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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

196 works between 2007 and 2025

101 - 120 of 196 works

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

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

2018

Other Outputs

Genetic analyses of medication-use and implications for precision medicine

Wu, Yeda, Byrne, Enda M., Zheng, Zhili, Kemper, Kathryn E., Yengo, Loic, Mallett, Andrew J., Yang, Jian, Visscher, Peter M. and Wray, Naomi R. (2018). Genetic analyses of medication-use and implications for precision medicine. doi: 10.1101/501049

Genetic analyses of medication-use and implications for precision medicine

2018

Journal Article

Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

Arnau-Soler, Aleix, Adams, Mark J., Hayward, Caroline, Thomson, Pippa A., Porteous, David, Campbell, Archie, Smith, Blair H., Black, Corri, Padmanabhan, Sandosh, McIntosh, Andrew, 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, Bækvad-Hansen, Marie, Beekman, Aartjan T.F., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas H.R., Bryois, Julien, Buttenschøn, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na ... Sullivan, Patrick F. (2018). Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. PLoS ONE, 13 (12) e0209160, e0209160. doi: 10.1371/journal.pone.0209160

Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

2018

Journal Article

Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling

Elia, Josephine, Ungal, Grace, Kao, Charlly, Ambrosini, Alexander, De Jesus-Rosario, Nilsa, Larsen, Lene, Chiavacci, Rosetta, Wang, Tiancheng, Kurian, Christine, Titchen, Kanani, Sykes, Brian, Hwang, Sharon, Kumar, Bhumi, Potts, Jacqueline, Davis, Joshua, Malatack, Jeffrey, Slattery, Emma, Moorthy, Ganesh, Zuppa, Athena, Weller, Andrew, Byrne, Enda, Li, Yun R., Kraft, Walter K. and Hakonarson, Hakon (2018). Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling. Nature Communications, 9 (1) 4, 1-9. doi: 10.1038/s41467-017-02244-2

Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling

2018

Journal Article

PPD ACT: an app-based genetic study of postpartum depression

Guintivano, Jerry, Krohn, Holly, Lewis, Carol, Byrne, Enda M., Henders, Anjali K., Ploner, Alexander, Kirk, Katherine, Martin, Nicholas G., Milgrom, Jeannette, Wray, Naomi R., Sullivan, Patrick F. and Meltzer-Brody, Samantha (2018). PPD ACT: an app-based genetic study of postpartum depression. Translational Psychiatry, 8 (1) 260, 260. doi: 10.1038/s41398-018-0305-5

PPD ACT: an app-based genetic study of postpartum depression

2018

Journal Article

Is schizophrenia a risk factor for breast cancer?—evidence from genetic data

Byrne, Enda M., Ferreira, Manuel A.R., Xue, Angli, Lindström, Sara, Jiang, Xia, Yang, Jian, Easton, Douglas F., Wray, Naomi R. and Chenevix-Trench, Georgia (2018). Is schizophrenia a risk factor for breast cancer?—evidence from genetic data. Schizophrenia Bulletin, 45 (6), 1251-1256. doi: 10.1093/schbul/sby162

Is schizophrenia a risk factor for breast cancer?—evidence from genetic data

2018

Other Outputs

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. (2018). Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. doi: 10.1101/433367

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

2018

Journal Article

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L., Ota, Vanessa K., Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J., Patel, Hamel, Hall, Lynsey S., O'Reilly, Paul F., Belangero, Sintia, Bressan, Rodrigo A., Breen, Gerome, 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. ... Major Depressive Disorder and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology, 1 (163) 163. doi: 10.1038/s42003-018-0155-y

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

2018

Other Outputs

Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

Mullins, Niamh, Bigdeli, Tim B., Børglum, Anders D, Coleman, Jonathan R I, Demontis, Ditte, Fanous, Ayman H., Mehta, Divya, Power, Robert A., Ripke, Stephan, Stahl, Eli A, Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan R, Forstner, Andreas J, Reif, Andreas, Koller, Anna C, Świątkowska, Beata, Baune, Bernhard T, Müller-Myhsok, Bertram, Konte, Bettina, Penninx, Brenda WJH, Pato, Carlos, Zai, Clement, Rujescu, Dan, Quested, Digby, Levinson, Douglas F, Binder, Elisabeth B, Byrne, Enda M ... Lewis, Cathryn M (2018). Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores. doi: 10.1101/416008

Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

2018

Journal Article

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till M. F., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bryois, Julien, Buttenschon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan I. R., Colodro-Conde, Lucia, Couvy-Duchesne, Baptiste, Craddock, Nick, Crawford, Gregory E., Crowley, Cheynna A. ... Sullivan, Patrick F. (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50 (5), 668-+. doi: 10.1038/s41588-018-0090-3

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

2018

Other Outputs

Genome-wide association analyses of chronotype in 697,828 individuals provides new insights into circadian rhythms in humans and links to disease

Jones, Samuel E., Lane, Jacqueline M., Wood, Andrew R., van Hees, Vincent T., Tyrrell, Jessica, Beaumont, Robin N., Jefferies, Aaron, Dashti, Hassan S., Hillsdon, Melvyn, Ruth, Katherine S., Tuke, Marcus A., Yaghootkar, Hanieh, Sharp, Seth, 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., Team, the 23andMe Research, Lawlor, Debbie A., Frayling, Timothy M. ... Weedon, Michael N. (2018). Genome-wide association analyses of chronotype in 697,828 individuals provides new insights into circadian rhythms in humans and links to disease. doi: 10.1101/303941

Genome-wide association analyses of chronotype in 697,828 individuals provides new insights into circadian rhythms in humans and links to disease

2018

Conference Publication

PHENOTYPIC AND GENETIC ASSOCIATIONS BETWEEN SCHIZOPHRENIA AND RETINAL VESSEL DIAMETER

Meier, Madeline, Byrne, Enda, Martin, Nicholas, Wong, Tien and Sim, Xueling (2018). PHENOTYPIC AND GENETIC ASSOCIATIONS BETWEEN SCHIZOPHRENIA AND RETINAL VESSEL DIAMETER. 6th Biennial Conference of the Schizophrenia-International-Research-Society (SIRS), Florence Italy, Apr 04-08, 2018. OXFORD: OXFORD UNIV PRESS.

PHENOTYPIC AND GENETIC ASSOCIATIONS BETWEEN SCHIZOPHRENIA AND RETINAL VESSEL DIAMETER

2018

Journal Article

7.4 PHENOTYPIC AND GENETIC ASSOCIATIONS BETWEEN SCHIZOPHRENIA AND RETINAL VESSEL DIAMETER

Meier, Madeline, Byrne, Enda, Martin, Nicholas, Wong, Tien and Sim, Xueling (2018). 7.4 PHENOTYPIC AND GENETIC ASSOCIATIONS BETWEEN SCHIZOPHRENIA AND RETINAL VESSEL DIAMETER. Schizophrenia Bulletin, 44 (suppl_1). doi: 10.1093/schbul/sby014.026

7.4 PHENOTYPIC AND GENETIC ASSOCIATIONS BETWEEN SCHIZOPHRENIA AND RETINAL VESSEL DIAMETER

2018

Journal Article

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Pardiñas, Antonio F, Holmans, Peter, Pocklington, Andrew J, Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E, Bishop, Sophie, Cameron, Darren, Hamshere, Marian L, Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H, McCarroll, Steven A, Baune, Bernhard T, Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C, Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M, Plomin, Robert, Porteous, David J, Wray, Naomi R, Caballero, Armando ... CRESTAR Consortium (2018). Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics, 50 (3), 381-389. doi: 10.1038/s41588-018-0059-2

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

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

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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

    Genetics of Neurodevelopmental Disorders and associated comorbidities

    Principal Advisor

    Other advisors: Dr Allan McRae

  • 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

    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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