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Dr Enda Byrne
Dr

Enda Byrne

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Overview

Background

The objective of my research is to improve understanding of the genetic etiology and biological mechanisms underlying risk of common psychiatric disorders, particularly those with onset during childhood and adolescence. As a Senior Research Fellow at the Child Health Research Centre, I lead a number of domestic and international collaborations that evaluate the association between polygenic risk scores, environmental variables and behaviour during childhood and adolescence. My group applies innovative statistical methods to large longitudinal datasets with information from infancy through to adulthood and to evaluate genetic and environmental contributions to risk to mental health problems. In addition, our research focuses on the potential clinical utility of polygenic risk scores in psychiatry. I have contributed to major advances in understanding of the etiology of a number of psychiatric disorders, with a major focus on depression

PhD and Honours projects are available in the group. Please contact me for more information.

Availability

Dr Enda Byrne is:
Available for supervision

Qualifications

  • Doctor of Philosophy, The University of Queensland

Research interests

  • Genomic Technologies

  • Statistical and Computational methods

Research impacts

My research has contributed to advances in a number of fields through the identification of previously unknown genetic variants that contribute to risk to complex disorders. The identification of these variants opens up new avenues for developing drug targets to target the biological pathways in which they are found.

Works

Search Professor Enda Byrne’s works on UQ eSpace

187 works between 2007 and 2025

81 - 100 of 187 works

2019

Journal Article

Identification of common genetic risk variants for autism spectrum disorder

Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel ... Børglum, Anders D. (2019). Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics, 51 (3), 431-444. doi: 10.1038/s41588-019-0344-8

Identification of common genetic risk variants for autism spectrum disorder

2019

Journal Article

Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

Arnau-Soler, Aleix, Macdonald-Dunlop, Erin, Adams, Mark J., Clarke, Toni-Kim, MacIntyre, Donald J., Milburn, Keith, Navrady, Lauren, Hayward, Caroline, McIntosh, Andrew M., Thomson, Pippa A., Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Agerbo, Esben, Air, Tracy M., Andlauer, Till F. M., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan T. F., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas H. R., Bryois, Julien, Buttenscon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na ... Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2019). Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Translational Psychiatry, 9 (1) 14. doi: 10.1038/s41398-018-0360-y

Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

2019

Journal Article

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

Howard, David M., Adams, Mark J., Clarke, Toni-Kim, Hafferty, Jonathan D., Gibson, Jude, Shirali, Masoud, Coleman, Jonathan R. I., Hagenaars, Saskia P., Ward, Joey, Wigmore, Eleanor M., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Xu, Eileen Y., Whalley, Heather C., Marioni, Riccardo E., Porteous, David J., Davies, Gail, Deary, Ian J., Hemani, Gibran, Berger, Klaus, Teismann, Henning, Rawal, Rajesh, Arolt, Volker, Baune, Bernhard T., Dannlowski, Udo, Domschke, Katharina, Tian, Chao, Hinds, David A. ... McIntosh, Andrew M. (2019). Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. Nature Neuroscience, 22 (3), 343-352. doi: 10.1038/s41593-018-0326-7

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

2019

Journal Article

Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms

Jones, Samuel E., Lane, Jacqueline M., Wood, Andrew R., van Hees, Vincent T., Tyrrell, Jessica, Beaumont, Robin N., Jeffries, Aaron R., Dashti, Hassan S., Hillsdon, Melvyn, Ruth, Katherine S., Tuke, Marcus A., Yaghootkar, Hanieh, Sharp, Seth A., Jie, Yingjie, Thompson, William D., Harrison, Jamie W., Dawes, Amy, Byrne, Enda M., Tiemeier, Henning, Allebrandt, Karla V., Bowden, Jack, Ray, David W., Freathy, Rachel M., Murray, Anna, Mazzotti, Diego R., Gehrman, Philip R., Lawlor, Debbie A., Frayling, Timothy M., Rutter, Martin K. ... Weedon, Michael N. (2019). Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms. Nature Communications, 10 (1) 343, 343. doi: 10.1038/s41467-018-08259-7

Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms

2019

Conference Publication

Conditional genome-wide association analysis identifies genetic variants

Byrne, E. (2019). Conditional genome-wide association analysis identifies genetic variants. 21st Annual ISBD Conference: Global Advances in Bipolar Disorder and Depression, Sydney, Australia, 20-23 March 2019. Hoboken, NJ United States: Wiley-Blackwell Publishing.

Conditional genome-wide association analysis identifies genetic variants

2019

Conference Publication

Identification of genetic risk factors for postpartum depression

Guintivano, Jerry, Byrne, Enda, Watson, Hunna, Wray, Naomi, Meltzer-Brody, Samantha and Sullivan, Patrick (2019). Identification of genetic risk factors for postpartum depression. 27th World Congress of Psychiatric Genetics, Los Angeles, United States, 26-31 October 2019. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2019.07.194

Identification of genetic risk factors for postpartum depression

2019

Conference Publication

Integrative analysis of genome-wide association study results of attention-deficit/hyperactivity disorder (ADHD) and human fetal brain methylation data reveals novel genes associated with ADHD

Hammerschlag, Anke, Byrne, Enda, Bartels, Meike, Wray, Naomi and Middeldorp, Christel M. (2019). Integrative analysis of genome-wide association study results of attention-deficit/hyperactivity disorder (ADHD) and human fetal brain methylation data reveals novel genes associated with ADHD. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October 2018. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2018.08.063

Integrative analysis of genome-wide association study results of attention-deficit/hyperactivity disorder (ADHD) and human fetal brain methylation data reveals novel genes associated with ADHD

2019

Conference Publication

Genetic risk for depression and treatment response in the Australian genetics of depression study

Byrne, Enda, Medland, Sarah E., Hickie, Ian, Martin, Nicholas G. and Wray, Naomi (2019). Genetic risk for depression and treatment response in the Australian genetics of depression study. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, United States, 26-31 October 2019. Amsterdam, The Netherlands: Elsevier . doi: 10.1016/j.euroneuro.2019.07.109

Genetic risk for depression and treatment response in the Australian genetics of depression study

2019

Journal Article

Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

Foo, Jerome C., Streit, Fabian, Frank, Josef, Witt, Stephanie H., Treutlein, Jens, Baune, Bernhard T., Moebus, Susanne, Joeckel, Karl-Heinz, Forstner, Andreas J., Noethen, Markus M., Rietschel, Marcella, Sartorius, Alexander, Kranaster, Laura, Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F. M., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan T. F., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas H. R. ... Sullivan, Patrick F. (2019). Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 180 (1), 35-45. doi: 10.1002/ajmg.b.32700

Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

2019

Journal Article

Sleep disorders and risk of incident depression: a population case-control study

Byrne, Enda M., Timmerman, Allan, Wray, Naomi R. and Agerbo, Esben (2019). Sleep disorders and risk of incident depression: a population case-control study. Twin Research and Human Genetics, 22 (03) PII S1832427419000227, 140-146. doi: 10.1017/thg.2019.22

Sleep disorders and risk of incident depression: a population case-control study

2019

Conference Publication

Examining the shared genetics between educational attainment and depression: results from the Australian Genetics of Depression Study

Mitchell, Brittany, Renteria, Miguel E., Byrne, Enda, Conde, Lucia Colodro, Han, Xikun, Medland, Sarah E., Wray, Naomi and Martin, Nick (2019). Examining the shared genetics between educational attainment and depression: results from the Australian Genetics of Depression Study. 27th World Congress of Psychiatric Genetics, Los Angeles, United States, 26-31 October 2019. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2019.07.172

Examining the shared genetics between educational attainment and depression: results from the Australian Genetics of Depression Study

2019

Conference Publication

Genetic risk scores and postpartum psychiatric disorders

Bauer, Anna, Liu, Xiaoqin, Byrne, Enda, Sullivan, Patrick, Wray, Naomi, Agerbo, Esben, Nyegaard, Mette, Ingstrup, Katja, Johannsen, Benedicte, Maegbaek, Merete, Wang, Yunpeng, Nordentoft, Merete, Mortensen, Preben Bo, Munk-Olsen, Trine and Meltzer-Brody, Samantha (2019). Genetic risk scores and postpartum psychiatric disorders. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October 2018. Amsterdam, The Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2018.08.048

Genetic risk scores and postpartum psychiatric disorders

2019

Conference Publication

Validating GWA associations in psychiatric disorders with functional genomic data

Trzaskowski, Maciej, Byrne, Enda, Yang, Jian and Wray, Naomi (2019). Validating GWA associations in psychiatric disorders with functional genomic data. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, United States, 13-17 October 2017. Amsterdam, The Netherlands: Elsevier . doi: 10.1016/j.euroneuro.2017.08.019

Validating GWA associations in psychiatric disorders with functional genomic data

2019

Conference Publication

Exploring the heterogeneity of depression: stressful life events and depressive symptoms

Conde, Lucia Colodro, Couvy-Duchesne, Baptiste, Byrne, Enda, Campos, Adrian, Martin, Nick and Medland, Sarah (2019). Exploring the heterogeneity of depression: stressful life events and depressive symptoms. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, United States, 26-31 October 2019. Amsterdam, The Netherlands: Elsevier . doi: 10.1016/j.euroneuro.2019.08.109

Exploring the heterogeneity of depression: stressful life events and depressive symptoms

2019

Conference Publication

Assessing clinical, demographic and genetic risk factors for treatment attributed suicidality in > 20,000 Australian adults on antidepressants

Campos, Adrian, Renteria, Miguel E., Byrne, Enda, Medland, Sarah E., Wray, Naomi, Hickie, Ian B. and Martin, Nick (2019). Assessing clinical, demographic and genetic risk factors for treatment attributed suicidality in > 20,000 Australian adults on antidepressants. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, United States, 26-31 October 2019. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2019.07.212

Assessing clinical, demographic and genetic risk factors for treatment attributed suicidality in > 20,000 Australian adults on antidepressants

2019

Conference Publication

Sleep disorders and risk of incident depression: a population case-control study

Byrne, Enda, Wray, Naomi and Agerbo, Esben (2019). Sleep disorders and risk of incident depression: a population case-control study. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, United States, 13-17 October 2017. Amsterdam, The Netherlands: Elsevier . doi: 10.1016/j.euroneuro.2017.08.343

Sleep disorders and risk of incident depression: a population case-control study

2019

Conference Publication

INVESTIGATING CAUSAL RELATIONSHIPS BETWEEN MAJOR DEPRESSIVE DISORDER AND GENETICALLY CORRELATED TRAITS USING MENDELIAN RANDOMISATION

Byrne, Enda, Trzaskowski, Maciej and Wray, Naomi (2019). INVESTIGATING CAUSAL RELATIONSHIPS BETWEEN MAJOR DEPRESSIVE DISORDER AND GENETICALLY CORRELATED TRAITS USING MENDELIAN RANDOMISATION. 25th World Congress of Psychiatric Genetics (WCPG), Orlando Fl, Oct 13-17, 2017. AMSTERDAM: ELSEVIER SCIENCE BV. doi: 10.1016/j.euroneuro.2017.08.020

INVESTIGATING CAUSAL RELATIONSHIPS BETWEEN MAJOR DEPRESSIVE DISORDER AND GENETICALLY CORRELATED TRAITS USING MENDELIAN RANDOMISATION

2019

Conference Publication

Comprehensive evaluation of enrichment for circadian clock gene sets in psychiatric traits: specific enrichment in clinical response to lithium

Papiol, Sergi, Heilbronner, Urs, Hou, Liping, McCarthy, Michael, Nievergelt, Caroline, Byrne, Enda, McMahon, Francis and Schulze, Thomas (2019). Comprehensive evaluation of enrichment for circadian clock gene sets in psychiatric traits: specific enrichment in clinical response to lithium. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, United States, 13-17 October 2017. Amsterdam, The Netherlands: Elsevier . doi: 10.1016/j.euroneuro.2017.08.270

Comprehensive evaluation of enrichment for circadian clock gene sets in psychiatric traits: specific enrichment in clinical response to lithium

2019

Conference Publication

A direct test of the diathesis-stress model for depression

Conde, Lucia Colodro, Couvy-Duchesne, Baptiste, Zhu, Gu, Coventry, William, Byrne, Enda, Gordon, Scott, Wright, Margaret, Montgomery, Grant, Madden, Pamela, Ripke, Stephan, Eaves, Lindon, Heath, Andrew, Wray, Naomi, Medland, Sarah E. and Martin, Nick (2019). A direct test of the diathesis-stress model for depression. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL United States, 13-17 October 2017. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2017.08.045

A direct test of the diathesis-stress model for depression

2019

Conference Publication

Genomic structural equation models of major depression symptoms

Adams, Mark, Grotzinger, Andrew, Jermy, Bradley, Thorp, Jackson, Nivard, Michel, Byrne, Enda, Hickie, Ian, Martin, Nick, Medland, Sarah, Wray, Naomi, Tucker-Drob, Elliot, Lewis, Cathryn, Derks, Eske and McIntosh, Andrew (2019). Genomic structural equation models of major depression symptoms. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, United States, 26-31 October 2019. Amsterdam, The Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2019.08.042

Genomic structural equation models of major depression symptoms

Funding

Current funding

  • 2023 - 2027
    Enabling pharmacogenomics in the Australian context: improving the accuracy of clinical utility and cost effectiveness analyses (MRFF externally administered by QIMR)
    Queensland Institute of Medical Research
    Open grant
  • 2022 - 2027
    Youth-GEMs: Gene Environment interactions in Mental health trajectories of Youth
    NHMRC European Union Collaborative Research Grants
    Open grant
  • 2022 - 2027
    Gene Environment interactions in Mental health trajectories of Youth - YOUTH-GEMs (EU grant administered by Maastricht University)
    Maastricht University
    Open grant
  • 2020 - 2025
    Australian Pharmacogenomics Diversity Project: Examining the evidence and improving the performance of pharmacogenomics in the Australian context (MRFF grant administered by QIMR Berghofer)
    Queensland Institute of Medical Research
    Open grant

Past funding

  • 2019 - 2024
    Postpartum Depression: Action Towards Causes and Treatment
    Research Donation Generic
    Open grant
  • 2018 - 2022
    Postpartum Depression: Action Towards Causes and Treatment
    NHMRC Project Grant
    Open grant
  • 2015 - 2019
    Tackling heterogeneity in the etiology of major depressive disorder (NHMRC Project Grant administered by QIMR)
    Queensland Institute of Medical Research
    Open grant
  • 2014 - 2017
    Discovering deep sleep genes and determining their roles for preserving cognitive functions
    NHMRC Project Grant
    Open grant
  • 2013 - 2017
    NHMRC Early Career Fellowship (CJ Martin - Overseas Biomedical Fellowship): Using new genomic technologies, statistical and computational methods to uncover the genetic aetiology of complex traits
    NHMRC Training (Postdoctoral) Fellowship
    Open grant

Supervision

Availability

Dr Enda Byrne is:
Available for supervision

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

Available projects

  • Gene Environment interactions in Mental health trajectories of Youth (Youth-GEMs)

    Mental health problems are common in young people, with life-long enduring impacts on individuals, families and societies. More than 63% of mental disorders throughout the life span emerge before 24 years of age, peaking at 14.5-18 years. Adolescence and young adulthood represent a critical period that forecasts the level of mental wellbeing over lifetime and interventions early in life may be critical in preventing later mental illness.

    The Child and Youth Mental Health Group is part of an Australian and European Union-funded consortium called Youth-GEMs that seeks to characterise and model trajectories of mental health in youth. In collaboration with researchers from universities in Europe, this project will combine datasets from longitudinal cohort studies from around the world to investigate the interplay between genetic, epigenetic, and environmental risk in influencing mental health across development.

    This project will involve advanced data analytics and statistical inference and will involve combining and analysing different types of data including genetic, clinical and environmental data. The ultimate goal is to develop predictive tools that can be used to aid clinical decision-making in youth mental health.

    We are seeking a motivated PhD scholar with a background in genetics, biomedical science, psychology, data science, machine learning or a related field to join our team and work closely with collaborators overseas on this project. There is also the possibility to spend time overseas at one of the collaborating labs.

Supervision history

Current supervision

  • Doctor Philosophy

    Gene Environment interactions in Mental health trajectories of Youth

    Principal Advisor

  • Doctor Philosophy

    Genetics of childhood onset psychiatric symptoms, their persistence and comorbidity with other traits

    Principal Advisor

    Other advisors: Professor Naomi Wray

  • Doctor Philosophy

    Genetics of Neurodevelopmental Disorders and associated comorbidities

    Principal Advisor

    Other advisors: Dr Allan McRae

  • Doctor Philosophy

    ELUCIDATING LIFESTYLE AND GENETIC FACTORS UNDERLYING DEPRESSION HETEROGENEITY AND TREATMENT RESPONSE

    Associate Advisor

    Other advisors: Professor Naomi Wray

  • Doctor Philosophy

    Multi-Omic Analyses of a Clinical Trial Cohort of Young People at Ultra-High Risk for Psychosis

    Associate Advisor

    Other advisors: Dr Allan McRae, Professor Naomi Wray

Completed supervision

Media

Enquiries

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