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Professor David Evans
Professor

David Evans

Email: 
Phone: 
+61 7 334 62617

Overview

Background

David Evans is an NHMRC Leadership Fellow and Professor of Statistical Genetics at the University of Queensland Institute for Molecular Bioscience. He is a winner of the NHMRC Marshall and Warren Award.

He completed his PhD in Statistical Genetics at the University of Queensland in 2003, before undertaking a four-year post-doctoral fellowship at the Wellcome Trust Centre for Human Genetics, University of Oxford where he worked as part of the The International HapMap Consortium and co-led the analysis of four diseases within the first Wellcome Trust Case Control Consortium. In 2007 he moved to take up a Senior Lecturer position at the University of Bristol where he led much of the genome-wide association studies work in the Avon Longitudinal Study of Parents and Children (ALSPAC). In 2013 he returned to take up a chair at the University of Queensland whilst continuing to lead an MRC Programme in statistical genetics at the University of Bristol.

His research interests include the genetic mapping of complex traits and diseases (including birthweight and other perinatal traits, osteoporosis, ankylosing spondylitis, sepsis, laterality) and the development of statistical methodologies in genetic epidemiology including approaches for gene mapping, individual risk prediction, causal modelling and dissecting the genetic architecture of complex traits. He has a particular interest in Mendelian randomization and has used it and other causal methods to investigate the Developmental Origins of Health and Disease (DOHaD)- the idea that adverse intrauterine exposures lead to increased risk of disease in later life.

He is Academic Codirector at the NIH funded International Workshop on Statistical Genetics Methods and is faculty on the European Programme in Educational Epidemiology.

He is Associate Editor at the International Journal of Epidemiology and Behavior Genetics journals.

Availability

Professor David Evans is:
Available for supervision
Media expert

Qualifications

  • Bachelor (Honours), The University of Queensland
  • Doctor of Philosophy, The University of Queensland

Research interests

  • Gestational Diabetes

  • Developmental Origins of Health and Disease (DOHaD)

  • Mendelian randomization

  • Genome-wide association studies

  • Causal Modeling

  • Sepsis

  • Osteoporosis

  • Ankylosing Spondylitis

Works

Search Professor David Evans’s works on UQ eSpace

508 works between 1997 and 2026

41 - 60 of 508 works

2024

Journal Article

A note on modelling bidirectional feedback loops in Mendelian randomization studies

Hwang, Liang-Dar and Evans, David M. (2024). A note on modelling bidirectional feedback loops in Mendelian randomization studies. Behavior Genetics, 54 (4), 367-373. doi: 10.1007/s10519-024-10183-0

A note on modelling bidirectional feedback loops in Mendelian randomization studies

2024

Journal Article

Ribosomal DNA copy number variation associates with hematological profiles and renal function in the UK Biobank

Rodriguez-Algarra, Francisco, Evans, David M. and Rakyan, Vardhman K. (2024). Ribosomal DNA copy number variation associates with hematological profiles and renal function in the UK Biobank. Cell Genomics, 4 (6) 100562, 100562. doi: 10.1016/j.xgen.2024.100562

Ribosomal DNA copy number variation associates with hematological profiles and renal function in the UK Biobank

2024

Journal Article

A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans

Moksnes, Marta R., Hansen, Ailin F., Wolford, Brooke N., Thomas, Laurent F., Rasheed, Humaira, Simić, Anica, Bhatta, Laxmi, Brantsæter, Anne Lise, Surakka, Ida, Zhou, Wei, Magnus, Per, Njølstad, Pål R., Andreassen, Ole A., Syversen, Tore, Zheng, Jie, Fritsche, Lars G., Evans, David M., Warrington, Nicole M., Nøst, Therese H., Åsvold, Bjørn Olav, Flaten, Trond Peder, Willer, Cristen J., Hveem, Kristian and Brumpton, Ben M. (2024). A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans. Communications Biology, 7 (1) 432, 432. doi: 10.1038/s42003-024-06101-z

A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans

2024

Journal Article

Estimating disease heritability from complex pedigrees allowing for ascertainment and covariates

Speed, Doug and Evans, David M. (2024). Estimating disease heritability from complex pedigrees allowing for ascertainment and covariates. The American Journal of Human Genetics, 111 (4), 680-690. doi: 10.1016/j.ajhg.2024.02.010

Estimating disease heritability from complex pedigrees allowing for ascertainment and covariates

2024

Journal Article

Maternal plasma cortisol’s effect on offspring birth weight: a Mendelian Randomisation study

Thompson, W. D., Reynolds, R. M., Beaumont, R. N., Warrington, N. M., Tyrrell, J., Wood, A. R., Evans, D. M., McDonald, T. J., Hattersley, A. H., Freathy, R. M., Lawlor, D. A. and Borges, M. C. (2024). Maternal plasma cortisol’s effect on offspring birth weight: a Mendelian Randomisation study. BMC Pregnancy and Childbirth, 24 (1) 65, 1-11. doi: 10.1186/s12884-024-06250-3

Maternal plasma cortisol’s effect on offspring birth weight: a Mendelian Randomisation study

2024

Other Outputs

Hwang_2024_NatCommun

Hwang, Daniel and Evans, David (2024). Hwang_2024_NatCommun. The University of Queensland. (Dataset) doi: 10.48610/9f69854

Hwang_2024_NatCommun

2024

Journal Article

A genome-wide association study of serum metabolite profiles in septic shock patients

Daubney, Emily R., D’Urso, Shannon, Cuellar-Partida, Gabriel, Rajbhandari, Dorrilyn, Peach, Elizabeth, de Guzman, Erika, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Cohen, Jeremy, Schirra, Horst Joachim, Venkatesh, Balasubramanian and Evans, David M. (2024). A genome-wide association study of serum metabolite profiles in septic shock patients. Critical Care Explorations, 6 (1) e1030, e1030. doi: 10.1097/cce.0000000000001030

A genome-wide association study of serum metabolite profiles in septic shock patients

2023

Journal Article

One-year and 18-month outcomes in nAMD patient eyes switched to brolucizumab alone versus to brolucizumab alternating with other anti-VEGF agents

Coney, Joseph M., Mccoy, Jasmyne E., Sinha, Samriddhi Buxy, Sonbolian, Nina, Zhou, Lujia, Hull, Thomas P., Lewis, Shawn A., Miller, David G., Novak, Michael A., Pendergast, Scott, Pham, Hang, Platt, Sean M., Rao, Llewelyn J., Schartman, Jerome P., Singerman, Lawrence J., Donkor, Richard, Fink, Margaret, Zubricky, Ryan and Karcher, Helene (2023). One-year and 18-month outcomes in nAMD patient eyes switched to brolucizumab alone versus to brolucizumab alternating with other anti-VEGF agents. Clinical Ophthalmology, 17, 3601-3611. doi: 10.2147/OPTH.S432957

One-year and 18-month outcomes in nAMD patient eyes switched to brolucizumab alone versus to brolucizumab alternating with other anti-VEGF agents

2023

Journal Article

Targeted investigational oncology agents in the NCI-60: a phenotypic systems-based resource

Morris, Joel, Kunkel, Mark W., White, Stephen L., Wishka, Donn G., Lopez, Omar D., Bowles, Lori, Brady, Penny Sellers, Ramsey, Patricia, Grams, Julie, Rohrer, Tiffany, Martin, Karen, Dexheimer, Thomas S., Coussens, Nathan P., Evans, David, Risbood, Prabhakar, Sonkin, Dmitriy, Williams, John D., Polley, Eric C., Collins, Jerry M., Doroshow, James H. and Teicher, Beverly A. (2023). Targeted investigational oncology agents in the NCI-60: a phenotypic systems-based resource. Molecular Cancer Therapeutics, 22 (11), 1270-1279. doi: 10.1158/1535-7163.MCT-23-0267

Targeted investigational oncology agents in the NCI-60: a phenotypic systems-based resource

2023

Journal Article

Intrauterine growth and offspring neurodevelopmental traits: a Mendelian randomization analysis of the Norwegian mother, father and child cohort study (MoBa)

D’Urso, Shannon, Moen, Gunn-Helen, Hwang, Liang-Dar, Hannigan, Laurie J., Corfield, Elizabeth C., Ask, Helga, Johannson, Stefan, Njølstad, Pål Rasmus, Beaumont, Robin N., Freathy, Rachel M., Evans, David M. and Havdahl, Alexandra (2023). Intrauterine growth and offspring neurodevelopmental traits: a Mendelian randomization analysis of the Norwegian mother, father and child cohort study (MoBa). JAMA Psychiatry, 81 (2), 144-156. doi: 10.1001/jamapsychiatry.2023.3872

Intrauterine growth and offspring neurodevelopmental traits: a Mendelian randomization analysis of the Norwegian mother, father and child cohort study (MoBa)

2023

Journal Article

Partitioning genetic effects on birthweight at classical human leukocyte antigen loci into maternal and fetal components, using structural equation modelling

Wang, Geng, Warrington, Nicole M. and Evans, David M. (2023). Partitioning genetic effects on birthweight at classical human leukocyte antigen loci into maternal and fetal components, using structural equation modelling. International Journal of Epidemiology, 53 (1) dyad142, 1-9. doi: 10.1093/ije/dyad142

Partitioning genetic effects on birthweight at classical human leukocyte antigen loci into maternal and fetal components, using structural equation modelling

2023

Journal Article

Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

Beaumont, Robin N., Flatley, Christopher, Vaudel, Marc, Wu, Xiaoping, Chen, Jing, Moen, Gunn-Helen, Skotte, Line, Helgeland, Øyvind, Solé-Navais, Pol, Banasik, Karina, Albiñana, Clara, Ronkainen, Justiina, Fadista, João, Stinson, Sara Elizabeth, Trajanoska, Katerina, Wang, Carol A., Westergaard, David, Srinivasan, Sundararajan, Sánchez-Soriano, Carlos, Bilbao, Jose Ramon, Allard, Catherine, Groleau, Marika, Kuulasmaa, Teemu, Leirer, Daniel J., White, Frédérique, Jacques, Pierre-Étienne, Cheng, Haoxiang, Hao, Ke, Andreassen, Ole A. ... The Early Growth Genetics (EGG) Consortium (2023). Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Nature Genetics, 55 (11), 1807-1819. doi: 10.1038/s41588-023-01520-w

Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

2023

Journal Article

Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study

Howe, Laurence J., Rasheed, Humaira, Jones, Paul R., Boomsma, Dorret I., Evans, David M., Giannelis, Alexandros, Hayward, Caroline, Hopper, John L., Hughes, Amanda, Lahtinen, Hannu, Li, Shuai, Lind, Penelope A., Martin, Nicholas G., Martikainen, Pekka, Medland, Sarah E., Morris, Tim T., Nivard, Michel G., Pingault, Jean-Baptiste, Silventoinen, Karri, Smith, Jennifer A., Willoughby, Emily A., Wilson, James F., Ahlskog, Rafael, Andreassen, Ole A., Ask, Helga, Campbell, Archie, Cheesman, Rosa, Cho, Yoonsu, Christensen, Kaare ... Within Family Consortium (2023). Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study. International Journal of Epidemiology, 52 (5), 1579-1591. doi: 10.1093/ije/dyad079

Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study

2023

Journal Article

Understanding national variations in reusable packaging: commercial drivers, regulatory factors, and provisioning systems

Beswick-Parsons, Rorie, Jackson, Peter and Evans, David M. (2023). Understanding national variations in reusable packaging: commercial drivers, regulatory factors, and provisioning systems. Geoforum, 145 103844, 1-12. doi: 10.1016/j.geoforum.2023.103844

Understanding national variations in reusable packaging: commercial drivers, regulatory factors, and provisioning systems

2023

Journal Article

The identification of distinct protective and susceptibility mechanisms for hip osteoarthritis: findings from a genome-wide association study meta-analysis of minimum joint space width and Mendelian randomisation cluster analyses

Faber, Benjamin G., Frysz, Monika, Boer, Cindy G., Evans, Daniel S., Ebsim, Raja, Flynn, Kaitlyn A., Lundberg, Mischa, Southam, Lorraine, Hartley, April, Saunders, Fiona R., Lindner, Claudia, Gregory, Jennifer S., Aspden, Richard M., Lane, Nancy E., Harvey, Nicholas C., Evans, David M., Zeggini, Eleftheria, Davey Smith, George, Cootes, Timothy, Van Meurs, Joyce, Kemp, John P. and Tobias, Jonathan H. (2023). The identification of distinct protective and susceptibility mechanisms for hip osteoarthritis: findings from a genome-wide association study meta-analysis of minimum joint space width and Mendelian randomisation cluster analyses. eBioMedicine, 95 104759, 104759. doi: 10.1016/j.ebiom.2023.104759

The identification of distinct protective and susceptibility mechanisms for hip osteoarthritis: findings from a genome-wide association study meta-analysis of minimum joint space width and Mendelian randomisation cluster analyses

2023

Journal Article

Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis

Medina-Gomez, Carolina, Mullin, Benjamin H., Chesi, Alessandra, Prijatelj, Vid, Kemp, John P., Shochat-Carvalho, Chen, Trajanoska, Katerina, Wang, Carol, Joro, Raimo, Evans, Tavia E., Schraut, Katharina E., Li-Gao, Ruifang, Ahluwalia, Tarunveer S., Zillikens, M. Carola, Zhu, Kun, Mook-Kanamori, Dennis O., Evans, Daniel S., Nethander, Maria, Knol, Maria J., Thorleifsson, Gudmar, Prokic, Ivana, Zemel, Babette, Broer, Linda, McGuigan, Fiona E., van Schoor, Natasja M., Reppe, Sjur, Pawlak, Mikolaj A., Ralston, Stuart H., van der Velde, Nathalie ... Rivadeneira, Fernando (2023). Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis. Communications Biology, 6 (1) 691, 1-12. doi: 10.1038/s42003-023-04869-0

Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis

2023

Journal Article

Real-world frequency and management of ocular adverse events in eyes with neovascular age-related macular degeneration treated with brolucizumab

Zubricky, Ryan, McCoy, Jasmyne, Donkor, Richard, Miller, David G., Sonbolian, Nina, Heaney, Andrew, Bilano, Ver, Karcher, Helene and Coney, Joseph M. (2023). Real-world frequency and management of ocular adverse events in eyes with neovascular age-related macular degeneration treated with brolucizumab. Ophthalmology and Therapy, 12 (5), 2397-2408. doi: 10.1007/s40123-023-00741-w

Real-world frequency and management of ocular adverse events in eyes with neovascular age-related macular degeneration treated with brolucizumab

2023

Journal Article

Insulin and body mass index decrease serum soluble leptin receptor levels in humans

Sommer, Christine, Vangberg, Kjersti G., Moen, Gunn-Helen, Evans, David M., Lee-Ødegård, Sindre, Blom-Høgestøl, Ingvild K., Sletner, Line, Jenum, Anne K., Drevon, Christian A., Gulseth, Hanne L. and Birkeland, Kåre I. (2023). Insulin and body mass index decrease serum soluble leptin receptor levels in humans. The Journal of Clinical Endocrinology and Metabolism, 108 (5), 1110-1119. doi: 10.1210/clinem/dgac699

Insulin and body mass index decrease serum soluble leptin receptor levels in humans

2023

Journal Article

Production and consumption in agri-food transformations: rethinking integrative perspectives

Beacham, Jonathan D. and Evans, David M. (2023). Production and consumption in agri-food transformations: rethinking integrative perspectives. Sociologia Ruralis, 63 (2), 309-327. doi: 10.1111/soru.12423

Production and consumption in agri-food transformations: rethinking integrative perspectives

2023

Journal Article

Do environmental effects indexed by parental genetic variation influence common psychiatric symptoms in childhood?

Jami, Eshim S., Hammerschlag, Anke R., Sallis, Hannah M., Qiao, Zhen, Andreassen, Ole A., Magnus, Per M., Njølstad, Pål R., Havdahl, Alexandra, Pingault, Jean-Baptiste, Evans, David M., Munafò, Marcus R., Ystrom, Eivind, Bartels, Meike and Middeldorp, Christel (2023). Do environmental effects indexed by parental genetic variation influence common psychiatric symptoms in childhood?. Translational Psychiatry, 13 (1) 94, 1-6. doi: 10.1038/s41398-023-02348-y

Do environmental effects indexed by parental genetic variation influence common psychiatric symptoms in childhood?

Funding

Current funding

  • 2023 - 2027
    Developing and Applying Mendelian Randomization Methods to Facilitate Drug Discovery and Solve Intractable Problems in Medical Research
    NHMRC Investigator Grants
    Open grant

Past funding

  • 2020 - 2024
    Developing and Applying Statistical Genetics Methods to Elucidate the Developmental Origins of Health and Disease
    NHMRC IDEAS Grants
    Open grant
  • 2019 - 2022
    Identifying maternal and fetal genetic determinants of infant birthweight and their relationship to offspring cardiometabolic risk
    NHMRC Project Grant
    Open grant
  • 2018 - 2024
    The role of size, shape and structure of bones and joints, in explaining common musculoskeletal diseases (Wellcome Trust Grant administered by University of Bristol)
    University of Bristol
    Open grant
  • 2018 - 2022
    Developing and applying statistical genetics methods to identify genes, molecular biomarkers and environmental agents that causally affect risk of complex musculoskeletal diseases
    NHMRC Research Fellowship
    Open grant
  • 2018 - 2020
    Enhancing host defence mechanisms in severe bacterial infections
    NHMRC Project Grant
    Open grant
  • 2017 - 2021
    Development and application of a Mendelian randomization framework aimed at dissecting the biological basis of ankylosing spondylitis and other complex diseases
    NHMRC Project Grant
    Open grant
  • 2017 - 2020
    Using Methods in Genetic Epidemiology to Elucidate the Relationship Between Viral Infection and Risk of Autoimmune Disease
    NHMRC Project Grant
    Open grant
  • 2016
    Establishing a gnotobiotic germ-free mouse facility
    UQ Major Equipment and Infrastructure
    Open grant
  • 2015 - 2016
    A biomarker for sepsis to thwart antibiotic overuse in the intensive care unit
    Royal Brisbane and Women's Hospital
    Open grant
  • 2015
    Bivariate genome-wide association study of birth weight and endophenotypes related to five diseases in later life
    UWA-UQ Bilateral Research Collaboration Award
    Open grant
  • 2015 - 2017
    Finding novel genetic associations in Ankylosing Spondylitis
    University of Oxford
    Open grant
  • 2015 - 2018
    Gene expression profiling in critically ill patients with septic shock: The ADRENAL-GEPS Study
    NHMRC Project Grant
    Open grant
  • 2015 - 2018
    Novel ways of utilizing genome-wide DNA methylation data from peripheral blood samples in genetic epidemiology
    NHMRC Project Grant
    Open grant
  • 2014
    Calibration of single channel and liquid handling robots
    UQ Major Equipment and Infrastructure
    Open grant
  • 2014 - 2016
    Dissecting the great ophthalmic masquerade: The Global Giant Cell Arteritis Genomics Consortium (NHMRC Project Grant administered by the Centre for Eye Research Australia)
    Centre for Eye Research Australia
    Open grant
  • 2014
    Multiplex High Throughput Bio-plex Protein Assay Platform
    UQ Major Equipment and Infrastructure
    Open grant
  • 2012 - 2018
    Clinical Researcher Training
    Research Donation Generic
    Open grant

Supervision

Availability

Professor David Evans is:
Available for supervision

Looking for a supervisor? Read our advice on how to choose a supervisor.

Available projects

  • Sometimes Correlation DOES Equal Causation: Developing Statistical Methods to Determine Causality Using Genetic Data

    There is a well-known mantra that correlation does not necessarily equal causation. This is why randomized controlled trials in which participants are physically randomized into treatment and placebo groups are the gold standard for assessing causality in epidemiological investigations. However, what is less appreciated is that strong evidence for causality can sometimes be obtained using observational data only. In particular, genotypes are randomly transmitted from parents to their offspring independent of the environment and other confounding factors, meaning that genotypes associated with particular traits can be used like natural “randomized controlled trials” to examine whether these traits causally affect risk of disease.

    The aim of this PhD project is to develop statistical methods to assess causality using observational data alone. The successful candidate will gain experience across a wide range of advanced statistical genetics methodologies including Mendelian randomization (a way of using genetic variants to investigate putatively causal relationships), structural equation modelling, genome-wide association analysis (GWAS), genetic restricted maximum likelihood (G-REML) analysis of genome-wide data which can be used to partition variation in phenotypes into genetic and environmental sources of variation, and instrumental variables analysis (using natural “experiments” to obtain information on causality from observational data). The candidate will apply the new statistical methods that they develop to large genetically informative datasets like the UK Biobank (500,000 individuals with genome-wide SNP data).

  • Using Genetics To Unravel The Developmental Origins of Health and Disease (DOHaD)

    During the final winter of the Second World War, a German blockade of food supplies to the occupied Netherlands precipitated a severe famine known as the Dutch Hunger Winter of 1944–45. This tragic episode created an unprecedented natural experiment for studying how severe nutritional deprivation during pregnancy can influence the long term health of the offspring of these mothers across their life course.

    Genetic approaches such as Mendelian randomization provide another powerful natural experiment, using inherited genetic variants as proxies for potentially causal exposures. This allows researchers to investigate whether factors experienced during development or later in life have a causal influence on health and disease, helping to disentangle causation from correlation.

    The aim of this PhD project is to develop and apply statistical genetic methods to assess the impact of adverse maternal exposures during pregnancy on increased risk of disease in offspring.

  • Understanding the Causes and Consequences of Gestational Diabetes

    Gestational diabetes mellitus (GDM) is a form of diabetes that develops during pregnancy, arising when the body cannot produce enough insulin to meet the increased demands of pregnancy and resulting in elevated blood glucose levels. Women who experience GDM have a substantially increased risk of developing type 2 diabetes later in life, with estimates suggesting a 7–10-fold higher risk compared with women without GDM.

    This PhD project will use Mendelian randomization and large scale genetic studies to investigate the causes and consequences of gestational diabetes, identifying potentially modifiable risk factors and clarifying its longer-term impact on the health of mothers and their children. The project will harness genetic data to help disentangle causal relationships from correlation and uncover new insights into the developmental and lifelong pathways linking gestational diabetes with later disease.

Supervision history

Current supervision

  • Doctor Philosophy

    Understanding the genetic epidemiology of women's reproductive health

    Principal Advisor

    Other advisors: Dr Gunn-Helen Moen

  • Doctor Philosophy

    Using genetics to predict drug efficacy and on-target side effects of pharmacological agents

    Principal Advisor

    Other advisors: Professor Glenn King, Associate Professor Sonia Shah

  • Doctor Philosophy

    Genetics of sensory nutrition - using genetics to understand how taste and olfactory perception influences eating behaviour and health

    Associate Advisor

    Other advisors: Dr Brooke Devlin, Dr Daniel Hwang

  • Doctor Philosophy

    Investigating the relationship between adverse perinatal environments and the development of childhood depression and anxiety using statistical genetics methods

    Associate Advisor

    Other advisors: Dr Daniel Hwang

Completed supervision

Media

Enquiries

Contact Professor David Evans directly for media enquiries about:

  • Genetics
  • Genome-wide association
  • Mendelian randomization
  • Twin Studies

Need help?

For help with finding experts, story ideas and media enquiries, contact our Media team:

communications@uq.edu.au