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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

381 - 400 of 803 works

2014

Journal Article

Common genetic variants explain the majority of the correlation between height and intelligence: The generation scotland study

Marioni, Riccardo E., Batty, G. David, Hayward, Caroline, Kerr, Shona M., Campbell, Archie, Hocking, Lynne J., Porteous, David J., Visscher, Peter M. and Deary, Ian J. (2014). Common genetic variants explain the majority of the correlation between height and intelligence: The generation scotland study. Behavior Genetics, 44 (2), 91-96. doi: 10.1007/s10519-014-9644-z

Common genetic variants explain the majority of the correlation between height and intelligence: The generation scotland study

2014

Journal Article

Novel risk loci for rheumatoid arthritis in han chinese and congruence with risk variants in europeans

Jiang, Lei, Yin, Jian, Ye, Lingying, Yang, Jian, Hemani, Gibran, Liu, Ai-Jun, Zou, Hejian, He, Dongyi, Sun, Lingyun, Zeng, Xiaofeng, Li, Zhanguo, Zheng Yi, Lin, Yiping, Liu, Yi, Fang, Yongfei, Xu, Jianhua, Li, Yinong, Dai, Shengming, Guan, Jianlong, Jiang, Lindi, Wei, Qianghua, Wang, Yi, Li, Yang, Huang, Cibo, Zuo, Xiaoxia, Liu, Yu, Wu, Xin, Zhang, Libin, Zhou, Ling ... Xu, Huji (2014). Novel risk loci for rheumatoid arthritis in han chinese and congruence with risk variants in europeans. Arthritis and Rheumatology, 66 (5), 1121-1132. doi: 10.1002/art.38353

Novel risk loci for rheumatoid arthritis in han chinese and congruence with risk variants in europeans

2013

Journal Article

Author reply to A commentary on Pitfalls of predicting complex traits from SNPs

Wray, Naomi R., Yang, Jian, Hayes, Ben J., Price, Alkes L., Goddard, Michael E. and Visscher, Peter M. (2013). Author reply to A commentary on Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics, 14 (12), 894-894. doi: 10.1038/nrg3457-c2

Author reply to A commentary on Pitfalls of predicting complex traits from SNPs

2013

Journal Article

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability

Derks, Eske M., Ayub, Muhammad, Chambert, Kimberly, Del Favero, Jurgen, Johnstone, Mandy, Macgregor, Stuart, Maclean, Alan, McKechanie, Andrew G., McRae, Allan F., Moran, Jennifer L., Pickard, Benjamin S., Purcell, Shaun, Sklar, Pamela, St Clair, David M., Wray, Naomi R., Visscher, Peter M. and Blackwood, Douglas H. R. (2013). A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 162 (8), 847-854. doi: 10.1002/ajmg.b.32189

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability

2013

Journal Article

Schizophrenia genetic variants are not associated with intelligence

Terwisscha van Scheltinga, A. F., Bakker, S. C., Van Haren, N. E. M., Derks, E. M., Buizer-Voskamp, J. E., Cahn, W., Ripke, S., Ophoff, R. A., Kahn, R. S., Psychiatric Genomic-Wide Association Study (GWAS) Consortium, Visscher, P. M., Mowry, B. J., Brown, M. A., McGrath, J. J. and McLean, Duncan E. (2013). Schizophrenia genetic variants are not associated with intelligence. Psychological Medicine, 43 (12), 2563-2570. doi: 10.1017/S0033291713000196

Schizophrenia genetic variants are not associated with intelligence

2013

Journal Article

Estimation and partition of heritability in human populations using whole-genome analysis methods

Vinkhuyzen, Anna A.E., Wray, Naomi R., Yang, Jiang, Goddard, Michael E. and Visscher, Peter M. (2013). Estimation and partition of heritability in human populations using whole-genome analysis methods. Annual Review of Genetics, Review in Advance: 47 (5), 93-113. doi: 10.1146/annurev-genet-111212-133258

Estimation and partition of heritability in human populations using whole-genome analysis methods

2013

Journal Article

Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs

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

Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs

2013

Journal Article

Stromatolitic knobs in Storr's Lake (San Salvador, Bahamas): a model system for formation and alteration of laminae

Dupraz, C., Fowler, A., Tobias, C. and Visscher, P. T. (2013). Stromatolitic knobs in Storr's Lake (San Salvador, Bahamas): a model system for formation and alteration of laminae. Geobiology, 11 (6), 527-548. doi: 10.1111/gbi.12063

Stromatolitic knobs in Storr's Lake (San Salvador, Bahamas): a model system for formation and alteration of laminae

2013

Journal Article

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'

Robinson, E. B., Howrigan, D., Yang, J., Ripke, S., Anttila, V., Duncan, L. E., Jostins, L., Barrett, J. C., Medland, S. E., Macarthur, D. G., Breen, G., O'Donovan, M. C., Wray, N. R., Devlin, B., Daly, M. J., Visscher, P. M., Sullivan, P. F. and Neale, B. M. (2013). Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'. Molecular Psychiatry, 19 (8), 859-861. doi: 10.1038/mp.2013.125

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'

2013

Journal Article

A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk

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

A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk

2013

Journal Article

Systematic identification of trans eQTLs as putative drivers of known disease associations

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. ... 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

Systematic identification of trans eQTLs as putative drivers of known disease associations

2013

Journal Article

What if we had whole-genome sequence data for millions of individuals?

Visscher, Peter and Gibson, Greg (2013). What if we had whole-genome sequence data for millions of individuals?. Genome Medicine, 5 (80) 80, 80.1-80.3. doi: 10.1186/gm484

What if we had whole-genome sequence data for millions of individuals?

2013

Journal Article

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent

de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, Bryan J., Goddard, Michael E., O'Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, The International Schizophrenia Consortium, The Molecular Genetics of Schizophrenia Collaboration, Visscher, Peter M., Wray, Naomi R. and Keller, Matthew C. (2013). Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. American Journal of Human Genetics, 93 (3), 463-470. doi: 10.1016/j.ajhg.2013.07.007

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent

2013

Journal Article

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Lee, S. Hong, Ripke, Stephan, Neale, Benjamin M., Faraone, Stephen V., Purcell, Shaun M., 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., Backlund, Lena, Badner, Judith A., Bailey, Anthony J., Banaschewski, Tobias, Barchas, Jack D., Barnes, Michael R., Barrett, Thomas B., Bass, Nicholas ... Wray, Naomi R. (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 45 (9), 984-995. doi: 10.1038/ng.2711

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

2013

Journal Article

Where GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophrenia

McGrath, John J., Mortensen, Preben Bo, Visscher, Peter M. and Wray, Naomi R. (2013). Where GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophrenia. Schizophrenia Bulletin, 39 (5), 955-959. doi: 10.1093/schbul/sbt108

Where GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophrenia

2013

Journal Article

Meta-analysis of gene-level associations for rare variants based on single-variant statistics

Hu, Yi-Juan, Berndt, Sonja I., Gustafsson, Stefan, Ganna, Andrea, Hirschhorn, Joel, North, Kari E., Ingelsson, Erik, Lin, Dan-Yu, Collins, Francis S., Berndt, Sonja I., Gustafsson, Stefan, Ma¨gi, Reedik, Ganna, Andrea, Wheeler, Eleanor, Feitosa, Mary F., Justice, Anne E., Monda, Keri L., Croteau-Chonka, Damien C., Day, Felix R., Esko, To˜nu, Fall, Tove, Ferreira, Teresa, Gentilini, Davide, Jackson, Anne U., Luan, Jian’an, Randall, Joshua C., Vedantam, Sailaja, Willer, Cristen J., Winkler, Thomas W. ... Ingelsson, Erik (2013). Meta-analysis of gene-level associations for rare variants based on single-variant statistics. American Journal of Human Genetics, 93 (2), 236-248. doi: 10.1016/j.ajhg.2013.06.011

Meta-analysis of gene-level associations for rare variants based on single-variant statistics

2013

Journal Article

Introgression and the fate of domesticated genes in a wild mammal population

Feulner, Philine G. D., Gratten, Jacob, Kijas, James W., Visscher, Peter M., Pemberton, Josephine M. and Slate, Jon (2013). Introgression and the fate of domesticated genes in a wild mammal population. Molecular Ecology, 22 (16), 4210-4221. doi: 10.1111/mec.12378

Introgression and the fate of domesticated genes in a wild mammal population

2013

Journal Article

Commentary: height and Mendel's theory: the long and the short of it

Visscher, Peter M. (2013). Commentary: height and Mendel's theory: the long and the short of it. International Journal of Epidemiology, 42 (4) dyt069, 944-945. doi: 10.1093/ije/dyt069

Commentary: height and Mendel's theory: the long and the short of it

2013

Journal Article

From personalized to public health genomics

Gibson, Greg and Visscher, Peter M. (2013). From personalized to public health genomics. Genome Medicine, 5 (60) 60, 1-2. doi: 10.1186/gm464

From personalized to public health genomics

2013

Journal Article

Pitfalls of predicting complex traits from SNPs

Wray, Naomi R., Yang, Jian, Hayes, Ben J., Price, Alkes L., Goddard, Michael E. and Visscher, Peter M. (2013). Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics, 14 (7), 507-515. doi: 10.1038/nrg3457

Pitfalls of predicting complex traits from SNPs

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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