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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

201 - 220 of 818 works

2018

Conference Publication

The genetic liability for insomnia is associated with the number of awakenings during sleep in young and healthy individuals

Ghaemmaghami, P., Muto, V., Jaspar, M., Meyer, C., Elansary, M., Van Egroo, M., Berthomier, C., Lambot, E., Brandewinder, M., Luxen, A., Degueldre, C., Salmon, E., Archer, S., Phillips, C., Dijk, D. -J., Visscher, P., Posthuma, D., Van Someren, E., Collette, F., Georges, M., Maquet, P. and Vandewalle, G. (2018). The genetic liability for insomnia is associated with the number of awakenings during sleep in young and healthy individuals. 24th Congress of the European-Sleep-Research-Society (ESRS), Basel Switzerland, Sep 25-28, 2018. HOBOKEN: WILEY.

The genetic liability for insomnia is associated with the number of awakenings during sleep in young and healthy individuals

2018

Journal Article

Oligo-Miocene lacustrine microbial and metazoan buildups from the Limagne Basin (French Massif Central)

Roche, Adeline, Vennin, Emmanuelle, Bouton, Anthony, Olivier, Nicolas, Wattinne, Aurelia, Bundeleva, Irina, Deconinck, Jean-Francois, Virgone, Aurelien, Gaucher, Eric C. and Visscher, Pieter T. (2018). Oligo-Miocene lacustrine microbial and metazoan buildups from the Limagne Basin (French Massif Central). Palaeogeography Palaeoclimatology Palaeoecology, 504, 34-59. doi: 10.1016/j.palaeo.2018.05.001

Oligo-Miocene lacustrine microbial and metazoan buildups from the Limagne Basin (French Massif Central)

2018

Other Outputs

Epigenetic signatures of starting and stopping smoking

McCartney, Daniel L, Stevenson, Anna J, Hillary, Robert F, Walker, Rosie M, Bermingham, Mairead L, Morris, Stewart W, Clarke, Toni-Kim, Campbell, Archie, Murray, Alison D, Whalley, Heather C, Porteous, David J, Visscher, Peter M, McIntosh, Andrew M, Evans, Kathryn L, Deary, Ian J and Marioni, Riccardo E (2018). Epigenetic signatures of starting and stopping smoking. doi: 10.1101/402453

Epigenetic signatures of starting and stopping smoking

2018

Journal Article

Evolutionary history and adaptation of a human pygmy population of Flores Island, Indonesia

Tucci, Serena, Vohr, Samuel H., McCoy, Rajiv C., Vernot, Benjamin, Robinson, Matthew R., Barbieri, Chiara, Nelson, Brad J., Fu, Wenqing, Purnomo, Gludhug A., Sudoyo, Herawati, Eichler, Evan E., Barbujani, Guido, Visscher, Peter M., Akey, Joshua M. and Green, Richard E. (2018). Evolutionary history and adaptation of a human pygmy population of Flores Island, Indonesia. Science, 361 (6401), 511-515. doi: 10.1126/science.aar8486

Evolutionary history and adaptation of a human pygmy population of Flores Island, Indonesia

2018

Journal Article

Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

Xue, Angli, Wu, Yang, Zhu, Zhihong, Zhang, Futao, Kemper, Kathryn E., Zheng, Zhili, Yengo, Loic, Lloyd-Jones, Luke R., Sidorenko, Julia, Wu, Yeda, eQTLGen Consortium, McRae, Allan F., Visscher, Peter M., Zeng, Jian and Yang, Jian (2018). Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Nature Communications, 9 (1) 2941, 2941. doi: 10.1038/s41467-018-04951-w

Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

2018

Journal Article

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Lee, James J., Wedow, Robbee, Okbay, Aysu, Kong, Edward, Maghzian, Omeed, Zacher, Meghan, Nguyen-Viet, Tuan Anh, Bowers, Peter, Sidorenko, Julia, Karlsson Linnér, Richard, Fontana, Mark Alan, Kundu, Tushar, Lee, Chanwook, Li, Hui, Li, Ruoxi, Royer, Rebecca, Timshel, Pascal N., Walters, Raymond K., Willoughby, Emily A., Yengo, Loïc, 23andMe Research Team, COGENT (Cognitive Genomics Consortium), Social Science Genetic Association Consortium, Alver, Maris, Bao, Yanchun, Clark, David W., Day, Felix R., Furlotte, Nicholas A., Joshi, Peter K. ... Cesarini, David (2018). Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nature Genetics, 50 (8), 1112-1121. doi: 10.1038/s41588-018-0147-3

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

2018

Journal Article

Formation of stromatolite lamina at the interface of oxygenic-anoxygenic photosynthesis

Pace, A., Bourillot, R., Bouton, A., Vennin, E., Braissant, O., Dupraz, C., Duteil, T., Bundeleva, I., Patrier, P., Galaup, S., Yokoyama, Y., Franceschi, M., Virgone, A. and Visscher, P. T. (2018). Formation of stromatolite lamina at the interface of oxygenic-anoxygenic photosynthesis. Geobiology, 16 (4), 378-398. doi: 10.1111/gbi.12281

Formation of stromatolite lamina at the interface of oxygenic-anoxygenic photosynthesis

2018

Journal Article

Misestimation of heritability and prediction accuracy of male-pattern baldness

Yap, Chloe X., Sirodenko, Julia, Marioni, Riccardo E., Yengo, Loic, Wray, Naomi R. and Visscher, Peter M. (2018). Misestimation of heritability and prediction accuracy of male-pattern baldness. Nature Communications, 9 (1) 2537, 2537. doi: 10.1038/s41467-018-04807-3

Misestimation of heritability and prediction accuracy of male-pattern baldness

2018

Journal Article

A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework

LeBlanc, Marissa, Zuber, Verena, Thompson, Wesley K., Andreassen, Ole A., Frigessi, Arnoldo, Andreassen, Bettina Kulle, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David, Huang, Hailiang, Pers, Tune, Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Bene, Judit, Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard ... Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium (2018). A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework. BMC Genomics, 19 (1) 494. doi: 10.1186/s12864-018-4859-7

A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework

2018

Journal Article

Distribution, redox state and (bio)geochemical implications of arsenic in present day microbialites of Laguna Brava, Salar de Atacama

Sancho-Tomas, Maria, Somogyi, Andrea, Medjoubi, Kadda, Bergamaschi, Antoine, Visscher, Pieter T., Van Driessche, Alexander E. S., Gerard, Emmanuelle, Farias, Maria E., Contreras, Manuel and Philippot, Pascal (2018). Distribution, redox state and (bio)geochemical implications of arsenic in present day microbialites of Laguna Brava, Salar de Atacama. Chemical Geology, 490, 13-21. doi: 10.1016/j.chemgeo.2018.04.029

Distribution, redox state and (bio)geochemical implications of arsenic in present day microbialites of Laguna Brava, Salar de Atacama

2018

Journal Article

Common disease is more complex than implied by the core gene omnigenic model

Wray, Naomi R., Wijmenga, Cisca, Sullivan, Patrick F., Yang, Jian and Visscher, Peter M. (2018). Common disease is more complex than implied by the core gene omnigenic model. Cell, 173 (7), 1573-1580. doi: 10.1016/j.cell.2018.05.051

Common disease is more complex than implied by the core gene omnigenic model

2018

Journal Article

Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes

Ruderfer, Douglas M., Ripke, Stephan, McQuillin, Andrew, Boocock, James, Stahl, Eli A., Pavlides, Jennifer M. Whitehead, Mullins, Niamh, Charney, Alexander W., Ori, Anil P.S., Loohuis, Loes M. Olde, Domenici, Enrico, Di Florio, Arianna, Papiol, Sergi, Kalman, Janos L., Trubetskoy, Vassily, Adolfsson, Rolf, Agartz, Ingrid, Agerbo, Esben, Akil, Huda, Albani, Diego, Albus, Margot, Alda, Martin, Alexander, Madeline, Alliey-Rodriguez, Ney, Als, Thomas D., Amin, Farooq, Anjorin, Adebayo, Arranz, Maria J., Awasthi, Swapnil ... Kendler, Kenneth S. (2018). Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes. Cell, 173 (7), 1705-1715.e16. doi: 10.1016/j.cell.2018.05.046

Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes

2018

Journal Article

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Qi, Ting, Wu, Yang, Zeng, Jian, Zhang, Futao, Xue, Angli, Jiang, Longda, Zhu, Zhihong, Kemper, Kathryn, Yengo, Loic, Zheng, Zhili, eQTLGen Consortium, Marioni, Riccardo E., Montgomery, Grant W., Deary, Ian J., Wray, Naomi R., Visscher, Peter M., McRae, Allan F. and Yang, Jian (2018). Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood. Nature Communications, 9 (1) 2282, 2282. doi: 10.1038/s41467-018-04558-1

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

2018

Journal Article

Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans

Cuellar Partida, Gabriel, Laurin, Charles, Ring, Susan M., Gaunt, Tom R., McRae, Allan, Visscher, Peter M., Montgomery, Grant W., Martin, Nicholas G., Hemani, Gibran, Suderman, Matthew, Relton, Caroline L., Davey Smith, George and Evans, David M. (2018). Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans. Human Molecular Genetics, 27 (16), 2927-2939. doi: 10.1093/hmg/ddy206

Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans

2018

Journal Article

GWAS on family history of Alzheimer's disease

Marioni, Riccardo E., Harris, Sarah E., Zhang, Qian, McRae, Allan F., Hagenaars, Saskia P., Hill, W. David, Davies, Gail, Ritchie, Craig W., Gale, Catharine R., Starr, John M., Goate, Alison M., Porteous, David J., Yang, Jian, Evans, Kathryn L., Deary, Ian J., Wray, Naomi R. and Visscher, Peter M. (2018). GWAS on family history of Alzheimer's disease. Translational Psychiatry, 8 (1) 99, 99. doi: 10.1038/s41398-018-0150-6

GWAS on family history of Alzheimer's disease

2018

Journal Article

Erratum: evidence of directional and stabilizing selection in contemporary humans (Proceedings of the National Academy of Sciences of the United States of America (2017) 115 (151–156) DOI: 10.1073/pnas.1707227114)

Sanjak, Jaleal S., Sidorenko, Julia, Robinson, Matthew R., Thornton, Kevin R. and Visscher, Peter M. (2018). Erratum: evidence of directional and stabilizing selection in contemporary humans (Proceedings of the National Academy of Sciences of the United States of America (2017) 115 (151–156) DOI: 10.1073/pnas.1707227114). Proceedings of the National Academy of Sciences of the United States of America, 115 (20). doi: 10.1073/pnas.1806837115

Erratum: evidence of directional and stabilizing selection in contemporary humans (Proceedings of the National Academy of Sciences of the United States of America (2017) 115 (151–156) DOI: 10.1073/pnas.1707227114)

2018

Journal Article

Global genetic differentiation of complex traits shaped by natural selection in humans

Guo, Jing, Wu, Yang, Zhu, Zhihong, Zheng, Zhili, Trzaskowski, Maciej, Zeng, Jian, Robinson, Matthew R., Visscher, Peter M. and Yang, Jian (2018). Global genetic differentiation of complex traits shaped by natural selection in humans. Nature Communications, 9 (1) 1865, 1865. doi: 10.1038/s41467-018-04191-y

Global genetic differentiation of complex traits shaped by natural selection in humans

2018

Journal Article

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till M. F., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bryois, Julien, Buttenschon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan I. R., Colodro-Conde, Lucia, Couvy-Duchesne, Baptiste, Craddock, Nick, Crawford, Gregory E., Crowley, Cheynna A. ... Sullivan, Patrick F. (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50 (5), 668-+. doi: 10.1038/s41588-018-0090-3

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

2018

Journal Article

Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

Evans, Luke M., Tahmasbi, Rasool, Vrieze, Scott I., Abecasis, Gonçalo R., Das, Sayantan, Gazal, Steven, Bjelland, Douglas W., de Candia, Teresa R., Haplotype Reference Consortium, Goddard, Michael E., Neale, Benjamin M., Yang, Jian, Visscher, Peter M. and Keller, Matthew C. (2018). Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits. Nature genetics, 50 (5), 737-745. doi: 10.1038/s41588-018-0108-x

Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

2018

Journal Article

Signatures of negative selection in the genetic architecture of human complex traits

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. Nature Genetics, 50 (5), 746-753. doi: 10.1038/s41588-018-0101-4

Signatures of negative selection in the genetic architecture of human complex traits

Supervision

Availability

Professor Peter Visscher is:
Not available for supervision

Supervision history

Current supervision

Completed supervision

Media

Enquiries

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