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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

421 - 440 of 803 works

2013

Journal Article

Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season

Parnell, Grant P., Gatt, Prudence N., McKay, Fiona C., Schibeci, Stephen, Krupa, Malgorzata, Powell, Joseph E., Visscher, Peter M., Montgomery, Grant W., Lechner-Scott, Jeannette, Broadley, Simon, Liddle, Christopher, Slee, Mark, Vucic, Steve, Stewart, Graeme J. and Booth, David R. (2013). Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season. Multiple Sclerosis, 20 (6), 675-685. doi: 10.1177/1352458513507819

Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season

2013

Journal Article

Genetic and nongenetic variation revealed for the principal components of human gene expression

Goldinger, Anita, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2013). Genetic and nongenetic variation revealed for the principal components of human gene expression. Genetics, 195 (3), 1117-1128. doi: 10.1534/genetics.113.153221

Genetic and nongenetic variation revealed for the principal components of human gene expression

2013

Conference Publication

Are SNPs associated with educational attainment also associated with cognitive function?

Rietveld, Cornelius, Koellinger, Philipp, Benjamin, Daniel, Cesarini, David, Davey-Smith, George, Davies, Gail, Deary, Ian, Johannesson, Magnus, Plomin, Robert, Posthuma, D. and Visscher, Peter (2013). Are SNPs associated with educational attainment also associated with cognitive function?. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, 28 June-02 July 2013. New York, NY United States: Springer New York LLC. doi: 10.1007/s10519-013-9623-9

Are SNPs associated with educational attainment also associated with cognitive function?

2013

Journal Article

Estimation of SNP heritability from dense genotype data

Lee, S. Hong, Yang, Jian, Chen, Guo-Bo, Ripke, Stephan, Stahl, Eli A., Hultman, Christina M., Sklar, Pamela, Visscher, Peter M., Sullivan, Patrick F., Goddard, Michael E. and Wray, Naomi (2013). Estimation of SNP heritability from dense genotype data. American Journal Of Human Genetics, 93 (6), 1151-1155. doi: 10.1016/j.ajhg.2013.10.015

Estimation of SNP heritability from dense genotype data

2012

Journal Article

A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing

Davies, G., Harris, S. E., Reynolds, C. A., Payton, A., Knight, H. M., Liewald, D. C., Lopez, L. M., Luciano, M., Gow, A. J., Corley, J., Henderson, R., Murray, C., Pattie, A., Fox, H. C., Redmond, P., Lutz, M. W., Chiba-Falek, O., Linnertz, C., Saith, S., Haggarty, P., McNeill, G., Ke, X., Ollier, W., Horan, M., Roses, A. D., Ponting, C. P., Porteous, D. J., Tenesa, A., Pickles, A. ... Deary, I. J. (2012). A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing. Molecular Psychiatry, 19 (1), 76-87. doi: 10.1038/mp.2012.159

A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing

2012

Journal Article

Seventy-five genetic loci influencing the human red blood cell

van der Harst, Pim, Zhang, Weihua, Leach, Irene Mateo, Rendon, Augusto, Verweij, Niek, Sehmi, Joban, Paul, Dirk S., Elling, Ulrich, Allayee, Hooman, Li, Xinzhong, Radhakrishnan, Aparna, Tan, Sian-Tsung, Voss, Katrin, Weichenberger, Christian X., Albers, Cornelis A., Al-Hussani, Abtehale, Asselbergs, Folkert W., Ciullo, Marina, Danjou, Fabrice, Dina, Christian, Esko, Tonu, Evans, David M., Franke, Lude, Goegele, Martin, Hartiala, Jaana, Hersch, Micha, Holm, Hilma, Hottenga, Jouke-Jan, Kanoni, Stavroula ... Chambers, John C. (2012). Seventy-five genetic loci influencing the human red blood cell. Nature, 492 (7429), 369-375. doi: 10.1038/nature11677

Seventy-five genetic loci influencing the human red blood cell

2012

Conference Publication

Additive genetic variation in risk to schizophrenia across African American and European American populations

de Candia, Teresa, Lee, Hong, Yang, Jian, Browning, Brian, Gejman, Pablo, Levinson, Douglas, Hewitt, John, Visscher, Peter, Wray, Naomi and Keller, Matthew (2012). Additive genetic variation in risk to schizophrenia across African American and European American populations. 42nd Annual Meeting of the Behavior-Genetics-Association, Edinburgh Scotland, Jun 22-25, 2012.

Additive genetic variation in risk to schizophrenia across African American and European American populations

2012

Journal Article

Reclassify controls at your own risk

Witte, John S. and Visscher, Peter M. (2012). Reclassify controls at your own risk. Epidemiology, 23 (6), 910-911. doi: 10.1097/EDE.0b013e31826cc118

Reclassify controls at your own risk

2012

Journal Article

Inside the alkalinity engine: the role of electron donors in the organomineralization potential of sulfate-reducing bacteria

Gallagher, K. L., Kading, T. J., Braissant, O., Dupraz, C. and Visscher, P. T. (2012). Inside the alkalinity engine: the role of electron donors in the organomineralization potential of sulfate-reducing bacteria. Geobiology, 10 (6), 518-530. doi: 10.1111/j.1472-4669.2012.00342.x

Inside the alkalinity engine: the role of electron donors in the organomineralization potential of sulfate-reducing bacteria

2012

Journal Article

Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding

Verweij, Karin J. H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Raback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kahonen, Mika, Viikari, Jorma, Raikkonen, Katri, Eriksson, Johan G., Keltikangas-Jarvinen, Liisa, Lehtimaki, Terho, Martin, Nicholas G., Jarvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C. and Zietsch, Brendan P. (2012). Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding. Evolution, 66 (10), 3238-3251. doi: 10.1111/j.1558-5646.2012.01679.x

Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding

2012

Journal Article

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

Lee, S. H., Yang, J., Goddard, M. E., Visscher, P. M. and Wray, N. R. (2012). Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Bioinformatics, 28 (19) bts474, 2540-2542. doi: 10.1093/bioinformatics/bts474

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

2012

Journal Article

Effect of Inorganic and Organic Ligands on the Bioavailability of Methylmercury as Determined by Using a <i>mer-lux</i> Bioreporter

Ndu, Udonna, Mason, Robert P., Zhang, Huan, Lin, Senjie and Visscher, Pieter T. (2012). Effect of Inorganic and Organic Ligands on the Bioavailability of Methylmercury as Determined by Using a mer-lux Bioreporter. Applied and Environmental Microbiology, 78 (20), 7276-7282. doi: 10.1128/AEM.00362-12

Effect of Inorganic and Organic Ligands on the Bioavailability of Methylmercury as Determined by Using a <i>mer-lux</i> Bioreporter

2012

Journal Article

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

Lips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., International Schizophrenia Consortium, Holmans, P. A., O'Donovan, M. C., Purcell, S. M., Smit, A. B., Verhage, M., Sullivan, P. F., Visscher, P. M. and Posthuma, D. (2012). Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry, 17 (10), 996-1006. doi: 10.1038/mp.2011.117

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

2012

Journal Article

A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

Surakka, Ida, Whitfield, John B., Perola, Markus, Visscher, Peter M., Montgomery, Grant W., Falchi, Mario, Willemsen, Gonneke, de Geus, Eco J. C., Magnusson, Patrik K. E., Christensen, Kaare, Sorensen, Thorild I. A., Pietilainen, Kirsi H., Rantanen, Taina, Silander, Kaisa, Widen, Elisabeth, Muilu, Juhu, Rahman, Iffat, Liljedahl, Ulrika, Syvanen, Ann-Christine, Palotie, Aarno, Kaprio, Jaakko, Kyvik, Kirsten O., Pedersen, Nancy L., Boomsma, Dorret I., Spector, Tim, Martin, Nicolas G., Ripatti, Samuli and Peltonen, Leena (2012). A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin Research and Human Genetics, 15 (6), 691-699. doi: 10.1017/thg.2012.63

A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

2012

Journal Article

FTO genotype is associated with phenotypic variability of body mass index

Yang, Jian, Loos, Ruth J., Powell, Joseph E., Medland, Sarah E, Speliotes, Elizabeth K., Chasman, Daniel I., Rose, Lynda M., Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Magi, Reedik, Waite, Lindsay, Vernon Smith, Albert, Yerges-Armstrong, Laura M., Monda, Keri L., Hadley, David, Mahajan, Anubha, Li, Guo, Kapur, Karen, Vitart, Veronique, Huffman, Jennifer E., Wang, Sophie R., Palmer, Cameron, Esko, To˜nu, Fischer, Krista, Hua Zhao, Jing, Demirkan, Ayse, Isaacs, Aaron, Feitosa, Mary F., Luan, Jian’an ... Visscher, Peter (2012). FTO genotype is associated with phenotypic variability of body mass index. Nature, 490 (7419), 267-272. doi: 10.1038/nature11401

FTO genotype is associated with phenotypic variability of body mass index

2012

Journal Article

Multivariate genetic analyses of cognition and academic achievement from two population samples of 174,000 and 166,000 school children

Calvin, Catherine M., Deary, Ian J., Webbink, Dinand, Smith, Pauline, Fernandes, Cres, Lee, Sang Hong, Luciano, Michelle and Visscher, Peter M. (2012). Multivariate genetic analyses of cognition and academic achievement from two population samples of 174,000 and 166,000 school children. Behavior Genetics, 42 (5), 699-710. doi: 10.1007/s10519-012-9549-7

Multivariate genetic analyses of cognition and academic achievement from two population samples of 174,000 and 166,000 school children

2012

Journal Article

Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence

Gordon, Lavinia, Joo, Jihoon E., Powell, Joseph E., Ollikainen, Miina, Novakovic, Boris, Li, Xin, Andronikos, Roberta, Cruickshank, Mark N., Conneely, Karen N., Smith, Alicia K., Alisch, Reid S., Morley, Ruth, Visscher, Peter M., Craig, Jeffrey M. and Saffery, Richard (2012). Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence. Genome Research, 22 (8), 1395-1406. doi: 10.1101/gr.136598.111

Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence

2012

Journal Article

Comparing linkage and association analyses in sheep points to a better way of doing GWAS

Kemper, Kathryn E., Daetwyler, Hans D., Visscher, Peter M. and Goddard, Michael E. (2012). Comparing linkage and association analyses in sheep points to a better way of doing GWAS. Genetics Research, 94 (4), 191-203. doi: 10.1017/S0016672312000365

Comparing linkage and association analyses in sheep points to a better way of doing GWAS

2012

Journal Article

Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease

Tang, Weihong, Schwienbacher, Christine, Lopez, Lorna M., Ben-Shlomo, Yoav, Oudot-Mellakh, Tiphaine, Johnson, Andrew D., Samani, Nilesh J., Basu, Saonli, Goegele, Martin, Davies, Gail, Lowe, Gordon D. O., Tregouet, David-Alexandre, Tan, Adrian, Pankow, James S., Tenesa, Albert, Levy, Daniel, Volpato, Claudia B., Rumley, Ann, Gow, Alan J., Minelli, Cosetta, Yarnell, John W. G., Porteous, David J., Starr, John M., Gallacher, John, Boerwinkle, Eric, Visscher, Peter M., Pramstaller, Peter P., Cushman, Mary, Emilsson, Valur ... Folsom, Aaron R. (2012). Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease. American Journal of Human Genetics, 91 (1), 152-162. doi: 10.1016/j.ajhg.2012.05.009

Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease

2012

Journal Article

Potential importance of physiologically diverse benthic foraminifera in sedimentary nitrate storage and respiration

Bernhard, Joan M., Casciotti, Karen L., McIlvin, Matthew R., Beaudoin, David J., Visscher, Pieter T. and Edgcomb, Virginia P. (2012). Potential importance of physiologically diverse benthic foraminifera in sedimentary nitrate storage and respiration. Journal of Geophysical Research-Biogeosciences, 117 G03002. doi: 10.1029/2012JG001949

Potential importance of physiologically diverse benthic foraminifera in sedimentary nitrate storage and respiration

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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