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Professor Peter Visscher
Professor

Peter Visscher

Email: 
Phone: 
+61 7 344 37045

Overview

Background

Visscher joined the University of Queensland in 2011, where he is Professor of Quantitative Genetics. He is a Laureate Fellow of the Australian Research Council. Visscher was elected a Fellow of the Australian Academy of Science in 2010, a Fellow of the Royal Society (London) in 2018 and a Foreign Member of the Royal Netherlands Academy of Arts and Sciences in 2018.

Visscher’s research is about genetic variation for complex traits (including quantitative traits and disease) in populations, with the broad aim to understand and quantify the causes and consequences of human trait variation.

Prof Peter Visscher, Prof Naomi Wray and Prof Jian Yang together comprise the Executive Team of the Program in Complex Trait Genomics (PCTG). PCTG comprises a critical mass of more than 30 post-doctoral researchers plus research assistants and students, all supported by external grant funding. Their skills lie in the ability to develop and apply statistical methods within the framework of quantitative, population and statistical genetics and to use theory to understand and predict results from data analyses. They play leading roles in the international research consortia. The focus of current research activities is in the detection and fine-mapping of loci underlying complex traits (including common disease), based upon theoretical studies and applications of methods to large datasets, in population genetics studies using theoretical approaches and high-density genetic marker data, and in systems genomics studies.

Availability

Professor Peter Visscher is:
Not available for supervision

Fields of research

Qualifications

  • Masters (Coursework) of Science, University of Edinburgh
  • Doctor of Philosophy, University of Edinburgh

Research impacts

Visscher's research focuses on understanding individual differences betweeen people in traits that are important for health outcomes and ageing. A better understanding of the genes that underlie variation in risk to diseases may lead to better treatments.

Works

Search Professor Peter Visscher’s works on UQ eSpace

818 works between 1987 and 2025

341 - 360 of 818 works

2015

Journal Article

Improving phenotypic prediction by combining genetic and epigenetic associations

Shah, Sonia, Bonder, Marc J., Marioni, Riccardo E., Zhu, Zhihong, McRae, Allan F., Zhernakova, Alexandra, Harris, Sarah E., Liewald, Dave, Henders, Anjali K., Mendelson, Michael M., Liu, Chunyu, Joehanes, Roby, Liang, Liming, Levy, Daniel, Martin, Nicholas G., Starr, John M., Wijmenga, Cisca, Wray, Naomi R., Yang, Jian, Montgomery, Grant W., Franke, Luke, Deary, Ian J., Visscher, Peter M. and BIOS Consortium (2015). Improving phenotypic prediction by combining genetic and epigenetic associations. American Journal of Human Genetics, 97 (1), 75-85. doi: 10.1016/j.ajhg.2015.05.014

Improving phenotypic prediction by combining genetic and epigenetic associations

2015

Journal Article

Genetic variation links creativity to psychiatric disorders

Keller, Matthew C. and Visscher, Peter M. (2015). Genetic variation links creativity to psychiatric disorders. Nature Neuroscience, 18 (7), 928-929. doi: 10.1038/nn.4047

Genetic variation links creativity to psychiatric disorders

2015

Journal Article

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

He, Ji, Tang, Lu, Benyamin, Beben, Shah, Sonia, Hemani, Gib, Liu, Rong, Ye, Shan, Liu, Xiaolu, Ma, Yan, Zhang, Huagang, Cremin, Katie, Leo, Paul, Wray, Naomi R., Visscher, Peter M., Xu, Huji, Brown, Matthew A., Bartlett, Perry F., Mangelsdorf, Marie and Fan, Dongsheng (2015). C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis. Neurobiology of Aging, 36 (9) 2660.e1, 2660.e1-2660.e8. doi: 10.1016/j.neurobiolaging.2015.06.002

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

2015

Journal Article

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

Lu, Yi, Cuellar-Partida, Gabriel, Painter, Jodie N., Nyholt, Dale R., Morris, Andrew P., Fasching, Peter A., Hein, Alexander, Burghaus, Stefanie, Beckmann, Matthias W., Lambrechts, Diether, Van Nieuwenhuysen, Els, Vergote, Ignace, Vanderstichele, Adriaan, Doherty, Jennifer Anne, Rossing, Mary Anne, Wicklund, Kristine G., Chang-Claude, Jenny, Eilber, Ursula, Rudolph, Anja, Wang-Gohrke, Shan, Goodman, Marc T., Bogdanova, Natalia, Doerk, Thilo, Duerst, Matthias, Hillemanns, Peter, Runnebaum, Ingo B., Antonenkova, Natalia, Butzow, Ralf, Leminen, Arto ... Visscher, Peter M. (2015). Shared genetics underlying epidemiological association between endometriosis and ovarian cancer. Human Molecular Genetics, 24 (20), 5955-5964. doi: 10.1093/hmg/ddv306

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

2015

Journal Article

Human fertility, molecular genetics, and natural selection in modern societies

Tropf, Felix C., Stulp, Gert, Barban, Nicola, Visscher, Peter M., Yang, Jian, Snieder, Harold and Mills, Melinda C. (2015). Human fertility, molecular genetics, and natural selection in modern societies. Plos One, 10 (6) e0126821, 1-14. doi: 10.1371/journal.pone.0126821

Human fertility, molecular genetics, and natural selection in modern societies

2015

Journal Article

Meta-analysis of the heritability of human traits based on fifty years of twin studies

Polderman, Tinca J. C., Benyamin, Beben, de Leeuw, Christiaan A, Sullivan, Patrick F., van Bochoven, Arjen, Visscher, Peter M. and Posthuma, Danielle (2015). Meta-analysis of the heritability of human traits based on fifty years of twin studies. Nature Genetics, 47 (7), 702-709. doi: 10.1038/ng.3285

Meta-analysis of the heritability of human traits based on fifty years of twin studies

2015

Journal Article

Mixed model with correction for case-control ascertainment increases association power

Hayeck, Tristan J., Zaitlen, Noah A., Loh, Po-Ru, Vilhjalmsson, Bjarni, Pollack, Samuela, Gusev, Alexander, Yang, Jian, Chen, Guo-Bo, Goddard, Michael E., Visscher, Peter M., Patterson, Nick and Price, Alkes L. (2015). Mixed model with correction for case-control ascertainment increases association power. American Journal of Human Genetics, 96 (5), 720-730. doi: 10.1016/j.ajhg.2015.03.004

Mixed model with correction for case-control ascertainment increases association power

2015

Journal Article

Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model

Moser, Gerhard, Lee, Sang Hong, Hayes, Ben J., Goddard, Michael E., Wray, Naomi R. and Visscher, Peter M. (2015). Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model. PLoS Genetics, 11 (4) e1004969, 1-22. doi: 10.1371/journal.pgen.1004969

Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model

2015

Journal Article

Quantitative genetics of disease traits

Wray, N. R. and Visscher, P. M. (2015). Quantitative genetics of disease traits. Journal of Animal Breeding and Genetics, 132 (2), 198-203. doi: 10.1111/jbg.12153

Quantitative genetics of disease traits

2015

Journal Article

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014)

Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jianan, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haelldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2015). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014). Nature Communications, 6 (1) 6542, 1-1. doi: 10.1038/ncomms7542

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014)

2015

Journal Article

Whole-genome sequence-based analysis of thyroid function

Taylor, Peter N., Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J., Traglia, Michela, Brown, Suzanne J., Mullin, Benjamin H., Shihab, Hashem A., Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R., Beilby, John P., Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D., Hui, Jennie, Lim, Ee M., McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R. B., Bell, Jordana T., Yuan, Wei ... Yang, Jian (2015). Whole-genome sequence-based analysis of thyroid function. Nature Communications, 6 (1) 5681, 5681.1-5681.10. doi: 10.1038/ncomms6681

Whole-genome sequence-based analysis of thyroid function

2015

Journal Article

Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci

Rahmioglu, Nilufer, Macgregor, Stuart, Drong, Alexander W., Hedman, Asa K., Harris, Holly R., Randall, Joshua C., Prokopenko, Inga, Nyholt, Dale R., Morris, Andrew P., Montgomery, Grant W., Missmer, Stacey A., Lindgren, Cecilia M., Zondervan, Krina T., The International Endogene Consortium and Visscher, Peter M. (2015). Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci. Human Molecular Genetics, 24 (4), 1185-1199. doi: 10.1093/hmg/ddu516

Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci

2015

Journal Article

Genetic studies of body mass index yield new insights for obesity biology

Locke, Adam E., Kahali, Bratati, Berndt, Sonja I., Justice, Anne E., Pers, Tune H., Day, Felix R., Powell, Corey, Vedantam, Sailaja, Buchkovich, Martin L., Yang, Jian, Croteau-Chonka, Damien C., Esko, Tonu, Fall, Tove, Ferreira, Teresa, Gustafsson, Stefan, Kutalik, Zoltán, Luan, Jian'an, Mägi, Reedik, Randall, Joshua C., Winkler, Thomas W., Wood, Andrew R., Workalemahu, Tsegaselassie, Faul, Jessica D., Smith, Jennifer A., Zhao, Jing Hua, Zhao, Wei, Chen, Jin, Fehrmann, Rudolf, Hedman, Asa K. ... Shah, Sonia (2015). Genetic studies of body mass index yield new insights for obesity biology. Nature, 518 (7538), 197-206. doi: 10.1038/nature14177

Genetic studies of body mass index yield new insights for obesity biology

2015

Journal Article

Dominance Genetic Variation Contributes Little to the Missing Heritability for Human Complex Traits

Zhu, Zhihong, Bakshi, Andrew, Vinkhuyzen, Anna A. E., Hemani, Gibran, Lee, Sang Hong, Nolte, Ilja M., vanVliet-Ostaptchouk, Jana V., Snieder, Harold, Esko, Tonu, Milani, Lili, Magi, Reedik, Metspalu, Andres, Hill, William G., Weir, Bruce S., Goddard, Michael E., Visscher, Peter M. and Yang, Jian (2015). Dominance Genetic Variation Contributes Little to the Missing Heritability for Human Complex Traits. American Journal of Human Genetics, 96 (3), 377-385. doi: 10.1016/j.ajhg.2015.01.001

Dominance Genetic Variation Contributes Little to the Missing Heritability for Human Complex Traits

2015

Journal Article

New genetic loci link adipose and insulin biology to body fat distribution

Shungin, Dmitry, Winkler, Thomas W, Croteau-Chonka, Damien C, Ferreira, Teresa, Locke, Adam E, Magi, Reedik, Strawbridge, Rona J, Pers, Tune H, Fischer, Krista, Justice, Anne E, Workalemahu, Tsegaselassie, Wu, Joseph M.W, Buchkovich, Martin L, Heard-Costa, Nancy L, Roman, Tamara S, Drong, Alexander W, Song, Ci, Gustafsson, Stefan, Day, Felix R, Esko, Tonu, Fall, Tove, Kutalik, Zoltan, Luan, Jian'an, Randall, Joshua C, Scherag, Andre, Vedantam, Sailaja, Wood, Andrew R, Chen, Jin, Fehrmann, Rudolf ... Shah, Sonia (2015). New genetic loci link adipose and insulin biology to body fat distribution. Nature, 518 (7538), 187-196. doi: 10.1038/nature14132

New genetic loci link adipose and insulin biology to body fat distribution

2015

Journal Article

Large autosomal copy-number differences within unselected monozygotic twin pairs are rare

Mcrae, Allan F., Visscher, Peter M., Montgomery, Grant W. and Martin, Nicholas G. (2015). Large autosomal copy-number differences within unselected monozygotic twin pairs are rare. Twin Research and Human Genetics, 18 (1), 13-18. doi: 10.1017/thg.2014.85

Large autosomal copy-number differences within unselected monozygotic twin pairs are rare

2015

Journal Article

DNA methylation age of blood predicts all-cause mortality in later life

Marioni, Riccardo E., Shah, Sonia, McRae, Allan F., Chen, Brian H., Colicino, Elena, 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., Feinberg, Andrew P., Fallin, M. Daniele, Multhaup, Michael L., Jaffe, Andrew E., Joehanes, Roby, Schwartz, Joel, Just, Allan C., Lunetta, Kathryn L., Murabito, Joanne M., Starr, John M., Horvath, Steve, Baccarelli, Andrea A., Levy, Daniel, Visscher, Peter M. ... Deary, Ian J. (2015). DNA methylation age of blood predicts all-cause mortality in later life. Genome Biology, 16 (1) 25, 25.1-25.12. doi: 10.1186/s13059-015-0584-6

DNA methylation age of blood predicts all-cause mortality in later life

2015

Journal Article

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

O'Dushlaine, Colm, Rossin, Lizzy, Lee, Phil H., Duncan, Laramie, Parikshak, Neelroop N., Newhouse, Stephen, Ripke, Stephan, Neale, Benjamin M., Purcell, Shaun M., Posthuma, Danielle, Nurnberger, John I., Lee, S. Hong, Faraone, Stephen V., Perlis, Roy H., Mowry, Bryan J, Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H. ... Breen, Gerome (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience, 18 (2), 199-209. doi: 10.1038/nn.3922

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

2015

Journal Article

A general unified framework to assess the sampling variance of heritability estimates using pedigree or marker-based relationships

Visscher, Peter M. and Goddard, Michael E. (2015). A general unified framework to assess the sampling variance of heritability estimates using pedigree or marker-based relationships. Genetics, 199 (1), 223-232. doi: 10.1534/genetics.114.171017

A general unified framework to assess the sampling variance of heritability estimates using pedigree or marker-based relationships

2015

Conference Publication

Pleiotropy with educational attainment: results based on a GWAS with 300,000 individuals

Beauchamp, Jonathan, Turley, Patrick, Fontana, Mark, Okbay, Aysu, Lee, James, Rietveld, Cornelius, de Vlaming, Ronald, Visscher, Peter, Esko, Tonu, Koellinger, Philipp, Cesarini, David and Benjamin, Daniel (2015). Pleiotropy with educational attainment: results based on a GWAS with 300,000 individuals. 45th Annual Meeting of the Behavior-Genetics-Association, San Diego, CA, United States, 20 June 2015. New York, NY, United States: Springer .

Pleiotropy with educational attainment: results based on a GWAS with 300,000 individuals

Supervision

Availability

Professor Peter Visscher is:
Not available for supervision

Supervision history

Current supervision

Completed supervision

Media

Enquiries

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