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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

441 - 460 of 803 works

2012

Journal Article

Evidence of inbreeding depression on human height

McQuillan, Ruth, Eklund, Niina, Pirastu, Nicola, Kuningas, Maris, McEvoy, Brian P., Esko, Tonu, Corre, Tanguy, Davies, Gail, Kaakinen, Marika, Lyytikainen, Leo-Pekka, Kristiansson, Kati, Havulinna, Aki S., Gogele, Martin, Vitart, Veronique, Tenesa, Albert, Aulchenko, Yurii, Hayward, Caroline, Johansson, Asa, Boban, Mladen, Ulivi, Sheila, Robino, Antonietta, Boraska, Vesna, Igl, Wilmar, Wild, Sarah H., Zgaga, Lina, Amin, Najaf, Theodoratou, Evropi, Polasek, Ozren, Girotto, Giorgia ... Wilson, James F. (2012). Evidence of inbreeding depression on human height. Plos Genetics, 8 (7) e1002655, e1002655. doi: 10.1371/journal.pgen.1002655

Evidence of inbreeding depression on human height

2012

Journal Article

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs (vol 44, pg 247, 2012)

Lee, S. Hong, DeCandia, Teresa R., Ripke, Stephan, Yang, Jian, Sullivan, Patrick F., Goddard, Michael E., Keller, Matthew C., Visscher, Peter M. and Wray, Naomi R. (2012). Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs (vol 44, pg 247, 2012). Nature Genetics, 44 (7), 831-831. doi: 10.1038/ng0712-831a

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs (vol 44, pg 247, 2012)

2012

Journal Article

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012)

Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012). Translational Psychiatry, 2 (5) e125, e125-e125. doi: 10.1038/tp.2012.49

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012)

2012

Conference Publication

Genome-Wide Estimation and Partitioning of Genetic (Co)Variation for Crohn's Disease and Ulcerative Colitis Tagged by Common SNPs

Lee, Hong, Montgomery, Grant, Radford-Smith, Graham and Visscher, Peter M. (2012). Genome-Wide Estimation and Partitioning of Genetic (Co)Variation for Crohn's Disease and Ulcerative Colitis Tagged by Common SNPs. Digestive Disease Week (DDW), San Diego Ca, May 19-22, 2012. PHILADELPHIA: W B SAUNDERS CO-ELSEVIER INC.

Genome-Wide Estimation and Partitioning of Genetic (Co)Variation for Crohn's Disease and Ulcerative Colitis Tagged by Common SNPs

2012

Journal Article

The genetic architecture of economic and political preferences

Benjamin, Daniel J., Cesarini, David, van der Loos, Matthijs, Dawes, Christopher T., Koellinger, Philipp d., Magnusson, Patrik K. E., Chabris, Christopher F., Conley, Dalton, Laibson, David, Johannesson, Magnus and Visscher, Peter M. (2012). The genetic architecture of economic and political preferences. Proceedings of the National Academy of Sciences of the United States of America, 109 (21), 8026-8031. doi: 10.1073/pnas.1120666109

The genetic architecture of economic and political preferences

2012

Journal Article

Genetic architecture of body size in mammals

Kemper, Kathryn E., Visscher, Peter M. and Goddard, Michael E. (2012). Genetic architecture of body size in mammals. Genome Biology, 13 (4) 244, 1-13. doi: 10.1186/gb-2012-13-4-244

Genetic architecture of body size in mammals

2012

Journal Article

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion

Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2 (e102) 201227, e102-e102. doi: 10.1038/tp.2012.27

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion

2012

Journal Article

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

Yang, Jian, Ferreira, Teresa, Morris, Andrew P., Medland, Sarah E., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Weedon, Michael N., Loos, Ruth J., Frayling, Timothy M., McCarthy, Mark I., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M., Genetic Invest ANthropometric Trai and DIAbet Genetics Replication Meta-A (2012). Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics, 44 (4), 369-375. doi: 10.1038/ng.2213

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

2012

Journal Article

The Brisbane systems genetics study: genetical genomics meets complex trait genetics

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, e35430.1-e35430.9. doi: 10.1371/journal.pone.0035430

The Brisbane systems genetics study: genetical genomics meets complex trait genetics

2012

Journal Article

A better coefficient of determination for genetic profile analysis

Lee, Sang Hong, Goddard, Michael E., Wray, Naomi R. and Visscher, Peter M. (2012). A better coefficient of determination for genetic profile analysis. Genetic Epidemiology, 36 (3), 214-224. doi: 10.1002/gepi.21614

A better coefficient of determination for genetic profile analysis

2012

Journal Article

Deleterious GRM1 mutations in schizophrenia

Ayoub, Mohammed Akli, Angelicheva, Dora, Vile, David, Chandler, David, Morar, Bharti, Cavanaugh, Juleen A., Visscher, Peter M., Jablensky, Assen, Pfleger, Kevin D. G. and Kalaydjieva, Luba (2012). Deleterious GRM1 mutations in schizophrenia. PLoS One, 7 (3) e32849, e32849. doi: 10.1371/journal.pone.0032849

Deleterious GRM1 mutations in schizophrenia

2012

Journal Article

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

Lee, S. Hong, DeCandia, Teresa R., Ripke, Stephan, Yang, Jian, Sullivan, Patrick F ., Goddard, Michael E ., Keller, Matthew C ., Visscher, Peter M ., Wray, Naomi R., Schizophrenia Psychiat Genome-Wide, Int Schizophrenia Consortium ISC, Mol Genetics Schizophrenia and Mowry, Bryan (2012). Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nature Genetics, 44 (3), 247-250. doi: 10.1038/ng.1108

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

2012

Journal Article

Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent

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 (3), 456-466. doi: 10.1101/gr.126540.111

Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent

2012

Journal Article

A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia

Jia, Peilin, Wang, Lily, Fanous, Ayman H., Chen, Xiangning, Kendler, Kenneth S., Zhao, Zhongming, Morris, Derek W., O'Dushlaine, Colm T., Kenny, Elaine, Quinn, Emma M., Gill, Michael, Corvin, Aiden, O'Donovan, Michael C., Kirov, George K., Craddock, Nick J., Holmans, Peter A., Williams, Nigel M., Georgieva, Lucy, Nikolov, Ivan, Norton, N., Williams, H., Toncheva, Draga, Milanova, Vihra, Owen, Michael J., Hultman, Christina M., Lichtenstein, Paul, Thelander, Emma F., Sullivan, Patrick, McQuillin, Andrew ... Sklar, Pamela (2012). A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia. Journal of Medical Genetics, 49 (2), 96-103. doi: 10.1136/jmedgenet-2011-100397

A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia

2012

Journal Article

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

Richards, A. L., Jones, L., Moskvina, V., Kirov, G., Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration, International Schizophrenia Consortium (ISC), Purcell, S., Visscher, P. M., Craddock, N., Owen, M. J., O'Donovan, M. C., Holmans, P. and Mowry, B.J. (2012). Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry, 17 (2), 193-201. doi: 10.1038/mp.2011.11

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

2012

Journal Article

Genetic contributions to stability and change in intelligence from childhood to old age

Deary, Ian J., Yang, Jian, Davies, Gail, Harris, Sarah E., Tenesa, Albert, Liewald, David, Luciano, Michelle, Lopez, Lorna M., Gow, Alan J., Corley, Janie, Redmond, Paul, Fox, Helen C., Rowe, Suzanne J., Haggarty, Paul, McNeill, Gerald, Goddard, Michael E., Porteous, David J., Whalley, Lawrence J., Starr, John M. and Visscher, Peter M. (2012). Genetic contributions to stability and change in intelligence from childhood to old age. Nature, 482 (7384), 212-215. doi: 10.1038/nature10781

Genetic contributions to stability and change in intelligence from childhood to old age

2012

Journal Article

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses

Visscher, Peter, Goddard, M. E., Derks, E. M. and Wray, Naomi (2012). Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. Molecular Psychiatry, 17 (5), 474-485. doi: 10.1038/mp.2011.65

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses

2012

Journal Article

Quantification of Inbreeding Due to Distant Ancestors and Its Detection Using Dense Single Nucleotide Polymorphism Data (vol 189, pg 237, 2011)

Keller, M. C., Visscher, P. M. and Goddard, M. E. (2012). Quantification of Inbreeding Due to Distant Ancestors and Its Detection Using Dense Single Nucleotide Polymorphism Data (vol 189, pg 237, 2011). Genetics, 190 (1), 283-283.

Quantification of Inbreeding Due to Distant Ancestors and Its Detection Using Dense Single Nucleotide Polymorphism Data (vol 189, pg 237, 2011)

2012

Conference Publication

The genetic architecture of economic and political preferences

Benjamin, Daniel, Cesarini, David, van der Loos, Matthijs, Dawes, Chris, Koellinger, Philipp, Magnusson, Patrik, Chabris, Chris, Conley, Dalton, Laibson, David, Johannesson, Magnus and Visscher, Peter (2012). The genetic architecture of economic and political preferences. 42nd Annual Meeting of the Behavior Genetics Association, Edinburgh Scotland, 22-25 June 2012. New York, NY United States: Springer New York LLC.

The genetic architecture of economic and political preferences

2012

Journal Article

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

Stolk L., Perry J.R.B., Chasman D.I., He C., Mangino M., Sulem P., Barbalic M., Broer L., Byrne E.M., Ernst F., Esko T., Franceschini N., Gudbjartsson D.F., Hottenga J.-J., Kraft P., McArdle P.F., Porcu E., Shin S.-Y., Smith A.V., Van Wingerden S., Zhai G., Zhuang W.V., Albrecht E., Alizadeh B.Z., Aspelund T., Bandinelli S., Lauc L.B., Beckmann J.S., Boban M. ... Lunetta K.L. (2012). Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, 44 (3), 260-268. doi: 10.1038/ng.1051

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

Funding

Current funding

  • 2019 - 2025
    Causes and consequence of human trait variation
    ARC Australian Laureate Fellowships
    Open grant

Past funding

  • 2022 - 2025
    Genetic architecture and evolution of complex traits across populations
    ARC Discovery Projects
    Open grant
  • 2018 - 2024
    Estimating the genetic and environmental architecture of psychiatric disorders (NIH Grant administered by the University of Colorado)
    University of Colorado
    Open grant
  • 2017 - 2023
    Complex trait genomics
    NHMRC Program Grant
    Open grant
  • 2016 - 2019
    Genetic analysis of the relationship between parental age and risk of psychiatric disorders
    NHMRC Project Grant
    Open grant
  • 2016 - 2019
    Phenotypic profiling from DNA using genetic and epigenetic information
    ARC Discovery Projects
    Open grant
  • 2016 - 2018
    The genetics of ageing in human populations
    ARC Discovery Projects
    Open grant
  • 2015 - 2019
    Sporadic ALS Australian Systems Genomics Consortium (SALSA-SGC)
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2015 - 2020
    Analysis of Genome-Wide Data in the Health and Retirement Study (NIH grant administered by the University of Southern California)
    University of Southern California
    Open grant
  • 2015 - 2019
    1/2 A Large-Scale Schizophrenia Association Study in Sweden (NIH grant administered by the University of North Carolina at Chapel Hill)
    University of North Carolina
    Open grant
  • 2015 - 2017
    Increasing the power of GxE detection by using multi-locus genome-wide predictors (NIH grant administered by Harvard Medical School)
    Harvard Medical School
    Open grant
  • 2015 - 2019
    NHMRC Research Fellowship: Neurogenetics and Statistical Genomics
    NHMRC Research Fellowship
    Open grant
  • 2014
    Deciphering the genetic code of diseases
    National Computational Merit Allocation Scheme
    Open grant
  • 2014
    Trans-ethnic and trans-omic statistical analyses to identify new ALS risk variants
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2013 - 2018
    Estimating the Frequencies and Population Specificities of Risk Alleles (NIH grant administered by the University of Colorado)
    University of Colorado
    Open grant
  • 2013 - 2016
    CAGE: Consortium for the Architecture of Gene Expression
    NHMRC Project Grant
    Open grant
  • 2013 - 2015
    Estimation and partitioning of the still-missing heritability for complex disease
    NHMRC Project Grant
    Open grant
  • 2013 - 2016
    Estimation of non-additive genetic variance for complex traits using genome-wide SNP and sequence data
    ARC Discovery Projects
    Open grant
  • 2013 - 2016
    Exploiting SNP data in epidemiology and genetics through multivariate analysis of complex traits
    NHMRC Project Grant
    Open grant
  • 2013 - 2015
    The genetic architecture and evolution of quantitative traits (ARC Discovery Project administered by the University of Melbourne)
    University of Melbourne
    Open grant
  • 2012 - 2018
    Statistical and Quantitative Genetics (NIH Grant administered by the University of Washington)
    University of Washington (Seattle)
    Open grant
  • 2012 - 2017
    Statistical genetic analyses of social and economic outcomes
    Stockholm School of Economics
    Open grant
  • 2012 - 2017
    Belgian Medical Genomics Initiative (BeMGI)
    University of Liege
    Open grant
  • 2012
    Explaining the Dark Matter of Genome-wide Association Studies for Complex Disease
    NHMRC Project Grant
    Open grant
  • 2011 - 2014
    Better Methods for Individual Risk Prediction of Complex Traits in Human Populations
    NHMRC Project Grant
    Open grant
  • 2011 - 2014
    NHMRC Research Fellowship (SPRF)
    NHMRC Research Fellowship
    Open grant
  • 2011 - 2017
    Theoretical Population Genetics (NIH Subcontract administered by the University of Washington)
    University of Washington (Seattle)
    Open grant
  • 2010 - 2013
    Identifying eQTLs and endophenotyping known CNVs in a large Australian schizophrenia sample
    NHMRC Project Grant
    Open grant
  • 2010 - 2012
    Why is most of the genetic variance for complex traits undetected by large powerful screens of common variants? (ARC Discovery Project administered by The University of Melbourne)
    University of Melbourne
    Open grant
  • 2007 - 2009
    Maximising knowledge from dense SNP data using multi-locus analysis
    ARC Discovery Projects
    Open grant

Supervision

Availability

Professor Peter Visscher is:
Not available for supervision

Supervision history

Current supervision

  • Doctor Philosophy

    Statistical methods and application to analyses genome and trait data from large biobanks

    Principal Advisor

    Other advisors: Dr Kathryn Kemper, Professor Loic Yengo

  • Doctor Philosophy

    Genetic architecture and evolution of complex traits across populations in humans

    Associate Advisor

    Other advisors: Professor Naomi Wray, Dr Fleur Garton, Dr Jian Zeng

  • Doctor Philosophy

    Integrating GWAS and molecular QTL data to dissect genetic architecture and improve polygenic prediction

    Associate Advisor

    Other advisors: Dr Jian Zeng

Completed supervision

Media

Enquiries

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