Skip to menu Skip to content Skip to footer
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

  • Mendelian randomization

  • Genome-wide association studies

  • Causal Modeling

  • Developmental Origins of Health and Disease (DOHaD)

  • Laterality

  • Sepsis

  • Osteoporosis

  • Ankylosing Spondylitis

Works

Search Professor David Evans’s works on UQ eSpace

413 works between 1997 and 2024

61 - 80 of 413 works

2021

Journal Article

Genome-wide association study of circulating interleukin 6 levels identifies novel loci

Ahluwalia, Tarunveer S., Prins, Bram P., Abdollahi, Mohammadreza, Armstrong, Nicola J., Aslibekyan, Stella, Bain, Lisa, Jefferis, Barbara, Baumert, Jens, Beekman, Marian, Ben-Shlomo, Yoav, Bis, Joshua C., Mitchell, Braxton D., de Geus, Eco, Delgado, Graciela E., Marek, Diana, Eriksson, Joel, Kajantie, Eero, Kanoni, Stavroula, Kemp, John P., Lu, Chen, Marioni, Riccardo E., McLachlan, Stela, Milaneschi, Yuri, Nolte, Ilja M., Petrelis, Alexandros M., Porcu, Eleonora, Sabater-Lleal, Maria, Naderi, Elnaz, Seppälä, Ilkka ... CHARGE Inflammation Working Group (2021). Genome-wide association study of circulating interleukin 6 levels identifies novel loci. Human Molecular Genetics, 30 (5), 393-409. doi: 10.1093/hmg/ddab023

Genome-wide association study of circulating interleukin 6 levels identifies novel loci

2021

Journal Article

Direct and indirect effects of maternal, paternal, and offspring genotypes: Trio-GCTA

Eilertsen, Espen Moen, Jami, Eshim Shahid, McAdams, Tom A., Hannigan, Laurie J., Havdahl, Alexandra S., Magnus, Per, Evans, David M. and Ystrom, Eivind (2021). Direct and indirect effects of maternal, paternal, and offspring genotypes: Trio-GCTA. Behavior Genetics, 51 (2), 154-161. doi: 10.1007/s10519-020-10036-6

Direct and indirect effects of maternal, paternal, and offspring genotypes: Trio-GCTA

2021

Journal Article

Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color

Simcoe, Mark, Valdes, Ana, Liu, Fan, Furlotte, Nicholas A., Evans, David M., Hemani, Gibran, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Vuckovic, Dragana, Girotto, Giorgia, Sala, Cinzia, Catamo, Eulalia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex, Wu, Wenting, Kraft, Peter, Hammond, Christopher J., Shi, Yuan, Chen, Yan ... the International Visible Trait Genetics Consortium (2021). Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color. Science Advances, 7 (11) abd1239, eabd1239. doi: 10.1126/sciadv.abd1239

Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color

2021

Journal Article

The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption

Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics, 51 (3), 223-236. doi: 10.1007/s10519-021-10044-0

The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption

2021

Journal Article

Modeling parent-specific genetic nurture in families with missing parental genotypes: application to birthweight and BMI

Tubbs, Justin D., Hwang, Liang-Dar, Luong, Justin, Evans, David M. and Sham, Pak C. (2021). Modeling parent-specific genetic nurture in families with missing parental genotypes: application to birthweight and BMI. Behavior Genetics, 51 (3), 289-300. doi: 10.1007/s10519-020-10040-w

Modeling parent-specific genetic nurture in families with missing parental genotypes: application to birthweight and BMI

2021

Journal Article

Variants associated with HHIP expression have sexdifferential effects on lung function

Fawcett, Katherine A., Obeidat, Ma'en, Melbourne, Carl, Shrine, Nick, Guyatt, Anna L., John, Catherine, Luan, Jian'an, Richmond, Anne, Moksnes, Marta R., Granell, Raquel, Weiss, Stefan, Imboden, Medea, May-Wilson, Sebastian, Hysi, Pirro, Boutin, Thibaud S., Portas, Laura, Flexeder, Claudia, Harris, Sarah E., Wang, Carol A., Lyytikäinen, Leo-Pekka, Palviainen, Teemu, Foong, Rachel E., Keidel, Dirk, Minelli, Cosetta, Langenberg, Claudia, Bossé, Yohan, Berge, Maarten Van den, Sin, Don D., Hao, Ke ... Wain, Louise V. (2021). Variants associated with HHIP expression have sexdifferential effects on lung function. Wellcome Open Research, 5, 1-20. doi: 10.12688/WELLCOMEOPENRES.15846.2

Variants associated with HHIP expression have sexdifferential effects on lung function

2020

Journal Article

Investigating the causal effect of maternal vitamin B12 and folate levels on offspring birthweight

Moen, Gunn-Helen, Beaumont, Robin N., Grarup, Niels, Sommer, Christine, Shields, Beverley M., Lawlor, Deborah A., Freathy, Rachel M., Evans, David M. and Warrington, Nicole M. (2020). Investigating the causal effect of maternal vitamin B12 and folate levels on offspring birthweight. International Journal of Epidemiology, 50 (1), 179-189. doi: 10.1093/ije/dyaa256

Investigating the causal effect of maternal vitamin B12 and folate levels on offspring birthweight

2020

Journal Article

A cautionary note on using Mendelian randomization to examine the Barker hypothesis and Developmental Origins of Health and Disease (DOHaD)

D'Urso, Shannon, Wang, Geng, Hwang, Liang-Dar, Moen, Gunn-Helen, Warrington, Nicole M. and Evans, David M. (2020). A cautionary note on using Mendelian randomization to examine the Barker hypothesis and Developmental Origins of Health and Disease (DOHaD). Journal of Developmental Origins of Health and Disease, 12 (5) PII S2040174420001105, 1-6. doi: 10.1017/S2040174420001105

A cautionary note on using Mendelian randomization to examine the Barker hypothesis and Developmental Origins of Health and Disease (DOHaD)

2020

Journal Article

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

Brumpton, Ben, Sanderson, Eleanor, Heilbron, Karl, Hartwig, Fernando Pires, Harrison, Sean, Vie, Gunnhild Åberge, Cho, Yoonsu, Howe, Laura D., Hughes, Amanda, Boomsma, Dorret I., Havdahl, Alexandra, Hopper, John, Neale, Michael, Nivard, Michel G., Pedersen, Nancy L., Reynolds, Chandra A., Tucker-Drob, Elliot M., Grotzinger, Andrew, Howe, Laurence, Morris, Tim, Li, Shuai, Brumpton, Ben, Sanderson, Eleanor, Heilbron, Karl, Hartwig, Fernando Pires, Harrison, Sean, Vie, Gunnhild Åberge, Cho, Yoonsu, Howe, Laura D. ... Davies, Neil M. (2020). Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses. Nature Communications, 11 (1) 3519, 3519. doi: 10.1038/s41467-020-17117-4

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

2020

Conference Publication

Do maternal intrauterine environmental influences that lower offspring birthweight causally increase offspring cardiometabolic risk factors in later life? A Mendelian randomization study of 45,849 genotyped parent offspring pairs in the HUNT study using the OpenMx software

Moen, Gunn-Helen, Brumpton, Ben, Willer, Cristen, Asvold, Bjorn Olav, Birkeland, Kare, Neale, Michael C., Freathy, Rachel M., Smith, George Davey, Lawlor, Deborah A., Kirkpatrick, Robert M., Warrington, Nicole M. and Evans, David M. (2020). Do maternal intrauterine environmental influences that lower offspring birthweight causally increase offspring cardiometabolic risk factors in later life? A Mendelian randomization study of 45,849 genotyped parent offspring pairs in the HUNT study using the OpenMx software. 50th Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 26, 2020. NEW YORK: SPRINGER.

Do maternal intrauterine environmental influences that lower offspring birthweight causally increase offspring cardiometabolic risk factors in later life? A Mendelian randomization study of 45,849 genotyped parent offspring pairs in the HUNT study using the OpenMx software

2020

Journal Article

Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

Moen, Gunn-Helen, Brumpton, Ben, Willer, Cristen, Åsvold, Bjørn Olav, Birkeland, Kåre I., Wang, Geng, Neale, Michael C., Freathy, Rachel M., Smith, George Davey, Lawlor, Deborah A., Kirkpatrick, Robert M., Warrington, Nicole M. and Evans, David M. (2020). Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort. Nature Communications, 11 (1) 5404, 5404. doi: 10.1038/s41467-020-19257-z

Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

2020

Journal Article

Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs

Hwang, Liang-Dar, Tubbs, Justin D., Luong, Justin, Lundberg, Mischa, Moen, Gunn-Helen, Wang, Geng, Warrington, Nicole M., Sham, Pak C., Cuellar-Partida, Gabriel and Evans, David M. (2020). Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs. PLoS Genetics, 16 (10) e1009154, e1009154. doi: 10.1371/journal.pgen.1009154

Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs

2020

Journal Article

The Boulder Workshop Question Box

Evans, David M. (2020). The Boulder Workshop Question Box. Behavior Genetics, 51 (3), 181-190. doi: 10.1007/s10519-020-10022-y

The Boulder Workshop Question Box

2020

Journal Article

Genome-wide association study identifies 48 common genetic variants associated with handedness

Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali ... Medland, Sarah E. (2020). Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), 59-70. doi: 10.1038/s41562-020-00956-y

Genome-wide association study identifies 48 common genetic variants associated with handedness

2020

Journal Article

Plasma cortisol, aldosterone, and ascorbic acid concentrations in patients with septic shock do not predict treatment effect of hydrocortisone on mortality. A nested cohort study

Cohen, Jeremy, Bellomo, Rinaldo, Billot, Laurent, Burrell, Louise M., Evans, David M., Finfer, Simon, Hammond, Naomi E., Li, Qiang, Liu, David, McArthur, Colin, McWhinney, Brett, Moore, John, Myburgh, John, Peake, Sandra, Pretorius, Carel, Rajbhandari, Dorrilyn, Rhodes, Andrew, Saxena, Manoj, Ungerer, Jacobus P. J., Young, Morag J. and Venkatesh, Balasubramanian (2020). Plasma cortisol, aldosterone, and ascorbic acid concentrations in patients with septic shock do not predict treatment effect of hydrocortisone on mortality. A nested cohort study. American Journal of Respiratory and Critical Care Medicine, 202 (5), 700-707. doi: 10.1164/rccm.202002-0281OC

Plasma cortisol, aldosterone, and ascorbic acid concentrations in patients with septic shock do not predict treatment effect of hydrocortisone on mortality. A nested cohort study

2020

Journal Article

Tasting as a social practice: a methodological experiment in making taste public

Jackson, Peter, Evans, David, Truninger, Monica, Baptista, Joao and Nunes, Nadia Carvalho (2020). Tasting as a social practice: a methodological experiment in making taste public. Social & Cultural Geography, 23 (5), 739-756. doi: 10.1080/14649365.2020.1809013

Tasting as a social practice: a methodological experiment in making taste public

2020

Journal Article

Septic shock: a genomewide association study and polygenic risk score analysis

D'Urso, Shannon, Rajbhandari, Dorrilyn, Peach, Elizabeth, De Guzman, Erika, Li, Qiang, Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Ligthart, Symen, Brown, Matthew A., Powell, Joseph, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Blumenthal, Antje, Cohen, Jeremy, Venkatesh, Balasubramanian, Cuellar-Partida, Gabriel and Evans, David M. (2020). Septic shock: a genomewide association study and polygenic risk score analysis. Twin Research and Human Genetics, 23 (4) PII S1832427420000602, 204-213. doi: 10.1017/thg.2020.60

Septic shock: a genomewide association study and polygenic risk score analysis

2020

Journal Article

Development of a polygenic risk score to improve screening for fracture risk: a genetic risk prediction study

Forgetta, Vincenzo, Keller-Baruch, Julyan, Forest, Marie, Durand, Audrey, Bhatnagar, Sahir, Kemp, John P., Nethander, Maria, Evans, Daniel, Morris, John A., Kiel, Douglas P., Rivadeneira, Fernando, Johansson, Helena, Harvey, Nicholas C., Mellström, Dan, Karlsson, Magnus, Cooper, Cyrus, Evans, David M., Clarke, Robert, Kanis, John A., Orwoll, Eric, McCloskey, Eugene V., Ohlsson, Claes, Pineau, Joelle, Leslie, William D., Greenwood, Celia M. T. and Richards, J. Brent (2020). Development of a polygenic risk score to improve screening for fracture risk: a genetic risk prediction study. PLOS Medicine, 17 (7) e1003152, e1003152. doi: 10.1371/journal.pmed.1003152

Development of a polygenic risk score to improve screening for fracture risk: a genetic risk prediction study

2020

Journal Article

RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro

Loh, Nellie Y., Minchin, James E. N., Pinnick, Katherine E., Verma, Manu, Todorčević, Marijana, Denton, Nathan, Moustafa, Julia El-Sayed, Kemp, John P., Gregson, Celia L., Evans, David M., Neville, Matt J., Small, Kerrin S., McCarthy, Mark I., Mahajan, Anubha, Rawls, John F., Karpe, Fredrik and Christodoulides, Constantinos (2020). RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro. Nature Communications, 11 (1) 2797, 1-15. doi: 10.1038/s41467-020-16592-z

RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro

2020

Journal Article

Proxy gene-by-environment Mendelian randomization for assessing causal effects of maternal exposures on offspring outcomes

Hwang, Liang-Dar and Evans, David M. (2020). Proxy gene-by-environment Mendelian randomization for assessing causal effects of maternal exposures on offspring outcomes. International Journal of Epidemiology, 49 (4), 1218-1220. doi: 10.1093/ije/dyaa069

Proxy gene-by-environment Mendelian randomization for assessing causal effects of maternal exposures on offspring outcomes

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
  • 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

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 - 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

Before you email them, read our advice on how to contact 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).

Supervision history

Current supervision

  • Doctor Philosophy

    Harnessing Genetically Informative Within-Family Research Designs for Deeper Insights into the Intrauterine Developmental Period and Downstream Effects on Offspring Neurodevelopmental Outcomes

    Principal Advisor

    Other advisors: Dr Daniel Hwang, Dr Gunn-Helen Moen

  • Doctor Philosophy

    Multi-omic Approaches to Understanding Septic Shock

    Principal Advisor

    Other advisors: Dr Daniel Hwang

  • Doctor Philosophy

    Developing and Applying Statistical Genetics Methods to Elucidate the Developmental Origins of Health and Disease

    Principal Advisor

    Other advisors: Dr Nicole Warrington

  • Doctor Philosophy

    Investigating the association between maternal and fetal HLA-KIR genotypes and offspring birth weight

    Principal Advisor

  • Doctor Philosophy

    Understanding the genetic epidemiology of women's reproductive health

    Principal Advisor

    Other advisors: Dr Gunn-Helen Moen

  • Doctor Philosophy

    Using multi-omics approaches to characterise determinants of early growth trajectories and their consequences on later life health

    Associate Advisor

    Other advisors: Honorary Professor Jake Gratten, Dr Nicole Warrington

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