zealand Sheep Genomics Program in the Biochemistry Department at the University of Otago and pioneered the introduction of genome mapping methods in farm animals. He moved to Australia in 1999 and joined the Queensland Institute of Medical Research where he ran a successful genome mapping program for human complex disease. In 2016, he moved to the University of Queensland and holds joint appointments at the Institute for Molecular Bioscience (IMB) and the Queensland Brain Institute (QBI). He is a National Health and Medical Research Council Principal Research Fellow and was elected a Fellow the Society for Reproductive Biology in 2012, Fellow of the Australian Academy of Health and Medical Sciences in 2015, and Honorary Fellow of the Royal Society of New Zealand in 2016. His research focusses on discovery of critical genes and pathways increasing risk for common diseases especially reproductive diseases including endometriosis.

Research Impacts

Professor Montgomery has made substantial contributions to the worldwide effort to map genomic regions contributing to risk for complex traits and diseases, including endometriosis, age at menarche and menopause, cancers of the reproductive tract, melanoma and inflammatory bowel disease. He is conducting systems genetics and functional studies to identify the genes and pathways affected by these genetic risk factors. His work has identified possible target genes and functional consequences of genetic risk factors in genomic regions associated with endometriosis providing novel insights into the causes of this important disease. He is Patron of the Endometriosis Association (QLD) Inc (QENDO) and has worked closely with QENDO, other patient groups, clinicians and politicians to help develop the National Action Plan for Endometriosis. He is on the Executive Committee of the National Endometriosis Clinical and Scientific Trials (NECST) Network. He is also Director of the UQ Genome Innovation Hub developing novel methods and pipelines for genomics in health and agriculature that can be widely applied in programs across The University of Queensland.

Qualifications

  • PhD, Massey University

Publications

  • Mortlock, Sally, Kendarsari, Raden I., Fung, Jenny N., Gibson, Greg, Yang, Fei, Restuadi, Restuadi, Girling, Jane E., Holdsworth-Carson, Sarah J., Teh, Wan Tinn, Lukowski, Samuel W., Healey, Martin, Qi, Ting, Rogers, Peter A. W., Yang, Jian, McKinnon, Brett and Montgomery, Grant W. (2020). Tissue specific regulation of transcription in endometrium and association with disease. Human Reproduction, 35 (2), 377-393. doi: 10.1093/humrep/dez279

  • Xu, Jun, Falconer, Caitlin, Nguyen, Quan, Crawford, Joanna, McKinnon, Brett D., Mortlock, Sally, Senabouth, Anne, Andersen, Stacey, Chiu, Han Sheng, Jiang, Longda, Palpant, Nathan J., Yang, Jian, Mueller, Michael D., Hewitt, Alex W., Pébay, Alice, Montgomery, Grant W., Powell, Joseph E. and Coin, Lachlan J. M. (2019). Genotype-free demultiplexing of pooled single-cell RNA-seq. Genome Biology, 20 (1) 290, 290. doi: 10.1186/s13059-019-1852-7

  • Montgomery, Grant W., Mortlock, Sally and Giudice, Linda C. (2019). Should genetics now be considered the pre-eminent etiologic factor in endometriosis?. Journal of Minimally Invasive Gynecology, 27 (2), 280-286. doi: 10.1016/j.jmig.2019.10.020

  • Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N. and Martin, N. G. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4

  • Mortlock, Sally, Restuadi, Restuadi, Levien, Rupert, Girling, Jane E., Holdsworth-Carson, Sarah J., Healey, Martin, Zhu, Zhihong, Qi, Ting, Wu, Yang, Lukowski, Samuel W., Rogers, Peter A. W., Yang, Jian, McRae, Allan F., Fung, Jenny N. and Montgomery, Grant W. (2019). Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseases. Clinical Epigenetics, 11 (1) 49, 49. doi: 10.1186/s13148-019-0648-7

  • Gabbett, Michael T., Laporte, Johanna, Sekar, Renuka, Nandini, Adayapalam, McGrath, Pauline, Sapkota, Yadav, Jiang, Peiyong, Zhang, Haiqiang, Burgess, Trent, Montgomery, Grant W., Chiu, Rossa and Fisk, Nicholas M. (2019). Molecular support for heterogonesis resulting in sesquizygotic twinning. New England Journal of Medicine, 380 (9), 842-849. doi: 10.1056/nejmoa1701313

  • Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Liu, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, M. Arfan, Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart, Sturm, Richard A. and Hewitt, Alex W. (2019). Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10 (1) 299, 299. doi: 10.1038/s41467-018-08078-w

  • Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Lui, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, Arfan M., Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart, Sturm, Richard A. and Hewitt, Alex W. (2018). Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 9 (1) 4774, 4774. doi: 10.1038/s41467-018-06649-5

  • Gajbhiye, Rahul, Fung, Jenny N. and Montgomery, Grant W. (2018). Complex genetics of female fertility. npj Genomic Medicine, 3 (1) 29, 29. doi: 10.1038/s41525-018-0068-1

  • Fung, Jenny N., Mortlock, Sally, Girling, Jane E., Holdsworth-Carson, Sarah J., Teh, Wan Tinn, Zhu, Zhihong, Lukowski, Samuel W., McKinnon, Brett D., McRae, Allan, Yang, Jian, Healey, Martin, Powell, Joseph E., Rogers, Peter A. W. and Montgomery, Grant W (2018). Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome. Scientific Reports, 8 (1) 11424, 11424. doi: 10.1038/s41598-018-29462-y

  • Fung, Jenny N. and Montgomery, Grant W. (2018). Genetics of endometriosis: state of the art on genetic risk factors for endometriosis. Best Practice & Research: Clinical Obstetrics & Gynaecology, 50, 61-71. doi: 10.1016/j.bpobgyn.2018.01.012

  • Fung, Jenny N., Girling, Jane E., Lukowski, Samuel W., Sapkota, Yadav, Wallace, Leanne, Holdsworth-Carson, Sarah J., Henders, Anjali K., Healey, Martin, Rogers, Peter A. W., Powell, Joseph E. and Montgomery, Grant W. (2017). The genetic regulation of transcription in human endometrial tissue. Human Reproduction, 32 (4), 893-904. doi: 10.1093/humrep/dex006

  • Lloyd-Jones, Luke R., Holloway, Alexander, McRae, Allan, Yang, Jian, Small, Kerrin, Zeng, Biao, Bakshi, Andrew, Metspalu, Andres, Dermitzakis, Manolis, Gibson, Greg, Spector, Tim, Montgomery, Grant, Esko, Tonu, Visscher, Peter M. and Powell, Joseph E. (2017). The genetic architecture of gene expression in peripheral blood. American Journal of Human Genetics, 100 (2), 228-237. doi: 10.1016/j.ajhg.2016.12.008

  • Powell, Joseph E., Fung, Jenny N., Shakhbazov, Konstantin, Sapkota, Yadav, Cloonan, Nicole, Hemani, Gibran, Hillman, Kristine M., Kaufmann, Susanne, Luong, Hien T., Bowdler, Lisa, Painter, Jodie N., Holdsworth-Carson, Sarah J., Visscher, Peter M., Dinger, Marcel E., Healey, Martin, Nyholt, Dale R., French, Juliet D., Edwards, Stacey L., Rogers, Peter A. W. and Montgomery, Grant W. (2016). Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. Human Molecular Genetics, 25 (22), 5046-5058. doi: 10.1093/hmg/ddw320

  • Cheng, Timothy H. T., Thompson, Deborah J., O'Mara, Tracy A., Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Webb, Penelope M., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W., Nyholt, Dale R., Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Dennis, Joe, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander, Ekici, Arif B. and Hall, Per (2016). Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics, 48 (6), 667-674. doi: 10.1038/ng.3562

  • Mbarek, Hamdi, Steinberg, Stacy, Nyholt, Dale R., Gordon, Scott D., Miller, Michael B., McRae, Allan F, Hottenga, Jouke Jan, Day, Felix R., Willemsen, Gonneke, de Geus, Eco J., Davies, Gareth E, Martin, Hilary C, Penninx, Brenda W, Jansen, Rick, McAloney, Kerrie, Vink, Jacqueline M., Kaprio, Jaakko, Plomin, Robert, Spector, Tim D., Magnusson, Patrik K., Reversade, Bruno, Harris, R. Alan, Aagaard, Kjersti, Kristjansson, Ragnar P., Olafsson, Isleifur, Eyjolfsson, Gudmundur Ingi, Sigurdardottir, Olof, Iacono, William G., Lambalk, Cornelis B, Montgomery, Grant W. and McGue , Matt (2016). Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility. American Journal of Human Genetics, 98 (5), 898-908. doi: 10.1016/j.ajhg.2016.03.008

  • Zhu, Zhihong, Zhang, Futao, Hu, Han, Bakshi, Andrew, Robinson, Matthew R., Powell, Joseph E., Montgomery,Grant W., Goddard, Michael E., Wray, Naomi R., Visscher, Peter M. and Yang, Jian (2016). Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. Nature Genetics, 48 (5), 481-487. doi: 10.1038/ng.3538

  • Day, Felix R., Ruth, Katherine S., Thompson, Deborah J., Lunetta, Kathryn L., Pervjakova, Natalia, Chasman, Daniel I., Stolk, Lisette, Finucane, Hilary K., Sulem, Patrick, Bulik-Sullivan, Brendan, Esko, Tonu, Johnson, Andrew D., Elks, Cathy E., Franceschini, Nora, He, Chunyan, Altmaier, Elisabeth, Brody, Jennifer A., Franke, Lude L., Huffman, Jennifer E., Keller, Margaux F., McArdle, Patrick F., Nutile, Teresa, Porcu, Eleonora, Robino, Antonietta, Rose, Lynda M., Schick, Ursula M., Smith, Jennifer A., Teumer, Alexander, Traglia, Michela, Vuckovic, Dragana and Yao, Jie (2015). Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nature Genetics, 47 (11), 1294-1305. doi: 10.1038/ng.3412

  • Fung, Jenny N., Holdsworth-Carson, Sarah J., Sapkota, Yadav, Zhao, Zhen Zhen, Jones, Lincoln, Girling, Jane E., Paiva, Premila, Healey, Martin, Nyholt, Dale R., Rogers, Peter A. W. and Montgomery, Grant W. (2015). Functional evaluation of genetic variants associated with endometriosis near GREB1. Human Reproduction, 30 (5), 1263-1275. doi: 10.1093/humrep/dev051

  • Fung, Jenny N., Rogers, Peter A. W. and Montgomery, Grant W. (2015). Identifying the biological basis of GWAS hits for endometriosis. Biology of Reproduction, 92 (4) 87 doi: 10.1095/biolreprod.114.126458

  • Painter J.N., O'Mara T.A., Batra J., Cheng T., Lose F.A., Dennis J., Michailidou K., Tyrer J.P., Ahmed S., Ferguson K., Healey C.S., Kaufmann S., Hillman K.M., Walpole C., Moya L., Pollock P., Jones A., Howarth K., Martin L., Gorman M., Hodgson S., De Polanco M.M.E., Sans M., Carracedo A., Castellvi-Bel S., Rojas-Martinez A., Santos E., Teixeira M.R., Carvajal-Carmona L., Shu X.-O. and Long J. (2015). Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 (5), 1478-1492. doi: 10.1093/hmg/ddu552

  • Shah, Sonia, McRae, Allan F., Marioni, Riccardo E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Starr, John M., Wray, Naomi R., Deary, Ian J. and Visscher, Peter M. (2014). Genetic and environmental exposures constrain epigenetic drift over the human life course. Genome Research, 24 (11), 1725-1733. doi: 10.1101/gr.176933.114

  • Perry, John R. B., Day, Felix, Elks, Cathy E., Sulem, Patrick, Thompson, Deborah J., Ferreira, Teresa, He, Chunyan, Chasman, Daniel I., Esko, Toenu, Thorleifsson, Gudmar, Albrecht, Eva, Ang, Wei Q., Corre, Tanguy, Cousminer, Diana L., Feenstra, Bjarke, Franceschini, Nora, Ganna, Andrea, Johnson, Andrew D., Kjellqvist, Sanela, Lunetta, Kathryn L., McMahon, George, Nolte, Ilja M., Paternoster, Lavinia, Porcu, Eleonora, Smith, Albert V., Stolk, Lisette, Teumer, Alexander, Tsernikova, Natalia, Tikkanen, Emmi, Ulivi, Sheila and Wagner, Erin K. (2014). Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature, 514 (7520), 92-97. doi: 10.1038/nature13545

  • Rahmioglu, Nilufer, Nyholt, Dale R., Morris, Andrew P., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2014). Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Human Reproduction Update, 20 (5) dmu015, 702-716. doi: 10.1093/humupd/dmu015

  • McRae, Allan F., Powell, Joseph E., Henders, Anjali K., Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2014). Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biology, 15 (5), 1-10. doi: 10.1186/gb-2014-15-5-r73

  • Westra, Harm-Jan, Peters, Marjolein J., Esko, Tonu, Yaghootkar, Hanieh, Schurmann, Claudia, Kettunen, Johannes, Christiansen, Mark W., Fairfax, Benjamin P., Schramm, Katharina, Powell, Joseph E., Zhernakova, Alexandra, Zhernakova, Daria V., Veldink, Jan H., Van den Berg, Leonard H., Karjalainen, Juha, Withoff, Sebo, Uitterlinden, Andre G., Hofman, Albert, Rivadeneira, Fernando, Hoen, Peter A. C't, Reinmaa, Eva, Fischer, Krista, Nelis, Mari, Milani, Lili, Melzer, David, Ferrucci, Luigi, Singleton, Andrew B., Hernandez, Dena G., Nalls, Michael A., Homuth, Georg and Nauck, Matthias (2013). Systematic identification of trans eQTLs as putative drivers of known disease associations. Nature Genetics, 45 (10), 1238-U195. doi: 10.1038/ng.2756

  • Nyholt, Dale R., Low, Siew-Kee, Anderson, Carl A., Painter, Jodie N., Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Kenichi, Nakamura, Yusuke, Zondervan, Krina T., Zembutsu, Hitoshi and Montgomery, Grant W. (2012). Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics, 44 (12), 1355-1359. doi: 10.1038/ng.2445

  • Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Wright, Margaret J., Martin, Nicholas G., Dermitzakis, Emmanouil T., Montgomery, Grant W. and Visscher, Peter M. (2012). Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22 (3), 456-466. doi: 10.1101/gr.126540.111

  • Stolk L., Perry J.R.B., Chasman D.I., He C., Mangino M., Sulem P., Barbalic M., Broer L., Byrne E.M., Ernst F., Esko T., Franceschini N., Gudbjartsson D.F., Hottenga J.-J., Kraft P., McArdle P.F., Porcu E., Shin S.-Y., Smith A.V., Van Wingerden S., Zhai G., Zhuang W.V., Albrecht E., Alizadeh B.Z., Aspelund T., Bandinelli S., Lauc L.B., Beckmann J.S., Boban M., Boerwinkle E. and Broekmans F.J. (2012). Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, 44 (3), 260-268. doi: 10.1038/ng.1051

  • Painter, JN, Anderson, CA, Nyholt, DR, Macgregor, S, Lin, JH, Lee, SH, Lambert, A, Zhao, ZZ, Roseman, F, Guo, Q, Gordon, SD, Wallace, L, Henders, AK, Visscher, PM, Kraft, P, Martin, NG, Morris, AP, Treloar, SA, Kennedy, SH, Missmer, SA, Montgomery, GW and Zondervan, KT (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics, 43 (1), 51-54. doi: 10.1038/ng.731

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Grants

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Supervision

  • Doctor Philosophy

  • Doctor Philosophy

  • (2014) Doctor Philosophy

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Publications

Featured Publications

  • Mortlock, Sally, Kendarsari, Raden I., Fung, Jenny N., Gibson, Greg, Yang, Fei, Restuadi, Restuadi, Girling, Jane E., Holdsworth-Carson, Sarah J., Teh, Wan Tinn, Lukowski, Samuel W., Healey, Martin, Qi, Ting, Rogers, Peter A. W., Yang, Jian, McKinnon, Brett and Montgomery, Grant W. (2020). Tissue specific regulation of transcription in endometrium and association with disease. Human Reproduction, 35 (2), 377-393. doi: 10.1093/humrep/dez279

  • Xu, Jun, Falconer, Caitlin, Nguyen, Quan, Crawford, Joanna, McKinnon, Brett D., Mortlock, Sally, Senabouth, Anne, Andersen, Stacey, Chiu, Han Sheng, Jiang, Longda, Palpant, Nathan J., Yang, Jian, Mueller, Michael D., Hewitt, Alex W., Pébay, Alice, Montgomery, Grant W., Powell, Joseph E. and Coin, Lachlan J. M. (2019). Genotype-free demultiplexing of pooled single-cell RNA-seq. Genome Biology, 20 (1) 290, 290. doi: 10.1186/s13059-019-1852-7

  • Montgomery, Grant W., Mortlock, Sally and Giudice, Linda C. (2019). Should genetics now be considered the pre-eminent etiologic factor in endometriosis?. Journal of Minimally Invasive Gynecology, 27 (2), 280-286. doi: 10.1016/j.jmig.2019.10.020

  • Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N. and Martin, N. G. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4

  • Mortlock, Sally, Restuadi, Restuadi, Levien, Rupert, Girling, Jane E., Holdsworth-Carson, Sarah J., Healey, Martin, Zhu, Zhihong, Qi, Ting, Wu, Yang, Lukowski, Samuel W., Rogers, Peter A. W., Yang, Jian, McRae, Allan F., Fung, Jenny N. and Montgomery, Grant W. (2019). Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseases. Clinical Epigenetics, 11 (1) 49, 49. doi: 10.1186/s13148-019-0648-7

  • Gabbett, Michael T., Laporte, Johanna, Sekar, Renuka, Nandini, Adayapalam, McGrath, Pauline, Sapkota, Yadav, Jiang, Peiyong, Zhang, Haiqiang, Burgess, Trent, Montgomery, Grant W., Chiu, Rossa and Fisk, Nicholas M. (2019). Molecular support for heterogonesis resulting in sesquizygotic twinning. New England Journal of Medicine, 380 (9), 842-849. doi: 10.1056/nejmoa1701313

  • Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Liu, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, M. Arfan, Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart, Sturm, Richard A. and Hewitt, Alex W. (2019). Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10 (1) 299, 299. doi: 10.1038/s41467-018-08078-w

  • Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Lui, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, Arfan M., Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart, Sturm, Richard A. and Hewitt, Alex W. (2018). Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 9 (1) 4774, 4774. doi: 10.1038/s41467-018-06649-5

  • Gajbhiye, Rahul, Fung, Jenny N. and Montgomery, Grant W. (2018). Complex genetics of female fertility. npj Genomic Medicine, 3 (1) 29, 29. doi: 10.1038/s41525-018-0068-1

  • Fung, Jenny N., Mortlock, Sally, Girling, Jane E., Holdsworth-Carson, Sarah J., Teh, Wan Tinn, Zhu, Zhihong, Lukowski, Samuel W., McKinnon, Brett D., McRae, Allan, Yang, Jian, Healey, Martin, Powell, Joseph E., Rogers, Peter A. W. and Montgomery, Grant W (2018). Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome. Scientific Reports, 8 (1) 11424, 11424. doi: 10.1038/s41598-018-29462-y

  • Fung, Jenny N. and Montgomery, Grant W. (2018). Genetics of endometriosis: state of the art on genetic risk factors for endometriosis. Best Practice & Research: Clinical Obstetrics & Gynaecology, 50, 61-71. doi: 10.1016/j.bpobgyn.2018.01.012

  • Fung, Jenny N., Girling, Jane E., Lukowski, Samuel W., Sapkota, Yadav, Wallace, Leanne, Holdsworth-Carson, Sarah J., Henders, Anjali K., Healey, Martin, Rogers, Peter A. W., Powell, Joseph E. and Montgomery, Grant W. (2017). The genetic regulation of transcription in human endometrial tissue. Human Reproduction, 32 (4), 893-904. doi: 10.1093/humrep/dex006

  • Lloyd-Jones, Luke R., Holloway, Alexander, McRae, Allan, Yang, Jian, Small, Kerrin, Zeng, Biao, Bakshi, Andrew, Metspalu, Andres, Dermitzakis, Manolis, Gibson, Greg, Spector, Tim, Montgomery, Grant, Esko, Tonu, Visscher, Peter M. and Powell, Joseph E. (2017). The genetic architecture of gene expression in peripheral blood. American Journal of Human Genetics, 100 (2), 228-237. doi: 10.1016/j.ajhg.2016.12.008

  • Powell, Joseph E., Fung, Jenny N., Shakhbazov, Konstantin, Sapkota, Yadav, Cloonan, Nicole, Hemani, Gibran, Hillman, Kristine M., Kaufmann, Susanne, Luong, Hien T., Bowdler, Lisa, Painter, Jodie N., Holdsworth-Carson, Sarah J., Visscher, Peter M., Dinger, Marcel E., Healey, Martin, Nyholt, Dale R., French, Juliet D., Edwards, Stacey L., Rogers, Peter A. W. and Montgomery, Grant W. (2016). Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. Human Molecular Genetics, 25 (22), 5046-5058. doi: 10.1093/hmg/ddw320

  • Cheng, Timothy H. T., Thompson, Deborah J., O'Mara, Tracy A., Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Webb, Penelope M., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W., Nyholt, Dale R., Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Dennis, Joe, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander, Ekici, Arif B. and Hall, Per (2016). Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics, 48 (6), 667-674. doi: 10.1038/ng.3562

  • Mbarek, Hamdi, Steinberg, Stacy, Nyholt, Dale R., Gordon, Scott D., Miller, Michael B., McRae, Allan F, Hottenga, Jouke Jan, Day, Felix R., Willemsen, Gonneke, de Geus, Eco J., Davies, Gareth E, Martin, Hilary C, Penninx, Brenda W, Jansen, Rick, McAloney, Kerrie, Vink, Jacqueline M., Kaprio, Jaakko, Plomin, Robert, Spector, Tim D., Magnusson, Patrik K., Reversade, Bruno, Harris, R. Alan, Aagaard, Kjersti, Kristjansson, Ragnar P., Olafsson, Isleifur, Eyjolfsson, Gudmundur Ingi, Sigurdardottir, Olof, Iacono, William G., Lambalk, Cornelis B, Montgomery, Grant W. and McGue , Matt (2016). Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility. American Journal of Human Genetics, 98 (5), 898-908. doi: 10.1016/j.ajhg.2016.03.008

  • Zhu, Zhihong, Zhang, Futao, Hu, Han, Bakshi, Andrew, Robinson, Matthew R., Powell, Joseph E., Montgomery,Grant W., Goddard, Michael E., Wray, Naomi R., Visscher, Peter M. and Yang, Jian (2016). Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. Nature Genetics, 48 (5), 481-487. doi: 10.1038/ng.3538

  • Day, Felix R., Ruth, Katherine S., Thompson, Deborah J., Lunetta, Kathryn L., Pervjakova, Natalia, Chasman, Daniel I., Stolk, Lisette, Finucane, Hilary K., Sulem, Patrick, Bulik-Sullivan, Brendan, Esko, Tonu, Johnson, Andrew D., Elks, Cathy E., Franceschini, Nora, He, Chunyan, Altmaier, Elisabeth, Brody, Jennifer A., Franke, Lude L., Huffman, Jennifer E., Keller, Margaux F., McArdle, Patrick F., Nutile, Teresa, Porcu, Eleonora, Robino, Antonietta, Rose, Lynda M., Schick, Ursula M., Smith, Jennifer A., Teumer, Alexander, Traglia, Michela, Vuckovic, Dragana and Yao, Jie (2015). Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nature Genetics, 47 (11), 1294-1305. doi: 10.1038/ng.3412

  • Fung, Jenny N., Holdsworth-Carson, Sarah J., Sapkota, Yadav, Zhao, Zhen Zhen, Jones, Lincoln, Girling, Jane E., Paiva, Premila, Healey, Martin, Nyholt, Dale R., Rogers, Peter A. W. and Montgomery, Grant W. (2015). Functional evaluation of genetic variants associated with endometriosis near GREB1. Human Reproduction, 30 (5), 1263-1275. doi: 10.1093/humrep/dev051

  • Fung, Jenny N., Rogers, Peter A. W. and Montgomery, Grant W. (2015). Identifying the biological basis of GWAS hits for endometriosis. Biology of Reproduction, 92 (4) 87 doi: 10.1095/biolreprod.114.126458

  • Painter J.N., O'Mara T.A., Batra J., Cheng T., Lose F.A., Dennis J., Michailidou K., Tyrer J.P., Ahmed S., Ferguson K., Healey C.S., Kaufmann S., Hillman K.M., Walpole C., Moya L., Pollock P., Jones A., Howarth K., Martin L., Gorman M., Hodgson S., De Polanco M.M.E., Sans M., Carracedo A., Castellvi-Bel S., Rojas-Martinez A., Santos E., Teixeira M.R., Carvajal-Carmona L., Shu X.-O. and Long J. (2015). Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 (5), 1478-1492. doi: 10.1093/hmg/ddu552

  • Shah, Sonia, McRae, Allan F., Marioni, Riccardo E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Starr, John M., Wray, Naomi R., Deary, Ian J. and Visscher, Peter M. (2014). Genetic and environmental exposures constrain epigenetic drift over the human life course. Genome Research, 24 (11), 1725-1733. doi: 10.1101/gr.176933.114

  • Perry, John R. B., Day, Felix, Elks, Cathy E., Sulem, Patrick, Thompson, Deborah J., Ferreira, Teresa, He, Chunyan, Chasman, Daniel I., Esko, Toenu, Thorleifsson, Gudmar, Albrecht, Eva, Ang, Wei Q., Corre, Tanguy, Cousminer, Diana L., Feenstra, Bjarke, Franceschini, Nora, Ganna, Andrea, Johnson, Andrew D., Kjellqvist, Sanela, Lunetta, Kathryn L., McMahon, George, Nolte, Ilja M., Paternoster, Lavinia, Porcu, Eleonora, Smith, Albert V., Stolk, Lisette, Teumer, Alexander, Tsernikova, Natalia, Tikkanen, Emmi, Ulivi, Sheila and Wagner, Erin K. (2014). Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature, 514 (7520), 92-97. doi: 10.1038/nature13545

  • Rahmioglu, Nilufer, Nyholt, Dale R., Morris, Andrew P., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2014). Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Human Reproduction Update, 20 (5) dmu015, 702-716. doi: 10.1093/humupd/dmu015

  • McRae, Allan F., Powell, Joseph E., Henders, Anjali K., Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2014). Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biology, 15 (5), 1-10. doi: 10.1186/gb-2014-15-5-r73

  • Westra, Harm-Jan, Peters, Marjolein J., Esko, Tonu, Yaghootkar, Hanieh, Schurmann, Claudia, Kettunen, Johannes, Christiansen, Mark W., Fairfax, Benjamin P., Schramm, Katharina, Powell, Joseph E., Zhernakova, Alexandra, Zhernakova, Daria V., Veldink, Jan H., Van den Berg, Leonard H., Karjalainen, Juha, Withoff, Sebo, Uitterlinden, Andre G., Hofman, Albert, Rivadeneira, Fernando, Hoen, Peter A. C't, Reinmaa, Eva, Fischer, Krista, Nelis, Mari, Milani, Lili, Melzer, David, Ferrucci, Luigi, Singleton, Andrew B., Hernandez, Dena G., Nalls, Michael A., Homuth, Georg and Nauck, Matthias (2013). Systematic identification of trans eQTLs as putative drivers of known disease associations. Nature Genetics, 45 (10), 1238-U195. doi: 10.1038/ng.2756

  • Nyholt, Dale R., Low, Siew-Kee, Anderson, Carl A., Painter, Jodie N., Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Kenichi, Nakamura, Yusuke, Zondervan, Krina T., Zembutsu, Hitoshi and Montgomery, Grant W. (2012). Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics, 44 (12), 1355-1359. doi: 10.1038/ng.2445

  • Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Wright, Margaret J., Martin, Nicholas G., Dermitzakis, Emmanouil T., Montgomery, Grant W. and Visscher, Peter M. (2012). Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22 (3), 456-466. doi: 10.1101/gr.126540.111

  • Stolk L., Perry J.R.B., Chasman D.I., He C., Mangino M., Sulem P., Barbalic M., Broer L., Byrne E.M., Ernst F., Esko T., Franceschini N., Gudbjartsson D.F., Hottenga J.-J., Kraft P., McArdle P.F., Porcu E., Shin S.-Y., Smith A.V., Van Wingerden S., Zhai G., Zhuang W.V., Albrecht E., Alizadeh B.Z., Aspelund T., Bandinelli S., Lauc L.B., Beckmann J.S., Boban M., Boerwinkle E. and Broekmans F.J. (2012). Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, 44 (3), 260-268. doi: 10.1038/ng.1051

  • Painter, JN, Anderson, CA, Nyholt, DR, Macgregor, S, Lin, JH, Lee, SH, Lambert, A, Zhao, ZZ, Roseman, F, Guo, Q, Gordon, SD, Wallace, L, Henders, AK, Visscher, PM, Kraft, P, Martin, NG, Morris, AP, Treloar, SA, Kennedy, SH, Missmer, SA, Montgomery, GW and Zondervan, KT (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics, 43 (1), 51-54. doi: 10.1038/ng.731

Book Chapter

  • Giudice, Linda C., Burney, Richard O., Becker, Christian, Missmer, Stacey, Montgomery, Grant, Rahmioglu, Nilufer, Rogers, Peter A. W. and Zondervan, Krina (2018). Genetics and genomics of endometriosis. Human Reproductive and Prenatal Genetics. (pp. 399-426) Amsterdam, Netherlands: Elsevier. doi: 10.1016/B978-0-12-813570-9.00018-8

  • Lee, Sang Hong, Sapkota, Yadav, Fung, Jenny and Montgomery, Grant W. (2017). Genetic biomarkers for endometriosis. Biomarkers for Endometriosis: State of the Art. (pp. 83-93) Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-59856-7_5

  • Painter, Jodie N., Medland, Sarah J., Montgomery, Grant W. and Hall, Judith G. (2013). Twins and twinning. Emery and Rimoin's principles and practice of medical genetics. (pp. 1-20) London, United Kingdom: Elsevier. doi: 10.1016/B978-0-12-383834-6.00020-3

  • Painter, Jodie N., Zondervan, Krina T. and Montgomery, Grant W. (2012). Understanding the pathogenesis of endometriosis: gene mapping studies. Endometriosis: science and practice. (pp. 54-64) edited by Linda C. Giudice, Johannes L. H. Evers and David L. Healy. Chichester, West Sussex, United Kingdom: Blackwell Publishing. doi: 10.1002/9781444398519.ch6

  • Wray, Naomi R., Coventry, William L., James, Michael R., Montgomery, Grant W., Eaves, Lindon J. and Martin, Nicholas G. (2008). Use of Monozygotic Twins to Investigate the Relationship between 5HTTLPR Genotype, Depression and Stressful Life Events: An Application of Item Response Theory. Genetic Effects on Environmental Vulnerability to Disease. (pp. 48-59) wiley. doi: 10.1002/9780470696781.ch4

  • Wray, Naomi R., Coventry, William L., James, Michael R., Montgomery, Grant W., Eaves, Lindon J. and Martin, Nicholas G. (2008). Use of monozygotic twins to investigate the relationship between 5HTTLPR genotype, depression and stressful life events: an application of item response theory. Genetic effects on environmental vulnerability to disease. (pp. 48-67) Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9780470696781.ch4

Journal Article

  • Shen, Xueyi, Howard, David M., Adams, Mark J., Hill, W. David, Clarke, Toni-Kim, Adams, Mark J., Clarke, Toni-Kim, McIntosh, Andrew M., Deary, Ian J., Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Agerbo, Esben, Air, Tracy M., Andlauer, Till F. M., Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan T. F., Bigdeli, Tim B., Binder, Elisabeth B., Bryois, Julien, Buttenschøn, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Coleman, Jonathan R. I. and Colodro-Conde, Lucía (2020). A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank. Nature Communications, 11 (1) 2301 doi: 10.1038/s41467-020-16022-0

  • Montgomery, Grant W. (2020). The genetics of endometriosis. Twin Research and Human Genetics, 23 (2), 1-2. doi: 10.1017/thg.2020.36

  • Landi, Maria Teresa, GenoMEL Consortium, Bishop, D. Timothy, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Menin, Chiara, Martinez, Jacobo, Hadjisavvas, Andreas, Song, Lei, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Goldstein, Alisa M., Potrony, Miriam, Kypreou, Katerina P., Pastorino, Lorenza, Queirolo, Paola, Pellegrini, Cristina, Cattaneo, Laura, Zawistowski, Matthew, Gimenez-Xavier, Pol and Rodriguez, Arantxa (2020). Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5), 494-504. doi: 10.1038/s41588-020-0611-8

  • Montgomery, Grant W., Mortlock, Sally and Giudice, Linda C. (2020). Author's reply. Journal of Minimally Invasive Gynecology doi: 10.1016/j.jmig.2020.04.021

  • Amare, Azmeraw T., Schubert, Klaus Oliver, Hou, Liping, Clark, Scott R., Papiol, Sergi, Cearns, Micah, Heilbronner, Urs, Degenhardt, Franziska, Tekola-Ayele, Fasil, Hsu, Yi-Hsiang, Shekhtman, Tatyana, Adli, Mazda, Akula, Nirmala, Akiyama, Kazufumi, Ardau, Raffaella, Arias, Bárbara, Aubry, Jean-Michel, Backlund, Lena, Bhattacharjee, Abesh Kumar, Bellivier, Frank, Benabarre, Antonio, Bengesser, Susanne, Biernacka, Joanna M., Birner, Armin, Brichant-Petitjean, Clara, Cervantes, Pablo, Chen, Hsi-Chung, Chillotti, Caterina, Cichon, Sven, Cruceanu, Cristiana and Czerski, Piotr M. (2020). Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Molecular Psychiatry doi: 10.1038/s41380-020-0689-5

  • Vallerga, Costanza L., Zhang, Futao, Fowdar, Javed, McRae, Allan F., Qi, Ting, Nabais, Marta F., Zhang, Qian, Kassam, Irfahan, Henders, Anjali K., Wallace, Leanne, Montgomery, Grant, Chuang, Yu-Hsuan, Horvath, Steve, Ritz, Beate, Halliday, Glenda, Hickie, Ian, Kwok, John B., Pearson, John, Pitcher, Toni, Kennedy, Martin, Bentley, Steven R., Silburn, Peter A., Yang, Jian, Wray, Naomi R., Lewis, Simon J. G., Anderson, Tim, Dalrymple-Alford, John, Mellick, George D., Visscher, Peter M. and Gratten, Jacob (2020). Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson’s disease. Nature Communications, 11 (1) 1238, 1238. doi: 10.1038/s41467-020-15065-7

  • Li, Chen, Stoma, Svetlana, Lotta, Luca A., Warner, Sophie, Albrecht, Eva, Allione, Alessandra, Arp, Pascal P., Broer, Linda, Buxton, Jessica L., Da Silva Couto Alves, Alexessander, Deelen, Joris, Fedko, Iryna O., Gordon, Scott D., Jiang, Tao, Karlsson, Robert, Kerrison, Nicola, Loe, Taylor K., Mangino, Massimo, Milaneschi, Yuri, Miraglio, Benjamin, Pervjakova, Natalia, Russo, Alessia, Surakka, Ida, van der Spek, Ashley, Verhoeven, Josine E., Amin, Najaf, Beekman, Marian, Blakemore, Alexandra I., Canzian, Federico, Hamby, Stephen E. and Hottenga, Jouke-Jan (2020). Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere Length. American Journal of Human Genetics, 106 (3), 389-404. doi: 10.1016/j.ajhg.2020.02.006

  • Adewuyi, Emmanuel O., Sapkota, Yadav, Auta, Asa, Yoshihara, Kosuke, Nyegaard, Mette, Griffiths, Lyn R., Montgomery, Grant W., Chasman, Daniel I. and Nyholt, Dale R. (2020). Shared molecular genetic mechanisms underlie endometriosis and migraine comorbidity. Genes, 11 (3) 268, 268. doi: 10.3390/genes11030268

  • Mortlock, Sally, Kendarsari, Raden I., Fung, Jenny N., Gibson, Greg, Yang, Fei, Restuadi, Restuadi, Girling, Jane E., Holdsworth-Carson, Sarah J., Teh, Wan Tinn, Lukowski, Samuel W., Healey, Martin, Qi, Ting, Rogers, Peter A. W., Yang, Jian, McKinnon, Brett and Montgomery, Grant W. (2020). Tissue specific regulation of transcription in endometrium and association with disease. Human Reproduction, 35 (2), 377-393. doi: 10.1093/humrep/dez279

  • Craig, Jamie E., Han, Xikun, Qassim, Ayub, Hassall, Mark, Cooke Bailey, Jessica N., Kinzy, Tyler G., Khawaja, Anthony P., An, Jiyuan, Marshall, Henry, Gharahkhani, Puya, Igo, Robert P., Graham, Stuart L., Healey, Paul R., Ong, Jue-Sheng, Zhou, Tiger, Siggs, Owen, Law, Matthew H., Souzeau, Emmanuelle, Ridge, Bronwyn, Hysi, Pirro G., Burdon, Kathryn P., Mills, Richard A., Landers, John, Ruddle, Jonathan B., Agar, Ashish, Galanopoulos, Anna, White, Andrew J. R., Willoughby, Colin E., Andrew, Nicholas H., Best, Stephen and Vincent, Andrea L. (2020). Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Nature Genetics, 52 (2), 160-166. doi: 10.1038/s41588-019-0556-y

  • Dube, Umber, Ibanez, Laura, Budde, John P., Benitez, Bruno A., Davis, Albert A., Harari, Oscar, Iles, Mark M., Law, Matthew H., Brown, Kevin M., Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Bryc, Katarzyna, Elson, Sarah L., Fontanillas, Pierre, Furlotte, Nicholas A., Hinds, David A., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McCreight, Jennifer C., McIntyre, Matthew H., Mountain, Joanna L., Noblin, Elizabeth S., Northover, Carrie A. M., Pitts, Steven J., Sathirapongsasuti, J. Fah, Sazonova, Olga V., Shelton, Janie F. and Shringarpure, Suyash (2020). Correction to: Overlapping genetic architecture between Parkinson disease and melanoma (Acta Neuropathologica, (2020), 139, 2, (347-364), 10.1007/s00401-019-02110-z). Acta Neuropathologica, 139 (5), 963-963. doi: 10.1007/s00401-020-02143-9

  • Bryois, Julien, Skene, Nathan G., Hansen, Thomas Folkmann, Kogelman, Lisette J. A., Watson, Hunna J., Liu, Zijing, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Baker, Jessica, Bergen, Andrew, Berrettini, Wade, Birgegård, Andreas, Boden, Joseph, Boehm, Ilka, Boni, Claudette, Boraska Perica, Vesna, Brandt, Harry, Breen, Gerome, Bryois, Julien, Buehren, Katharina, Bulik, Cynthia, Burghardt, Roland, Cassina, Matteo, Cichon, Sven, Clementi, Maurizio, Coleman, Jonathan, Cone, Roger, Courtet, Philippe and Crawford, Steven (2020). Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease. Nature Genetics, 52 (5), 482-493. doi: 10.1038/s41588-020-0610-9

  • Holdsworth-Carson, Sarah J, Chung, Jessica, Sloggett, Clare, Mortlock, Sally, Fung, Jenny N., Montgomery, Grant W., Dior, Uri P., Healey, Martin, Rogers, Peter A.W. and Girling, Jane E. (2020). Obesity does not alter endometrial gene expression in women with endometriosis. Reproductive BioMedicine Online, 41 (1), 113-118. doi: 10.1016/j.rbmo.2020.03.015

  • Munn-Chernoff, Melissa A., Johnson, Emma C., Chou, Yi-Ling, Coleman, Jonathan R.I., Thornton, Laura M., Walters, Raymond K., Yilmaz, Zeynep, Baker, Jessica H., Hübel, Christopher, Gordon, Scott, Medland, Sarah E., Watson, Hunna J., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Adan, Roger A.H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Boraska Perica, Vesna, Buehren, Katharina and Burghardt, Roland (2020). Shared genetic risk between eating disorder- and substance-use-related phenotypes: evidence from genome-wide association studies. Addiction Biology e12880, e12880. doi: 10.1111/adb.12880

  • Tanaka, Keisuke, Mayne, Leah, Khalil, Akram, Baartz, David, Eriksson, Lars, Mortlock, Sally-Anne, Montgomery, Grant, McKinnon, Brett and Amoako, Akwasi A. (2020). The role of the endocannabinoid system in aetiopathogenesis of endometriosis: a potential therapeutic target. European Journal of Obstetrics and Gynecology and Reproductive Biology, 244, 87-94. doi: 10.1016/j.ejogrb.2019.11.012

  • Xu, Jun, Falconer, Caitlin, Nguyen, Quan, Crawford, Joanna, McKinnon, Brett D., Mortlock, Sally, Senabouth, Anne, Andersen, Stacey, Chiu, Han Sheng, Jiang, Longda, Palpant, Nathan J., Yang, Jian, Mueller, Michael D., Hewitt, Alex W., Pébay, Alice, Montgomery, Grant W., Powell, Joseph E. and Coin, Lachlan J. M. (2019). Genotype-free demultiplexing of pooled single-cell RNA-seq. Genome Biology, 20 (1) 290, 290. doi: 10.1186/s13059-019-1852-7

  • Lee, Phil H., Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A., Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M., Nivard, Michel G., Grotzinger, Andrew D., Posthuma, Danielle, Wang, Meg M.-J., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K., Anney, Richard J.L., Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Cook, Edwin H., Coppola, Giovanni, Derks, Eske M., Hoekstra, Pieter J., Kaprio, Jaakko, Keski-Rahkonen, Anna, Kirov, George, Kranzler, Henry R., Luykx, Jurjen J., Rohde, Luis A. and Zai, Clement C. (2019). Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders. Cell, 179 (7), 1469-1482.e11. doi: 10.1016/j.cell.2019.11.020

  • Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli, Bras, Jose, Young, Emily, von Coelln, Rainer, Simón-Sánchez, Javier, Schulte, Claudia, Sharma, Manu, Krohn, Lynne, Pihlstrøm, Lasse, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Faghri, Faraz, Gibbs, J Raphael, Hernandez, Dena G, Scholz, Sonja W, Botia, Juan A, Martinez, Maria, Corvol, Jean-Christophe, Lesage, Suzanne, Jankovic, Joseph and Shulman, Lisa M (2019). Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18 (12), 1091-1102. doi: 10.1016/S1474-4422(19)30320-5

  • Czamara, Darina, Eraslan, Gökçen, Page, Christian M., Lahti, Jari, Lahti-Pulkkinen, Marius, Hämäläinen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M., Reynolds, Rebecca M., Nystad, Wenche, Håberg, Siri E., London, Stephanie J., O’Donnell, Kieran J., Garg, Elika, Meaney, Michael J., Entringer, Sonja, Wadhwa, Pathik D., Buss, Claudia, Jones, Meaghan J., Lin, David T. S., MacIsaac, Julie L., Kobor, Michael S., Koen, Nastassja, Zar, Heather J., Koenen, Karestan C., Dalvie, Shareefa, Stein, Dan J., Kondofersky, Ivan, Müller, Nikola S. and Theis, Fabian J. (2019). Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications, 10 (1) 2548 doi: 10.1038/s41467-019-10461-0

  • Andlauer, Till F. M., Guzman-Parra, Jose, Streit, Fabian, Strohmaier, Jana, González, Maria José, Gil Flores, Susana, Cabaleiro Fabeiro, Francisco J., del Río Noriega, Francisco, Perez, Fermin Perez, Haro González, Jesus, Orozco Diaz, Guillermo, de Diego-Otero, Yolanda, Moreno-Küstner, Berta, Auburger, Georg, Degenhardt, Franziska, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoffmann, Per, Frank, Josef, Foo, Jerome C., Treutlein, Jens, Witt, Stephanie H., Cichon, Sven, Kogevinas, Manolis, Stahl, Eli A, Breen, Gerome, Forstner, Andreas J, McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily and Mattheisen, Manuel (2019). Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Molecular Psychiatry doi: 10.1038/s41380-019-0558-2

  • Montgomery, Grant W., Mortlock, Sally and Giudice, Linda C. (2019). Should genetics now be considered the pre-eminent etiologic factor in endometriosis?. Journal of Minimally Invasive Gynecology, 27 (2), 280-286. doi: 10.1016/j.jmig.2019.10.020

  • Coleman, Jonathan R.I., Gaspar, Héléna A., Bryois, Julien, Byrne, Enda M., Forstner, Andreas J., Holmans, Peter A., de Leeuw, Christiaan A., Mattheisen, Manuel, McQuillin, Andrew, Whitehead Pavlides, Jennifer M., Pers, Tune H., Ripke, Stephan, Stahl, Eli A., Steinberg, Stacy, Trubetskoy, Vassily, Trzaskowski, Maciej, Wang, Yunpeng, Abbott, Liam, Abdellaoui, Abdel, Adams, Mark J., Adolfsson, Annelie Nordin, Agerbo, Esben, Akil, Huda, Albani, Diego, Alliey-Rodriguez, Ney, Als, Thomas D., Andlauer, Till F.M., Anjorin, Adebayo, Antilla, Verneri, Van der Auwera, Sandra and Awasthi, Swapnil (2019). The genetics of the mood disorder spectrum: Genome-wide association analyses of more than 185,000 cases and 439,000 controls. Biological Psychiatry doi: 10.1016/j.biopsych.2019.10.015

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  • Luciano, Michelle, Huffman, Jennifer E., Arias-Vasquez, Alejandro, Vinkhuyzen, Anna A. E., Middeldorp, Christel M., Giegling, Ina, Payton, Antony, Davies, Gail, Zgaga, Lina, Janzing, Joost, Ke, Xiayi, Galesloot, Tessel, Hartmann, Annette M., Ollier, William, Tenesa, Albert, Hayward, Caroline, Verhagen, Maaike, Montgomery, Grant W., Hottenga, Jouke-Jan, Konte, Bettina, Starr, John M., Vitart, Veronique, Vos, Pieter E., Madden, Pamela A. F., Willemsen, Gonneke, Konnerth, Heike, Horan, Michael A., Porteous, David J., Campbell, Harry, Vermeulen, Sita H. and Heath, Andrew C. (2012). Genome-wide association uncovers shared genetic effects among personality traits and mood states. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B (6), 684-695. doi: 10.1002/ajmg.b.32072

  • Rahmioglu, Nilufer, Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2012). Insights into assessing the genetics of endometriosis. Current Obstetrics and Gynecology Reports, 1 (3), 124-137. doi: 10.1007/s13669-012-0016-5

  • Whitehall, Vicki L. J., Rickman, Celestine, Bond, Catherine E., Ramsnes, Ingunn, Greco, Sonia A., Umapathy, Aarti, McKeone, Diane, Faleiro, Rebecca J., Buttenshaw, Ron L., Worthley, Daniel L., Nayler, Sam, Zhao, Zhen Zhen, Montgomery, Grant W., Mallitt, Kylie-Ann, Jass, Jeremy R., Matsubara, Nagahide, Notohara, Kenji, Ishii, Tatsuhiro and Leggett, Barbara A. (2012). Oncogenic PIK3CA mutations in colorectal cancers and polyps. International Journal of Cancer, 131 (4), 813-820. doi: 10.1002/ijc.26440

  • Hartz, Sarah M., Short, Susan E., Saccone, Nancy L., Culverhouse, Robert, Chen, LiShiun, Schwantes-An, Tae-Hwi, Coon, Hilary, Han, Younghun, Stephens, Sarah H., Sun, Juzhong, Chen, Xiangning, Ducci, Francesca, Dueker, Nicole, Franceschini, Nora, Frank, Josef, Geller, Frank, Guobjartsson, Daniel, Hansel, Nadia N., Jiang, Chenhui, Keskitalo-Vuokko, Kaisu, Liu, Zhen, Lyytikainen, Leo-Pekka, Michel, Martha, Rawal, Rajesh, Hum, Sc, Rosenberger, Albert, Scheet, Paul, Shaffer, John R., Teumer, Alexander, Thompson, John R. and Vink, Jacqueline M. (2012). Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry, 69 (8), 854-861. doi: 10.1001/archgenpsychiatry.2012.124

  • Verweij, Karin J. H., Vinkhuyzen, Anna A. E., Benyamin, Beben, Lynskey, Michael T., Quaye, Lydia, Agrawal, Arpana, Gordon, Scott D., Montgomery, Grant W., Madden, Pamela A. F., Heath, Andrew C., Spector, Andrew C., Martin, Nicholas G. and Medland, Sarah E. (2012). The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. Addiction Biology, 18 (5), 846-850. doi: 10.1111/j.1369-1600.2012.00478.x

  • Yuen, Hiu-Fung, Abramczykd, Olga, Montgomery, Grant, Chan, Ka-Kui, Huang, Yu-Han, Sasazuki, Takehiko, Shirasawa, Senji, Gopesh, Srivastava, Chan, Kwok-Wah, Fennell, Dean, Janne, Pasi, El-Tanani, Mohamed and Murray, James T. (2012). Impact of oncogenic driver mutations on feedback between the PI3K and MEK pathways in cancer cells. Bioscience Reports, 32 (4), 413-422. doi: 10.1042/BSR20120050

  • Byrne, Enda M., Johnson, Julie, McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Gehrman, Philip R., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Chenevix-Trench, Georgia and Martin, Nicholas G. (2012). A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Sleep, 35 (7), 967-975. doi: 10.5665/sleep.1962

  • Agrawal, Arpana, Nelson, Elliot C., Littlefield, Andrew K., Bucholz, Kathleen K., Degenhardt, Louisa, Henders, Anjali K., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Pergadia, Michele L., Sher, Kenneth J., Heath, Andrew C. and Lynskey, Michael T. (2012). Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression. Archives of General Psychiatry, 69 (7), 732-740. doi: 10.1001/archgenpsychiatry.2011.2273

  • McQuillan, Ruth, Eklund, Niina, Pirastu, Nicola, Kuningas, Maris, McEvoy, Brian P., Esko, Tonu, Corre, Tanguy, Davies, Gail, Kaakinen, Marika, Lyytikainen, Leo-Pekka, Kristiansson, Kati, Havulinna, Aki S., Gogele, Martin, Vitart, Veronique, Tenesa, Albert, Aulchenko, Yurii, Hayward, Caroline, Johansson, Asa, Boban, Mladen, Ulivi, Sheila, Robino, Antonietta, Boraska, Vesna, Igl, Wilmar, Wild, Sarah H., Zgaga, Lina, Amin, Najaf, Theodoratou, Evropi, Polasek, Ozren, Girotto, Giorgia, Lopez, Lorna M. and Sala, Cinzia (2012). Evidence of inbreeding depression on human height. Plos Genetics, 8 (7) e1002655, e1002655. doi: 10.1371/journal.pgen.1002655

  • Bloom, A. Joseph, Harari, Oscar, Martinez, Maribel, Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Rice, John P., Murphy, Sharon E., Bierut, Laura J. and Goate, Alison (2012). Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6. Human Molecular Genetics, 21 (13) dds114, 3050-3062. doi: 10.1093/hmg/dds114

  • Chiang, Ming-Chang, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Johnson, Kori, Montgomery, Grant W., Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J., Shapshak, Paul and Thompson, Paul M. (2012). Gene network effects on brain microstructure and intellectual performance identified in 472 twins. Journal of Neuroscience, 32 (25), 8732-8745. doi: 10.1523/JNEUROSCI.5993-11.2012

  • Hibar, Derrek P., Jahanshad, Neda, Stein, Jason L., Kohannim, Omid, Toga, Arthur W., Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins. Twin Research and Human Genetics, 15 (3), 286-295. doi: 10.1017/thg.2012.15

  • Verbrugghe, Phebe, Bouwer, Sonja, Wiltshire, Steven, Carter, Kim, Chandler, David, Cooper, Matthew, Morar, Bharti, Razif, Muhammad F. M., Henders, Anjali, Badcock, Johanna C., Dragovic, Milan, Carr, Vaughan, Almeida, Osvaldo P., Flicker, Leon, Montgomery, Grant, Jablensky, Assen and Kalaydjieva, Luba (2012). Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 159 B (4), 392-404. doi: 10.1002/ajmg.b.32042

  • Li, Rui, Brockschmidt, Felix F., Kiefer, Amy K., Stefansson, Hreinn, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Glass, Daniel, Medland, Sarah E., Dimitriou, Maria, Waterworth, Dawn, Tung, Joyce Y., Geller, Frank, Heilmann, Stefanie, Hillmer, Axel M., Bataille, Veronique, Eigelshoven, Sibylle, Hanneken, Sandra, Moebus, Susanne, Herold, Christine, den Heijer, Martin, Montgomery, Grant W., Deloukas, Panos, Eriksson, Nicholas, Heath, Andrew C., Becker, Tim, Sulem, Patrick, Mangino, Massimo, Vollenweider, Peter and Spector, Tim D. (2012). Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genetics, 8 (5) e1002746, 222-224. doi: 10.1371/journal.pgen.1002746

  • Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012). Translational Psychiatry, 2 (5) e125, e125-e125. doi: 10.1038/tp.2012.49

  • Service, S. K., Verweij, K. J. H., Lahti, J., Congdon, E., Ekelund, J., Hintsanen, M., Raikkonen, K., Lehtimaki, T., Kahonen, M., Widen, E., Taanila, A., Veijola, J., Heath, A. C., Madden, P. A. F., Montgomery, G. W., Sabatti, C., Jarvelin, M-R, Palotie, A., Raitakari, O., Viikari, J., Martin, N. G., Eriksson, J. G., Keltikangas-Jarvinen, L., Wray, N. R. and Freimer, N. B. (2012). A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales. Translational Psychiatry, 2 (5) e116, e116-e116. doi:10.1038/tp.2012.37

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  • Stein, Jason L., Medland, Sarah E., Vasquez, Alejandro Arias, Hibar, Derrek P., Senstad, Rudy E., Winkler, Anderson M., Toro, Roberto, Appel, Katja, Bartecek, Richard, Bergmann, Ørjan, Bernard, Manon, Brown, Andrew A., Cannon, Dara M., Chakravarty, M. Mallar, Christoforou, Andrea, Domin, Martin, Grimm, Oliver, Hollinshead, Marisa, Holmes, Avram J., Homuth, Georg, Hottenga, Jouke-Jan, Langan, Camilla, Lopez, Lorna M., Hansell, Narelle K., Hwang, Kristy S., Kim, Sungeun, Laje, Gonzalo, Lee, Phil H., Liu, Xinmin, Loth, Eva and Lourdusamy, Anbarasu (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, 44 (5), 552-561. doi: 10.1038/ng.2250

  • Verweij, Karin J. H., Zietsch, Brendan P., Liu, Jimmy Z., Medland, Sarah E., Lynskey, Michael T., Madden, Pamela A. F., Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C. and Martin, Nicholas G. (2012). No association of candidate genes with cannabis use in a large sample of Australian twin families. Addiction Biology, 17 (3), 687-690. doi: 10.1111/j.1369-1600.2011.00320.x

  • Hollis-Moffatt, Jade E., Phipps-Green, Amanda J., Chapman, Brett, Jones, Gregory T., van Rij, Andre, Gow, Peter J., Harrison, Andrew A., Highton, John, Jones, Peter B., Montgomery, Grant W., Stamp, Lisa K., Dalbeth, Nicola and Merriman, Tony R. (2012). The renal urate transporter SLC17A1 locus: confirmation of association with gout. Arthritis Research and Therapy, 14 (2) R92 doi: 10.1186/ar3816

  • Middelberg, Rita P. S., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein. PLoS ONE, 7 (4) e35605, e35605. doi: 10.1371/journal.pone.0035605

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  • Jahanshad, Neda, Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Whitfield, John B., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2012). Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene. Proceedings of the National Academy of Sciences of USA, 109 (14), E851-E859. doi: 10.1073/pnas.1105543109

  • Dennis, Emily L., Jahanshad, Neda, Rudie, Jeffrey D., Brown, Jesse A., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant, Martin, Nicholas G., Wright, Margaret J., Bookheimer, Susan Y., Dapretto, Mirella, Toga, Arthur W. and Thompson, Paul M. (2012). Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2. Brain Connectivity, 1 (6), 447-460. doi: 10.1089/brain.2011.0064

  • Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2 (e102) 201227, e102-e102. doi: 10.1038/tp.2012.27

  • Yang, Jian, Ferreira, Teresa, Morris, Andrew P., Medland, Sarah E., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Weedon, Michael N., Loos, Ruth J., Frayling, Timothy M., McCarthy, Mark I., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M., Genetic Invest ANthropometric Trai and DIAbet Genetics Replication Meta-A (2012). Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics, 44 (4), 369-375. doi: 10.1038/ng.2213

  • Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Caracella, Anthony, Smith, Sara, Wright, Margaret J., Whitfield, John B., Dermitzakis, Emmanouil T., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2012). The Brisbane systems genetics study: genetical genomics meets complex trait genetics. PLoS One, 7 (4) e35430, e35430.1-e35430.9. doi: 10.1371/journal.pone.0035430

  • Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Wright, Margaret J., Martin, Nicholas G., Dermitzakis, Emmanouil T., Montgomery, Grant W. and Visscher, Peter M. (2012). Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22 (3), 456-466. doi: 10.1101/gr.126540.111

  • Tomlinson, Ian P. M., Houlston, Richard S., Montgomery, Grant W., Sieber, Oliver M. and Dunlop, Malcolm G. (2012). Investigation of the effects of DNA repair gene polymorphisms on the risk of colorectal cancer. Mutagenesis, 27 (2), 219-223. doi: 10.1093/mutage/ger070

  • Spain, Sarah L., Carvajal-Carmona, Luis G., Howarth, Kimberley M., Jones, Angela M., Su, Zhan, Cazier, Jean-Baptiste, Williams, Jennet, Aaltonen, Lauri A., Pharoah, Paul, Kerr, David J., Cheadle, Jeremy, Li, Li, Casey, Graham, Vodicka, Pavel, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Morreau, Hans, van Wezel, Tom, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, Dunlop, Malcolm, Houlston, Richard S. and Tomlinson, Ian P. M. (2012). Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. Human Molecular Genetics, 21 (4) ddr523, 934-946. doi: 10.1093/hmg/ddr523

  • O'Callaghan, Michael E., MacLennan, Alastair H., Gibson, Catherine S., McMichael, Gai L., Haan, Eric A., Broadbent, Jessica L., Goldwater, Paul N., Painter, Jodie N., Montgomery, Grant W. and Dekker, Gus A. (2012). Fetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study. Pediatrics, 129 (2), E414-E423. doi: 10.1542/peds.2011-0739

  • Law, Matthew H., Montgomery, Grant W., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Hayward, Nicholas K., MacGregor, Stuart and Q-MEGA and AMFS Investigators (2012). Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. Journal of Investigative Dermatology, 132 (2), 485-487. doi: 10.1038/jid.2011.322

  • Paternoster, Lavinia, Standl, Marie, Chen, Chi-Mei, Ramasamy, Adaikalavan, Bonnelykke, Klaus, Duijts, Liesbeth, Ferreira, Manuel A., Alves, Alexessander C., Thyssen, Jacob P., Albrecht, Eva, Baurecht, Hansjorg, Feenstra, Bjarke, Sleiman, Patrick M. A., Hysi, Piro, Warrington, Nicole M., Curjuric, Ivan, Myhre, Ronny, Curtin, John A., Groen-Blokhuis, Maria M., Kerkhof, Marjan, Saaf, Annika, Franke, Andre, Ellinghaus, David, Folster-Holst, Regina, Dermitzakis, Emmanouil, Montgomery, Stephen B., Prokisch, Holger, Heim, Katharina, Hartikainen, Anna-Lisa, Pouta, Anneli and Pekkanen, Juha (2012). Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nature Genetics, 44 (2), 187-192. doi: 10.1038/ng.1017

  • Knaapila, Antti, Zhu, Gu, Medland, Sarah E., Wysocki, Charles J., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Reed, Danielle R. (2012). A genome-wide study on the perception of the odorants androstenone and galaxolide. Chemical Senses, 37 (6), 541-552. doi: 10.1093/chemse/bjs008

  • Rao, Fangwen, Chiron, Stephane, Wei, Zhiyun, Fung, Maple M., Chen, Yuqing, Wen, Gen, Khandrika, Srikrishna, Ziegler, Michael G., Benyamin, Beben, Montgomery, Grant, Whitfield, John B., Martin, Nicholas G., Waalen, Jill, Hamiltoni, Bruce A., Mahata, Sushil K. and O'Connor, Daniel T. (2012). Genetic variation within a metabolic motif in the chromogranin A promoter: Pleiotropic influence on cardiometabolic risk traits in twins. American Journal of Hypertension, 25 (1), 29-40. doi: 10.1038/ajh.2011.163

  • Wray, N. R., Pergadia, M. L., Blackwood, D. H. R., Penninx, B. W. J. H., Gordon, S. D., Nyholt, D. R., Ripke, S., MacIntyre, D. J., McGhee, K. A., MacLean, A. W., Smit, J. H., Hottenga, J. J., Willemsen, G., Middeldorp, C. M., De Geus, E. J. C., Lewis, C. M., McGuffin, P., Hickie, I. B., Van Den Oord, E. J. C. G., Liu, J. Z., MacGregor, S., McEvoy, B. P., Byrne, E. M., Medland, S. E., Statham, D. J., Henders, A. K., Heath, A. C., Montgomery, G. W., Martin, N. G., Boomsma, D. I. and Madden, P. A. F. (2012). Genome-wide association study of major depressive disorder: New results, meta-analysis, and lessons learned. Molecular Psychiatry, 17 (1), 36-48. doi: 10.1038/mp.2010.109

  • Middelberg, Rita P., Benyamin, Beben, de Moor, Marleen H. M., Warrington, Nicole M., Gordon, Scott, Henders, Anjali K., Medland, Sarah E., Nyholt, Dale R., de Geus, Eco J. C., Hottenga, Jouke J., Willemsen, Gonneke, Beilin, Lawrence J., Mori, Trevor A., Wright, Margaret J., Heath, Andrew C., Madden, Pamela A. F., Boomsma, Dorret I., Pennell, Craig E., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Loci affecting gamma-glutamyl transferase in adults and adolescents show age x SNP interaction and cardiometabolic disease associations. Human Molecular Genetics, 21 (2) ddr478, 446-455. doi: 10.1093/hmg/ddr478

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  • Kvaskoff, Marina, Whiteman, David C., Zhao, Zhen Z., Montgomery, Grant W., Martin, Nicholas G., Hayward, Nicholas K. and Duffy, David L. (2011). Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma. Twin Research and Human Genetics, 14 (5), 422-432. doi: 10.1375/twin.14.5.422

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  • Larsson, Mats, Duffy, David L., Zhu, Gu, Liu, Jimmy Z., Macgregor, Stuart, McRae, Allan F., Wright, Margaret J., Sturm, Richard A., Mackey, David A., Montgomery, Grant W., Martin, Nicholas G. and Medland, Sarah E. (2011). GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern development. American Journal of Human Genetics, 89 (2), 334-343. doi: 10.1016/j.ajhg.2011.07.011

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  • Martin, Nicolas W., Medland, Sarah E., Verweij, Karin J. H., Lee, S. Hong, Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Educational Attainment: A Genome Wide Association Study in 9538 Australians. PLoS One, 6 (6) e20128, e20128.1-e20128.8. doi: 10.1371/journal.pone.0020128

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  • Luciano, Michelle, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample. Twin Research and Human Genetics, 14 (3), 228-232. doi: 10.1375/twin.14.3.228

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  • Spurdle, Amanda B., Thompson, Deborah J., Ahmed, Shahana, Ferguson, Kaltin, Healey, Catherine S., O'Mara, Tracy, Walker, Logan C., Montgomery, Stephen B., Dermitzakis, Emmanouil T., The Australian National Endometrial Cancer Study Group, Fahey, Paul, Montgomery, Grant W., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Lambrechts, Diether, Coenegrachts, Lieve, Vergote, Ignace, Amant, Frederic, Salvesen, Helga B., Trovik, Jone, Njolstad, Tormund S., Helland, Harald, Scott, Rodney J., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, National Study of Endometrial Cancer Genetics Group and Tomlinson, Ian (2011). Genome-wide association study identifies a common variant associated with risk of endometrial cancer. Nature Genetics, 43 (5), 451-454. doi: 10.1038/ng.812

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  • Brennan, Patricia A., Hammen, Constance, Sylvers, Patrick, Bor, William, Najman, Jake, Lind, Penelope, Montgomery, Grant and Smith, Alicia K. (2011). Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes. Biological Psychology, 87 (1), 99-105. doi: 10.1016/j.biopsycho.2011.02.013

  • Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Aexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon, Hamshere, Marian and O'Donovan, Michael C. (2011). Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics, 88 (3), 372-381. doi: 10.1016/j.ajhg.2011.01.017

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  • Lind, Penelope A., Macgregor, Stuart, Vink, Jacqueline M., Pergadia, Michele L., Hansell, Narelle K., de Moor, Marleen H. M., Smit, August B., Hottenga, Jouke-Jan, Richter, Melinda M., Heath, Andrew C., Martin, Nicholas G., Willemsen, Gonneke, de Geus, Eco J. C., Vogelzangs,Nicole, Penninx, Brenda W., Whitfield, John B., Montgomery, Grant W., Boomsma, Dorret I. and Madden, Pamela A. F. (2010). A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Research And Human Genetics, 13 (1), 10-29. doi: 10.1375/twin.13.1.10

  • Hoekstra, Chantal, Willemsen, Gonneke, van Beijsterveldt, Toos, Lambalk, Cornelius B., Montgomery, Grant W. and Boomsma, Dorret I. (2010). Body composition, smoking, and spontaneous dizygotic twinning. Fertility and Sterility, 93 (3), 885-893. doi: 10.1016/j.fertnstert.2008.10.012

  • Duffy, David L., Zhao, Zhen Z., Sturm, Richard A., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2010). Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma. Journal of Investigative Dermatology, 130 (2), 520-528. doi: 10.1038/jid.2009.258

  • Ferreira, Mar, Mangino, M, Brumme, CJ, Zhao, ZZ, Medland, SE, Wright, MJ, Nyholt, DR, Gordon, S, Campbell, M, McEvoy, BP, Henders, A, Evans, DM, Lanchbury, JS, Pereyra, F, Walker, BD, Haas, DW, Soranzo, N, Spector, TD, de Bakker, PIW, Frazer, IH, Montgomery, GW, Martin, NG and Int HIV Controllers Study (2010). Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. American Journal of Human Genetics, 86 (1) 88-92. doi:10.1016/j.ajhg.2009.12.008

  • Nelson, Elliot C., Agrawal, Arpana, Pergadia, Michele L., Wang, Jen C., Whitfield, John B., Saccone, F. Scott, Kern, Jason, Grant, Julia D., Schrage, Andrew J., Rice, John P., Montgomery, Grant W., Heath, Andrew C, Goate, Alison M., Martin, Nicholas G. and Madden, Pamela A. F. (2010). H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence. Addiction Biology, 15 (1), 1-11. doi: 10.1111/j.1369-1600.2009.00181.x

  • Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Gordon, Scott D., Lind, Penelope A., Pergadia, Michele L., Montgomery, Grant W., Madden, Pamela A. F., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2010). Linkage analysis of alcohol dependence symptoms in the community. Alcoholism: Clinical and Experimental Research, 34 (1), 158-163. doi: 10.1111/j.1530-0277.2009.01077.x

  • Prodoehl, Mark J., Hatzirodos, Nicholas, Irving-Rodgers, Helen F., Zhao, Zhen Z., Painter, Jodie N., Hickey, Theresa E., Gibson, Mark A., Rainey, William E., Carr, Bruce R., Mason, Helen D., Norman, Robert J., Montgomery, Grant W. and Rodgers, Raymond J. (2009). Genetic and gene expression analyses of the polycystic ovary syndrome candidate gene fibrillin-3 and other fibrillin family members in human ovaries. Molecular Human Reproduction, 15 (12) gap072, 829-841. doi: 10.1093/molehr/gap072

  • Medland, S, Nyholt, D, Painter, JN, McEnvoy, BP, Allan McRae, Zhu, G, Gordon, SD, Ferreira, MAR, Wright, MJ, Henders, AK, Campbell MJ, Duffy, D, Hansell, N K, Macgregor, S, Slutske, WS, Heath, AC, Montgomery, GW and Martin, NG (2009). Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics, 85 (5), 750-755. doi: 10.1016/j.ajhg.2009.10.009

  • William L. Coventry, Michael R. James, Lindon J. Eaves, Scott D. Gordon, Nathan A. Gillespie, Leanne Ryan, Andrew C. Heath, Grant W. Montgomery, Nicholas G. Martin and Naomi R. Wray (2009). Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 153b (3), 757-765. doi: 10.1002/ajmg.b.31044

  • Benyamin, B, Ferreira, MAR, Willemsen, G, Gordon, S, Middelberg, RPS, McEvoy, BP, Hottenga, JJ, Henders, AK, Campbell, MJ, Wallace, L, Frazer, IH, Heath, AC, de Geus, EJC, Nyholt, DR, Visscher, PM, Penninx, BW, Boomsma, DI, Martin, NG, Montgomery, GW and Whitfield, JB (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics, 41 (11), 1173-1175. doi: 10.1038/ng.456

  • Visscher, Peter M. and Montgomery, Grant W. (2009). Genome-wide Association Studies and Human Disease From Trickle to Flood. Jama-Journal of the American Medical Association, 302 (18), 2028-2029. doi: 10.1001/jama.2009.1643

  • Ferreira, MAR, Hottenga, JJ, Warrington, NM, Medland, SE, Willemsen, G, Lawrence, RW, Gordon, S, de Geus, EJC, Henders, AK, Smit, JH, Campbell, MJ, Wallace, L, Evans, DM, Wright, MJ, Nyholt, DR, James, AL, Beilby, JP, Penninx, BW, Palmer, LJ, Frazer, IH, Montgomery, GW, Martin, NG and Boomsma, DI (2009). Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (5), 745-749. doi: 10.1016/j.ajhg.2009.10.005

  • Ferreira, M. A. R., Zhao, Z. Z., Thomsen, S. F., James, M., Evans, D. M., Postmus, P. E., Kyvik, K. O., Backer, V., Boomsma, D. I., Martin, N. G., Montgomery, G. W. and Duffy, D. L. (2009). Association and interaction analyses of eight genes under asthma linkage peaks. Allergy, 64 (11), 1623-1628. doi: 10.1111/j.1398-9995.2009.02091.x

  • Sun, Cong, Zhu, Gu, Wong, Tien Y, Hewitt, Alex W, Ruddle, Jonathan B, Hodgson, Lauren, Montgomery, Grant W, Young, Terri L, Hammond, Christopher J, Craig, Jamie E, Martin, Nicholas G, He, Mingguang and Mackey, David A. (2009). Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study. Hypertension, 54 (4), 788-795. doi: 10.1161/HYPERTENSIONAHA.109.132902

  • Jamie E. Craig, Alex W. Hewitt, Amy E. McMellon, Anjali K. Henders, Lingjun Ma, Leanne Wallace, Shiwani Sharma, Kathryn P. Burdon, Peter M. Visscher, Grant W. Montgomery and Stuart MacGregor (2009). Rapid inexpensive genome-wide association using pooled whole blood. Genome Research, 19 (11), 2075-2080. doi: 10.1101/gr.094680.109

  • E. M. Byrne, A. F. McRae, D. L. Duffy, Z. Z. Zhao, N. G. Martin, J. B. Whitfield, P. M. Visscher and G. W. Montgomery (2009). Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia, 52 (11), 2359-2368. doi: 10.1007/s00125-009-1510-9

  • Naomi R. Wray, Michael R. James, Scott D. Gordon, Troy Dumenil, Leanne Ryan, William L. Coventry, Dixie J. Statham, Michele L. Pergadia, Pamela A.F. Madden, Andrew C. Heath, Grant W. Montgomery and Nicholas G. Martin (2009). Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures. Biological Psychiatry, 66 (5), 468-476. doi: 10.1016/j.biopsych.2009.04.030

  • Byrne, EM, McRae, AF, Duffy, DL, Zhao, ZZ, Martin, NG, Wright, MJ, Montgomery, GW and Visscher, PM (2009). Association Study of Common Mitochondrial Variants and Cognitive Ability. BEHAVIOR GENETICS, 39 (5), 504-512. doi: 10.1007/s10519-009-9276-x

  • J Kettunen, M Perola, N G Martin, B K Cornes, S G Wilson, G W Montgomery, B Benyamin, J R Harris, D Boomsma, G Willemsen, J-J Hottenga, P E Slagboom, K Christensen, K O Kyvik, T I A Sørensen, N L Pedersen, P K E Magnusson, T Andrew, T D Spector, E Widen, K Silventoinen, J Kaprio, A Palotie and L Peltonen (2009). Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci. International Journal of Obesity, 33 (11), 1235-1242. doi: 10.1038/ijo.2009.168

  • Matthew C. Keller, Allan F. McRae, Julie M. McGaughran, Peter M. Visscher, Nicholas G. Martin and Grant W. Montgomery (2009). Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.. American Journal of Medical Genetics. Part A, 149A (8), 1823-1826. doi: 10.1002/ajmg.a.32973

  • Bishop, DT, Demenais, F, Iles, MM, Harland, M, Taylor, JC, Corda, E, Randerson-Moor, J, Aitken, JF, Avril, MF, Azizi, E, Bakker, B, Bianchi-Scarra, G, Bressac-de Paillerets, B, Calista, D, Cannon-Albright, LA, Chin-A-Woeng, T, Debniak, T, Galore-Haskel, G, Ghiorzo, P, Gut, I, Hansson, J, Hocevar, M, Hoiom, V, Hopper, JL, Ingvar, C, Kanetsky, PA, Kefford, RF, Landi, MT, Lang, J, Lubinski, J and Mackie, R (2009). Genome-wide association study identifies three loci associated with melanoma risk. Nature Genetics, 41 (8), 920-925. doi: 10.1038/ng.411

  • Falchi, M, Bataille, V, Hayward, NK, Duffy, DL, Bishop, JAN, Pastinen, T, Cervino, A, Zhao, ZZ, Deloukas, P, Soranzo, N, Elder, DE, Barrett, JH, Martin, NG, Bishop, DT, Montgomery, GW and Spector, TD (2009). Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nature Genetics, 41 (8), 915-919. doi: 10.1038/ng.410

  • Cornes, Belinda K., Medland, Sarah E., Lind, Penelope A., Nyholt, Dale R., Montgomery, Grant W. and Martin, Nicholas G. (2009). Genetic variation in female BMI increases with number of children born but failure to replicate association between GN beta 3 variants and increased BMI in parous females. Twin Research and Human Genetics, 12 (3), 276-285. doi: 10.1375/twin.12.3.276

  • Brian P. McEvoy, Grant W. Montgomery, Allan F. McRae, Samuli Ripatti, Markus Perola, Tim D. Spector, Lynn Cherkas, Kourosh R. Ahmadi, Dorret Boomsma, Gonneke Willemsen, Jouke J. Hottenga, Nancy L. Pedersen, Patrik K.E. Magnusson, Kirsten Ohm Kyvik, Kaare Christensen, Jaakko Kaprio, Kauko Heikkilä, Aarno Palotie, Elisabeth Widen, Juha Muilu, Ann-Christine Syvänen, Ulrika Liljedahl, Orla Hardiman, Simon Cronin, Leena Peltonen, Nicholas G. Martin and Peter M. Visscher (2009). Geographical structure and differential natural selection among North European populations. Genome Research, 19 (5), 804-814. doi: 10.1101/gr.083394.108

  • Zhao, ZZ, Duffy, DL, Thomas, SA, Martin, NG, Hayward, NK and Montgomery, GW (2009). Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma. Melanoma Research, 19 (2), 80-85. doi: 10.1097/CMR.0b013e328322fc45

  • Rogers, Peter A. W., D'Hooghe, Thomas M., Fazleabas, Asgerally, Gargett, Caroline E., Giudice, Linda C., Montgomery, Grant W., Rombauts, Luk, Salamonsen, Lois A. and Zondervan, Krina T. (2009). Priorities for endometriosis research: recommendations from an international consensus workshop. Reproductive Sciences, 16 (4), 335-346. doi: 10.1177/1933719108330568

  • Woo, Jean, Tong, Stephen, Campbell, Megan J., Wallace, Leanne, Meagher, Simon, Montgomery, Grant W., Chao, Fay, Chan, Weng and Vollenhoven, Beverley (2009). Two Corpora Lutea Seen at 6-13 Weeks' Gestation Infers Dizygosity Among Spontaneous Same-Sexed Dichorionic Twins. Twin Research and Human Genetics, 12 (2), 180-182. doi: 10.1375/twin.12.2.180

  • Agrawal, Arpana, Pergadia, Michele L., Balasubramanian, Sumitra, Saccone, Scott F., Hinrichs, Anthony L., Saccone, Nancy L., Breslau, Naomi, Johnson, Eric O., Hatsukami, Dorothy, Martin, Nicholas G., Montgomery, Grant W., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A.F. (2009). Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerstrom test for nicotine dependence. Addiction, 104 (3), 471-477. doi: 10.1111/j.1360-0443.2008.02445.x

  • Nelson, E. C., Agrawal, A., Pergadia, M. L., Lynskey, M. T., Todorov, A. A., Wang, J. C., Todd, R. D., Martin, N. G., Heath, A. C., Goate, A. M., Montgomery, G. W. and Madden, P. A. F. (2009). Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults. Molecular Psychiatry, 14 (3), 234-235. doi: 10.1038/mp.2008.81

  • Andrew J. Birley, Michael R. James, Peter A. Dickson, Grant W. Montgomery, Andrew C. Heath, Nicholas G. Martin and John B. Whitfield (2009). ADH single nucleotide polymorphism associations with alcohol metabolism in vivo. Human Molecular Genetics, 18 (8), 1533-1542. doi: 10.1093/hmg/ddp060

  • Stuart Macgregor, Penelope A. Lind, Kathleen K. Bucholz, Narelle K. Hansell, Pamela A.F. Madden, Melinda M. Richter, Grant W. Montgomery, Nicholas G. Martin, Andrew C. Heath and John B. Whitfield (2009). Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. Human Molecular Genetics, 18 (3), 580-593. doi: 10.1093/hmg/ddn372

  • Nyholt, Dale R., Gillespie, Nathan G., Merikangas, Kathleen R., Treloar, Susan A., Martin, Nicholas G. and Montgomery, Grant W. (2009). Common genetic influences underlie comorbidity of migraine and endometriosis. Genetic Epidemiology, 33 (2), 105-113. doi: 10.1002/gepi.20361

  • Michele L. Pergadia, Arpana Agrawal, Anu Loukola, Grant W. Montgomery, Ulla Broms, Scott F. Saccone, Jen C. Wang, Alexandre A. Todorov, Kauko Heikkilä, Dixie J. Statham, Anjali K. Henders, Megan J. Campbell, John P. Rice, Richard D. Todd, Andrew C. Heath, Alison M. Goate, Leena Peltonen, Jaakko Kaprio, Nicholas G. Martin and Pamela A.F. Madden (2009). Genetic linkage findings for DSM-IV nicotine withdrawal in two populations. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 150b (7), 950-959. doi: 10.1002/ajmg.b.30924

  • Narelle K. Hansell, Arpana Agrawal, John B. Whitfield, Katherine I. Morley, Scott D. Gordon, Penelope A. Lind, Michele L. Pergadia, Grant W. Montgomery, Pamela A. F. Madden, Richard D. Todd, Andrew C. Heath and Nicholas G. Martin (2009). Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?. Alcoholism: Clinical and Experimental Research, 33 (4), 729-739. doi: 10.1111/j.1530-0277.2008.00890.x

  • Zachary A Kaminsky, Thomas Tang, Sun-Chong Wang, Carolyn Ptak, Gabriel H T Oh, Albert H C Wong, Laura A Feldcamp, Carl Virtanen, Jonas Halfvarson, Curt Tysk, Allan F McRae, Peter M Visscher, Grant W Montgomery, Irving I Gottesman, Nicholas G Martin and Art Petronis (2009). DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics, 41 (2), 240-245. doi: 10.1038/ng.286

  • Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011

  • Cornes, B., Lind, P. A., Medland, S. E., Montgomery, G. W ., Nyholt, D. R. and Martin, N. G . (2009). Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction. International Journal of Obesity, 33 (1), 75-79. doi: 10.1038/ijo.2008.223

  • Hoekstra, Chantal, Willemsen, Gonneke, van Beijsterveldt, Toos C. E. M., Montgomery, Grant W. and Boomsma, Dorret I. (2008). Familial twinning and fertility in Dutch mothers of twins. American Journal of Medical Genetics, Part A, 146A (24), 3147-3156. doi: 10.1002/ajmg.a.32585

  • Agrawal, Arpana, Morley, Katherine I., Hansell, Narelle K., Pergadia, Michele L., Montgomery, Grant W., Statham, Dixie J., Todd, Richard D., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John, Martin, Nicholas G. and Lynskey, Michael T. (2008). Autosomal linkage analysis for cannabis use behaviors in Australian adults. Drug and Alcohol Dependence, 98 (3), 185-190. doi: 10.1016/j.drugalcdep.2008.05.009

  • Middelberg, Rita P., Gordon, Scott D., Zhu, Gu, McRae, Allan, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2008). Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence. Twin Research and Human Genetics, 11 (6), 603-620. doi: 10.1375/twin.11.6.603

  • Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Farkkila, Markus, Hamalainen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Goebel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W. M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M. J. M., Kubisch, Christian and Martin, Nicholas G. (2008). A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics, 17 (21), 3318-3331. doi: 10.1093/hmg/ddn227

  • Bates, Timothy C., Luciano, Michelle, Lind, Penelope A., Wright, Margaret J., Montgomery, Grant W. and Martin, Nicholas G. (2008). Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language. Intelligence, 36 (6), 689-693. doi: 10.1016/j.intell.2008.04.001

  • Hillmer, Axel M., Brockschmidt, Felix F., Hanneken, Sandra, Eigelshoven, Sibylle, Steffens, Michael, Flaquer, Antonia, Herms, Stefan, Becker, Tim, Kortuem, Anne-Katrin, Nyholt, Dale R., Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Muehleisen, Thomas W., Alblas, Margrieta A., Moebus, Susanne, Joeckel, Karl-Heinz, Broecker-Preuss, Martina, Erbel, Raimund, Reinartz, Roman, Betz, Regina C., Cichon, Sven, Propping, Peter, Baur, Max P., Wienker, Thomas F., Kruse, Roland and Noethen, Markus M. (2008). Susceptibility variants for male-pattern baldness on chromosome 20p11. Nature Genetics, 40 (11), 1279-1281. doi: 10.1038/ng.228

  • Byrne, Enda M., Mcrae, Allan F., Zhao, Zhen-Zhen, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies. European Journal of Human Genetics, 16 (11), 1396-1403. doi: 10.1038/ejhg.2008.117

  • Peters, Kirsten, Wiltshire, Steven, Henders, Anjali K., Dragovic, Milan, Badcock, Johanna C., Chandler, David, Howell, Sarah, Ellis, Chris, Bouwer, Sonja, Montgomery, Grant W., Palmer, Lyle J., Kalaydjieva, Luba and Jablensky, Assen (2008). Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B (7), 1159-1166. doi: 10.1002/ajmg.b.30741

  • Anderson, Carl A., Zhu, Gu, Falchi, Mario, van den Berg, Stéphanie M., Treloar, Susan A., Spector, Timothy D., Martin, Nicholas G., Boomsma, Dorret I., Visscher, Peter M. and Montgomery, Grant W. (2008). A genome-wide linkage scan for age at menarche in three populations of European descent. Journal of Clinical Endocrinology and Metabolism., 93 (10), 3965-3970. doi: 10.1210/jc.2007-2568

  • Fowler, Elizabeth V., Doecke, James, Simms, Lisa A., Zhao, Zhen Zhen, Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Florin, Timothy H., Montgomery, Grant W., Cavanaugh, Juleen A. and Radford-Smith, Graham L. (2008). ATG16L1 T300A shows strong associations with disease subgroups in a large Australian IBD population: Further support for significant disease heterogeneity. The American Journal of Gastroenterology, 103 (10), 2519-2526. doi: 10.1111/j.1572-0241.2008.02023.x

  • Lind, Penelope A., Macgregor, Stuart, Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G. and Whitfield, John B. (2008). The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample. Alcoholism: Clinical and Experimental Research, 32 (10), 1721-1731. doi: 10.1111/j.1530-0277.2008.00768.x

  • Zhao, Zhen Zhen, Painter, Jodie N., Palmer, James S., Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Boomsma, Dorret I., Martin, Nicholas G., Duffy, David L. and Montgomery, Grant W. (2008). Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning. Human Reproduction, 23 (10), 2372-2379. doi: 10.1093/humrep/den268

  • Macgregor, Stuart, Hottenga, Jouke-Jan, Lind, Penelope A., Suchiman, H. Eka D., Willemsen, Gonneke, Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G., Visscher, Peter M. and Boomsma, Dorret I. (2008). Vitamin D receptor gene polymorphisms have negligible effect on human height. Twin Research and Human Genetics, 11 (5), 488-494. doi: 10.1375/twin.11.5.488

  • Zhao, Zhen Zhen, Nyholt, Dale R., Thomas, Shane, Treloar, Susan A. and Montgomery, Grant W. (2008). Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis. Molecular Human Reproduction, 14 (9), 531-538. doi: 10.1093/molehr/gan043

  • Montgomery, Grant W., Nyholt, Dale R., Zhao, Zhen Zhen, Treloar, Susan A., Painter, Jodie N., Missmer, Stacey A., Zondervan, Krina T. and Kennedy, Stephen H. (2008). The search for genes contributing to endometriosis risk. Human Reproduction Update, 14 (5), 447-457. doi: 10.1093/humupd/dmn016

  • Luciano, Michelle, Lind, Penelope A., Deary, Ian J., Payton, Antony, Posthuma, Danielle, Butcher, Lee M., Bochdanovits, Zoltan, Whalley, Lawrence J., Visscher, Peter M., Harris, Sarah E., Polderman, Tinca J.C., Davis, Oliver S.P., Wright, Margaret J., Starr, John M., de Geus, Eco J.C., Bates, Timothy C., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G. and Plomin, Robert (2008). Erratum: Testing replication of a 5-SNP set for general cognitive ability in six population samples (European Journal of Human Genetics (2008) 10.1038/ejhg.2008.100). European Journal of Human Genetics, 16 (8), 1025-1025. doi: 10.1038/ejhg.2008.124

  • Middeldorp, CM, Sullivan, PF, Wray, NR, Hottenga, JJ, de Geus, EJC, van den Berg, M, Montgomery, GW, Coventry, WL, Statham, DJ, Andrews, G, Slagboom, PE, Boomsma, DI and Martin, NG (2008). Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 150B (3), 352-358. doi: 10.1002/ajmg.b.30817

  • Brown, K. M., MacGregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D. C., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Newton Bishop, J., Kefford, R. F., Giles, G. G. and Armstrong, B. K. (2008). Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics, 40 (7), 838-840. doi: 10.1038/ng.163

  • Zhao, Zhu Zhen, Pollock, Pamela M., Thomas, Shane, Treloar, Susan A., Nyholt, Dale R. and Montgomery, Grant W. (2008). Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk. Human Reproduction, 23 (7), 1661-1668. doi: 10.1093/humrep/den035

  • Whitfield, John B., Day, Veronica, Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Montgomery, Grant W. (2008). Measuring carbohydrate-deficient transferrin by direct immunoassay: factors affecting diagnostic sensitivity for excessive alcohol intake. Clinical Chemistry, 54 (7), 1158-1165. doi: 10.1373/clinchem.2007.101733

  • Agrawal, Arpana, Pergadia, Michele. L., Saccone, Scott F., Lynskey, Michael T., Wang, Jen C., Martin, Nicholas G., Statham, Dixie, Henders, Anjali, Campbell, Megan, Garcia, Robertino, Broms, Ulla, Todd, Richard D., Goate, Alison M., Rice, John, Kaprio, Jaakko, Heath, Andrew C., Montgomery, Grant W. and Madden, Pamela A. F. (2008). An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project. Archives of General Psychiatry, 65 (6), 713-722. doi: 10.1001/archpsyc.65.6.713

  • Agrawal, Arpana, Pergadia, Michele L., Saccone, Scott F., Hinrichs, Anthony L., Lessov-Schlaggar, Christina N., Saccone, Nancy L., Neuman, Rosalind J., Breslau, Naomi, Johnson, Eric, Hatsukami, Dorothy, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A. F. (2008). Gamma-aminobutyric acid receptor genes and nicotine dependence: Evidence for association from a case-control study. Addiction, 103 (6), 1027-1038. doi: 10.1111/j.1360-0443.2008.02236.x

  • Zhu, Gu, Hewitt, Alex W., Ruddle, Jonathan B., Kearns, Lisa S., Brown, Shayne A., Mackinnon, Jane R., Chen, Christine Y., Hammond, Christopher J., Craig, Jamie E., Montgomery, Grant W., Martin, Nicholas G. and Mackey, David A. (2008). Genetic Dissection of Myopia Evidence for Linkage of Ocular Axial Length to Chromosome 5q. Ophthalmology, 115 (6), 1053-1057. doi: 10.1016/j.ophtha.2007.08.013

  • van Beijsterveldt, C. E. M. Toos, Hoekstra, Chantal, Schats, Roel, Montgomery, Grant W., Willemsen, Gonneke and Boomsma, Dorret I. (2008). Mode of conception of twin pregnancies: willingness to reply to survey items and comparison of survey data to hospital records. Twin Research and Human Genetics, 11 (3), 349-351. doi: 10.1375/twin.11.3.349

  • McRae, Allan F., Byrne, Enda M., Zhao, Zhen Zhen, Montgomery, Grant W. and Visscher, Peter M. (2008). Power and SNP tagging in whole mitochondrial genome association studies. Genome Research, 18 (6), 911-917. doi: 10.1101/gr.074872.107

  • Anttila, Verneri, Nyholt, Dale R., Kallela, Mikko, Artto, Ville, Vepsalainen, Salli, Jakkula, Eveliina, Wennerstrom, Annika, Tikka-Kleemola, Paeivi, Kaunisto, Mari A., Hamalainen, Eija, Widen, Elisabeth, Terwilliger, Joseph, Merikangas, Kathleen, Montgomery, Grant W., Martin, Nicholas G., Daly, Mark, Kaprio, Jaakko, Peltonen, Leena, Farkkila, Markus, Wessman, Maija and Palotie, Aarno (2008). Consistently replicating locus linked to migraine on 10q22-q23. American Journal of Human Genetics, 82 (5), 1051-1063. doi: 10.1016/j.ajhg.2008.03.003

  • Han, J., Kraft, P., Nan, H., Guo, Q., Chen, C., Qureshi, A., Hankinson, S.E., Hu, F.B., Duffy, D., Zhao, Z.Z., Martin, N. G., Montgomery, G., Hayward, N., Thomas, G., Hoover, R.N., Chanock, S. and Hunter, D.J. (2008). A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. Plos Genetics, 4 (5) e1000074, e1000074. doi: 10.1371/journal.pgen.1000074

  • Shekar, Sri N., Duffy, David L., Frudakis, Tony, Montgomery, Grant W., James, Michael R., Sturm, Richard A. and Martin, Nicholas G. (2008). Spectrophotometric methods for quantifying pigmentation in human hair - influence of MC1R genotype and environment. Photochemistry and Photobiology, 84 (3), 719-726. doi: 10.1111/j.1751-1097.2007.00237.x

  • Lind, Penelope A., MacGregor, Stuart, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G. and Whitfield, John B. (2008). Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the Alcohol Challenge Twin Study. Twin Research and Human Genetics, 11 (2), 174-182. doi: 10.1375/twin.11.2.174

  • Benyamin, Beben, Perola, Markus, Cornes, Belinda K., Madden, Pamela A. F., Palotie, Aarno, Nyholt, Dale R., Montgomery, Grant W., Peltonen, Leena, Martin, Nicholas G. and Visscher, Peter M. (2008). Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs. European Journal of Human Genetics, 16 (4), 516-524. doi: 10.1038/sj.ejhg.5201992

  • Shekar, Sri N., Duffy, David L., Frudakis, Tony, Sturm, Richard A., Zhao, Zhen Z., Montgomery, Grant W. and Martin, Nicholas G. (2008). Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: The effects of OCA2 and HERC2. Journal of Investigative Dermatology, 128 (12), 2807-2814. doi: 10.1038/jid.2008.147

  • Sturm, Richard A., Duffy, David L., Zhao, Zhen Zhen, Leite, Fabio P.N., Stark, Mitchell S., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2008). A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour. The American Journal of Human Genetics, 82 (2), 424-431. doi: 10.1016/j.ajhg.2007.11.005

  • Birley, Andrew J., James, Michael R., Dickson, Peter A., Montgomery, Grant W., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2008). Association of the gastric alcohol dehydrogenase gene Adh7 with variation in alcohol metabolism. Human Molecular Genetics, 17 (2), 179-189. doi: 10.1093/hmg/ddm295

  • Wray, Naomi R., James, Michael R., Handoko, Herlina Y., Dumenil, Troy, Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008). Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression. Psychiatric Genetics, 18 (5), 219-225. doi: 10.1097/YPG.0b013e3283050aee

  • Wray, Naomi, James, Michael R., Dumenil, Troy, Handoko, Herlina Y., Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008). Association study of candidate variants of COMT with neuroticism, anxiety and depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B (7), 1314-1318. doi: 10.1002/ajmg.b.30744

  • Zhao, Zhen Zhen, Nyholt, Dale R., Le, Lien, Treloar, Susan A. and Montgomery, Grant W. (2008). Common variation in the CYP17A1 and IFIT1 genes on chromosome 10 does not contribute to the risk of endometriosis. The Open Reproductive Science Journal, 1, 35-40. doi: 10.2174/1874255600801010035

  • Hoekstra, Chantal, Zhao, Zhen Zhen, Lambalk, Cornelius B., Willemsen, Gonneke, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2008). Dizygotic twinning. Human Reproduction Update, 14 (1), 37-47. doi: 10.1093/humupd/dmm036

  • Wray, Naomi R., Middeldorp, Christel M., Birley, Andrew J., Gordon, Scott D., Sullivan, Patrick F., Visscher, Peter M., Nyholt, Dale R, Willemsen, Gonneke, de Geus, Eco J.C., Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G. and Boomsma, Dorret I. (2008). Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands. Archives of General Psychiatry, 65 (6), 649-658. doi: 10.1001/archpsyc.65.6.649

  • Macgregor, Stuart, Zhao, Zhen Zhen, Henders, Anjali, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays. Nucleic Acids Research, 36 (6) e35, 291-296. doi: 10.1093/nar/gkm1060

  • Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas (2008). QTLs identified for P3 amplitude in a non-clinical sample: Importance of neurodevelopmental and neurotransmitter genes. Biological Psychiatry, 63 (9), 864-873. doi: 10.1016/j.biopsych.2007.09.002

  • Doecke, J D, Zhao, Z Z, Stark, M S, Green, A C, Hayward, N K, Montgomery, G W, Webb, P M and Whiteman, D C (2008). Single nucleotide polymorphisms in obesity-related genes and the risk of esophageal cancers. Cancer Epidemiology, Biomarkers & Prevention, 17 (4), 1007-1012. doi: 10.1158/1055-9965.EPI-08-0023

  • Luciano, Michelle, Lind, Penelope A., Deary, Ian J., Payton, Antony, Posthuma, Danielle, Butcher, Lee M., Bochdanovits, Zoltan, Whalley, Lawrence J., Visscher, Peter M., Harris, Sarah E., Polderman, Tinca J. C., Davis, Oliver S. P., Wright, Margaret J., Starr, John M., de Geus, Eco J. C., Bates, Timothy C., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G. and Plomin, Robert (2008). Testing replication of a 5-SNP set for general cognitive ability in six population samples. European Journal of Human Genetics, 16 (11), 1388-1395. doi: 10.1038/ejhg.2008.100

  • Ellis, MK, Zhao, ZZ, Chen, HG, Montgomery, GW, Li, YS and McManus, DP (2007). Analysis of the 5q31-33 locus shows an association between single nucleotide polymorphism variants in the IL-5 gene and symptomatic infection with the human blood fluke, Schistosoma japonicum. Journal of Immunology, 179 (12), 8366-8371. doi: 10.4049/jimmunol.179.12.8366

  • Visscher, Peter M., Macgregor, Stuart, Benyamin, Beben, Zhu, Gu, Gordon, Scott, Medland, Sarah, Hill, William G., Hottenga, Jouke-Jan, Willemsen, Gonneke, Boomsma, Dorret I., Liu, Yao-Zhong, Deng, Hong-Wen, Montgomery, Grant W. and Martin, Nicholas G. (2007). Genome partitioning of genetic variation for height from 11,214 sibling pairs. American Journal of Human Genetics, 81 (5), 1104-1110. doi: 10.1086/522934

  • Luciano, Michelle, Lind, Penelope A., Duffy, David L., Castles, Anne, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2007). A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biological Psychiatry, 62 (7), 811-817. doi: 10.1016/j.biopsych.2007.03.007

  • Zhao, Zhen Zhen, Nyholt, Dale R., Le, Lien, Thomas, Shane, Engwerda, Christian, Randall, Louise, Treloar, Susan A. and Montgomery, Grant W. (2007). Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample. Human Reproduction, 22 (9), 2389-2397. doi: 10.1093/humrep/dem182

  • Medland, Sarah E., Loesch, Danuta Z., Mdzewski, Bogdan, Zhu, Gu, Montgomery, Grant W. and Martin, Nicholas G. (2007). Linkage analysis of a model quantitative trait in humans: Finger ridge count shows significant multivariate linkage to 5q14.1. PLoS Genetics, 3 (9), 1736-1744. doi: 10.1371/journal.pgen.0030165

  • Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Montgomery, Grant W., Ferreira, Manuel A. R., Duffy, David L., Neale, Michael C., Heijmans, Bas T., Heath, Andrew C. and Martin, Nicholas G. (2007). Evidence of genetic effects on blood lead concentration. Environmental Health Perspectives, 115 (8), 1224-1230. doi: 10.1289/ehp.8847

  • Treloar, S. A., Zhao, Z. Z., Le, L., Zondervan, K. T., Martin, N. G., Kennedy, S., Nyholt, D. R. and Montgomery, G. W. (2007). Variants in EMX2 and PTEN do not contribute to risk of endometriosis. Molecular Human Reproduction, 13 (8), 587-594. doi: 10.1093/molehr/gam023

  • Perola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick G., Visscher, Peter M., Montgomery, Grant W., Benyamin, Beben, Harris, Jennifer R., Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Karre, Kyvik, Kirsten Ohm, Sorensen, Thorkild I., Pedersen, Nancy L., Magnusson, Patrik K., Spector, Tim D., Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno, Peltonen, Leena and GenomEUtwin Project (2007). Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci. PLoS Genetics, 3 (6), 1019-1028. doi: 10.1371/journal.pgen.0030097

  • Perola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick, Visscher, Peter M., Montgomery, Grant W., Benyamin, Beben, Harris, Jennifer R, Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Kaare, Ohm Kyvik, Kirsten, Sørensen, Thorkild I. A., Pedersen, Nancy L., Magnusson, Patrik K.E., Spector, Tim D, Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno and Peltonen, Leena (2007). Combined genome scans for body stature in 6602 European twins: evidence for common Caucasian loci. PLoS Genetics, 3 (6), 1019-1028. doi: 10.1371/journal.pgen.0030097

  • Souter, Vivienne L., Parisi, Melissa A., Nyholt, Dale R., Kapur, Raj P., Henders, Anjali K., Opheim, Kent E., Gunther, Daniel F., Mitchell, Michael E., Glass, Ian A. and Montgomery, Grant W. (2007). A case of true hermaphroditism reveals an unusual mechanism of twinning. Human Genetics, 121 (2), 179-185. doi: 10.1007/s00439-006-0279-x

  • Hansell, N. K., James, M. R., Duffy, D. L., Birley, A. J., Luciano, M., Geffen, G. M., Wright, M. J., Montgomery, G. W. and Martin, N. G. (2007). Effect of the BDNF V166M polymorphism on working memory in healthy adolescents. Genes, Brain and Behavior, 6 (3), 260-268. doi: 10.1111/j.1601-183X.2006.00254.x

  • Wray, Naomi R., James, Michael R., Mah, Steven P., Nelson, Matthew, Andrews, Gavin, Sullivan, Patrick F., Montgomery, Grant W., Birley, Andrew J., Braun, Andreas and Martin, Nicholas G. (2007). Anxiety and comorbid measures associated with PLXNA2. Archives of General Psychiatry, 64 (3), 318-326. doi: 10.1001/archpsyc.64.3.318

  • Mekel-Bobrov, Nitzan, Posthuma, Danielle, Gilbert, Sandra L., Lind, Penelope, Gosso, M. Florencia, Luciano, Michelle, Harris, Sarah E., Bates, Timothy C., Polderman, Tinca J., Whalley, Lawrence J., Fox, Helen, Starr, John M., Evans, Patrick D., Montgomery, Grant W., Fernandes, Croydon, Heutink, Peter, Martin, Nicholas G., Boomsma, Dorret I., Deary, Ian J., Wright, Margaret J., de Geus, Eco J. and Lahn, Bruce T. (2007). The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence. Human Molecular Genetics, 16 (6), 600-608. doi: 10.1093/hmg/ddl487

  • Luciano, M., Ghu, Z., Kirk, K. M., Gordon, S. D., Heath, A. C., Montgomery, G. W. and Martin, N. G. (2007). "No thanks, it keeps me awake". The genetics of coffee-attributed sleep disturbance. Sleep, 30 (10), 1378-1386. doi: 10.1093/sleep/30.10.1378

  • Zhu, Gu, Montgomery, Grant W., James, Michael R., Trent, Jeff M., Hayward, Nicholas K., Martin, Nicholas G. and Duffy, David L. (2007). A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions. European Journal of Human Genetics, 15 (1), 94-102. doi: 10.1038/sj.ejhg.5201729

  • Duffy, D. L., Montgomery, G. W., Chen, W., Zhao, Z. Z., Le, L., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2007). A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. American Journal of Human Genetics, 80 (2), 241-252. doi: 10.1086/510885

  • Saccone, S. F., Hinrichs, A. L., Saccone, N. L., Chase, G. A., Konvicka, K., Madden, P. A., Breslau, N., Johnson, E. O., Hatsukami, D., Pomerleau, O., Swan, G. E., Goate, A. M., Rutter, J., Bertelsen, S., Fox, L., Fugman, D., Martin, N. G., Montgomery, G. W., Wang, J. C., Ballinger, D. G., Rice, J. P. and Bierut, L. J. (2007). Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. Human Molecular Genetics, 16 (1), 36-49. doi: 10.1093/hmg/ddl438

  • Saccone, Scott F., Pergadia, Michele L., Loukola, Anu, Broms, Ula, Montgomery, Grant W., Wang, Jen C., Agrawal, Arpana, Dick, Danielle M., Heath, Andrew C., Todorov, Alexandre A., Maunu, Heidi, Heikkila, Kauko, Morley, Katherine I., Rice, John P., Todd, Richard D., Kaprio, Jaakko, Peltonen, Leena, Martin, Nicholas G., Goate, Alison M. and Madden, Pamela A. (2007). Genetic linkage to chromosome 22q12 for a heavy-smoking quantitative trait in two independent samples. American Journal of Human Genetics, 80 (5), 856-866. doi: 10.1086/513703

  • Iliadou, A., Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2007). Genomewide scans of red cell indices suggest linkage on chromosome 6q23. Journal of Medical Genetics, 44 (1), 24-30. doi: 10.1136/jmg.2006.043521

  • Bierut, L. J., Madden, P. A., Breslau, N., Johnson, E. O., Hatsukami, D., Pomerleau, O. F., Swan, G. E., Rutter, J., Bertelsen, S., Fox, L., Fugman, D., Goate, A. M., Hinrichs, A. L., Konvicka, K., Martin, N. G., Montgomery, G. W., Saccone, N. L., Saccone, S. F., Wang, J. C., Chase, G. A., Rice, J. P. and Ballinger, D. G. (2007). Novel genes identified in a high-density genome wide association study for nicotine dependence. Human Molecular Genetics, 16 (1), 24-35. doi: 10.1093/hmg/ddl441

  • Zondervan, K. T., Treloar, S. A., Lin, J., Weeks, D. E., Nyholt, D. R., Mangion, J., MacKay, I. J., Cardon, L. R., Martin, N. G., Kennedy, S. H. and Montgomery, G. W. (2007). Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15. Human Reproduction, 22 (3), 717-728. doi: 10.1093/humrep/del446

  • Spring, Kevin, Zhao, Zhen Zhen, Karamatic, Rozemary, Walsh, Michael, Whitehall, Vicki, Pike, Tanya, Simms, Lisa, Young, Joanne, James, Michael, Montgomery, Grant, Appleyard, Mark, Hewett, David, Togashi, Kazutomo, Jass, Jeremy and Leggett, Barbara (2006). High prevalence of sessile serrated adenomas with BRAF mutations: A prospective study of patients undergoing colonoscopy. Gastroenterology, 131 (5), 1400-1407. doi: 10.1053/j.gastro.2006.08.038

  • Cornes, B. K., Medland, S. E., Ferreira, M. A.R., Morley, K. I., Duffy, D. L., Heijmans, B. T., Montgomery, G. W. and Martin, N. G. (2006). Erratum: A sex-limited genome scan for body mass index in an unselected sample (Twin Research and Human Genetics (2005) 8, 6 (616-632)). Twin Research and Human Genetics, 9 (3) doi: 10.1375/twin.9.3.ii

  • Visscher, Peter M., Medland, Sarah E., Ferreira, Manuel A. R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006). Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. Plos Genetics, 2 (3), 316-325. doi: 10.1371/journal.pgen.0020041

  • Visscher, Peter M., Medland, Sarah E., Ferreira, Manuel A.R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006). Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. PLoS Genetics, 2 (3), 316-325. doi: 10.1371/journal.pgen.0020041

  • Shekar, Sri Niranjan, Duffy, David L., Montgomery, Grant W. and Martin, Nicholas G. (2006). A genome scan for epidermal skin pattern in adolescent twins reveals suggestive linkage on 12p13.31. Journal of Investigative Dermatology, 126 (2), 277-282. doi: 10.1038/sj.jid.5700067

  • Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas G. (2006). A linkage study of academic skills defined by the Queensland Core Skills Test. Behavior Genetics, 36 (1), 56-64. doi: 10.1007/s10519-005-9013-z

  • Morley, Katherine I., Medland, Sarah E., Ferreira, Manuel A. R., Lynskey, Michael T., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2006). A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin families. Behavior Genetics, 36 (1), 87-99. doi: 10.1007/s10519-005-9004-0

  • Macgregor, S., Visscher, P. M. and Montgomery, G. (2006). Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates. Nucleic Acids Research, 34 (7) e55 doi: 10.1093/nar/gkl136

  • Valle, Anne, OConnor, Daniel T., Taylor, Palmer, Zhu, Gu, Montgomery, Grant W., Slagboom, P. Eline, Martin, Nicholas G. and Whitfield, John B. (2006). Butyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity. Clinical Chemistry, 52 (6), 1014-1020. doi: 10.1373/clinchem.2005.065052

  • Dickson, Peter A., James, Michael R., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Whitfield, John B. and Birley, Andrew J. (2006). Effects of Variation at the ALDH2 Locus on Alcohol Metabolism, Sensitivity, Consumption, and Dependence in Europeans. Alcoholism - Clinical And Experimental Research, 30 (7), 1093-1100. doi: 10.1111/j.1530-0277.2006.00128.x

  • Sullivan, Patrick F., Montgomery, Grant W., Hottenga, Jouke J., Wray, Naomi R., Boomsma, Dorret I. and Martin, Nicholas G. (2006). Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers. Twin Research And Human Genetics, 9 (4), 600-602. doi: 10.1375/183242706778025026

  • Middelberg, Rita P., Martin, Nicholas G., Montgomery, Grant W. and Whitfield, John B. (2006). Genome-wide linkage scan for loci influencing plasma triglycerides. Clinica Chimica Acta, 374 (1-2), 87-92. doi: 10.1016/j.cca.2006.05.033

  • Luciano, M., Wright, M. J., Duffy, D. L., Wainwright, M. A., Zhu, G., Evans, D. M., Geffen, G. M., Montgomery, G. W. and Martin, N. G. (2006). Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q. Behavior Genetics, 36 (1), 45-55. doi: 10.1007/s10519-005-9003-1

  • Montgomery, Grant W., Zhu, Gu, Hottenga, Jouke J., Duffy, David L., Heath, Andrew C., Boomsma, Dorret I., Martin, Nicholas G. and Visscher, Peter M. (2006). HLA and Genomewide Allele Sharing in Dizygotic Twins. American Journal of Human Genetics, 79 (6), 1052-1058. doi: 10.1086/510136

  • Zhao, Z. Z., Nyholt, D. R., Le, L., Martin, N. G., James, M. R., Treloar, S. A. and Montgomery, G. W. (2006). KRAS variation and risk of endometriosis. Molecular Human Reproduction, 12 (11), 671-676. doi: 10.1093/molehr/gal078

  • Hansell, N. K., Medland, S. E., Ferreira, A. R., Geffen, G. M., Zhu, G., Montgomery, G. W., Duffy, D. L., Wright, M.J. and Martin, N. G. (2006). Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task. Behavior Genetics, 36 (1), 29-44. doi: 10.1007/s10519-005-9002-2

  • Palmer, J. S., Zhao, Z. Z., Hoekstra, C., Hayward, N. K., Webb, P. M., Whiteman, D. C., Martin, N. G., Boomsma, D. I., Duffy, D. L. and Montgomery, G. W. (2006). Novel variants in growth differentiation factor 9 in mothers of dizygotic twins. Journal of Clinical Endocrinology And Metabolism, 91 (11), 4713-4716. doi: 10.1210/jc.2006-0970

  • James, Michael R., Dumeni, Troy, Stark, Mitchell S., Duffy, David L., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2006). Rapid screening of 4000 individuals for germ-line variations in the BRAF gene. Clinical Chemistry, 52 (9), 1675-1678. doi: 10.1373/clinchem.2006.070169

  • James, Michael R., Roth, Richard B., Shi, Michael M., Kammerer, Stefan, Nelson, Matthew R., Stark, Mitchell S., Dumenil, Troy, Montgomery, Grant W., Hayward, Nicholas K., Martin, Nicholas G., Braun, Andreas and Duffy, David L. (2005). BRAF Polymorphisms and Risk of Melanocytic Neoplasia. Journal of Investigative Dermatology, 125 (6), 1252-1258. doi: 10.1111/j.0022-202X.2005.23937.x

  • Cornes, BK, Medland, SE, Ferreira, MAR, Morley, KI, Duffy, DL, Heijmans, BT, Montgomery, GW and Martin, NG (2005). Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families. Twin Research and Human Genetics, 8 (6), 616-632. doi: 10.1375/183242705774860240

  • Medland, Sarah E., Duffy, David L., Spurdle, Amanda B., Wright, Margaret J., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2005). Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females. Behavior Genetics, 35 (6), 735-744. doi: 10.1007/s10519-005-6187-3

  • Nyholt, Dale R., Morley, Katherine I., Ferreira, Manual A. R., Medland, Sarah E., Boomsma, Dorret I., Heath, Andrew C., Merikangas, Kathleen R., Montgomery, Grant W. and Martin, Nicholas G. (2005). Genomewide significant linkage to migrainous Hheadache on chromosome 5q21. American Journal Of Human Genetics, 77 (3), 500-512. doi: 10.1086/444510

  • Zhao, Zhen Zhen, Nyholt, Dale R., James, Michael R., Mayne, Renee, Treloar, Susan A. and Montgomery, Grant W. (2005). A comparison of DNA pools constructed following whole genome amplification for two-stage SNP genotyping designs. Twin Research and Human Genetics, 8 (4), 353-361. doi: 10.1375/1832427054936718

  • Posthuma, Danielle, Luciano, Michelle, de Geus, Eco J. C., Wright, Margie J., Slagboom, P. Eline, Montgomery, Grant W., Boomsma, Dorret I. and Martin, Nicholas G. (2005). A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p. American Journal of Human Genetics, 77 (2), 318-326. doi: 10.1086/432647

  • Loehlin, JC, Medland, SE, Montgomery, GW and Martin, NG (2005). Eysenck's Psychoticism and the X-linked androgen receptor gene CAG polymorphism in additional Australian samples. Personality and Individual Differences, 39 (3), 661-667. doi: 10.1016/j.paid.2005.02.016

  • Treloar, Susan A., Zhao, Zhen Zhen, Armitage, Trudi, Duffy, David L., Wicks, Jacqueline, O'Connor, Daniel T., Martin, Nicholas G. and Montgomery, Grant W. (2005). Association between polymorphisms in the progesterone receptor gene and endometriosis. Molecular Human Reproduction, 11 (9), 641-647. doi: 10.1093/molehr/gah221

  • Montgomery, GW, Campbell, MJ, Dickson, P, Herbert, S, Siemering, K, Ewen-White, KR, Visscher, PM and Martin, NG (2005). Estimation of the rate of SNP genotyping errors from DNA extracted from different tissues. Twin Research and Human Genetics, 8 (4), 346-352. doi: 10.1375/1832427054936673

  • Dickson, PA, Montgomery, GW, Henders, A, Campbell, MJ, Martin, NG and James, MR (2005). Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan. Nucleic Acids Research, 33 (13), 1-4. doi: 10.1093/nar/gni126

  • Treloar, Susan A., Wicks, Jacqueline, Nyholt, Dale R., Montgomery, Grant W., Bahlo, Melanie, Smith, Vicki, Dawson, Gary, Mackay, Ian J., Weeks, Daniel E., Bennett, Simon T., Carey, Alisoun, Ewen-White, Kelly R., Duffy, David L., O'Connor, Daniel T., Barlow, David H., Martin, Nicholas G. and Kennedy, Stephen H. (2005). Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. American Journal of Human Genetics, 77 (3), 365-376. doi: 10.1086/432960

  • Hoekstra, Chantal, Meijer, Piet, Kluft, Cornelis, Heutink, Peter, Smit, Guus, de Geus, Eco, Smit, Jan H., van Bruggen, Angelique, Montgomery, Grant W. and Boomsma, Dorret I. (2004). Genetics of dizygotic twinning: a feasibility study for a biobank. Twin Research and Human Genetics, 7 (6), 556-563. doi: 10.1375/1369052042663751

  • Evans, DM, Zhu, G, Duffy, DL, Montgomery, GW, Frazer, IH and Martin, NG (2004). Major quantitative trait locus for eosinophil count is located on chromosome 2q. Journal of Allergy And Clinical Immunology, 114 (4), 826-830. doi: 10.1016/j.jaci.2004.05.060

  • Fleming, Jean S., Yu, Fu, McDonald, Robin M., Meyers, Stuart A., Montgomery, Grant W., Smith, John F. and Nicholson, Helen D. (2004). Effects of scrotal heating on sperm surface protein PH-20 expression in sheep. Molecular Reproduction and Development, 68 (1), 103-114. doi: 10.1002/mrd.20049

  • Montgomery, G. W., Zhao, Z. Z., Marsh, A. J., Mayne, R., Treloar, S. A., James, M., Martin, N. G., Boomsma, D. I. and Duffy, D. L. (2004). A deletion mutation in GDF9 in sisters with spontaneous DZ twins. Twin Research, 7 (6), 548-555. doi: 10.1375/1369052042663823

  • Zhu, G., Evans, D. M., Duffy, D. L., Montgomery, G. W., Medland, S. E., Gillespie, N. A., Ewen, K. R., Jewell, M., Liew, Y. W., Hayward, N. K., Sturm, R. A., Trent, J. M. and Martin, N. G. (2004). A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q. Twin Research, 7 (2), 197-210. doi: 10.1375/136905204323016186

  • Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2004). A major quantitative trait locus for CD4-CD8 ratio is located on chromosome 11. Genes and Immunity, 5 (7), 548-552. doi: 10.1038/sj.gene.6364126

  • James, Michael R., Hayward, Nicholas K., Dumenil, Troy, Montgomery, Grant W., Martin, Nicholas G. and Duffy, David L. (2004). Epidermal Growth Factor Gene (EGF) Polymorphism and Risk of Melanocytic Neoplasiay. Journal of Investigative Dermatology, 123 (4), 760-762. doi: 10.1111/j.0022-202X.2004.23305.x

  • Loehlin, John C., Jonsson, Erik G., Gustavsson, J. Petter, Schalling, Martin, Medland, Sarah E., Montgomery, Grant W. and Martin, Nicholas G. (2004). Gender diagnosticity and androgen receptor gene CAG repeat sequence. Twin Research, 7 (5), 456-461. doi: 10.1375/1369052042335359

  • Duffy, D. L., Box, N. F., Chen, W., Palmer, J. S., Montgomery, G. W., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2004). Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Human Molecular Genetics, 13 (4), 447-461. doi: 10.1093/hmg/ddh043

  • Evans, D. M., Zhu, G., Duffy, D. L., Montgomery, G. W., Frazer, IH and Martin, NG (2004). Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q. European Journal of Human Genetics, 12 (10), 835-842. doi: 10.1038/sj.ejhg.5201248

  • Souter, Vivienne L., Kapur, Raj P., Nyholt, Dale R., Skogerboe, Kristen, Myerson, David, Ton, Carl C., Opheim, Kent E., Easterling, Thomas R., Shields, Laurence E., Montgomery, Grant W. and Glass, Ian A. (2003). A report of dizygous monochorionic twins. New England Journal of Medicine, 349 (2), 154-158. doi: 10.1056/NEJMoa030050

  • Montgomery, Grant W., Zhao, Zhen Zehn, Morley, Katherine I., Marsh, Anna J., Boomsma, Dorret I., Martin, Nicholas G. and Duffy, David L. (2003). Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes. Human Reproduction, 18 (11), 2460-2464. doi: 10.1093/humrep/deg441

  • Zhu, Gu, Duffy, David L., Turner, David R., Ewen, Kelly R., Montgomery, Grant W. and Martin, Nicholas G. (2003). Linkage and Association Analysis of Radiation Damage Repair Genes XRCC3 and XRCC5 with Nevus Density in Adolescent Twins. Twin Research, 6 (4), 315-321. doi: 10.1375/136905203322296683

  • Gilfillan, Christopher P., Montgomery, Grant W., Zhu, Gu, Martin, Nicholas G., Groome, N. P. and Robertson, David M. (2003). Serum inhibin A and B concentrations during the menstrual cycle in mothers of spontaneous dizygotic twins. Twin Research, 6 (1), 27-33. doi: 10.1375/136905203762687870

  • Heath, Andrew C., Nyholt, Dale R., Neuman, Rosalind, Madden, Pamela A. F., Bucholz, Kathleen K., Todd, Richard D., Nelson, Elliot C., Montgomery, Grant W. and Martin, Nicholas G. (2003). Zygosity Diagnosis in the Absence of Genotypic Data: An Approach Using Latent Class Analysis. Twin Research and Human Genetics, 6 (1), 22-26. doi: 10.1375/136905203762687861

  • Haiman, Christopher A., Chen, Gary K., Vachon, Celine M., Canzian, Federico, Dunning, Alison, Millikan, Robert C., Wang, Xianshu, Ademuyiwa, Foluso, Ahmed, Shahana, Ambrosone, Christine B., Baglietto, Laura, Balleine, Rosemary, Bandera, Elisa V., Beckmann, Matthias W., Berg, Christine D., Bernstein, Leslie, Blomqvist, Carl, Blot, William J., Brauch, Hiltrud, Buring, Julie E., Carey, Lisa A., Carpenter, Jane E., Chang-Claude, Jenny, Chanock, Stephen J., Chasman, Daniel I., Clarke, Christine L., Cox, Angela, Cross, Simon S., Deming, Sandra L., Diasio, Robert B. and Dimopoulos, Athanasios M. (2002). Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature Genetics, 32 (2), 285-289. doi: 10.1038/ng985

  • Nestler, John E., Whitfield, John B., Williams, Terre Y., Zhu, Gu, Condon, Juliann, Kirk, Katherine M., Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2002). Genetics of Serum Dehydroepiandrosterone Sulfate and Its Relationship to Insulin in a Population-Based Cohort of Twin Subjects. Journal of Clinical Endocrinology And Metabolism, 87 (2), 682-686. doi: 10.1210/jc.87.2.682

  • Morley, KI and Montgomery, GW (2001). The genetics of cognitive processes: Candidate genes in humans and animals. Behavior Genetics, 31 (6), 511-531. doi: 10.1023/A:1013337209957

  • Montgomery, GW, Galloway, SM, Davis, GH and McNatty, KP (2001). Genes controlling ovulation rate in sheep. Reproduction, 121 (6), 843-852. doi: 10.1530/rep.0.1210843

  • Duffy, David L., Montgomery, Grant W., Hall, Jeff, Mayne, Carol, Healey, Sue C., Brown, Joy, Boomsma, Dorret I. and Martin, Nicholas G. (2001). Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecB. American Journal of Medical Genetics Part A, 100 (3), 182-186. doi: 10.1002/ajmg.1255

  • Wilson, T, Wu, XY, Juengel, JL, Ross, IK, Lumsden, JM, Lord, EA, Dodds, KG, Walling, GA, McEwan, JC, O'Connell, AR, McNatty, KP and Montgomery, GW (2001). Highly prolific Booroola sheep have a mutation in the intracellular kinase domain of bone morphogenetic protein IB receptor (ALK-6) that is expressed in both oocytes and granulosa cells. Biology of Reproduction, 64 (4), 1225-1235. doi: 10.1095/biolreprod64.4.1225

  • Montgomery, Grant W., Duffy, David L., Hall, Jeff, Kudo, Masataka, Martin, Nicholas G. and Hsueh, Aaron J. (2001). Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning. Lancet, 357 (9258), 773-774. doi: 10.1016/S0140-6736(00)04164-7

  • Duffy, David, Montgomery, Grant, Treloar, Susan, Birley, Andrew, Kirk, Katherine, Boomsma, Dorret, Beem, Leo, de Geus, Eco, Slagboom, Eline, Knighton, Joharna, Reed, Peter and Martin, Nicholas (2001). IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers. Nature Genetics, 28 (4), 315-315. doi: 10.1038/91074

  • Montgomery, Grant W., Duffy, David L., Hall, Jeff, Haddon, Barbara R., Kudo, Masataka, McGee, Elizabeth A., Palmer, James S., Hsueh, Aaron J., Boomsma, Dorrett I. and Martin, Nicholas G. (2000). Dizygotic Twinning Is Not Linked to Variation at the {alpha}-Inhibin Locus on Human Chromosome 2. Journal of Clinical Endocrinology & Metabolism, 85 (9), 3391-3395. doi: 10.1210/jc.85.9.3391

  • Jenkins, ZA, Henry, HM, Sise, JA and Montgomery, GW (2000). Follistatin (FST), growth hormone receptor (GHR) and prolactin receptor (PRLR) genes map to the same region of sheep chromosome 16. Animal Genetics, 31 (4), 280-280. doi: 10.1046/j.1365-2052.2000.00482.x

  • Galloway, SM, McNatty, KP, Cambridge, LM, Laitinen, MPE, Juengel, JL, Jokiranta, TS, McLaren, RJ, Luiro, K, Dodds, KG, Montgomery, GW, Beattie, AE, Davis, GH and Ritvos, O (2000). Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner. Nature Genetics, 25 (3), 279-283. doi: 10.1038/77033

  • Montgomery, GW (2000). Genome mapping in ruminants and map locations for genes influencing reproduction. Reviews of Reproduction, 5 (1), 25-37. doi: 10.1530/ror.0.0050025

  • Yang, L, Zhao, SH, Li, K, Peng, ZZ and Montgomery, GW (1999). Determination of genetic relationships among five indigenous Chinese goat breeds with six microsatellite markers. Animal Genetics, 30 (6), 452-455. doi: 10.1046/j.1365-2052.1999.00548.x

  • McLaren, RJ and Montgomery, GW (1999). Genomic imprinting of the insulin-like growth factor 2 gene in sheep. Mammalian Genome, 10 (6), 588-591. doi: 10.1007/s003359901050

  • Jenkins, ZA and Montgomery, GW (1999). Linkage mapping of genes encoding bone morphogenetic proteins 1, 4 and 5 in sheep. Animal Genetics, 30 (2), 163-164. doi: 10.1046/j.1365-2052.1999.00382-4.x

  • Lumsden, JM, Lord, EA, Hirst, KL, Dixon, MJ and Montgomery, GW (1999). Mapping of dentin-specific acidic phosphoprotein and integrin-binding sialoprotein in sheep defines an inversion breakpoint with respect to human chromosome 4Q. Genetics and Molecular Biology, 22 (1), 29-31. doi: 10.1590/S1415-47571999000100007

  • Jenkins, ZA and Montgomery, GW (1999). Genetic mapping of the ovine homologue of the mouse Hacl1 gene to sheep chromosome 1. Animal Genetics, 30 (1), 74-74. doi: 10.1046/j.1365-2052.1999.00323-12.x

  • Lumsden, JM, Lord, EA, Cato, SA, Richardson, TE, van Stijn, TC, Broom, MF, Patel, K and Montgomery, GW (1999). The application of AFLP fingerprinting to construct a YAC contig containing ADH2 and MTP on sheep chromosome 6. Cytogenetics and Cell Genetics, 84 (3-4), 225-229. doi: 10.1159/000015264

  • Henry, HM, Dodds, KG, Wuliji, T, Jenkins, ZA, Beattie, AE and Montgomery, GW (1998). A genome screen for QTL for wool traits in a Merino x Romney backcross flock (Reprinted). Wool Technology and Sheep Breeding, 46 (3), 213-217.

  • Lord, EA, Davis, GH, Dodds, KG, Henry, HM, Lumsden, JM and Montgomery, GW (1998). Identification of Booroola carriers using microsatellite markers (Reprinted). Wool Technology and Sheep Breeding, 46 (3), 245-249.

  • Broad, Thomas E., Hill, Diana F., Maddox, Jullian F., Montgomery, Grant W. and Nicholas, Frank W. (1998). The sheep gene map. ILAR Journal, 39 (2-3), 160-170. doi: 10.1093/ilar.39.2-3.160

  • McLaren, RJ, Rogers, GR, Davies, KP, Maddox, JF and Montgomery, GW (1997). Linkage mapping of wool keratin and keratin-associated protein genes in sheep. Mammalian Genome, 8 (12), 938-940. doi: 10.1007/s003359900616

  • Gootwine, E, Suttie, JM, McEwan, JC, Veenvliet, BA, Littlejohn, RP, Fennessy, PF and Montgomery, GW (1997). The physiological effects of natural variation in growth hormone gene copy number in ram lambs. Domestic Animal Endocrinology, 14 (6), 381-390. doi: 10.1016/S0739-7240(98)00043-5

  • Jenkins, ZA, Henry, HM, Galloway, SM, Dodds, KG and Montgomery, GW (1997). Comparative linkage mapping of genes on sheep chromosome 3 provides evidence of chromosomal rearrangements in the evolution of the Bovidae. Cytogenetics and Cell Genetics, 78 (3-4), 272-274. doi: 10.1159/000134670

  • Montgomery, G. W. and Kinghorn, B. P. (1997). Recent developments in gene mapping and progress towards marker-assisted selection in sheep. Australian Journal of Agriculture Research, 48 (6), 729-741. doi: 10.1071/A96153

  • Fleming, JS, Suttie, JM, Montgomery, GW, Gunn, J, Stuart, SK, Littlejohn, RP and Gootwine, E (1997). The effects of a duplication in the ovine growth hormone (GH) gene on gh expression in the pituitaries of ram lambs from lean and fat-selected sheep lines. Domestic Animal Endocrinology, 14 (1), 17-24. doi: 10.1016/S0739-7240(96)00098-7

  • Jenkins, ZA and Montgomery, GW (1996). Genetic mapping of the laminin gamma 2 gene on sheep Chromosome 12. Mammalian Genome, 7 (11), 868-869. doi: 10.1007/s003359900257

  • Andersson, L., Archibald, A., Ashburner, M., Audun, S., Barendse, W., Bitgood, J., Bottema, C., Broad, T., Brown, S., Burt, D., Charlier, C., Copeland, N., Davis, S., Davisson, M., Edwards, J., Eggen, A., Elgar, G., Eppig, J. T., Franklin, I., Grewe, P., Gill, T., Graves, J. A. M., Hawken, R., Hetzel, J., Hilyard, A., Jacob, H., Jaswinska, L., Jenkins, N., Kunz, H., Levan, G. and Lie, O. (1996). Comparative genome organization of vertebrates. Mammalian Genome, 7 (10), 717-734. doi: 10.1007/s003359900222

  • Escayg, AP, Hickford, JGH, Montgomery, GW, Dodds, KG and Bullock, DW (1996). Polymorphism at the ovine major histocompatibility complex class II loci. Animal Genetics, 27 (5), 305-312.

  • Lumsden, JM and Montgomery, GW (1996). Genetic mapping of the endothelin receptor type A gene on sheep Chromosome 17. Mammalian Genome, 7 (7), 560-561. doi: 10.1007/s003359900169

  • Lumsden, JM, Lord, EA and Montgomery, GW (1996). Characterization and linkage mapping often sheep microsatellite markers derived from a sheep x hamster cell hybrid. Animal Genetics, 27 (3), 203-206.

  • Lord, EA, Lumsden, JM, Dodds, KG, Henry, HM, Crawford, AM, Ansari, HA, Pearce, PD, Maher, DW, Stone, RT, Kappes, SM, Beattie, CW and Montgomery, GW (1996). The linkage map of sheep chromosome 6 compared with orthologous regions in other species. Mammalian Genome, 7 (5), 373-376. doi: 10.1007/s003359900107

  • Tebbutt, SJ, Broom, MF, vanStijn, TC, Montgomery, GW and Hill, DF (1996). Genetic and physical mapping of the ovine cystic fibrosis gene. Cytogenetics and Cell Genetics, 74 (4), 245-247. doi: 10.1159/000134425

  • Montgomery, G. W., Henry, H. M., Dodds, K. G., Beattie, A. E., Wuliji, T. and Crawford, A. M. (1996). Mapping the Horns (Ho) locus in sheep: A further locus controlling horn development in domestic animals. Journal of Heredity, 87 (5), 358-363. doi: 10.1093/oxfordjournals.jhered.a023014

  • Sise, JA, Hillyard, AL and Montgomery, GW (1996). The sheep gene map database (SheepBase) is now available on the World Wide Web. Mammalian Genome, 7 (1), 1-1. doi: 10.1007/s003359900001

  • MONTGOMERY, GW, TATE, ML, HENRY, HM, PENTY, JM and ROHAN, RM (1995). THE FOLLICLE-STIMULATING-HORMONE RECEPTOR AND LUTEINIZING-HORMONE RECEPTOR GENES ARE CLOSELY LINKED IN SHEEP AND DEER. Journal of Molecular Endocrinology, 15 (3), 259-265. doi: 10.1677/jme.0.0150259

  • MONTGOMERY, GW, PENTY, JM, HENRY, HM, SISE, JA, LORD, EA, DODDS, KG and HILL, DF (1995). SHEEP LINKAGE MAPPING - RFLP MARKERS FOR COMPARATIVE MAPPING STUDIES. Animal Genetics, 26 (4), 249-259. doi: 10.1111/j.1365-2052.1995.tb03252.x

  • CRAWFORD, AM, DODDS, KG, EDE, AJ, PIERSON, CA, MONTGOMERY, GW, GARMONSWAY, HG, BEATTIE, AE, DAVIES, K, MADDOX, JF, KAPPES, SW, STONE, RT, NGUYEN, TC, PENTY, JM, LORD, EA, BROOM, JE, BUITKAMP, J, SCHWAIGER, W, EPPLEN, JT, MATTHEW, P, MATTHEWS, ME, HULME, DJ, BEH, KJ, MCGRAW, RA and BEATTIE, CW (1995). AN AUTOSOMAL GENETIC-LINKAGE MAP OF THE SHEEP GENOME. Genetics, 140 (2), 703-724.

  • MONTGOMERY, GW, PENTY, JM, LORD, EA, BROOKS, J and MCNEILLY, AS (1995). THE GONADOTROPIN-RELEASING-HORMONE RECEPTOR MAPS TO SHEEP CHROMOSOME-6 OUTSIDE OF THE REGION OF THE FECB LOCUS. Mammalian Genome, 6 (6), 436-438. doi: 10.1007/BF00355648

  • PENTY, JM, LORD, EA, DODDS, KG, GALLOWAY, SM and MONTGOMERY, GW (1995). LINKAGE OF LHB AND MAG TO GPI ON SHEEP CHROMOSOME-14. Mammalian Genome, 6 (4), 299-300. doi: 10.1007/BF00352421

  • Crawford, A. M., Dodds, K. G., Ede, A. J., Pierson, C. A., Montgomery, G. W., Garmonsway, H. G., Beattie, A. E., Davies, K., Maddox, J. F., Kappes, S. W., Stone, R. T., Nguyen, T. C., Penty, J. M., Lord, E. A., Broom, J. E., Buitkamp, J., Schwaiger, W., Epplen, J. T. and Matthew, P. (1995). An autosomal genetic linkage map of the sheep genome. Genetics, 140 (2), 703-724.

  • Montgomery, G. W., Penty, J. M., Lord, E. A. and Broom, M. F. (1995). The search for the Booroola (FecB) mutation. Journal of reproduction and fertility. Supplement, 49, 113-121.

  • HANRAHAN, , PENTY, JM and MONTGOMERY, GW (1994). AN APAI POLYMORPHISM AT THE OVINE TISSUE INHIBITOR OF METALLOPROTEINASE LOCUS (TIMP). Animal Genetics, 25 (4), 287-287. doi: 10.1111/j.1365-2052.1994.tb00212.x

  • MONTGOMERY, GW, LORD, EA, PENTY, JM, DODDS, KG, BROAD, TE, CAMBRIDGE, L, SUNDEN, SLF, STONE, RT and CRAWFORD, AM (1994). THE BOOROOLA FECUNDITY (FECB) GENE MAPS TO SHEEP CHROMOSOME-6. Genomics, 22 (1), 148-153. doi: 10.1006/geno.1994.1355

  • CRAWFORD, AM, MONTGOMERY, GW, PIERSON, CA, BROWN, T, DODDS, KG, SUNDEN, SLF, HENRY, HM, EDE, AJ, SWARBRICK, PA, BERRYMAN, T, PENTY, JM and HILL, DF (1994). SHEEP LINKAGE MAPPING - 19 LINKAGE GROUPS DERIVED FROM THE ANALYSIS OF PATERNAL HALF-SIB FAMILIES. Genetics, 137 (2), 573-579.

  • SISE, JA, HANRAHAN, , MONTGOMERY, GW and HILL, DF (1994). GENETIC-LINKAGE OF PROTEOLIPID PROTEIN (PLP) AND THYROXINE-BINDING GLOBULIN (TBG) ON THE OVINE X-CHROMOSOME. Cytogenetics and Cell Genetics, 66 (4), 250-252. doi: 10.1159/000133705

  • PENTY, JM and MONTGOMERY, GW (1993). AN XBA RFLP AT THE OVINE BASIC FIBROBLAST GROWTH-FACTOR LOCUS (FGFB). Animal Genetics, 24 (4), 329-329. doi: 10.1111/j.1365-2052.1993.tb00328.x

  • GOOTWINE, E, SISE, JA, PENTY, JM and MONTGOMERY, GW (1993). THE DUPLICATED GENE COPY OF THE OVINE GROWTH-HORMONE GENE CONTAINS A PVUII POLYMORPHISM IN THE 2ND INTRON. Animal Genetics, 24 (4), 319-321. doi: 10.1111/j.1365-2052.1993.tb00321.x

  • MONTGOMERY, GW, CRAWFORD, AM, PENTY, JM, DODDS, KG, EDE, AJ, HENRY, HM, PIERSON, CA, LORD, EA, GALLOWAY, SM, SCHMACK, AE, SISE, JA, SWARBRICK, PA, HANRAHAN, , BUCHANAN, FC and HILL, DF (1993). THE OVINE BOOROOLA FECUNDITY GENE (FECB) IS LINKED TO MARKERS FROM A REGION OF HUMAN CHROMOSOME-4Q. Nature Genetics, 4 (4), 410-414. doi: 10.1038/ng0893-410

  • Escayg, A. P., Montgomery, G. W., Hickford, J. G. and Bullock, D. W. (1993). A BglII RFLP at the ovine MHC class II DRA locus. Animal Genetics, 24 (3), 217-217. doi: 10.1111/j.1365-2052.1993.tb00292.x

  • Dodds, K. G., Montgomery, G. W. and Tate, M. L. (1993). Testing for linkage between a marker locus and a major gene locus in half-sib families. Journal of Heredity, 84 (1), 43-48. doi: 10.1093/oxfordjournals.jhered.a111275

  • MONTGOMERY, GW, PENTY, JM, SISE, JA and TOU, HM (1992). GENES ENCODING THE ALPHA-CHAINS AND BETA-CHAINS OF FOLLICLE-STIMULATING-HORMONE ARE NOT SITES FOR THE BOOROOLA (FEC(B)) MUTATION IN SHEEP. Journal of Reproduction and Fertility, 95 (3), 895-901.

  • MONTGOMERY, GW, MCNATTY, KP and DAVIS, GH (1992). PHYSIOLOGY AND MOLECULAR-GENETICS OF MUTATIONS THAT INCREASE OVULATION RATE IN SHEEP. Endocrine Reviews, 13 (2), 309-328. doi: 10.1210/er.13.2.309

  • SISE, JA and MONTGOMERY, GW (1992). A PVUII POLYMORPHISM AT THE OVINE CORTICOTROPIN RELEASING HORMONE (CRH) LOCUS. Animal Genetics, 23 (1), 86-86. doi: 10.1111/j.1365-2052.1992.tb00241.x

  • TOU, HM, PENTY, JM and MONTGOMERY, GW (1992). A PVUII RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM AT THE OVINE UNCOUPLING PROTEIN LOCUS. Animal Genetics, 23 (1), 83-83. doi: 10.1111/j.1365-2052.1992.tb00238.x

  • TATE, ML, MANLY, HC, DODDS, KG and MONTGOMERY, GW (1992). GENETIC-LINKAGE ANALYSIS BETWEEN PROTEIN POLYMORPHISMS AND THE FEC(B) MAJOR GENE IN SHEEP. Animal Genetics, 23 (5), 417-424. doi: 10.1111/j.1365-2052.1992.tb02160.x

  • MONTGOMERY, GW, SISE, JA, PENTY, JM, TOU, HM and HILL, DF (1992). SHEEP LINKAGE MAPPING - RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM DETECTION WITH HETEROLOGOUS CDNA PROBES. Animal Genetics, 23 (5), 411-416. doi: 10.1111/j.1365-2052.1992.tb02159.x

  • PENTY, JM and MONTGOMERY, GW (1991). A MSPI RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM AT THE OVINE LOCUS FOR GLUCAGON. Animal Genetics, 22 (5), 440-440. doi: 10.1111/j.1365-2052.1991.tb00707.x

  • PENTY, JM and MONTGOMERY, GW (1991). A PSTI RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM AT THE OVINE LOCUS FOR POLY-UBIQUITIN. Animal Genetics, 22 (5), 438-438. doi: 10.1111/j.1365-2052.1991.tb00705.x

  • SISE, JA, TOU, HM and MONTGOMERY, GW (1991). A TAQI POLYMORPHISM AT THE OVINE ALPHA-INHIBIN LOCUS. Animal Genetics, 22 (2), 195-195. doi: 10.1111/j.1365-2052.1991.tb00666.x

  • PENTY, JM, SISE, JA and MONTGOMERY, GW (1991). RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS AT THE OVINE LOCUS FOR THE ALPHA-SUBUNIT OF PITUITARY GLYCOPROTEIN HORMONES. Animal Genetics, 22 (2), 198-198. doi: 10.1111/j.1365-2052.1991.tb00669.x

  • MONTGOMERY, GW, SISE, JA, GREENWOOD, PJ and FLEMING, JS (1990). THE BOOROOLA F-GENE MUTATION IN SHEEP IS NOT LOCATED CLOSE TO THE FSH-BETA GENE. Journal of Molecular Endocrinology, 5 (2), 167-173. doi: 10.1677/jme.0.0050167

  • Montgomery, G. W. and Sise, J. A. (1990). Extraction of dna from sheep white blood cells. New Zealand Journal of Agricultural Research, 33 (3), 437-441. doi: 10.1080/00288233.1990.10428440

  • BARRELL, GK and MONTGOMERY, GW (1989). ABSENCE OF CIRCADIAN PATTERNS OF SECRETION OF MELATONIN OR CORTISOL IN WEDDELL SEALS UNDER CONTINUOUS NATURAL DAYLIGHT. Journal of Endocrinology, 122 (2), 445-449. doi: 10.1677/joe.0.1220445

  • MONTGOMERY, GW, SCOTT, IC, LITTLEJOHN, RP, DAVIS, GH and PETERSON, AJ (1989). CONCENTRATIONS OF FSH ARE ELEVATED IN NEW-BORN EWE LAMBS CARRYING THE BOOROOLA F-GENE BUT NOT IN LAMBS FROM A PROLIFIC ROMNEY STRAIN. Reproduction Fertility and Development, 1 (4), 299-307. doi: 10.1071/RD9890299

  • Montgomery, G. W., Scott, I. C. and Johnstone, P. D. (1988). Seasonal changes in ovulation rate in coopworth ewes maintained at different liveweights. Animal Reproduction Science, 17 (3-4), 197-205. doi: 10.1016/0378-4320(88)90058-9

  • MONTGOMERY, GW, MARTIN, GB, LOCATELLI, A and PELLETIER, J (1987). EFFECT OF ADRENALECTOMY ON LH-RELEASE IN SHEEP DURING THE ANESTROUS SEASON. Journal of Endocrinology, 114 (3), 437-442. doi: 10.1677/joe.0.1140437

  • MONTGOMERY, GW, MARTIN, GB, BLANC, MR and PELLETIER, J (1987). SEASON INFLUENCES FSH CONCENTRATION IN OVARIECTOMIZED ILE-DE-FRANCE EWES. Journal of Reproduction and Fertility, 80 (1), 271-277. doi: 10.1530/jrf.0.0800271

  • MONTGOMERY, GW and HAWKER, H (1987). SEASONAL REPRODUCTION IN EWES SELECTED ON SEASONAL-CHANGES IN WOOL GROWTH. Journal of Reproduction and Fertility, 79 (1), 207-213. doi: 10.1530/jrf.0.0790207

  • MONTGOMERY, GW, SCOTT, IC and HUDSON, N (1985). AN INTERACTION BETWEEN SEASON OF CALVING AND NUTRITION ON THE RESUMPTION OF OVARIAN CYCLES IN POST-PARTUM BEEF-CATTLE. Journal of Reproduction and Fertility, 73 (1), 45-50. doi: 10.1530/jrf.0.0730045

  • MONTGOMERY, GW, MARTIN, GB and PELLETIER, J (1985). CHANGES IN PULSATILE LH-SECRETION AFTER OVARIECTOMY IN ILE-DE-FRANCE EWES IN 2 SEASONS. Journal of Reproduction and Fertility, 73 (1), 173-183. doi: 10.1530/jrf.0.0730173

  • MONTGOMERY, GW, MARTIN, GB, LEBARS, J and PELLETIER, J (1985). GONADOTROPIN-RELEASE IN OVARIECTOMIZED EWES FED DIFFERENT AMOUNTS OF COUMESTROL. Journal of Reproduction and Fertility, 73 (2), 457-463. doi: 10.1530/jrf.0.0730457

  • Caraty, A., Martin, G. B. and Montgomery, G. (1984). A new method for studying pituitary responsiveness in vivo using pulses of LH-RH analogue in ewes passively immunized against native LH-RH. Reproduction Nutrition Developpement, 24 (4), 439-448. doi: 10.1051/rnd:19840409

  • MCNATTY, KP, HUDSON, N, GIBB, M, HENDERSON, KM, LUN, S, HEATH, D and MONTGOMERY, GW (1984). SEASONAL DIFFERENCES IN OVARIAN ACTIVITY IN COWS. Journal of Endocrinology, 102 (2), 189-198. doi: 10.1677/joe.0.1020189

  • MCNATTY, KP, HEATH, DA, HENDERSON, KM, LUN, S, HURST, PR, ELLIS, LM, MONTGOMERY, GW, MORRISON, L and THURLEY, DC (1984). SOME ASPECTS OF THECAL AND GRANULOSA-CELL FUNCTION DURING FOLLICULAR DEVELOPMENT IN THE BOVINE OVARY. Journal of Reproduction and Fertility, 72 (1), 39-53.

  • Montgomery, G. W., Bray, A. R. and Kelly, R. W. (1983). Ovulation rates of first cross booroola compared with local breed ewes following differential feeding. Animal Reproduction Science, 6 (3), 209-215. doi: 10.1016/0378-4320(83)90039-8

  • Davis, G. H., Montgomery, G. W., Allison, A. J., Kelly, R. W. and Bray, A. R. (1982). Segregation of a major gene influencing fecundity in progeny of Booroola sheep. New Zealand Journal of Agricultural Research, 25 (4), 525-529. doi: 10.1080/00288233.1982.10425216

  • MONTGOMERY, GW (1982). INFLUENCE OF SUCKLING FREQUENCY AND BROMOCRYPTINE TREATMENT ON THE RESUMPTION OF OVARIAN CYCLES IN POSTPARTUM BEEF-CATTLE. Theriogenology, 17 (5), 551-563. doi: 10.1016/0093-691X(82)90181-9

  • MONTGOMERY, GW, FLUX, DS and GREENWAY, RM (1980). TRYPTOPHAN DEFICIENCY IN PIGS - CHANGES IN FOOD-INTAKE AND PLASMA-LEVELS OF GLUCOSE, AMINO-ACIDS, INSULIN AND GROWTH-HORMONE. Hormone and Metabolic Research, 12 (7), 304-309. doi: 10.1055/s-2007-996276

  • MONTGOMERY, GW, FLUX, DS and CARR, (1978). FEEDING PATTERNS IN PIGS - EFFECTS OF AMINO-ACID DEFICIENCY. Physiology & Behavior, 20 (6), 693-698. doi: 10.1016/0031-9384(78)90294-9

Conference Publication

  • Conde, Lucia Colodro, Couvy-Duchesne, Baptiste, Zhu, Gu, Coventry, William, Byrne, Enda, Gordon, Scott, Wright, Margaret, Montgomery, Grant, Madden, Pamela, Ripke, Stephan, Eaves, Lindon, Heath, Andrew, Wray, Naomi, Medland, Sarah E. and Martin, Nick (2019). A direct test of the diathesis-stress model for depression. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL United States, 13-17 October 2017. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2017.08.045

  • Holdsworth-Carson, Sarah J., Girling, Jane, Cann, Leonie, Healey, Martin, Fung, Jenny N., Montgomery, Grant and Rogers, Peter (2019). Expression and Cellular Localization of Endometriosis Risk Gene Long Intergenic Non-Coding RNA 339 (LINC00339). 66th Annual Scientific Meeting of the Society for Reproductive Investigation (SRI), Paris, France, 12-16 March 2019. Thousand Oaks, CA United States: Sage.

  • Holdsworth-Carson, Sarah J., Donoghue, Jacqueline, Colgrave, Eliza, Fung, Jenny N., Churchill, Molly, Healey, Martin, Montgomery, Grant, Girling, Jane and Rogers, Peter (2019). Generation of Immortalized Human Endometrial Stromal Cell Lines with Different Endometriosis Risk Genotypes. 66th Annual Scientific Meeting of the Society-for-Reproductive-Investigation (SRI), Paris, France, 12-16 March 2019. Thousand Oaks, CA, United States: Sage.

  • Mortlock, Sally, Fung, Jenny N., Girling, Jane E., Holdsworth-Carson, Sarah J., Healey, Martin, Lukowski, Samuel W., McKinnon, Brett D., Yang, Jian, McRae, Allan, Rogers, Peter A. W. and Montgomery, Grant W. (2019). Identifying Target Genes for Endometriosis through Integration of Genetic Effects on Transcription and Methylation in Human Endometrium. 66th Annual Scientific Meeting of the Society for Reproductive Investigation (SRI), Paris, France, 12-16 March 2019. Thousand Oaks, CA, United States: Sage.

  • Holdsworth-Carson, Sarah J., Chung, Jessica, Healey, Martin, Fung, Jenny N., Montgomery, Grant, Rogers, Peter and Girling, Jane (2019). Obesity Does Not Impact on Endometrial Gene Expression in Women with Endometriosis. 66th Annual Scientific Meeting of the Society-for-Reproductive-Investigation (SRI), Paris, France, 12-16 March 2019 . Thousand Oaks, CA, United States: Sage.

  • Fung, Jenny N., Mortlock, Sally, Girling, Jane E., Holdsworth-Carson, Sarah J., Teh, Wan Tinn, Healey, Martin, Rogers, Peter A. W. and Montgomery, Grant W. (2018). Dynamic changes in gene regulation in human endometrium. 65th Annual Scientific Meeting of the Society for Reproductive Investigation (SRI), San Diego CA, United States, 6-10 March 2018. Thousand Oaks, CA United States: Sage Publications.

  • Zeng, Jian, de Vlaming, Ronald, Wu, Yang, Robinson, Matthew R., Lloyd-Jones, Luke R., Yengo, Loic, Yap, Chloe X., Xue, Angli, Sidorenko, Julia, Mcrae, Allan F., Powell, Joseph E., Montgomery, Grant W., Metspalu, Andres, Esko, Tonu, Gibson, Greg, Wray, Naomi R., Visscher, Peter M. and Yang, Jian (2018). Signatures of negative selection in the genetic architecture of human complex traits. 48th Annual Meeting of the Behavior-Genetics-Association (BGA), Boston MA, United States, 20-23 June 2018. New York, NY United States: Springer New York.

  • Montgomery, Grant W., Fung, Jenny N., Holdsworth-Carson, Sarah J., Girling, Jane E., Franch, Juliet D., Edwards, Stacey L., Powell, Joseph E. and Rogers, Peter A. W. (2017). Endometriosis and Ovarian Cancer: Shared Genetic Risk and Common Mechanisms.. 64th Annual Scientific Meeting of the Society-for-Reproductive-Investigation (SRI), Orlando Fl, Mar 15-18, 2017. SAGE PUBLICATIONS INC.

  • Rogers, Peter A. W., Holdsworth-Carson, Sarah J., Fung, Jenny N., Colgrave, Eliza M., Paiva, Premila, Girling, Jane E. and Montgomery, Grant W. (2017). Expression Quantitative Trait Loci (eQTL) Approaches for Understanding the Genetics of Endometriosis.. 64th Annual Scientific Meeting of the Society-for-Reproductive-Investigation (SRI), Orlando Fl, Mar 15-18, 2017. SAGE PUBLICATIONS INC.

  • Conde, Lucia Colodro, Paternoster, Lavinia, Lind, Penelope, Painter, Jodie, Wright, Margaret, Montgomery, Grant, Martin, Nicholas, Nyholt, Dale and Medland, Sarah (2017). Genetic correlation between nausea and vomiting during pregnancy and major depressive disorder. 47th Annual Meeting of the Behavior-Genetics-Association (BGA), Oslo, Norway, 28 June-1 July 2017. New York, NY United States: Springer New York.

  • Conde, Lucia Colodro, Couvy-Duchesne, Baptiste, Lind, Penelope, Painter, Jodie, Wright, Margie, Montgomery, Grant, Nyholt, Dale and Medland, Sarah E. (2017). Genetic risk for major depressive disorder as a predictor of nausea and vomiting during pregnancy. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto, Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier.

  • Rogers, Peter A. W., Adamson, G. David, Al-Jefout, Moamar, Becker, Christian M., D'Hooghe, Thomas M., Dunselman, Gerard A. J., Fazleabas, Asgerally, Giudice, Linda C., Horne, Andrew W., Hull, M. Louise, Hummelshoj, Lone, Missmer, Stacey A., Montgomery, Grant W., Stratton, Pamela, Taylor, Robert N., Rombauts, Luk, Saunders, Philippa T., Vincent, Katy and Zondervan, Krina T. (2017). Research priorities for endometriosis: recommendations from a global consortium of investigators in endometriosis. 3rd International Consensus Workshop on Research Directions in Endometriosis, São Paulo, Brazil, 4 May 2014. Thousand Oaks, CA, United States: Sage Publications. doi: 10.1177/1933719116654991

  • Warrington, Nicole, Hemani, Gibran, Hysi, Pirro, Mangino, Massimo, McMahon, George, Hickey, Martha, Wolke, Dieter, Montgomery, Grant, Pennell, Craig, Spector, Tim, Martin, Nicholas, Medland, Sarah and Evans, David (2016). Genome-wide association study of 6,939 individuals identifies five novel loci and suggests that prenatal exposure to testosterone is not a major determinant of individual differences in 2D:4D finger ratio. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane Australia, Jun 20-23, 2016.

  • von Schuckmann, L. A., Law, M. H., Montgomery, G. W., Green, A. C. and van der Pols, J. C. (2015). Vitamin D receptor polymorphisms and keratinocyte skin cancers: a cohort study and meta-analysis. Australasian College of Dermatologists 48th Annual Scientific Meeting, Adelaide, Australia, 16 May 2015. Richmond, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/ajd.12337

  • Merriman, T., Phipps-Green, A., Topless, R., Merriman, M., Franklin, C., Jones, G., van Rij, A., Montgomery, G., Chapman, B., White, D., Stamp, L. and Dalbeth, N. (2014). Association analysis of 18 recently discovered serum urate loci with gout. 15th Annual European Congress of Rheumatology (EULAR), Paris, France, 11-14 June 2014. doi: 10.1136/annrheumdis-2014-eular.4679

  • Warstadt, Nicholus M., Jahanshad, Neda, Dennis, Emily L., Kohannim, Omid, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Wright, Margaret J. and Thompson, Paul M. (2014). Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure. Biomedical Imaging ISBI, Beijing, China, 29 April - 2 May, 2014. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2014.6867881

  • Dumenil, T. D., Klein, K., Wockner, L. F., Mckeone, D. M., Bowdler, L. M., Montgomery, G. W., Leggett, B. A. and Whitehall, V. L. J. (2014). Integrated genome wide DNA methylation and gene expression analysis identifies subgroups of colorectal cancer with distinct molecular and clinical features. Australian Gastroenterology Week 2014, Broadbeach, QLD Australia, 22‐24 October 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia.

  • Whitehall, V. L. J., Dumenil, T. D., Mckeone, D. M., Bond, C. E., Bettington, M. L., Buttenshaw, R. L., Bowdler, L., Montgomery, G. W., Wockner, L. F. and Leggett, B. A. (2014). Isocitrate Dehydrogenase 1 R132C mutation occurs exclusively in microsatellite stable colorectal cancers with the CpG island methylator phenotype. Australian Gastroenterology Week 2014, Broadbeach, QLD Australia, 22‐24 October 2014.

  • Ebejer, Jane, Medland, Sarah, Martin, Nick G., Wright, Margaret, Montgomery, Grant, Powell, Joseph, Visscher, Peter and Duffy, David (2013). Clarification of varying genetic expression and structure within adolescent monozygotic and dizygotic twins discordant for high and low attention and activity. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, 28 June-02 July 2013. New York, NY United States: Springer New York LLC. doi: 10.1007/s10519-013-9623-9

  • Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Weiner, Michael W. and Thompson, Paul M. (2013). Exhaustive search of the SNP-SNP interactome identifies epistatic effects on brain volume in two cohorts. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40760-4_75

  • Hibar, Derrek P., Medland, Sarah E., Stein, Jason L., Kim, Sungeun, Shen, Li, Saykin, Andrew J., de Zubicaray, Greig I., McMahon, Katie L, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Djurovic, Srdjan, Agartz, Ingrid A., Andreassen, Ole A. and Thompson, Paul M. (2013). Genetic clustering on the hippocampal surface for genome-wide association studies. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40763-5_85

  • Luciano, Michelle, Evans, David, Hansell, Narelle, Medland, Sarah, Montgomery, Grant, Martin, Nick G., Wright, Margaret and Bates, Timothy (2013). Genome-wide association for reading and language abilities in two population cohorts. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille, France, 28 June-2 July 2013. New York, NY United States: Springer New York.

  • Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Changes in Anatomical Brain Connectivity Between Ages 12 and 30: A HARDI Study of 484 Adolescents and Adults. 9th IEEE International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway NJ, United States: IEEE. doi: 10.1109/ISBI.2012.6235695

  • Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Diffusion imaging protocol effects on genetic associations. International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. NEW YORK: IEEE. doi: 10.1109/ISBI.2012.6235712

  • Jahanshad, Neda, Hibar, Derrek, Ryles, April, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansel, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235605

  • Lendon, Corinne, Handoko, Herlina, Pritchard, Antonia, Lind, Penelope, Bentham, Peter, Montgomery, Grant, Wray, Naomi, Khoo, Soo-Keat, Pachana, Nancy and Byrne, Gerard (2011). Evidence for the involvement of the RSG2 gene in risk for anxiety and related phenotypes in an elderly population not selected for this trait. Alzheimer's Imaging Consortium, Paris, France, July 16-21, 2011. Elsevier. doi: 10.1016/j.jalz.2011.09.153

  • Medland, S. E., Nyholt, D. R., Painter, J. N., McEvoy, B. P., McRae, A. F., Montgomery, G. W. and Martin, N. G. (2010). Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses. 6th World Congress for Hair Research, Cairns, QLD, Australia, 16-19 June 2010. Oxford, United Kingdom: Wiley-Blackwell. doi: 10.1111/j.1600-0625.2010.01097.x

  • Bates, Timothy C., Luciano, Michelle, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2010). Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics Association 40th Annual Meeting, Seoul, Korea, 2-5 June 2010. New York, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7

  • Martin, N., Madden, P., Pergadia, M., Nelson, E., Bucholz, K., Whitfield, J.B., Montgomery, G. and Heath, G. (2010). Genomewide association study of quantitative alcohol phenotypes in community-ascertained families. 2010 World Congress on International Society for Biomedical Research on Alcoholism, Paris, France, 13-16 September 2010. Hoboken, NJ, U.S.A.: Wiley-Blackwell Publishing. doi: 10.1111/j.1530-0277.2010.01292_3.x

  • Wray, Naomi R., Coventry, William L., James, Michael R., Montgomery, Grant W., Eaves, Lindon J. and Martin, Nicholas G. (2008). 4. Use of monozygotic twins to investigate the relationship between 5HTTLPR genotype, depression and stressful life events: An application of Item Response Theory.

  • Montgomery, G. W., Treloar, S. A., Kennedy, S. H. and Zondervan, K. T. (2008). Genetic variation and endometriosis risk. AGES XVIII Annual Scientific Meeting: Art and Science of Endometriosis. WCE 2008: 10th World Congress on Endometriosis, Melbourne, VIC, Australia, 11-14 March 2008. Malden, MA, U.S.A.: Blackwell Publishers.

  • Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2006). Genome-wide scan for loci influencing the P3: An endophenotype for psychopathology. World Congress on Alcohol Research (ISBRA 2006), Sydney, Australia, 10 - 13 September 2006. Oxford: Blackwell Publishing. doi: 10.1111/j.1530-0277.2006.00197.x

  • Treloar, Susan, Hadfield, Ruth, Montgomery, Grant, Lambert, ,Ann, Wicks, Jacki, Barlow, David H., O’Connor, Daniel T., Kennedy, Stephen and International Endogene Study Group (2002). The international endogene study: a collection of families for genetic research in endometriosis. New York: Elsevier. doi: 10.1016/S0015-0282(02)03341-1

Grants (Administered at UQ)

PhD and MPhil Supervision

Current Supervision

  • Doctor Philosophy — Principal Advisor

    Other advisors:

  • Doctor Philosophy — Principal Advisor

    Other advisors:

  • Doctor Philosophy — Associate Advisor

    Other advisors:

  • Doctor Philosophy — Associate Advisor

    Other advisors:

Completed Supervision