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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

803 works between 1987 and 2025

61 - 80 of 803 works

2021

Journal Article

Association of genetic variant at chromosome 12q23.1 with neuropathic pain susceptibility

Veluchamy, Abirami, Hebert, Harry L., van Zuydam, Natalie R., Pearson, Ewan R., Campbell, Archie, Hayward, Caroline, Meng, Weihua, McCarthy, Mark I., Bennett, David L. H., Palmer, Colin N. A. and Smith, Blair H. (2021). Association of genetic variant at chromosome 12q23.1 with neuropathic pain susceptibility. JAMA Network Open, 4 (12) e2136560, 1-14. doi: 10.1001/jamanetworkopen.2021.36560

Association of genetic variant at chromosome 12q23.1 with neuropathic pain susceptibility

2021

Journal Article

Creating and validating a DNA methylation-based proxy for interleukin-6

Stevenson, Anna J, Gadd, Danni A, Hillary, Robert F, McCartney, Daniel L, Campbell, Archie, Walker, Rosie M, Evans, Kathryn L, Harris, Sarah E, Spires-Jones, Tara L, McRae, Allan F, Visscher, Peter M, McIntosh, Andrew M, Deary, Ian J and Marioni, Riccardo E (2021). Creating and validating a DNA methylation-based proxy for interleukin-6. Journals of Gerontology - Series A Biological Sciences and Medical Sciences, 76 (12), 2284-2292. doi: 10.1093/gerona/glab046

Creating and validating a DNA methylation-based proxy for interleukin-6

2021

Journal Article

Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits

Patxot, Marion, Banos, Daniel Trejo, Kousathanas, Athanasios, Orliac, Etienne J., Ojavee, Sven E., Moser, Gerhard, Holloway, Alexander, Sidorenko, Julia, Kutalik, Zoltan, Mägi, Reedik, Visscher, Peter M., Rönnegård, Lars and Robinson, Matthew R. (2021). Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits. Nature Communications, 12 (1) 6972, 6972. doi: 10.1038/s41467-021-27258-9

Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits

2021

Journal Article

Autism-related dietary preferences mediate autism-gut microbiome associations

Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Wood, David L.A., Krause, Lutz, Tyson, Gene W., Restuadi, Restuadi, Wallace, Leanne, McLaren, Tiana, Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Frenk, Mira Levis, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Holtmann, Gerald, Strike, Lachlan T., de Zubicaray, Greig I. ... Gratten, Jacob (2021). Autism-related dietary preferences mediate autism-gut microbiome associations. Cell, 184 (24), 5916-5931.e17. doi: 10.1016/j.cell.2021.10.015

Autism-related dietary preferences mediate autism-gut microbiome associations

2021

Conference Publication

Resource Profile and User Guide of the Polygenic Index Repository

Becker, Joel, Burik, Casper A. P., Goldman, Grant, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Belsky, Daniel W., Linner, Richard Karlsson, Ahlskog, Rafael, Kleinman, Aaron, Hinds, David A., Caspi, Avshalom, Corcoran, David L., Moffitt, Terrie E., Poulton, Richie, Sugden, Karen, Williams, Benjamin S., Harris, Kathleen Mullan, Steptoe, Andrew, Ajnakina, Olesya, Milani, Lili, Esko, Tonu, Iacono, William G., McGue, Matt, Magnusson, Patrik K. E., Mallard, Travis T., Harden, K. Paige, Tucker-Drob, Elliot M., Herd, Pamela ... Okbay, Aysu (2021). Resource Profile and User Guide of the Polygenic Index Repository. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 29, 2021. NEW YORK: SPRINGER.

Resource Profile and User Guide of the Polygenic Index Repository

2021

Conference Publication

Polygenic prediction within and between families from a 3-million-person GWAS of educational attainment

Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hermon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Tian, Chao, Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David, Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton C., Koellinger, Philipp D., Johannesson, Magnus, Laibson, David I., Meyer, Michelle N., Lee, James J., Kong, Augustine ... Young, Alexander I. (2021). Polygenic prediction within and between families from a 3-million-person GWAS of educational attainment. Behavior Genetics Association 51st Annual Meeting, Online, 2021. New York, NY United States: Springer. doi: 10.1007/s10519-021-10087-3

Polygenic prediction within and between families from a 3-million-person GWAS of educational attainment

2021

Journal Article

A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts

Ni, Guiyan, Zeng, Jian, Revez, Joana A., Wang, Ying, Zheng, Zhili, Ge, Tian, Restuadi, Restuadi, Kiewa, Jacqueline, Nyholt, Dale R., Coleman, Jonathan R.I., Smoller, Jordan W., Yang, Jian, Visscher, Peter M. and Wray, Naomi R. (2021). A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts. Biological Psychiatry, 90 (9), 611-620. doi: 10.1016/j.biopsych.2021.04.018

A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts

2021

Journal Article

Problems with using polygenic scores to select embryos

Turley, Patrick, Meyer, Michelle N., Wang, Nancy, Cesarini, David, Hammonds, Evelynn, Martin, Alicia R., Neale, Benjamin M., Rehm, Heidi L., Wilkins-Haug, Louise, Benjamin, Daniel J., Hyman, Steven, Laibson, David and Visscher, Peter M. (2021). Problems with using polygenic scores to select embryos. Obstetrical and Gynecological Survey, 76 (10), 609-610. doi: 10.1097/OGX.0000000000000972

Problems with using polygenic scores to select embryos

2021

Journal Article

Discovery and implications of polygenicity of common diseases

Visscher, Peter M., Yengo, Loic, Cox, Nancy J. and Wray, Naomi R. (2021). Discovery and implications of polygenicity of common diseases. Science, 373 (6562), 1468-1473. doi: 10.1126/science.abi8206

Discovery and implications of polygenicity of common diseases

2021

Journal Article

The genomics of heart failure: design and rationale of the HERMES consortium

Lumbers, R. Thomas, Shah, Sonia, Lin, Honghuang, Czuba, Tomasz, Henry, Albert, Swerdlow, Daniel I., Mälarstig, Anders, Andersson, Charlotte, Verweij, Niek, Holmes, Michael V., Ärnlöv, Johan, Svensson, Per, Hemingway, Harry, Sallah, Neneh, Almgren, Peter, Aragam, Krishna G., Asselin, Geraldine, Backman, Joshua D., Biggs, Mary L., Bloom, Heather L., Boersma, Eric, Brandimarto, Jeffrey, Brown, Michael R., Brunner‐La Rocca, Hans‐Peter, Carey, David J., Chaffin, Mark D., Chasman, Daniel I., Chazara, Olympe, Chen, Xing ... Regeneron Genetics Center (2021). The genomics of heart failure: design and rationale of the HERMES consortium. ESC Heart Failure, 8 (6) ehf2.13517, 5531-5541. doi: 10.1002/ehf2.13517

The genomics of heart failure: design and rationale of the HERMES consortium

2021

Journal Article

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Võsa, Urmo, Claringbould, Annique, Westra, Harm-Jan, Bonder, Marc Jan, Deelen, Patrick, Zeng, Biao, Kirsten, Holger, Saha, Ashis, Kreuzhuber, Roman, Yazar, Seyhan, Brugge, Harm, Oelen, Roy, de Vries, Dylan H., van der Wijst, Monique G. P., Kasela, Silva, Pervjakova, Natalia, Alves, Isabel, Favé, Marie-Julie, Agbessi, Mawussé, Christiansen, Mark W., Jansen, Rick, Seppälä, Ilkka, Tong, Lin, Teumer, Alexander, Schramm, Katharina, Hemani, Gibran, Verlouw, Joost, Yaghootkar, Hanieh, Sönmez Flitman, Reyhan ... i2QTL Consortium (2021). Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nature Genetics, 53 (9), 1300-1310. doi: 10.1038/s41588-021-00913-z

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

2021

Journal Article

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

Min, Josine L., Hemani, Gibran, Hannon, Eilis, Dekkers, Koen F., Castillo-Fernandez, Juan, Luijk, René, Carnero-Montoro, Elena, Lawson, Daniel J., Burrows, Kimberley, Suderman, Matthew, Bretherick, Andrew D., Richardson, Tom G., Klughammer, Johanna, Iotchkova, Valentina, Sharp, Gemma, Al Khleifat, Ahmad, Shatunov, Aleksey, Iacoangeli, Alfredo, McArdle, Wendy L., Ho, Karen M., Kumar, Ashish, Söderhäll, Cilla, Soriano-Tárraga, Carolina, Giralt-Steinhauer, Eva, Kazmi, Nabila, Mason, Dan, McRae, Allan F., Corcoran, David L., Sugden, Karen ... BIOS Consortium (2021). Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. Nature Genetics, 53 (9), 1311-1321. doi: 10.1038/s41588-021-00923-x

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

2021

Journal Article

Phantom epistasis between unlinked loci

Hemani, Gibran, Powell, Joseph E., Wang, Huanwei, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Goddard, Michael E., Gibson, Greg, Yang, Jian and Visscher, Peter M. (2021). Phantom epistasis between unlinked loci. Nature, 596 (7871), E1-E3. doi: 10.1038/s41586-021-03765-z

Phantom epistasis between unlinked loci

2021

Journal Article

Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

van Blokland, Irene V., Lanting, Pauline, Ori, Anil P.S., Vonk, Judith M., Warmerdam, Robert C.A., Herkert, Johanna C., Boulogne, Floranne, Claringbould, Annique, Lopera-Maya, Esteban A., Bartels, Meike, Hottenga, Jouke-Jan, Ganna, Andrea, Karjalainen, Juha, Hayward, Caroline, Fawns-Ritchie, Chloe, Campbell, Archie, Porteous, David, Cirulli, Elizabeth T., Barrett, Kelly M. Schiabor, Riffle, Stephen, Bolze, Alexandre, White, Simon, Tanudjaja, Francisco, Wang, Xueqing, Ramirez, Jimmy M., Lim, Yan Wei, Lu, James T., Washington, Nicole L., de Geus, Eco J. C. ... Yengo, Loic (2021). Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility. PLoS One, 16 (8) e0255402, 1-18. doi: 10.1371/journal.pone.0255402

Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

2021

Journal Article

Genomic partitioning of inbreeding depression in humans

Yengo, Loic, Yang, Jian, Keller, Matthew C., Goddard, Michael E., Wray, Naomi R. and Visscher, Peter M. (2021). Genomic partitioning of inbreeding depression in humans. American Journal of Human Genetics, 108 (8), 1488-1501. doi: 10.1016/j.ajhg.2021.06.005

Genomic partitioning of inbreeding depression in humans

2021

Journal Article

Problems with using polygenic scores to select embryos

Turley, Patrick, Meyer, Michelle N., Wang, Nancy, Cesarini, David, Hammonds, Evelynn, Martin, Alicia R., Neale, Benjamin M., Rehm, Heidi L., Wilkins-Haug, Louise, Benjamin, Daniel J., Hyman, Steven, Laibson, David and Visscher, Peter M. (2021). Problems with using polygenic scores to select embryos. New England Journal of Medicine, 385 (1), 78-86. doi: 10.1056/NEJMsr2105065

Problems with using polygenic scores to select embryos

2021

Journal Article

Multi-omic and multi-species meta-analyses of nicotine consumption

Palmer, Rohan H. C., Benca-Bachman, Chelsie E., Huggett, Spencer B., Bubier, Jason A., McGeary, John E., Ramgiri, Nikhil, Srijeyanthan, Jenani, Yang, Jingjing, Visscher, Peter M., Yang, Jian, Knopik, Valerie S. and Chesler, Elissa J. (2021). Multi-omic and multi-species meta-analyses of nicotine consumption. Translational Psychiatry, 11 (1) 98, 98. doi: 10.1038/s41398-021-01231-y

Multi-omic and multi-species meta-analyses of nicotine consumption

2021

Journal Article

Gene action, genetic variation, and GWAS: A user-friendly web tool

Hivert, Valentin, Wray, Naomi R. and Visscher, Peter M. (2021). Gene action, genetic variation, and GWAS: A user-friendly web tool. PLoS Genetics, 17 (5) e1009548, 1-9. doi: 10.1371/journal.pgen.1009548

Gene action, genetic variation, and GWAS: A user-friendly web tool

2021

Journal Article

Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals (vol 108, pg 786, 2021)

Hivert, Valentin, Sidorenko, Julia, Rohart, Florian, Goddard, Michael E., Yang, Jian, Wray, Naomi R., Yengo, Loic and Visscher, Peter M. (2021). Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals (vol 108, pg 786, 2021). American Journal of Human Genetics, 108 (5), 962-962. doi: 10.1016/j.ajhg.2021.04.012

Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals (vol 108, pg 786, 2021)

2021

Journal Article

Cohort profile: DOLORisk Dundee: a longitudinal study of chronic neuropathic pain

Hebert, Harry L., Veluchamy, Abirami, Baskozos, Georgios, Fardo, Francesca, Van Ryckeghem, Dimitri M. L., Pascal, Mathilde M. V., Jones, Claire, Milburn, Keith, Pearson, Ewan R., Crombez, Geert, Bennett, David L. H., Meng, Weihua, Palmer, Colin N. A. and Smith, Blair H. (2021). Cohort profile: DOLORisk Dundee: a longitudinal study of chronic neuropathic pain. BMJ Open, 11 (5) e042887, 1-11. doi: 10.1136/bmjopen-2020-042887

Cohort profile: DOLORisk Dundee: a longitudinal study of chronic neuropathic pain

Supervision

Availability

Professor Peter Visscher is:
Not available for supervision

Supervision history

Current supervision

Completed supervision

Media

Enquiries

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