Dr Joseph Powell

Senior Research Fellow

Institute for Molecular Bioscience

Affiliate Senior Research Fellow

Queensland Brain Institute
+61 7 334 62611
+61 7 334 66393


Research Interests

  • Disease genomics background
    The last decade has seen a dramatic increase in our understanding of the role of genetic variation in common diseases. In particular, genome-wide association (GWA) studies have catalogued thousands of common genetic variants that affect human diseases. However, the intermediate molecular mechanisms by which this genetic variation predisposes individuals to disease are still poorly understood, impeding the development of effective therapeutic interventions. Research has shown that most GWA variants are not located in protein coding regions and are instead highly enriched for regulatory regions of the genome. This suggests that for most variants, the functional mechanism by which they affect disease susceptibility is via gene regulation. Thus, characterisation of the regulatory architecture of the human genome is essential, not only for understanding basic biology, but also for interpreting GWAS loci. The expression levels of most transcripts are highly heritable and expression quantitative trait loci (eQTL) can be mapped using GWA type approaches. However, the lack of comprehensive eQTL data from a wide variety of human tissues and cell types has resulted in eQTL databases that are biased towards the small group of tissues that are more readily accessible. The pathophysiology of most common diseases is restricted to a limited number of tissue types or organ systems. Therefore, to understand the mechanisms of disease susceptibility and develop preventative and targeted therapies, we ultimately require knowledge of genetic control of regulatory variation in many different tissues.
  • Research areas
    Broadly, our research is focused on three areas: 1. The investigation of differences in the genetic regulation of genes across tissues and cell types. We are interested in whether this can explain some of the tissue specific pathology of disease. 2. The development of novel methodology to provide flexible and efficient approaches to help determine the biological mechanisms underlying human disease. In silico methods are first used as a stepping-stone, prior to collaborating with colleagues to design molecular genomics studies to delineate the exact mechanisms. 3. The development of computational tools and apps to integrate methods and data to aid in the clinical diagnosis of disease using genomic information.

Research Impacts

IMB's computational genomics group, led by Dr Joseph Powell, uses large-scale, high-throughput genomic data to investigate how DNA sequence variants contribute to human disease. Our research engages sophisticated statistical methodology and the use of high performance computing resources for novel analyses and methods development. We are committed to both open-source and reproducible research practices.


  • Bachelor of Science (Honours), University of London
  • Masters of Science, University of Edinburgh
  • PhD - Statistical Genetics, University of Edinburgh


  • Robins, Chloe, McRae, Allan F., Powell, Joseph E., Wiener, Howard W., Aslibekyan, Stella, Kennedy, Elizabeth M., Absher, Devin M., Arnett, Donna K., Montgomery, Grant W., Visscher, Peter M., Cutler, David J. and Conneely, Karen N. (2017) Testing Two Evolutionary Theories of Human Aging with DNA Methylation Data. Genetics, 207 4: 1547-1560. doi:10.1534/genetics.117.300217

  • Lukowski, Samuel W., Lloyd-Jones, Luke R., Holloway, Alexander, Kirsten, Holger, Hemani, Gibran, Yang, Jian, Small, Kerrin, Zhao, Jing, Metspalu, Andres, Dermitzakis, Emmanouil T., Gibson, Greg, Spector, Timothy D., Thiery, Joachim, Scholz, Markus, Montgomery, Grant W., Esko, Tonu, Visscher, Peter M. and Powell, Joseph E. (2017) Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood. Nature Communications, 8 483: . doi:10.1038/s41467-017-00473-z

  • Zeng, Biao, Lloyd-Jones, Luke R., Holloway, Alexander, Marigorta, Urko M., Metspalu, Andres, Montgomery, Grant W., Esko, Tonu, Brigham, Kenneth L., Quyyumi, Arshed A., Idaghdour, Youssef, Yang, Jian, Visscher, Peter M., Powell, Joseph E. and Gibson, Greg (2017) Constraints on eQTL fine mapping in the presence of multisite local regulation of gene expression. G3: Genes Genomes Genetics, 7 8: 2533-2544. doi:10.1534/g3.117.043752

View all Publications


  • Doctor Philosophy

  • (2017) Doctor Philosophy

  • Doctor Philosophy

View all Supervision


Journal Article

  • Robins, Chloe, McRae, Allan F., Powell, Joseph E., Wiener, Howard W., Aslibekyan, Stella, Kennedy, Elizabeth M., Absher, Devin M., Arnett, Donna K., Montgomery, Grant W., Visscher, Peter M., Cutler, David J. and Conneely, Karen N. (2017) Testing Two Evolutionary Theories of Human Aging with DNA Methylation Data. Genetics, 207 4: 1547-1560. doi:10.1534/genetics.117.300217

  • Lukowski, Samuel W., Lloyd-Jones, Luke R., Holloway, Alexander, Kirsten, Holger, Hemani, Gibran, Yang, Jian, Small, Kerrin, Zhao, Jing, Metspalu, Andres, Dermitzakis, Emmanouil T., Gibson, Greg, Spector, Timothy D., Thiery, Joachim, Scholz, Markus, Montgomery, Grant W., Esko, Tonu, Visscher, Peter M. and Powell, Joseph E. (2017) Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood. Nature Communications, 8 483: . doi:10.1038/s41467-017-00473-z

  • Zeng, Biao, Lloyd-Jones, Luke R., Holloway, Alexander, Marigorta, Urko M., Metspalu, Andres, Montgomery, Grant W., Esko, Tonu, Brigham, Kenneth L., Quyyumi, Arshed A., Idaghdour, Youssef, Yang, Jian, Visscher, Peter M., Powell, Joseph E. and Gibson, Greg (2017) Constraints on eQTL fine mapping in the presence of multisite local regulation of gene expression. G3: Genes Genomes Genetics, 7 8: 2533-2544. doi:10.1534/g3.117.043752

  • 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

  • Gerring, Zachary F., Powell, Joseph E., Montgomery, Grant W. and Nyholt, Dale R. (2017) Genome-wide analysis of blood gene expression in migraine implicates immune-inflammatory pathways. Cephalalgia, . doi:10.1177/0333102416686769

  • 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

  • Kassam, Irfahan, Lloyd-Jones, Luke, Holloway, Alexander, Small, Kerrin S., Zeng, Biao, Bakshi, Andrew, Metspalu, Andres, Gibson, Greg, Spector, Tim D., Esko, Tonu, Montgomery, Grant W., Powell, Joseph E., Yang, Jian, Visscher, Peter M. and McRae, Allan F. (2016) Autosomal genetic control of human gene expression does not differ across the sexes. Genome Biology, 17 1: 248.1-248.10. doi:10.1186/s13059-016-1111-0

  • 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

  • Kassam, Irfahan, Qi, Tuan, Lloyd-Jones, Luke, Holloway, Alexander, Bonder, Marc Jan, Henders, Anjali K., Martin, Nicholas G., Powell, Joseph E., Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and McRae, Allan F. (2016) Evidence for mitochondrial genetic control of autosomal gene expression. Human Molecular Genetics, 25 24: 5332-5338. doi:10.1093/hmg/ddw347

  • Hung, Sandy S. C., Chrysostomou, Vicki, Li, Fan, Lim, Jeremiah K. H., Wang, Jiang-Hui, Powell, Joseph E., Tu, Leilei, Daniszewski, Maciej, Lo, Camden, Wong, Raymond C., Crowston, Jonathan G., Pebay, Alice, King, Anna E., Bui, Bang V., Liu, Guei-Sheung and Hewitt, Alex W. (2016) AAV-mediated CRISPR/Cas gene editing of retinal cells in vivo. Investigative Ophthalmology and Visual Science, 57 7: 3470-3476. doi:10.1167/iovs.16-19316

  • Gerring, Zachary, Rodriguez-Acevedo, Astrid J., Powell, Joseph E., Griffiths, Lyn R., Montgomery, Grant W. and Nyholt, Dale R. (2016) Blood gene expression studies in migraine: potential and caveats. Cephalalgia, 36 7: 669-678. doi:10.1177/0333102416628463

  • Holdsworth-Carson, Sarah J., Fung, Jenny N., Luong, Hien T. T., Sapkota, Yadav, Bowdler, Lisa M., Wallace, Leanne, Teh, Wan Tinn, Powell, Joseph E., Girling, Jane E., Healey, Martin, Montgomery, Grant W. and Rogers, Peter A. W. (2016) Endometrial vezatin and its association with endometriosis risk. Human Reproduction, 31 5: 999-1013. doi:10.1093/humrep/dew047

  • 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

  • Shakhbazov, Konstantin, Powell, Joseph E., Hemani, Gibran, Henders, Anjali K., Martin, Nicholas G., Visscher, Peter M., Montgomery, Grant W. and McRae, Allan F. (2016) Shared genetic control of expression and methylation in peripheral blood. BMC Genomics, 17 1: . doi:10.1186/s12864-016-2498-4

  • McKay, Fiona C., Gatt, Prudence N., Fewings, Nicole, Parnell, Grant P., Schibeci, Stephen D., Basuki, Monica A. I., Powell, Joseph E., Goldinger, Anita, Fabis-Pedrini, Marzena J., Kermode, Allan G., Burke, Therese, Vucic, Steve, Stewart, Graeme J. and Booth, David R. (2016) The low EOMES/TBX21 molecular phenotype in multiple sclerosis reflects CD56+ cell dysregulation and is affected by immunomodulatory therapies. Clinical Immunology, 163 96-107. doi:10.1016/j.clim.2015.12.015

  • Pilling, L.C., Joehanes, R., Kacprowski,T., Peters, M., Jansen, R., Karasik, D., Kiel, D.P., Harries, L.W., Teumer, A., Powell, J., Levy, D., Lin, H., Lunetta, K., Munson, P., Bandinelli, S., Henley, W., Hernandez, D., Singleton, A., Tanaka, T., van Grootheest, G., Hofman, A., Uitterlinden, A.G., Biffar, R., Glaser, S., Homuth, G., Malsch, C., Volker, U., Penninx, B., van Meurs, J.B.J., Ferrucci, L., Kocher, T., Murabito, J. and Melzer, D. (2016) Gene transcripts associated with muscle strength: A CHARGE meta-analysis of 7,781 persons. Physiological Genomics, 48 1: 1-11. doi:10.1152/physiolgenomics.00054.2015

  • Peters, Marjolein J., Joehanes, Roby, Pilling, Luke C., Schurmann, Claudia, Conneely, Karen N., Powell, Joseph, Reinmaa, Eva, Sutphin, George L., Zhernakova, Alexandra, Schramm, Katharina, Wilson, Yana A., Kobes, Sayuko, Tukiainen, Taru, Ramos, Yolande F., Goring, Harald H. H., Fornage, Myriam, Liu, Yongmei, Gharib, Sina A., Stranger, Barbara E., De Jager, Philip L., Aviv, Abraham, Levy, Daniel, Murabito, Joanne M., Munson, Peter J., Huan, Tianxiao, Hofman, Albert, Uitterlinden, Andre G., Rivadeneira, Fernando, Van Rooij, Jeroen, Stolk, Lisette, Broer, Linda, Verbiest, Michael M. P. J., Jhamai, Mila, Arp, Pascal, Metspalu, Andres, Tserel, Liina, Milani, Lili, Samani, Nilesh J., Peterson, Part, Kasela, Silva, Codd, Veryan, Peters, Annette, Ward-Caviness, Cavin K., Herder, Christian, Waldenberger, Melanie, Roden, Michael, Singmann, Paula, Zeilinger, Sonja, Illig, Thomas, Homuth, Georg, Grabe, Hans-Jorgen, Volzke, Henry, Steil, Leif, Kocher, Thomas, Murray, Anna, Melzer, David, Yaghootkar, Hanieh, Bandinelli, Stefania, Moses, Eric K., Kent, Jack W., Curran, Joanne E., Johnson, Matthew P., Williams-Blangero, Sarah, Westra, Harm-Jan, McRae, Allan F., Smith, Jennifer A., Kardia, Sharon L. R., Hovatta, Iiris, Perola, Markus, Ripatti, Samuli, Salomaa, Veikko, Henders, Anjali K., Martin, Nicholas G., Smith, Alicia K., Mehta, Divya, Binder, Elisabeth B., Nylocks, K. Maria, Kennedy, Elizabeth M., Klengel, Torsten, Ding, Jingzhong, Suchy-Dicey, Astrid M., Enquobahrie, Daniel A., Brody, Jennifer, Rotter, Jerome I., Chen, Yii-Der I., Houwing-Duistermaat, Jeanine, Kloppenburg, Margreet, Slagboom, P. Eline, Helmer, Quinta, Den Hollander, Wouter, Bean, Shannon, Raj, Towfique, Bakhshi, Noman, Wang, Qiao Ping, Oyston, Lisa J., Psaty, Bruce M., Tracy, Russell P., Montgomery, Grant W., Turner, Stephen T., Blangero, John, Meulenbelt, Ingrid, Ressler, Kerry J., Yang, Jian, Franke, Lude, Kettunen, Johannes, Visscher, Peter M., Neely, G. Gregory, Korstanje, Ron, Hanson, Robert L., Prokisch, Holger, Ferrucci, Luigi, Esko, Tonu, Teumer, Alexander, Van Meurs, Joyce B. J., Johnson, Andrew D., Nalls, Michael A., Hernandez, Dena G., Cookson, Mark R., Gibbs, Raphael J., Hardy, John, Ramasamy, Adaikalavan, Zonderman, Alan B., Dillman, Allissa, Traynor, Bryan, Smith, Colin, Longo, Dan L., Trabzuni, Daniah, Troncoso, Juan, Van Der Brug, Marcel, Weale, Michael E., O'Brien, Richard, Johnson, Robert, Walker, Robert, Zielke, Ronald H., Arepalli, Sampath, Ryten, Mina, Singleton, Andrew B. and NABEC/UKBEC Consortium (2015) The transcriptional landscape of age in human peripheral blood. Nature Communications, 6 8570.1-8570.14. doi:10.1038/ncomms9570

  • Robinson, Matthew R., Hemani, Gibran, Medina-Gomez, Carolina, Mezzavilla, Massimo, Esko, Tonu, Shakhbazov, Konstantin, Powell, Joseph E., Vinkhuyzen, Anna, Berndt, Sonja I., Gustafsson, Stefan, Justice, Anne E., Kahali, Bratati, Locke, Adam E., Pers, Tune H., Vedantam, Sailaja, Wood, Andrew R., van Rheenen, Wouter, Andreassen, Ole A., Gasparini, Paolo, Metspalu, Andres, van den Berg, Leonard H., Veldink, Jan H., Rivadeneira, Fernando, Werge, Thomas M., Abecasis, Goncalo R., Boomsma, Dorret I., Chasman, Daniel I., de Geus, Eco J. C., Frayling, Timothy M., Hirschhorn, Joel N., Hottenga, Jouke Jan, Ingelsson, Erik, Loos, Ruth J. F., Magnusson, Patrik K. E., Martin, Nicholas G., Montgomery, Grant W., North, Kari E., Pedersen, Nancy L., Spector, Timothy D., Speliotes, Elizabeth K., Goddard, Michael E., Yang, Jian and Visscher, Peter M. (2015) Population genetic differentiation of height and body mass index across Europe. Nature Genetics, 47 11: 1357-1361. doi:10.1038/ng.3401

  • Gibson, Greg, Powell, Joseph E. and Marigorta, Urko M. (2015) Expression quantitative trait locus analysis for translational medicine. Genome Medicine, 7 1: 1-14. doi:10.1186/s13073-015-0186-7

  • Goldinger, Anita, Shakhbazov, Konstantin, Henders, Anjali K., McRae, Allan F., Montgomery, Grant W. and Powell, Joseph E. (2015) Seasonal effects on gene expression. PLoS ONE, 10 5: 1-16. doi:10.1371/journal.pone.0126995

  • McGovern, Alice E, Driessen, Alexandria K, Simmons, David G, Powell, Joseph, Davis-Poynter, Nicholas, Farrell, Michael J and Mazzone, Stuart B (2015) Distinct brainstem and forebrain circuits receiving tracheal sensory neuron inputs revealed using a novel conditional anterograde transsynaptic viral tracing system.. Journal of Neuroscience, 35 18: 7041-7055. doi:10.1523/JNEUROSCI.5128-14.2015

  • Robinson, Philip C., Claushuis, Theodora A. M., Cortes, Adrian, Martin, Tammy M., Evans, David M., Leo, Paul, Mukhopadhyay, Pamela, Bradbury, Linda A., Cremin, Katie, Harris, Jessica, Maksymowych, Walter P., Inman, Robert D., Rahman, Proton, Haroon, Nigil, Gensler, Lianne, Powell, Joseph E., Van Der Horst-Bruinsma, Irene E., Hewitt, Alex W., Craig, Jamie E., Lim, Lyndell L., Wakefield, Denis, McCluskey, Peter, Voigt, Valentina, Fleming, Peter, Spondyloarthritis Research Consortium of Canada, Australio-Anglo-American Spondylitis Consortium, International Genetics of Ankylosing Spondylitis Consortium, Wellcome Trust Case Control Study 2, Degli-Esposti, Mariapia, Pointon, Jennifer J., Weisman, Michael H., Wordsworth, B. Paul, Reveille, John D., Rosenbaum, James T. and Brown, Matthew A. (2015) Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis. Arthritis and Rheumatology, 67 1: 140-151. doi:10.1002/art.38873

  • Wood, Andrew R., Esko, Tonu, Yang, Jian, Vedantam, Sailaja, Pers, Tune H., Gustafsson, Stefan, Chu, Audrey Y., Estrada, Karol, Luan, Jian'an, Kutalik, Zoltan, Amin, Najaf, Buchkovich, Martin L., Croteau-Chonka, Damien C., Day, Felix R., Duan, Yanan, Fall, Tove, Fehrmann, Rudolf, Ferreira, Teresa, Jackson, Anne U., Karjalainen, Juha, Lo, Ken Sin, Locke, Adam E., Magi, Reedik, Mihailov, Evelin, Porcu, Evelin, Randall, Joshua C., Scherag, Andre, Vinkhuyzen, Anne A. E., Westra, Harm-Jan, Winkler, Thomas W., Workalemahu, Tsegaselassie, Zhao, Jing Hua, Absher, Devin, Albrecht, Eva, Anderson, Denise, Baron, Jeffrey, Beekman, Marian, Demirkan, Ayse, Ehret, Georg B., Feenstra, Bjarke, Feitosa, Mary F., Fischer, Krista, Fraser, Ross M., Goel, Anuj, Gong, Jian, Justice, Anne E., Kanoni, Stavroula, Kleber, Marcus E., Kristiansson, Kati, Lim, Unhee, Lotay, Vaneet, Lui, Julian C., Mangino, Massimo, Leach, Irene Mateo, Medina-Gomez, Carolina, Nalls, Michael A., Nyholt, Dale R., Palmer, Cameron D., Pasko, Dorota, Pechlivanis, Sonali, Prokopenko, Inga, Ried, Janina S., Ripke, Stephan, Shungin, Dmitry, Stancakova, Alena, Strawbridge, Rona J., Sung, Yun Ju, Tanaka, Toshiko, Teumer, Alexander, Trompet, Stella, van der Laan, Sander W., van Setten, Jessica, Van Vliet-Ostaptchouk, Jana V., Wang, Zhaoming, Yengo, Loic, Zhang, Weihua, Afzal, Uzma, Arnlov, Johan, Arscott, Gillian M., Bandinelli, Stefania, Barrett, Amy, Bellis, Claire, Bennett, Amanda J., Berne, Christian, Bluher, Matthias, Bolton, Jennifer L., Bottcher, Yvonne, Boyd, Heather A., Bruinenberg, Marcel, Buckley, Brendan M., Buyske, Steven, Caspersen, Ida H., Chines, Peter S., Clarke, Robert, Claudi-Boehm, Simone, Cooper, Matthew, Daw, E. Warwick, De Jong, Pim A., Deelen, Joris, Delgado, Graciela, Denny, Josh C., Dhonukshe-Rutten, Rosalie, Dimitriou, Maria, Doney, Alex S. F., Dorr, Marcus, Eklund, Niina, Eury, Elodie, Folkersen, Lasse, Garcia, Melissa E., Geller, Frank, Giedraitis, Vilmantas, Go, Alan S., Grallert, Harald, Grammer, Tanja B., Grassler, Jurgen, Gronberg, Henrik, de Groot, Lisette C. P. G. M., Groves, Christopher J., Haessler, Jeffrey, Hall, Per, Haller, Toomas, Hallmans, Goran, Hannemann, Anke, Hartman, Catharina A., Hassinen, Maija, Hayward, Caroline, Heard-Costa, Nancy L., Helmer, Quinta, Hemani, Gibran, Henders, Anjali K., Hillege, Hans L., Hlatky, Mark A., Hoffmannm Wolfgang, Hoffmann, Per, Holmen, Oddgeir, Houwing-Duistermaat, Jeanine J., Illig, Thomas, Isaacs, Aaron, James, Alan L., Jeff, Jarina, Johansen, Berit, Johansson, Asa, Jolley, Jennifer, Juliusdottir, Thorhildur, Junttila, Juhani, Kho, Abel N., Kinnunen, Leena, Klopp, Norman, Kocher, Thomas, Kratzer, Wolfgang, Lichtner, Peter, Lind, Lars, Lindstrom, Jaana, Lobbens, Stephane, Lorentzon, Matthias, Lu, Yingchang, Lyssenko, Valeriya, Magnusson, Patrik K. E., Mahajan, Anubha, Maillard, Marc, McArdle, Wendy L., McKenzie, Colin A., McLachlan, Stela, McLaren, Paul J., Menni, Cristina, Merger, Sigrun, Milani, Lili, Moayyeri, Alireza, Monda, Keri L., Morken, Mario A., Muller, Gabriele, Muller-Nurasyid, Martina, Musk, Arthur W., Narisu, Narisu, Nauck, Matthias, Nolte, Ilja M., Nothen, Markus M., Oozageer, Laticia, Pilz, Stefan, Rayner, Nigel W., Renstrom, Frida, Robertson, Neil R., Rose, Lynda M., Roussel, Ronan, Sanna, Serena, Scharnagl, Hubert, Scholtens, Salome, Schumacher, Fredrick R., Schunkert, Heribert, Scott, Robert A., Sehmi, Joban, Seufferlein, Thomas, Shi, Jianxin, Silventoinen, Karri, Smit, Johannes H., Smith, Albert Vernon, Smolonska, Joanna, Stanton, Alice V., Stirrups, Kathleen, Stott, David J., Stringham, Heather M., Sundstrom, Johan, Swertz, Morris A., Syvanen, Ann-Christine, Tayo, Bamidele O., Thorleifsson, Gudmar, Tyrer, Jonathan P., van Dijk, Suzanne, van Schoor, Natasja M., van der Velde, Nathalie, van Heemst, Diana, van Oort, Floor V. A., Vermeulen, Sita H., Verweij, Niek, Vonk, Judith M., Waite, Lindsay L., Waldenberger, Melanie, Wennauer, Roman, Wilkens, Lynne R., Willenborg, Christina, Wilsgaard, Tom, Wojczynski, Mary K., Wong, Andrew, Wright, Alan F., Zhang, Qunyuan, Arveiler, Dominique, Bakker, Stephan J. L., Beilby, John, Bergman, Richard N., Bergmann, Sven, Biffar, Reiner, Blangero, John, Boomsma, Dorret I., Bornstein, Stefan R., Bovet, Pascal, Brambilla, Paolo, Brown, Morris J., Campbell, Harry, Caulfield, Mark J., Chakravarti, Aravinda, Collins, Rory, Collins, Francis S., Crawford, Dana C., Cupples, L. Adrienne, Danesh, John, de Faire, Ulf, den Ruijter Hester M., Erbel, Raimund, Erdmann, Jeanette, Eriksson, Johan G., Farrall, Martin, Ferrannini, Ele, Ferrieres, Jean, Ford, Ian, Forouhi, Nita G., Forrester, Terrence, Gansevoort, Ron T., Gejman, Pablo V., Gieger, Christian, Golay, Alain, Gottesman, Omri, Gudnason, Vilmundur, Gyllensten, Ulf, Haas, David W., Hall, Alistair S., Harris, Tamara B., Hattersley, Andrew T., Heath, Andrew C., Hengstenberg, Christian, Hicks, Andrew A., Hindorff, Lucia A., Hingorani, Aroon D., Hofman, Albert, Hovingh, G. Kees, Humphries, Steve E., Hunt, Steven C., Hypponen, Elina, Jacobs, Kevin B., Jarvelin, Marjo-Riitta, Jousilahti, Pekka, Jula, Antti M., Kaprio, Jaakko, Kastelein, John J. P., Kayser, Manfred, Kee, Frank, Keinanen-Kiukaanniemi, Sirkka M., Kiemeney, Lambertus A., Kooner, Jaspal S., Kooperberg, Charles, Koskinen, Seppo, Kovacs, Peter, Kraja, Aldi T., Kumari, Meena, Kuusisto, Johanna, Lakka, Timo A., Langenberg, Claudia, Le Marchandm Loic, Lehtimaki, Terho, Lupoli, Sara, Madden, Pamela A. F., Mannisto, Satu, Manunta, Paolo, Marette, Andre, Matise, Tara C., McKnight, Barbara, Meitinger, Thomas, Moll, Frans L., Montgomery, Grant W., Morris, Andrew D., Morris, Andrew P., Murray, Jeffrey C., Nelis, Mari, Ohlsson, Claes, Oldehinkel, Albertine J., Ong, Ken K., Ouwehand, Willem H., Pasterkamp, Gerard, Peters, Annette, Pramstaller, Peter P., Price, Jackie F., Qi, Lu, Raitakari, Olli T., Rankinen, Tuomo, Rao, D. C., Rice, Treva K., Ritchie, Marylyn, Rudan, Igor, Salomaa, Veikko, Samani, Nilesh J., Saramies, Jouko, Sarzynski, Mark A., Schwarz, Peter E. H., Sebert, Sylvain, Sever, Peter, Shuldiner, Alan R., Sinisalo, Juha, Steinthorsdottir, Valgerdur, Stolk, Ronald P., Tardif, Jean-Claude, Tonjes, Anke, Tremblay, Angelo, Tremoli, Elena, Virtamo, Jarmo, Vohl, Marie-Claude, Amouyel, Philippe, Asselbergs, Folkert W., Assimes, Themistocles L., Bochud, Murille, Boehm, Bernhard O., Boerwinkle, Eric, Bottinger, Erwin P., Bouchard, Claude, Cauchi, Stephane, Chambers, John C., Chanock, Stephen J., Cooper, Richard S., de Bakker Paul I. W., Dedoussis, George, Ferrucci, Luigi, Franks, Paul W., Froguel, Philippe, Groop, Leif C., Haiman, Christopher A., Hamsten, Anders, Hayes, M. Geoffrey, Hui, Jennie, Hunter, David J., Hveem, Kristian, Jukema, J. Wouter, Kaplan, Robert C., Kivimaki, Mika, Kuh, Diana, Laakso, Markku, Liu, Yongmei, Martin, Nicholas G., Marz, Winfried, Melbye, Mads, Moebus, Susanne, Munroe, Patricia B., Njolstad, Inger, Oostra, Ben A., Palmer, Colin N. A., Pedersen, Nancy L., Perola, Markus, Perusse, Louis, Peters, Ulrike, Powell, Joseph E., Power, Chris, Quertermous, Thomas, Rauramaa, Rainer, Reinmaa, Eva, Ridker, Paul M., Rivadeneira, Fernando, Rotter, Jerome I., Saaristo, Timo E., Saleheen, Danish, Schlessinger, David, Slagboom, P. Eline, Snieder, Harold, Spector, Tim D., Strauch, Konstantin, Stumvoll, Michael, Tuomilehto, Jaakko, Uusitupa, Matti, van der Harst, Pim, Volzke, Henry, Walker, Mark, Wareham, Nicholas J., Watkins, Hugh, Wichmann, H.-Erich, Wilson, James F., Zanen, Pieter, Deloukas, Panos, Heid, Iris M., Lindgren, Cecilia M., Mohlke, Karen L., Speliotes, Elizabeth K., Thorsteinsdottir, Unnur, Barroso, Ines, Fox, Caroline S., North, Kari E., Strachan, David P., Beckmann, Jacques S., Berndt, Sonja I., Boehnke, Michael, Borecki, Ingrid B., McCarthy, Mark I., Metspalu, Andres, Stefansson, Kari, Uitterlinden, Andre G., van Duijn Cornelia M., Franke, Lude, Willer, Cristen J., Price, Alkes L., Lettre, Guillaume, Loos, Ruth J. F., Weedon, Michael N., Ingelsson, Erik, O'Connell, Jeffrey R., Abecasis, Goncalo R., Chasman, Daniel I., Goddard, Michael E., Visscher, Peter M., Hirschhorn, Joel N. and Frayling, Timothy M. (2014) Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46 11: 1173-1186. doi:10.1038/ng.3097

  • Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jian'an, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haeldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer, Kiemeney, Lambertus A., Sweep, Fred C., Sala, Cinzia F., Schwienbacher, Christine, Pichler, Irene, Hui, Jennie, Demirkan, Ayse, Isaacs, Aaron, Amin, Najaf, Steri, Maristella, Waeber, Gerard, Verweij, Niek, Powell, Joseph E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Visscher, Peter M., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Hernandez, Dena, Bandinelli, Stefania, van der Harst, Pim, Uda, Manuela, Vollenweider, Peter, Scott, Robert A., Langenberg, Claudia, Wareham, Nicholas J., van Duijn, Cornelia, Beilby, John, Pramstaller, Peter P., Hicks, Andrew A., Ouwehand, Willem H., Oexle, Konrad, Gieger, Christian, Metspalu, Andres, Camaschella, Clara, Toniolo, Daniela, Swinkels, Dorine W. and Whitfield, John B. (2014) Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature Communications, 5 4926.1-4926.10. doi:10.1038/ncomms5926

  • Hemani, Gibran, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Yang, Jian, Gibson, Greg, Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2014) Another explanation for apparent epistasis: reply. Nature, 514 7520: E5-E6. doi:10.1038/nature13692

  • McKenzie, Marna, Henders, Anjali K., Caracella, Anthony, Wray, Naomi R. and Powell, Joseph E. (2014) Overlap of expression Quantitative Trait Loci (eQTL) in human brain and blood. BMC Medical Genomics, 7 1: 1-11. doi:10.1186/1755-8794-7-31

  • 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

  • Hemani, Gibran, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Yang, Jian, Gibson, Greg, Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2014) Detection and replication of epistasis influencing transcription in humans. Nature, 508 7495: 249-253. doi:10.1038/nature13005

  • Hemani, Gibran, Yang, Jian, Vinkhuyzen, Anna, Powell, Joseph E., Willemsen, Gonneke, Hottenga, Jouke-Jan, Abdellaoui, Abdel, Mangino, Massimo, Valdes, Ana M., Medland, Sarah E., Madden, Pamela A., Heath, Andrew C., Henders, Anjali K., Nyholt, Dale R., de Geus, Eco J. C., Magnusson, Patrik K. E., Ingelsson, Erik, Montgomery, Grant W., Spector, Timothy D., Boomsma, Dorret I., Pedersen, Nancy L., Martin, Nicholas G. and Visscher, Peter M. (2013) Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics, 93 5: 865-875. doi:10.1016/j.ajhg.2013.10.005

  • Revez, J. A., Bain, L., Chapman, B., Powell, J. E., Jansen, R., Duffy, D. L., Tung, J. Y., AAGC Collaborators, Penninx, B. W., Visscher, P. M., De Geus, E. J. C., Boomsma, D. I., Hinds, D. A., Martin, N. G., Montgomery, G. W., Ferreira, M. A. R., Danoy, Patrick and Brown, Matthew A. (2013) A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14 7: 441-446. doi:10.1038/gene.2013.38

  • Ripke, Stephan, O'Dushlaine, Colm, Chambert, Kimberly, Moran, Jennifer L., Kaehler, Anna K., Akterin, Susanne, Bergen, Sarah E., Collins, Ann L., Crowley, James J., Fromer, Menachem, Kim, Yunjung, Lee, Sang Hong, Magnusson, Patrik K. E., Sanchez, Nick, Stahl, Eli A., Williams, Stephanie, Wray, Naomi R., Xia, Kai, Bettella, Francesco, Borglum, Anders D., Bulik-Sullivan, Brendan K., Cormican, Paul, Craddock, Nick, de Leeuw, Christiaan, Durmishi, Naser, Gill, Michael, Golimbet, Vera, Hamshere, Marian L., Holmans, Peter, Hougaard, David M., Kendler, Kenneth S., Lin, Kuang, Morris, Derek W., Mors, Ole, Mortensen, Preben B., Neale, Benjamin M., O'Neill, Francis A., Owen, Michael J., Milovancevic, Milica Pejovic, Posthuma, Danielle, Powell, John, Richards, Alexander L., Riley, Brien P., Ruderfer, Douglas, Rujescu, Dan, Sigurdsson, Engilbert, Silagadze, Teimuraz, Smit, August B., Stefansson, Hreinn, Steinberg, Stacy, Suvisaari, Jaana, Tosato, Sarah, Verhage, Matthijs, Walters, James T., Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2,, Bramon, Elvira, Corvin, Aiden P., O'Donovan, Michael C., Stefansson, Kari, Scolnick, Edward, Purcell, Shaun, McCarroll, Steven A., Sklar, Pamela, Hultman, Christina M., Sullivan, Patrick F., Mowry, Bryan J., Nertney, Deborah A. and Brown, Matthew A (2013) Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics, 45 10: 1150-U282. doi:10.1038/ng.2742

  • 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, Nauck, Matthias, Radke, Doerte, Voelker, Uwe, Perola, Markus, Salomaa, Veikko, Brody, Jennifer, Suchy-Dicey, Astrid, Gharib, Sina A., Enquobahrie, Daniel A., Lumley, Thomas, Montgomery, Grant W., Makino, Seiko, Prokisch, Holger, Herder, Christian, Roden, Michael, Grallert, Harald, Meitinger, Thomas, Strauch, Konstantin, Li, Yang, Jansen, Ritsert C., Visscher, Peter M., Knight, Julian C., Psaty, Bruce M., Ripatti, Samuli, Teumer, Alexander, Frayling, Timothy M., Metspalu, Andres, van Meurs, Joyce B. J. and Franke, Lude (2013) Systematic identification of trans eQTLs as putative drivers of known disease associations. Nature Genetics, 45 10: 1238-U195. doi:10.1038/ng.2756

  • Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Kim, Jinhee, Hemani, Gibran, Martin, Nicholas G., Dermitzakis, Emmanouil T., Gibson, Greg, Montgomery, Grant W. and Visscher, Peter M. (2013) Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics, 9 5: e1003502.1-e1003502.10. doi:10.1371/journal.pgen.1003502

  • Luong, Hien T. T., Painter, Jodie N., Shakhbazov, Konstantin, Chapman, Brett, Henders, Anjali K., Powell, Joseph E, Nyholt, Dale R. and Montgomery, Grant W. (2013) Fine mapping of variants associated with endometriosis in the WNT4 region on chromosome 1p36. International Journal of Molecular Epidemiology and Genetics, 4 4: 193-206.

  • Goldinger, Anita, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2013) Genetic and nongenetic variation revealed for the principal components of human gene expression. Genetics, 195 3: 1117-1128. doi:10.1534/genetics.113.153221

  • Parnell, Grant P., Gatt, Prudence N., McKay, Fiona C., Schibeci, Stephen, Krupa, Malgorzata, Powell, Joseph E., Visscher, Peter M., Montgomery, Grant W., Lechner-Scott, Jeannette, Broadley, Simon, Liddle, Christopher, Slee, Mark, Vucic, Steve, Stewart, Graeme J. and Booth, David R. (2013) Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season. Multiple Sclerosis, 20 6: 675-685. doi:10.1177/1352458513507819

  • Yang, Jian, Loos, Ruth J., Powell, Joseph E., Medland, Sarah E, Speliotes, Elizabeth K., Chasman, Daniel I., Rose, Lynda M., Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Magi, Reedik, Waite, Lindsay, Vernon Smith, Albert, Yerges-Armstrong, Laura M., Monda, Keri L., Hadley, David, Mahajan, Anubha, Li, Guo, Kapur, Karen, Vitart, Veronique, Huffman, Jennifer E., Wang, Sophie R., Palmer, Cameron, Esko, To˜nu, Fischer, Krista, Hua Zhao, Jing, Demirkan, Ayse, Isaacs, Aaron, Feitosa, Mary F., Luan, Jian’an, Heard-Costa, Nancy L., White, Charles, Jackson, Anne U., Preuss, Michael, Ziegler, Andreas, Eriksson, Joel, Kutalik, Zoltan, Frau, Francesca, Nolte, Ilja M., Van Vliet-Ostaptchouk, Jana V., Hottenga, Jouke-Jan, Jacobs, Kevin B., Verweij, Niek, Goel, Anuj, Medina-Gomez, Carolina, Estrada, Karol, Lynn Bragg-Gresham, Jennifer, Sanna, Serena, Sidore, Carlo, Tyrer, Jonathan, Teumer, Alexander, Prokopenko, Inga, Mangino, Massimo, Lindgren, Cecilia M., Assimes, Themistocles L., Shuldiner, Alan R., Hui, Jennie, Beilby, John P., McArdle, Wendy L., Hall, Per, Haritunians, Talin, Zgaga, Lina, Kolcic, Ivana, Polasek, Ozren, Zemunik, Tatijana, Oostra, Ben A., Juhani Junttila, M. Juhani, Gronberg, Henrik, Schreiber, Stefan, Peters, Annette, Hicks, Andrew A., Stephens, Jonathan, Foad, Nicola S., Laitinen, Jaana, Pouta, Anneli, Kaakinen, Marika, Willemsen, Gonneke, Vink, Jacqueline M., Wild, Sarah H., Navis, Gerjan, Asselbergs, Folkert W., Homuth, Georg, John, Ulrich, Iribarren, Carlos, Harris, Tamara, Launer, Lenore, Gudnason, Vilmundur, O'Connell, Jeffrey R., Boerwinkle, Eric, Cadby, Gemma, Palmer, Lyle J., James, Alan L., Musk, Arthur W., Ingelsson, Erik, Psaty, Bruce M., Beckmann, Jacques S., Waeber, Gerard, Vollenweider, Peter, Hayward, Caroline, Wright, Alan F., Rudan, Igor, Groop, Leif C., Metspalu, Andres, Tee Khaw, Kay, van Duijn, Cornelia M., Borecki, Ingrid B., Province, Michael A., Wareham, Nicholas J., Tardif, Jean-Claude, Huikuri, Heikki V., Cupples, L. Adrienne, Atwood, Larry D., Fox, Caroline S., Boehnke, Michael, Collins, Francis S., Mohlke, Karen L., Erdmann, Jeanette, Schunkert, Heribert, Hengstenberg, Christian, Stark, Klaus, Lorentzon, Mattias, Ohlsson, Claes, Cusi, Daniele, Staessen, Jan A., Van der Klauw, Melanie M., Pramstaller, Peter P., Kathiresan, Sekar, Jolley, Jennifer D., Ripatti, Samuli, Jarvelin, Marjo-Riitta, de Geus, Eco J. C., Boomsma, Dorret I., Penninx, Brenda, Wilson, James F., Campbell, Harry, Chanock, Stephen J., van der Harst, Pim, Hamsten, Anders, Watkins, Hugh, Hofman, Albert, Witteman, Jacqueline C., Zillikens, M. Carola, Kiemeney, Lambertus A., Vermeulen, Sita H., Vermeulen, S. H., Abecasis, Goncalo R., Schlessinger, David, Schipf, Sabine, Stumvoll, Michael, Tonjes, Anke, Spector, Tim D., North, Kari E., Lettre, Guillaume, McCarthy, Mark I., Berndt, Sonja I., Heath, Andrew C., Madden, Pamela A. F., Nyholt, Dale, Montgomery, Grant, Martin, Nicolas, McKnight, Barbara, Strachan, David P., Hill, Willaim G., Snieder, Harold, Ridker, Paul M., Thorsteinsdottir, Unnur, Stefansson, Kari, Frayling, Timothy M., Hirschhorn, Joel N., Goddard, Michael E. and Visscher, Peter (2012) FTO genotype is associated with phenotypic variability of body mass index. Nature, 490 7419: 267-272. doi:10.1038/nature11401

  • Gordon, Lavinia, Joo, Jihoon E., Powell, Joseph E., Ollikainen, Miina, Novakovic, Boris, Li, Xin, Andronikos, Roberta, Cruickshank, Mark N., Conneely, Karen N., Smith, Alicia K., Alisch, Reid S., Morley, Ruth, Visscher, Peter M., Craig, Jeffrey M. and Saffery, Richard (2012) Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence. Genome Research, 22 8: 1395-1406. doi:10.1101/gr.136598.111

  • 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: e35430.1-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, 22 456-466. doi:10.1101/gr.126540.111

  • Maugeri, Narelle, Powell, Joseph E., 't Hoen, Peter A. C., de Geus, Eco J. C., Willemsen, Gonneke, Kattenberg, Mathijs, Henders, Anjali K., Wallace, Leanne, Penninx, Brenda, Hottenga, Jouke-Jan, Medland, Sarah E., Saviouk, Viatcheslav, Martin, Nicholas G., Visscher, Peter M., van Ommen, Gert-Jan B., Frazer, Ian H., Boomsma, Dorret I., Montgomery, Grant W. and Ferreira, Manuel A. R (2011) LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts. Human Mutation, 32 8: 873-876. doi:10.1002/humu.21536

  • McEvoy, Brian P., Powell, Joseph E., Goddard, Michael E. and Visscher, Peter M. (2011) Human population dispersal "Out of Africa" estimated from linkage disequilibrium and allele frequencies of SNPs. Genome Research, 21 6: 821-829. doi:10.1101/gr.119636.110

  • Powell, Joseph E., Visscher, Peter M. and Goddard, Michael E. (2010) Reconciling the analysis of IBD and IBS in complex trait studies. Nature Reviews Genetics, 11 11: 800-805. doi:10.1038/nrg2865

Conference Publication

  • McKay, Fiona, Gatt, Prudence N., Fewings, Nicole, Schibeci, Stephen D., Parnell, Grant, Basuki, Monica A. I., Powell, Joseph E., Goldinger, Anita, Fabis-Pedrini, Marzena J., Kermode, Allan G., Burke, Therese, Vucic, Steve, Stewart, Graeme J. and Booth, David R. (2015). Characterising the Molecular Phenotypes of MS: heredity, gene expression modules, dysregulated immune cell subsets and response to therapy. In: MS Research Australia Progress in MS Research Conference, Melbourne, VIC, Australia, (NP3-NP4). 29-30 October 2015. doi:10.1177/1352458515616527

  • 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. In: Behavior Genetics Association 43rd Annual Meeting Abstracts. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, (515-516). 28 June-02 July 2013. doi:10.1007/s10519-013-9623-9

  • Medland, Sarah, Verweij, Karin and Powell, Joseph (2012). Using openMx for GWAS. In: Behavior Genetics Association 42nd Annual Meeting Abstracts. 42nd Annual Meeting of the Behavior Genetics Association, Edinburgh Scotland, (952-952). 22-25 June 2012.

Grants (Administered at UQ)

PhD and MPhil Supervision

Current Supervision

  • Doctor Philosophy — Principal Advisor

  • Doctor Philosophy — Associate Advisor

    Other advisors:

  • Doctor Philosophy — Associate Advisor

Completed Supervision

  • (2017) Doctor Philosophy — Principal Advisor

    Other advisors: