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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

523 works between 1997 and 2026

81 - 100 of 523 works

2022

Conference Publication

Contributions of maternal classical HLA alleles to the risk of miscarriages and stillbirths

Brito Nunes, Caroline, Hwang, Liang-Dar, Wang, Geng, Leggatt, Graham, Moen, Gunn-Helen and Evans, David (2022). Contributions of maternal classical HLA alleles to the risk of miscarriages and stillbirths. Queensland Perinatal Consortium (QPaCt), Brisbane, QLD Australia, 15 December 2022.

Contributions of maternal classical HLA alleles to the risk of miscarriages and stillbirths

2022

Journal Article

Using genomic structural equation modeling to partition the genetic covariance between birthweight and cardiometabolic risk factors into maternal and offspring components in the Norwegian HUNT study

Moen, Gunn-Helen, Nivard, Michel, Bhatta, Laxmi, Warrington, Nicole M., Willer, Cristen, Åsvold, Bjørn Olav, Brumpton, Ben and Evans, David M. (2022). Using genomic structural equation modeling to partition the genetic covariance between birthweight and cardiometabolic risk factors into maternal and offspring components in the Norwegian HUNT study. Behavior Genetics, 53 (1), 1-13. doi: 10.1007/s10519-022-10116-9

Using genomic structural equation modeling to partition the genetic covariance between birthweight and cardiometabolic risk factors into maternal and offspring components in the Norwegian HUNT study

2022

Journal Article

Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk

D’Urso, Shannon, Arumugam, Pooja, Weider, Therese, Hwang, Liang-Dar, Bond, Tom A., Kemp, John P., Warrington, Nicole M., Evans, David M., O’Mara, Tracy A. and Moen, Gunn-Helen (2022). Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk. BMC Medicine, 20 (1) 419, 1-17. doi: 10.1186/s12916-022-02585-w

Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk

2022

Journal Article

Birth weight and cardiometabolic risk factors: a discordant twin study in the UK Biobank

Wang, Geng, Bond, Tom A., Warrington, Nicole M. and Evans, David M. (2022). Birth weight and cardiometabolic risk factors: a discordant twin study in the UK Biobank. Journal of Developmental Origins of Health and Disease, 14 (2) PII S2040174422000538, 1-7. doi: 10.1017/s2040174422000538

Birth weight and cardiometabolic risk factors: a discordant twin study in the UK Biobank

2022

Conference Publication

Using structural equation modelling to partition genetic effects on birth weight at human leukocyte antigen loci into maternal and fetal components

Wang, Geng, Warrington, Nicole M. and Evans, David M. (2022). Using structural equation modelling to partition genetic effects on birth weight at human leukocyte antigen loci into maternal and fetal components. International Genetic Epidemiology Society 2022 Annual Meeting, Paris, France, 7 - 9 September 2022. Hoboken, NJ, United States: John Wiley & Sons. doi: 10.1002/gepi.22503

Using structural equation modelling to partition genetic effects on birth weight at human leukocyte antigen loci into maternal and fetal components

2022

Conference Publication

Partitioning genetic effects on birth weight into maternal and fetal components at classical HLA loci

Wang, Geng, Warrington, Nicole M. and Evans, David M. (2022). Partitioning genetic effects on birth weight into maternal and fetal components at classical HLA loci. DOHaD World Congress 2022, Vancouver, BC, Canada, 27 - 31 August 2022.

Partitioning genetic effects on birth weight into maternal and fetal components at classical HLA loci

2022

Journal Article

Using adopted individuals to partition indirect maternal genetic effects into prenatal and postnatal effects on offspring phenotypes

Hwang, Liang-Dar, Moen, Gunn-Helen and Evans, David M. (2022). Using adopted individuals to partition indirect maternal genetic effects into prenatal and postnatal effects on offspring phenotypes. eLife, 11 e73671, 1-27. doi: 10.7554/elife.73671

Using adopted individuals to partition indirect maternal genetic effects into prenatal and postnatal effects on offspring phenotypes

2022

Journal Article

Evaluating indirect genetic effects of siblings using singletons

Howe, Laurence J., Evans, David M., Hemani, Gibran, Davey Smith, George and Davies, Neil M. (2022). Evaluating indirect genetic effects of siblings using singletons. PLOS Genetics, 18 (7) e1010247, 1-16. doi: 10.1371/journal.pgen.1010247

Evaluating indirect genetic effects of siblings using singletons

2022

Journal Article

Mendelian randomization study of maternal coffee consumption and its influence on birthweight, stillbirth, miscarriage, gestational age and pre-term birth

Brito Nunes, Caroline, Huang, Peiyuan, Wang, Geng, Lundberg, Mischa, D’Urso, Shannon, Wootton, Robyn E., Borges, Maria Carolina, Lawlor, Deborah A., Warrington, Nicole M., Evans, David M., Hwang, Liang-Dar and Moen, Gunn-Helen (2022). Mendelian randomization study of maternal coffee consumption and its influence on birthweight, stillbirth, miscarriage, gestational age and pre-term birth. International Journal of Epidemiology, 52 (1), 1-13. doi: 10.1093/ije/dyac121

Mendelian randomization study of maternal coffee consumption and its influence on birthweight, stillbirth, miscarriage, gestational age and pre-term birth

2022

Journal Article

Intravitreal nesvacumab (antiangiopoietin 2) plus aflibercept in diabetic macular edema Phase 2 RUBY randomized trial

Brown, David M., Boyer, David S., Csaky, Karl, Vitti, Robert, Perlee, Lorah, Chu, Karen W., Asmus, Friedrich, Leal, Sergio, Zeitz, Oliver, Cheng, Yenchieh, Schmelter, Thomas and Heier, Jeffrey S. (2022). Intravitreal nesvacumab (antiangiopoietin 2) plus aflibercept in diabetic macular edema Phase 2 RUBY randomized trial. Retina: The Journal of Retinal and Vitreous Diseases, 42 (6), 1111-1120. doi: 10.1097/IAE.0000000000003441

Intravitreal nesvacumab (antiangiopoietin 2) plus aflibercept in diabetic macular edema Phase 2 RUBY randomized trial

2022

Journal Article

Food geographies 'in,' 'of' and 'for' the Anthropocene: introducing the issue and main themes

Maye, Damian, Coles, Ben and Evans, David (2022). Food geographies 'in,' 'of' and 'for' the Anthropocene: introducing the issue and main themes. Geographical Journal, 188 (3), 310-317. doi: 10.1111/geoj.12456

Food geographies 'in,' 'of' and 'for' the Anthropocene: introducing the issue and main themes

2022

Journal Article

Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

Howe, Laurence J., Nivard, Michel G., Morris, Tim T., Hansen, Ailin F., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., Palviainen, Teemu, van der Zee, Matthijs D., Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M., Bielak, Lawrence F., Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A., Reynolds, Chandra A., Balbona, Jared V., Andreassen, Ole A., Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie ... Within Family Consortium (2022). Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Nature Genetics, 54 (5), 581-592. doi: 10.1038/s41588-022-01062-7

Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

2022

Journal Article

DNA methylation in peripheral tissues and left-handedness

Odintsova, Veronika V., Suderman, Matthew, Hagenbeek, Fiona A., Caramaschi, Doretta, Hottenga, Jouke-Jan, Pool, René, Dolan, Conor V., Ligthart, Lannie, van Beijsterveldt, Catharina E M, Willemsen, Gonneke, de Geus, Eco J C, Beck, Jeffrey J., Ehli, Erik A., Cuellar-Partida, Gabriel, Evans, David M., Medland, Sarah E., Relton, Caroline L., Boomsma, Dorret I. and van Dongen, Jenny (2022). DNA methylation in peripheral tissues and left-handedness. Scientific Reports, 12 (1) 5606, 5606. doi: 10.1038/s41598-022-08998-0

DNA methylation in peripheral tissues and left-handedness

2022

Journal Article

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K E, Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N. ... Social Science Genetic Association Consortium (2022). Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Nature Genetics, 54 (4), 437-449. doi: 10.1038/s41588-022-01016-z

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

2022

Journal Article

Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomisation using polygenic risk scores

Bond, Tom A., Richmond, Rebecca C., Karhunen, Ville, Cuellar-Partida, Gabriel, Borges, Maria Carolina, Zuber, Verena, Couto Alves, Alexessander, Mason, Dan, Yang, Tiffany C., Gunter, Marc J., Dehghan, Abbas, Tzoulaki, Ioanna, Sebert, Sylvain, Evans, David M., Lewin, Alex M., O’Reilly, Paul F., Lawlor, Deborah A. and Järvelin, Marjo-Riitta (2022). Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomisation using polygenic risk scores. BMC Medicine, 20 (1) 34, 1-16. doi: 10.1186/s12916-021-02216-w

Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomisation using polygenic risk scores

2022

Journal Article

Frequency and symptoms of intravitreal silicone oil droplets following Becton Dickinson and Norm-Ject bevacizumab injections

Miller, Chase W., Wilneff, Matt A., Wuller, Allison L., Platt, Sean M., Schartman, Jerome P., Lewis, Shawn A., Rao, Llewellyn J., Wuller, Shannon L. and Miller, David G. (2022). Frequency and symptoms of intravitreal silicone oil droplets following Becton Dickinson and Norm-Ject bevacizumab injections. Ophthalmic Surgery Lasers and Imaging Retina, 53 (2), 108-112. doi: 10.3928/23258160-20220124-03

Frequency and symptoms of intravitreal silicone oil droplets following Becton Dickinson and Norm-Ject bevacizumab injections

2022

Journal Article

Limb development genes underlie variation in human fingerprint patterns

Li, Jinxi, Glover, James D., Zhang, Haiguo, Peng, Meifang, Tan, Jingze, Mallick, Chandana Basu, Hou, Dan, Yang, Yajun, Wu, Sijie, Liu, Yu, Peng, Qianqian, Zheng, Shijie C., Crosse, Edie I., Medvinsky, Alexander, Anderson, Richard A., Brown, Helen, Yuan, Ziyu, Zhou, Shen, Xu, Yanqing, Kemp, John P., Ho, Yvonne Y.W., Loesch, Danuta Z., Wang, Lizhong, Li, Yingxiang, Tang, Senwei, Wu, Xiaoli, Walters, Robin G., Lin, Kuang, Meng, Ruogu ... Wang, Sijia (2022). Limb development genes underlie variation in human fingerprint patterns. Cell, 185 (1), 95-112.e18. doi: 10.1016/j.cell.2021.12.008

Limb development genes underlie variation in human fingerprint patterns

2022

Book Chapter

Integrating family-based and Mendelian randomization designs

Hwang, Liang-Dar, Davies, Neil M., Warrington, Nicole M. and Evans, David M. (2022). Integrating family-based and Mendelian randomization designs. Combining human genetics and causal inference to understand human disease and development. (pp. 137-150) edited by George Davey Smith, Rebecca Richmond and Jean-Baptiste Pingault. Cold Spring Harbor, NY, United States: Cold Spring Harbor Laboratory Press.

Integrating family-based and Mendelian randomization designs

2022

Journal Article

Investigating a potential causal relationship between maternal blood pressure during pregnancy and future offspring cardiometabolic health

Wang, Geng, Bhatta, Laxmi, Moen, Gunn-Helen, Hwang, Liang-Dar, Kemp, John P., Bond, Tom A., Åsvold, Bjørn Olav, Brumpton, Ben, Evans, David M. and Warrington, Nicole M. (2022). Investigating a potential causal relationship between maternal blood pressure during pregnancy and future offspring cardiometabolic health. Hypertension, 79 (1), 170-177. doi: 10.1161/hypertensionaha.121.17701

Investigating a potential causal relationship between maternal blood pressure during pregnancy and future offspring cardiometabolic health

2021

Journal Article

Fetal alleles predisposing to metabolically favourable adiposity are associated with higher birth weight

Thompson, William D., Beaumont, Robin N., Kuang, Alan, Warrington, Nicole M., Ji, Yingjie, Tyrrell, Jess, Wood, Andrew R., Scholtens, Denise, Knight, Bridget A., Evans, David M., Lowe, Bill L., Santorelli, Gillian, Azad, Raq, Mason, Dan, Hattersley, Andrew T., Frayling, Timothy M., Yaghootkar, Hanieh, Borges, Maria-Carolina, Lawlor, Deborah A. and Freathy, Rachel M. (2021). Fetal alleles predisposing to metabolically favourable adiposity are associated with higher birth weight. Human Molecular Genetics, 31 (11), 1762-1775. doi: 10.1093/hmg/ddab356

Fetal alleles predisposing to metabolically favourable adiposity are associated with higher birth weight

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

    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

    Understanding the genetic epidemiology of women's reproductive health

    Principal Advisor

    Other advisors: Dr Gunn-Helen Moen

  • 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?

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communications@uq.edu.au