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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

541 - 560 of 803 works

2009

Journal Article

Is there still a cognitive cost of being a twin in the UK?

Calvin, Catherine, Fernandes, Cres, Smith, Pauline, Visscher, Peter M. and Deary, Ian J. (2009). Is there still a cognitive cost of being a twin in the UK?. Intelligence, 37 (3), 243-248. doi: 10.1016/j.intell.2008.12.005

Is there still a cognitive cost of being a twin in the UK?

2009

Journal Article

Geographical structure and differential natural selection among North European populations

Brian P. McEvoy, Grant W. Montgomery, Allan F. McRae, Samuli Ripatti, Markus Perola, Tim D. Spector, Lynn Cherkas, Kourosh R. Ahmadi, Dorret Boomsma, Gonneke Willemsen, Jouke J. Hottenga, Nancy L. Pedersen, Patrik K.E. Magnusson, Kirsten Ohm Kyvik, Kaare Christensen, Jaakko Kaprio, Kauko Heikkilä, Aarno Palotie, Elisabeth Widen, Juha Muilu, Ann-Christine Syvänen, Ulrika Liljedahl, Orla Hardiman, Simon Cronin, Leena Peltonen, Nicholas G. Martin and Peter M. Visscher (2009). Geographical structure and differential natural selection among North European populations. Genome Research, 19 (5), 804-814. doi: 10.1101/gr.083394.108

Geographical structure and differential natural selection among North European populations

2009

Journal Article

QSAR Studies on <i>N</i>-aryl Derivative Activity Towards Alzheimer's Disease

Solomon, Kamalakaran Anand, Sundararajan, Srinivasan and Abirami, Veluchamy (2009). QSAR Studies on N-aryl Derivative Activity Towards Alzheimer's Disease. Molecules, 14 (4), 1448-1455. doi: 10.3390/molecules14041448

QSAR Studies on <i>N</i>-aryl Derivative Activity Towards Alzheimer's Disease

2009

Journal Article

Increased accuracy of artificial selection by using the realized relationship matrix. (vol 91, pg 47, 2009)

Hayes, B. J., Visscher, P. M. and Goddard, M. E. (2009). Increased accuracy of artificial selection by using the realized relationship matrix. (vol 91, pg 47, 2009). Genetics Research, 91 (2), 143-143. doi: 10.1017/S0016672309000111

Increased accuracy of artificial selection by using the realized relationship matrix. (vol 91, pg 47, 2009)

2009

Journal Article

Statistical genetics & statistical genomics: Where biology, epistemology, statistics, and computation collide

Allison, David B., Visscher, Peter M., Rosa, Guilherme J. M. and Amos, Christopher I. (2009). Statistical genetics & statistical genomics: Where biology, epistemology, statistics, and computation collide. Computational Statistics & Data Analysis, 53 (5), 1531-1534. doi: 10.1016/j.csda.2009.01.005

Statistical genetics & statistical genomics: Where biology, epistemology, statistics, and computation collide

2009

Journal Article

Cognitive Ability at Age 11 and 70 Years, Information Processing Speed, and APOE Variation: The Lothian Birth Cohort 1936 Study

Luciano, Michelle, Gow, Alan J., Harris, Sarah E., Hayward, Caroline, Allerhand, Mike, Starr, John M., Visscher, Peter M. and Deary, Ian J. (2009). Cognitive Ability at Age 11 and 70 Years, Information Processing Speed, and APOE Variation: The Lothian Birth Cohort 1936 Study. Psychology and Aging, 24 (1), 129-138. doi: 10.1037/a0014780

Cognitive Ability at Age 11 and 70 Years, Information Processing Speed, and APOE Variation: The Lothian Birth Cohort 1936 Study

2009

Journal Article

Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936

Houlihan, L. M., Harris, S. E., Luciano, M., Gow, A. J., Starr, J. M., Visscher, P. M. and Deary, I. J. (2009). Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936. Genes Brain and Behavior, 8 (2), 238-247. doi: 10.1111/j.1601-183X.2008.00470.x

Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936

2009

Journal Article

Variation in the dysbindin gene and normal cognitive function in three independent population samples

M. Luciano, F. Miyajima, P. A. Lind, T. C. Bates, M. Horan, S. E. Harris, M. J. Wright, W. E. Ollier, C. Hayward, N. Pendleton, A. J. Gow, P. M. Visscher, J. M. Starr, I. J. Deary, N. G. Martin and A. Payton (2009). Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes, Brain and Behavior, 8 (2), 218-227. doi: 10.1111/j.1601-183X.2008.00462.x

Variation in the dysbindin gene and normal cognitive function in three independent population samples

2009

Journal Article

Characteristics and turnover of exopolymeric substances in a hypersaline microbial mat

Braissant, Olivier, Decho, Alan W., Przekop, Kristen M., Gallagher, Kimberley L., Glunk, Christina, Dupraz, Christophe and Visscher, Pieter T. (2009). Characteristics and turnover of exopolymeric substances in a hypersaline microbial mat. Fems Microbiology Ecology, 67 (2), 293-307. doi: 10.1111/j.1574-6941.2008.00614.x

Characteristics and turnover of exopolymeric substances in a hypersaline microbial mat

2009

Journal Article

Increased accuracy of artificial selection by using the realized relationship matrix

Hayes, B. J., Visscher, P. M. and Goddard, M. E. (2009). Increased accuracy of artificial selection by using the realized relationship matrix. Genetics Research, 91 (1), 47-60. doi: 10.1017/S0016672308009981

Increased accuracy of artificial selection by using the realized relationship matrix

2009

Journal Article

Family-based genome-wide association studies

Benyamin, Beben, Visscher, Peter M. and McRae, Allan F. (2009). Family-based genome-wide association studies. Pharmacogenomics, 10 (2), 181-190. doi: 10.2217/14622416.10.2.181

Family-based genome-wide association studies

2009

Journal Article

Association Mapping in Outbred Populations: Power and Efficiency When Genotyping Parents and Phenotyping Progeny

Chenoweth, SF and Visscher, PM (2009). Association Mapping in Outbred Populations: Power and Efficiency When Genotyping Parents and Phenotyping Progeny. Genetics, 181 (2), 755-765. doi: 10.1534/genetics.108.099218

Association Mapping in Outbred Populations: Power and Efficiency When Genotyping Parents and Phenotyping Progeny

2009

Journal Article

Autoinducers extracted from microbial mats reveal a surprising diversity of <i>N</i>-acylhomoserine lactones (AHLs) and abundance changes that may relate to diel pH

Decho, Alan W., Visscher, Pieter T., Ferry, John, Kawaguchi, Tomohiro, He, Lijian, Przekop, Kristen M., Norman, R. Sean and Reid, R. Pamela (2009). Autoinducers extracted from microbial mats reveal a surprising diversity of N-acylhomoserine lactones (AHLs) and abundance changes that may relate to diel pH. Environmental Microbiology, 11 (2), 409-420. doi: 10.1111/j.1462-2920.2008.01780.x

Autoinducers extracted from microbial mats reveal a surprising diversity of <i>N</i>-acylhomoserine lactones (AHLs) and abundance changes that may relate to diel pH

2009

Journal Article

DNA methylation profiles in monozygotic and dizygotic twins

Zachary A Kaminsky, Thomas Tang, Sun-Chong Wang, Carolyn Ptak, Gabriel H T Oh, Albert H C Wong, Laura A Feldcamp, Carl Virtanen, Jonas Halfvarson, Curt Tysk, Allan F McRae, Peter M Visscher, Grant W Montgomery, Irving I Gottesman, Nicholas G Martin and Art Petronis (2009). DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics, 41 (2), 240-245. doi: 10.1038/ng.286

DNA methylation profiles in monozygotic and dizygotic twins

2009

Journal Article

Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011

Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

2009

Journal Article

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

Knight, Helen M., Pickard, Benjamin S., Maclean, Alan, Malloy, Mary P., Soares, Dinesh C., McRae, Allan F., Condie, Alison, White, Angela, Hawkins, William, McGhee, Kevin, van Beck, Margaret, MacIntyre, Donald J., Starr, John M., Deary, Ian J., Visscher, Peter M., Porteous, David J., Cannon, Ronald E., St Clair, David, Muir, Walter J. and Blackwood, Douglas H. R. (2009). A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression. American Journal of Human Genetics, 85 (6), 833-846. doi: 10.1016/j.ajhg.2009.11.003

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

2009

Journal Article

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

Evans, David M., Visscher, Peter M. and Wray, Naomi R. (2009). Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. Human Molecular Genetics, 18 (18), 3525-3531. doi: 10.1093/hmg/ddp295

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

2009

Journal Article

Apolipoprotein E is not Related to Memory Abilities at 70 Years of Age

Luciano, Michelle, Gow, Alan J., Taylor, Michelle D., Hayward, Caroline, Harris, Sarah E., Campbell, Harry, Porteous, David J., Starr, John M., Visscher, Peter M. and Deary, Ian J. (2009). Apolipoprotein E is not Related to Memory Abilities at 70 Years of Age. Behavior Genetics, 39 (1), 6-14. doi: 10.1007/s10519-008-9236-x

Apolipoprotein E is not Related to Memory Abilities at 70 Years of Age

2008

Journal Article

Divergence between human populations estimated from linkage disequilibrium

Sved, John A., McRae, Allan F. and Visscher, Peter M. (2008). Divergence between human populations estimated from linkage disequilibrium. American Journal of Human Genetics, 83 (6), 737-743. doi: 10.1016/j.ajhg.2008.10.019

Divergence between human populations estimated from linkage disequilibrium

2008

Journal Article

Common genetic components of obesity traits and serum leptin

Hasselbalch, Ann L., Benyamin, Beben, Visscher, Peter M., Heitmann, Berit L., Kyvik, Kirsten O. and Sorensen, Thorkild I. A. (2008). Common genetic components of obesity traits and serum leptin. Obesity, 16 (12), 2723-2729. doi: 10.1038/oby.2008.440

Common genetic components of obesity traits and serum leptin

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

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