Associate Professor Stuart Macgregor

Honorary Associate Professor

Royal Brisbane Clinical Unit
Faculty of Medicine

Overview

Publications

  • French, Juliet D., Johnatty, Sharon E., Lu, Yi, Beesley, Jonathan, Gao, Bo, Kalimutho, Murugan, Henderson, Michelle J., Russell, Amanda J., Kar, Siddhartha, Chen, Xiaoging, Hillman, Kristine M., Kaufmann, S, Sivakumaran H., O'Reilly, Martin, Wang, Chen, Korbie, Darren J., Lambrechts, Diether, Despierre, Evelyn, Van Nieuwenhuysen, Els, Lambrechts, Sandra, Vergote, Ignace, Karlan, Beth, Lester, Jenny, Orsulic, Sandra, Walsh, Christine, Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Matsuo, Keitaro, Hosono, Satoyo, Pisterer, Jacobus, Hillemanns, Peter, Nakanishi, Toru, Yatabe, Yasushi, Goodman, Marc T., Lurie, Galine, Matsuno, Rayna K., Thompson, Pamela J., Pejovic, Tanja, Bean, Yukie, Heitz, Florian, Harter, Philipp, Du Bois, Andreas, Schwaab, Ira, Hogdall, Estrid, Kjaer, Susanne K., Jensen, Allan, Hogdall, Claus, Lundvall, Lene, Engelholm, Svend Aage, Brown, Bob, Flanagan, James M., Metcalf, Michelle D., Siddiqui, Nadeem, Sellers, Thomas, Fridley, Brooke, Cunningham, Julie, Schildkraut, Joellen M., Iversen, Ed, Weber, Rachel Palmieri, Brennan, Donal, Berchuck, Andrew, Pharoah, Paul, Harnett, Paul, Norris, Murray D., Haber, Michelle, Goode, Ellen L., Lee, Jason S., Khanna, Kum Kum, Meyer, Kerstin B., Chenevix-Trench, Georgia, DeFazio, Anna, Edwards, Stacey L. and MacGregor, Stuart (2016) Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. Oncotarget, 7 6: 6353-6368. doi:10.18632/oncotarget.7047

  • Law, Matthew H., Rowe, Casey J., Montgomery, Grant W., Hayward, Nicholas K., MacGregor, Stuart and Khosrotehrani, Kiarash (2015) PARP1 polymorphisms play opposing roles in melanoma occurrence and survival. International Journal of Cancer, 136 10: 2488-2489. doi:10.1002/ijc.29280

  • Cheng C.-Y., Schache M., Ikram M.K., Young T.L., Guggenheim J.A., Vitart V., MacGregor S., Verhoeven V.J.M., Barathi V.A., Liao J., Hysi P.G., Bailey-Wilson J.E., St. Pourcain B., Kemp J.P., McMahon G., Timpson N.J., Evans D.M., Montgomery G.W., Mishra A., Wang Y.X., Wang J.J., Rochtchina E., Polasek O., Wright A.F., Amin N., Van Leeuwen E.M., Wilson J.F., Pennell C.E., Van Duijn C.M., De Jong P.T.V.M., Vingerling J.R., Zhou X., Chen P., Li R., Tay W.-T., Zheng Y., Chew M., Burdon K.P., Craig J.E., Iyengar S.K., Igo Jr. R.P., Lass Jr. J.H., Chew E.Y., Haller T., Mihailov E., Metspalu A., Wedenoja J., Simpson C.L., Wojciechowski R., Hohn R., Mirshahi A., Zeller T., Pfeiffer N., Lackner K.J., Bettecken T., Meitinger T., Oexle K., Pirastu M., Portas L., Nag A., Williams K.M., Yonova-Doing E., Klein R., Klein B.E., Hosseini S.M., Paterson A.D., Makela K.-M., Lehtimaki T., Kahonen M., Raitakari O., Yoshimura N., Matsuda F., Chen L.J., Pang C.P., Yip S.P., Yap M.K.H., Meguro A., Mizuki N., Inoko H., Foster P.J., Zhao J.H., Vithana E., Tai E.-S., Fan Q., Xu L., Campbell H., Fleck B., Rudan I., Aung T., Hofman A., Uitterlinden A.G., Bencic G., Khor C.-C., Forward H., Parssinen O., Mitchell P., Rivadeneira F., Hewitt A.W., Williams C., Oostra B.A., Teo Y.-Y., Hammond C.J., Stambolian D., MacKey D.A., Klaver C.C.W., Wong T.-Y., Saw S.-M. and Baird P.N. (2013) Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. American Journal of Human Genetics, 93 2: 264-277. doi:10.1016/j.ajhg.2013.06.016

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Supervision

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Publications

Journal Article

  • French, Juliet D., Johnatty, Sharon E., Lu, Yi, Beesley, Jonathan, Gao, Bo, Kalimutho, Murugan, Henderson, Michelle J., Russell, Amanda J., Kar, Siddhartha, Chen, Xiaoging, Hillman, Kristine M., Kaufmann, S, Sivakumaran H., O'Reilly, Martin, Wang, Chen, Korbie, Darren J., Lambrechts, Diether, Despierre, Evelyn, Van Nieuwenhuysen, Els, Lambrechts, Sandra, Vergote, Ignace, Karlan, Beth, Lester, Jenny, Orsulic, Sandra, Walsh, Christine, Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Matsuo, Keitaro, Hosono, Satoyo, Pisterer, Jacobus, Hillemanns, Peter, Nakanishi, Toru, Yatabe, Yasushi, Goodman, Marc T., Lurie, Galine, Matsuno, Rayna K., Thompson, Pamela J., Pejovic, Tanja, Bean, Yukie, Heitz, Florian, Harter, Philipp, Du Bois, Andreas, Schwaab, Ira, Hogdall, Estrid, Kjaer, Susanne K., Jensen, Allan, Hogdall, Claus, Lundvall, Lene, Engelholm, Svend Aage, Brown, Bob, Flanagan, James M., Metcalf, Michelle D., Siddiqui, Nadeem, Sellers, Thomas, Fridley, Brooke, Cunningham, Julie, Schildkraut, Joellen M., Iversen, Ed, Weber, Rachel Palmieri, Brennan, Donal, Berchuck, Andrew, Pharoah, Paul, Harnett, Paul, Norris, Murray D., Haber, Michelle, Goode, Ellen L., Lee, Jason S., Khanna, Kum Kum, Meyer, Kerstin B., Chenevix-Trench, Georgia, DeFazio, Anna, Edwards, Stacey L. and MacGregor, Stuart (2016) Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. Oncotarget, 7 6: 6353-6368. doi:10.18632/oncotarget.7047

  • Law, Matthew H., Rowe, Casey J., Montgomery, Grant W., Hayward, Nicholas K., MacGregor, Stuart and Khosrotehrani, Kiarash (2015) PARP1 polymorphisms play opposing roles in melanoma occurrence and survival. International Journal of Cancer, 136 10: 2488-2489. doi:10.1002/ijc.29280

  • Cheng C.-Y., Schache M., Ikram M.K., Young T.L., Guggenheim J.A., Vitart V., MacGregor S., Verhoeven V.J.M., Barathi V.A., Liao J., Hysi P.G., Bailey-Wilson J.E., St. Pourcain B., Kemp J.P., McMahon G., Timpson N.J., Evans D.M., Montgomery G.W., Mishra A., Wang Y.X., Wang J.J., Rochtchina E., Polasek O., Wright A.F., Amin N., Van Leeuwen E.M., Wilson J.F., Pennell C.E., Van Duijn C.M., De Jong P.T.V.M., Vingerling J.R., Zhou X., Chen P., Li R., Tay W.-T., Zheng Y., Chew M., Burdon K.P., Craig J.E., Iyengar S.K., Igo Jr. R.P., Lass Jr. J.H., Chew E.Y., Haller T., Mihailov E., Metspalu A., Wedenoja J., Simpson C.L., Wojciechowski R., Hohn R., Mirshahi A., Zeller T., Pfeiffer N., Lackner K.J., Bettecken T., Meitinger T., Oexle K., Pirastu M., Portas L., Nag A., Williams K.M., Yonova-Doing E., Klein R., Klein B.E., Hosseini S.M., Paterson A.D., Makela K.-M., Lehtimaki T., Kahonen M., Raitakari O., Yoshimura N., Matsuda F., Chen L.J., Pang C.P., Yip S.P., Yap M.K.H., Meguro A., Mizuki N., Inoko H., Foster P.J., Zhao J.H., Vithana E., Tai E.-S., Fan Q., Xu L., Campbell H., Fleck B., Rudan I., Aung T., Hofman A., Uitterlinden A.G., Bencic G., Khor C.-C., Forward H., Parssinen O., Mitchell P., Rivadeneira F., Hewitt A.W., Williams C., Oostra B.A., Teo Y.-Y., Hammond C.J., Stambolian D., MacKey D.A., Klaver C.C.W., Wong T.-Y., Saw S.-M. and Baird P.N. (2013) Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. American Journal of Human Genetics, 93 2: 264-277. doi:10.1016/j.ajhg.2013.06.016

  • Levine, D.M., Ek, W.E., Zhang, R., Liu, X., Onstad, L., Sather, C., Lao-Sirieix, P., Gammon, M.D., Corley, D.A., Shaheen, N.J., Bird, N.C., Hardie, L.J., Murray, L.J., Reid, B.J., Chow, W.-H., Risch ,H.A., Nyren, O., Ye, W., Liu, G., Romero, Y., Bernstein, L., Wu, A.H., Casson, A.G., Chanock, S.J., Harrington, P., Caldas, I., Debiram-Beecham, I., Caldas, C., Hayward, N.K., Pharoah, P.D., Fitzgerald, R.C., MacGregor, S., Whiteman, D.C. and Vaughan, T.L. (2013) A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. Nature Genetics, 45 12: 1487-1493. doi:10.1038/ng.2796

  • Iles M.M., Law M.H., Stacey S.N., Han J., Fang S., Pfeiffer R., Harland M., MacGregor S., Taylor J.C., Aben K.K., Akslen L.A., Avril M.-F., Azizi E., Bakker B., Benediktsdottir K.R., Bergman W., Scarra G.B., Brown K.M., Calista D., Chaudru V., Fargnoli M.C., Cust A.E., Demenais F., De Waal A.C., Debniak T., Elder D.E., Friedman E., Galan P., Ghiorzo P., Gillanders E.M., Goldstein A.M., Gruis N.A., Hansson J., Helsing P., Hocevar M., Hoiom V., Hopper J.L., Ingvar C., Janssen M., Jenkins M.A., Kanetsky P.A., Kiemeney L.A., Lang J., Lathrop G.M., Leachman S., Lee J.E., Lubinski J., MacKie R.M., Mann G.J., Martin N.G., Mayordomo J.I., Molven A., Mulder S., Nagore E., Novakovic S., Okamoto I., Olafsson J.H., Olsson H., Pehamberger H., Peris K., Grasa M.P., Planelles D., Puig S., Puig-Butille J.A., Randerson-Moor J., Requena C., Rivoltini L., Rodolfo M., Santinami M., Sigurgeirsson B., Snowden H., Song F., Sulem P., Thorisdottir K., Tuominen R., Van Belle P., Van Der Stoep N., Van Rossum M.M., Wei Q., Wendt J., Zelenika D., Zhang M., Landi M.T., Thorleifsson G., Bishop D.T., Amos C.I., Hayward N.K., Stefansson K., Bishop J.A.N. and Barrett J.H. (2013) A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics, 45 4: 428-432. doi:10.1038/ng.2571

  • Liu H., Wang L.-E., Liu Z., Chen W.V., Amos C.I., Lee J.E., Iles M.M., Law M.H., Barrett J.H., Montgomery G.W., Taylor J.C., Macgregor S., Cust A.E., Bishop J.A.N., Hayward N.K., Bishop D.T., Mann G.J., Affleck P. and Wei Q. (2013) Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk. Carcinogenesis, 34 4: 885-892. doi:10.1093/carcin/bgs407

  • Qian, J., Liu, H., Wei, S., Liu, Z., Li,Y., Wang, L..-E., Chen, W.V., Amos, C.I., Lee, J.E., Iles, M.M., Law, M.H., Cust, A.E., Barrett, J.H., Montgomery, G.W., Taylor, J., Bishop, J.A.N., Macgregor, S., Bishop, D.T., Mann, G.J., Hayward, N.K. and Wei, Q. (2013) Association between putative functional variants in the PSMB9 gene and risk of melanoma - re-analysis of published melanoma genome-wide association studies. Pigment Cell and Melanoma Research, 26 3: 392-401. doi:10.1111/pcmr.12069

  • Law, Matthew H., MacGregor, Stuart and Hayward, Nicholas K. (2012) Melanoma genetics: Recent findings take us beyond well-traveled pathways. Journal of Investigative Dermatology, 132 7: 1763-1774. doi:10.1038/jid.2012.75

  • 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

  • Yokoyama, Satoru, Woods, Susan L., Boyle, Glen M., Aoude, Lauren G., MacGregor, Stuart, Zismann, Victoria, Gartside, Michael, Cust, Anne E., Haq, Rizwan, Harland, Mark, Taylor, John C., Duffy, David L., Holohan, Kelly, Dutton-Regester, Ken, Palmer, Jane M., Bonazzi, Vanessa, Stark, Mitchell S., Symmons, Judith, Law, Matthew H., Schmidt, Christopher, Lanagan, Cathy, O'Connor, Linda, Holland, Elizabeth A., Schmid, Helen, Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Jenkins, Mark A., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Hopper, John L., Whiteman, David C., Pharoah, Paul D., Easton, Douglas F., Dunning, Alison M., Newton-Bishop, Julia A., Montgomery, Grant W., Martin, Nicholas G., Mann, Graham J., Bishop, D. Timothy, Tsao, Hensin, Trent, Jeffrey M., Fisher, David E., Hayward, Nicholas K. and Brown, Kevin M. (2011) A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 480 7375: 99-103. doi:10.1038/nature10630

  • Amos, Christopher I., Wang, Li-E, Lee, Jeffrey E., Gershenwald, Jeffrey E., Chen, Wei V., Fang, Shenying, Kosoy, Roman, Zhang, Mingfeng, Qureshi, Abrar A., Vattathil, Selina, Schacherer, Christopher W., Gardner, Julie M., Wang, Yuling, Bishop, D. Tim, Barrett, Jennifer H., MacGregor, Stuart, Hayward, Nicholas K., Martin, Nicholas G., Duffy, David L., Mann, Graham J., Cust, Anne, Hopper, John, Brown, Kevin M., Grimm, Elizabeth A., Xu, Yaji, Han, Younghun, Jing, Kaiyan, McHugh, Caitlin, Laurie, Cathy C., Doheny, Kim F., Pugh, Elizabeth W., Seldin, Michael F., Han, Jiali and Wei, Qingyi (2011) Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Human Molecular Genetics, 20 24: 5012-5023. doi:10.1093/hmg/ddr415

  • MacGregor, Stuart, Montgomery, Grant W., Liu, Jimmy Z., Zhao, Zhen Zhen, Henders, Anjali K., Stark, Mitchell, Schmid, Helen, Holland, Elizabeth A., Duffy, David L., Zhang, Mingfeng, Painter, Jodie N., Nyholt, Dale R., Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Cust, Anne E., Jenkins, Mark A., Whiteman, David C., Olsson, Hakan, Puig, Susana, Bianchi-Scarra, Giovanna, Hansson, Johan, Demenais, Florence, Landi, Maria Teresa, Debniak, Tadeusz, Mackie, Rona, Azizi, Esther, Bressac-de Paillerets, Brigitte, Goldstein, Alisa M., Kanetsky, Peter A., Gruis, Nelleke A., Elder, David E., Newton-Bishop, Julia A., Bishop, D. Timothy, Iles, Mark M., Helsing, Per, Amos, Christopher I., Wei, Qingyi, Wang, Li-E, Lee, Jeffrey E., Qureshi, Abrar A., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Han, Jiali, Hopper, John L., Trent, Jeffrey M., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Hayward, NK and Hayward, Nicholas K. (2011) Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature Genetics, 43 11: 1114-1118. doi:10.1038/ng.958

  • Beesley, Jonathan, Pickett, Hilda A., Johnatty,Sharon E., Dunning, Alison M., Chen, Xiaoqing, Li, Jun, Michailidou, Kyriaki, Lu, Yi, Rider, David N., Palmieri, Rachel T., Stutz, Michael D., Lambrechts, Diether, Despierre, Evelyn, Lambrechts, Sandrina, Vergote, Ignace, Chang-Claude, Jenny, Nickels, Stefan, Vrieling, Alina, Flesch-Janys, Dieter, Wang-Gohrke, Shan, Eilber, Ursula, Bogdanova, Natalia, Antonenkova, Natalia, Runnebaum, Ingo B., Dörk, Thilo, Goodman, Marc T., Lurie, Galina, Wilkens, Lynne R., Matsuno, Rayna K., Kiemeney, Lambertus A., Aben, Katja K.H., Marees, Tamara, Massuger, Leon F. A. G., Fridley, Brooke L., Vierkant, Robert A., Bandera, Elisa V., Olson, Sara H., Orlow, Irene, Rodriguez-Rodriguez, Lorna, Cook, Linda S., Le, Nhu D., Brooks-Wilson, Angela, Kelemen, Linda E., Campbell, Ian, Gayther, Simon A., Ramus, Susan J., Gentry-Maharaj, Aleksandra, Menon, Usha, Ahmed, Shahana, Baynes, Caroline, Pharoah, Paul D., kConFab Investigators, Australian Ovarian Cancer Study Group, ABCTB Investigators, Muir, Kenneth, Lophatananon, Artitaya, Chaiwerawattana, Arkom, Wiangnon, Surapon, Macgregor, Stuart, Easton, Douglas F., Reddel, Roger R., Goode, Ellen L., Chenevix-Trench, Georgia and on behalf of the Ovarian Cancer Association Consortium (2011) Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers. PLoS One, 6 9: e24987 .1-e24987 .6. doi:10.1371/journal.pone.0024987

  • Huang, R. Stephanie, Johnatty, Sharon E., Gamazon, Eric R., Im, Hae Kyung, Ziliak, Dana, Duan, Shiwei, Zhang, Wei, Kistner, Emily O., Chen, Peixian, Beesley, Jonathan, Mi, Shuangli, O'Donnell, Peter H., Fraiman, Yarden S., Das, Soma, Cox, Nancy J., Lu, Yi, MacGregor, Stuart, Goode, Ellen L., Vierkant, Robert A., Fridley, Brooke L., Hogdall, Estrid, Kjaer, Susanne K., Jensen, Allan, Moysich, Kirsten B., Grasela, Matthew, Odunsi, Kunle, Brown, Robert, Paul, Jim, Lambrechts, Diether, Despierre, Evelyn, Vergote, Ignace, Gross, Jenny, Karlan, Beth Y., deFazio, Anna, Chenevix-Trench, Georgia, for the Australian Ovarian Cancer Study Group and Dolan, M. Eileen (2011) Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients. Clinical Cancer Research, 17 16: 5490-5500. doi:10.1158/1078-0432.CCR-11-0724

  • Pharoah, Paul D. P., Palmieri, Rachel T., Ramus, Susan J., Gayther, Simon A., Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia, Antoniou, Antonis C., Beattie, Mary S., Beckmann, Matthias W., Birrer, Michael J., Bogdanova, Natalia, Bolton, Kelly L., Brewster, Wendy, Brooks-Wilson, Angela, Brown, Robert, Butzow, Ralf, Caldes, Trinidad, Caligo, Maria Adelaide, Campbell, Ian, Chang-Claude, Jenny, Chen, Y. Ann, Cook, Linda S., Couch, Fergus J., Cramer, Daniel W., Cunningham, Julie M., Despierre, Evelyn, Doherty, Jennifer A., Doerk, Thilo, Duerst, Matthias, Eccles, Diana M., Ekici, Arif B., Easton, Douglas, Fasching, Peter A., de Fazio, Anna, Fenstermacher, David A., Flanagan, James M., Fridley, Brooke L., Friedman, Eitan, Gao, Bo, Sinilnikova, Olga, Gentry-Maharaj, Aleksandra, Godwin, Andrew K., Goode, Ellen L., Goodman, Marc T., Gross, Jenny, Hansen, Thomas V. O., Harnett, Paul, Rookus, Matti, Heikkinen, Tuomas, Hein, Rebecca, Hogdall, Claus, Hogdall, Estrid, Iversen, Edwin S., Jakubowska, Anna, Johnatty, Sharon E., Karlan, Beth Y., Kauff, Noah D., Kaye, Stanley B., Chenevix-Trench, Georgia, Kelemen, Linda E., Kiemeney, Lambertus A., Kjaer, Susanne Krueger, Lambrechts, Diether, LaPolla, James P., Lazaro, Conxi, Le, Nhu D., Leminen, Arto, Leunen, Karin, Levine, Douglas A., Lu, Yi, Lundvall, Lene, Macgregor, Stuart, Marees, Tamara, Massuger, Leon F., McLaughlin, John R., Menon, Usha, Montagna, Marco, Moysich, Kirsten B., Narod, Steven A., Nathanson, Katherine L., Nedergaard, Lotte, Ness, Roberta B., Nevanlinna, Heli, Nickels, Stefan, Osorio, Ana, Paul, Jim, Pearce, Celeste Leigh, Phelan, Catherine M., Pike, Malcolm C., Radice, Paolo, Rossing, Mary Anne, Schildkraut, Joellen M., Sellers, Thomas A., Singer, Christian F., Song, Honglin, Stram, Daniel O., Sutphen, Rebecca, Lindblom, Annika, Terry, Kathryn L., Tsai, Ya-Yu, van Altena, Anne M., Vergote, Ignace, Vierkant, Robert A., Vitonis, Allison F., Walsh, Christine, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Wu, Anna H., Ziogas, Argyrios, Berchuck, Andrew and Risch, Harvey A. (2011) The role of KRAS rs61764370 in invasive epithelial ovarian cancer: Implications for clinical testing. Clinical Cancer Research, 17 11: 3742-3750. doi:10.1158/1078-0432.CCR-10-3405

  • 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

  • Barrett, Jennifer H., Iles, Mark M., Harland, Mark, Taylor, John C., Aitken, Joanne F., Andresen, Per Arne, Akslen, Lars A., Armstrong, Bruce K., Avril, Marie-Francoise, Azizi, Esther, Bakker, Bert, Bergman, Wilma, Bianchi-Scarrà, Giovanna, Bressac-de Paillerets, Brigitte, Calista, Donato, Cannon-Albright, Lisa A., Corda, Eve, Cust, Anne E., Dębniak, Tadeusz, Duffy, David, Dunning, Alison M., Easton, Douglas F., Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Giles, Graham G., Hansson, Johan, Hocevar, Marko, Höiom, Veronica, Hopper, John L., Ingvar, Christian, Janssen, Bart, Jenkins, Mark A., Jönsson, Göran, Malvehy, Josep, Martin, Nicholas G., Molven, Anders, Montgomery, Grant W., van Nieuwpoort, Frans A., Novakovic, Srdjan, Olsson, Håkan, Pastorino, Lorenza, Puig, Susana, Puig-Butille, Joan Anton, Randerson-Moor, Juliette, Snowden, Helen, Tuominen, Rainer, VanBelle, Patricia, van der Stoep, Nienke, Whiteman, David C., Zelenika, Diana, Han, Jiali, Fang, Shenying, Lee, Jeffrey E., Wei, Qingyi, Lathrop, G. Mark, Gillanders, Elizabeth M., Brown, Kevin M., Goldstein, Alisa M., Kanetsky, Peter A., Mann, Graham J., MacGregor, Stuart, Elder, David E., Amos, Christopher I., Hayward, Nicholas K., Gruis, Nelleke A., Demenais, Florence, Bishop, Julia A. and Bishop, D. Timothy (2011) Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics, 43 11: 1108-1113. doi:10.1038/ng.959

  • Hysi, Pirro G., Young, Terri L., Mackey, David A., Andrew, Toby, Fernandez-Medarde, Alberto, Solouki, Abbas M., Hewitt, Alex W., Macgregor, Stuart, Vingerling, Johannes R., Li, Yi-Ju, Ikram, M. Kamran, Fai, Lee Yiu, Sham, Pak C., Manyes, Lara, Porteros, Angel, Lopes, Margarida C., Carbonaro, Francis, Fahy, Samantha J., Martin, Nicholas G., van Diujn, Cornelia M., Spector, Timothy D., Rahi, Jugnoo S., Santos, Eugenio, Klaver, Caroline C. W. and Hammond, Christopher J. (2010) A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nature Genetics, 42 10: 902-905. doi:10.1038/ng.664

  • Thorleifsson, Gudmar, Walters, G. Bragi, Hewitt, Alex W., Masson, Gisli, Helgason, Agnar, DeWan, Andrew, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Gudjonsson, Sigurjon A., Magnusson, Kristinn P., Stefansson, Hreinn, Lam, Dennis S. C., Tam, Pancy O. S., Gudmundsdottir, Gudrun J., Southgate, Laura, Burdon, Kathryn P., Gottfredsdottir, Maria Soffia, Aldred, Micheala A., Mitchell, Paul, St Clair, David, Collier, David A., Tang, Nelson, Sveinsson, Orn, Macgregor, Stuart, Martin, Nicholas G., Cree, Angela J., Gibson, Jane, MacLeod, Alex, Jacob, Aby, Ennis, Sarah, Young,Terri L., Chan, Juliana C. N., Karwatowski, Wojciech S. S., Hammond, Christopher J., Thordarson, Kristjan, Zhang, Mingzhi, Wadelius, Claes, Lotery, Andrew J., Trembath, Richard C., Pang, Chi Pui, Hoh, Josephine, Craig, Jamie E., Kong, Augustine, Mackey, David A., Jonasson, Fridbert, Thorsteinsdottir, Unnur and Stefansson, Kari (2010) Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics, 42 10: 906-910. doi:10.1038/ng.661

  • Ikram, M. Kamran, Sim, Xueling, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B., Cheung, Ning, Liew, Gerald, Mitchell, Paul, Uitterlinden, Andrew G., Rivadeneira, Fernando, Hofman, Albert, de Jong, Paulus T. V. M., van Kuijn, Cornelia M., Kao, Linda, Cheng, Ching-Yu, Smith, Albert Vernon, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Jonasson, Fridbert, Eiriksdottir, Gudny, Aspelund, Thor, Global BPgen Consortium, Harris, Tamara B., Launer, Lenore J., Taylor, Kent D., Li, Xiaohui, Iyengar, Sudha K., Xi, Quansheng, Sivakumaran, Theru A., Mackey, David A., MacGregor, Stuart, Martin, Nicholas G., Young, Terri L., Bis, Josh C., Wiggins, Kerri L., Heckbert, Susan R., Hammond, Christopher J., Andrew, Toby, Fahy, Samantha, Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Islam, F. M. Amirul, Rotter, Jerome I., McAuley, Annie K., Boerwinkle, Eric, Tai, E. Shyong, Gudnason, Vilmundur, Siscovick, David S., Vingerling, Johannes R. and Wong, Tien Y. (2010) Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genetics, 6 10: 1-12. doi:10.1371/journal.pgen.1001184

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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

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  • Radka Kaneva, Vihra Milanova, Dora Angelicheva, Stuart MacGregor, Christian Kostov, Rositza Vladimirova, Spiridon Aleksiev, Mina Angelova, Vessela Stoyanova, Angeline Loh, Joachim Hallmayer, Luba Kalaydjieva and Assen Jablensky (2008) Bipolar disorder in the Bulgarian Gypsies: Genetic heterogeneity in a young founder population. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 150b 2: 191-201. doi:10.1002/ajmg.b.30775

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Grants (Administered at UQ)

PhD and MPhil Supervision

Current Supervision

  • Doctor Philosophy — Principal Advisor

  • Doctor Philosophy — Principal Advisor

Completed Supervision