Professor Naomi Wray
Professor

Naomi Wray

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Background

Naomi Wray is the Michael Davys Professor in the Department of Psychiatry, University of Oxford. She holds an appointment at the Institute for Molecular Bioscience (IMB) within the University of Queensland. She joined UQ Queensland Brain Institute in 2011 moving to the IMB in 2015. She was Head of the Centre for Population & Disease Genomics within IMB 2018-2023. Her Oxford appointment started in 2023.

Her research focuses on development and application of quantitative genetics and genomics methodologies across complex diseases, disorders and traits, but particularly psychiatric-related traits.

She is a National Health and Medical Research Council (NHMRC) Leadership Fellow, a Fellow of the Australian Academy of Science and a Fellow of the Australian Academy of Health and Medical Science. In 2020 she was awarded the NHMRC Elizabeth Blackburn Award for Leadership in Basic Science and the 2021 International Society of Psychiatric Genetics Ming Tsuang Lifetime Achievement Award. She is a Clarivate Highly Cited researcher.

She was Director of the Program in Complex Trait Genomics (PCTG) funded as an NHMRC Program Grant 2017-2022. She plays a key role in the International Psychiatric Genomics Consortium and established the sporadic ALS Australia systems genomics consortium (SALSA) funded by the MND Research Australia IceBucket Challenge and FightMND. She is a co-investigator on the Australian Genetics of Depression Study (AGDS) and is currently launching the AGDS-Cello project focussed on establishing a cell line resource from participants with a detailed history of anti-depressant use and response measures. She is part of an NHMRC Synergy (2023-2027) "Rhythms and blues: Personalising care for body clock dysfunction in mood disorders".

She is secretary of the International Society of Psychiatric Genetics, and is on the editorial advisory boards of JAMA Psychiatry, Neuron, Royal Society Open and Research Directions: Depression.

Availability

Professor Naomi Wray is:
Not available for supervision

Qualifications

  • Doctor of Philosophy, University of Edinburgh

Research interests

  • Genetics of complex genetic traits, disease and disorders

    Quantitative genetics methodology Genetics of Psychiatric Disorder Genetics of Motor Neurone Disease Genetics of Cognitive Ageing Systems Genomics

Search Professor Naomi Wray’s works on UQ eSpace

559 works between 1987 and 2025
All (559) Journal Article (466) Other Outputs (1) Conference Publication (88) Book Chapter (4)

1 - 20 of 559 works

2025

Journal Article

Population-representative inference for primary and secondary outcomes in extended case-cohort designs

Wimberley, Theresa, Plana-Ripoll, Oleguer, Pedersen, Carsten B., Pedersen, Marianne G., Dreier, Julie W., Christensen, Jakob, Horsdal, Henriette Thisted, Astrup, Aske, Thompson, Wesley K., Helenius, Dorte, McGrath, John J., Wray, Naomi R., Petersen, Liselotte Vogdrup, Vilhjálmsson, Bjarni, Mortensen, Preben B. and Agerbo, Esben (2025). Population-representative inference for primary and secondary outcomes in extended case-cohort designs. Discover public health, 22 (1) 599. doi: 10.1186/s12982-025-00888-w

Population-representative inference for primary and secondary outcomes in extended case-cohort designs

2025

Journal Article

Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids

Bentley, Amy R., Brown, Michael R., Musani, Solomon K., Schwander, Karen L., Winkler, Thomas W., Sims, Mario, Kilpeläinen, Tuomas O., Aschard, Hugues, Bartz, Traci M., Bielak, Lawrence F., Chai, Jin-Fang, Chitrala, Kumaraswamy Naidu, Franceschini, Nora, Graff, Mariaelisa, Guo, Xiuqing, Hartwig, Fernando P., Horimoto, Andrea R.V.R., Lim, Elise, Liu, Yongmei, Manning, Alisa K., Nolte, Ilja M., Noordam, Raymond, Richard, Melissa A., Smith, Albert V., Sung, Yun Ju, Vojinovic, Dina, Wang, Rujia, Wang, Yujie, Feitosa, Mary F. ... Fox, Ervin R. (2025). Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids. Translational Psychiatry, 15 (1) 207, 1. doi: 10.1038/s41398-025-03418-z

Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids

2025

Journal Article

Epigenetic profiles of tissue informative CpGs inform ALS disease status and progression

Caggiano, Christa, Morselli, Marco, Qian, Xiaoyu, Celona, Barbara, Thompson, Michael J., Wani, Shivangi, Tosevska, Anela, Taraszka, Kodi, Heuer, Galen, Ngo, Shyuan T., Steyn, Frederick J., Nestor, Peter J., Wallace, Leanne, Mccombe, Pamela, Heggie, Susan, Thorpe, Kathryn, Mcelligott, Caitlin, English, Gemyka, Henders, Anjali, Henderson, Robert, Lomen-Hoerth, Catherine, Wray, Naomi R., Mcrae, Allan F., Pellegrini, Matteo, Garton, Fleur C. and Zaitlen, Noah (2025). Epigenetic profiles of tissue informative CpGs inform ALS disease status and progression. Genome Medicine, 17 (1) 115. doi: 10.1186/s13073-025-01542-5

Epigenetic profiles of tissue informative CpGs inform ALS disease status and progression

2025

Conference Publication

Refined mitochondrial DNA copy number (MTDNA-CN) calling and analysis pipeline reveals nuclear genetic regulation of MTDNA-CN in blood and its lack of association with mood disorders

Wang, Xiaotong, McGrath, Isabelle, Li, Ang and Wray, Naomi (2025). Refined mitochondrial DNA copy number (MTDNA-CN) calling and analysis pipeline reveals nuclear genetic regulation of MTDNA-CN in blood and its lack of association with mood disorders. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.402

Refined mitochondrial DNA copy number (MTDNA-CN) calling and analysis pipeline reveals nuclear genetic regulation of MTDNA-CN in blood and its lack of association with mood disorders

2025

Conference Publication

Multi-ancestry conditional and joint analysis (MANC-COJO) of GWAS summary statistics

Wang, Xiaotong, Wang, Yong, Visscher, Peter, Wray, Naomi and Yengo, Loic (2025). Multi-ancestry conditional and joint analysis (MANC-COJO) of GWAS summary statistics. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.136

Multi-ancestry conditional and joint analysis (MANC-COJO) of GWAS summary statistics

2025

Conference Publication

BENCHMARKING METHODS INTEGRATING GWAS AND SINGLE-CELL TRANSCRIPTOMIC DATA FOR MAPPING TRAIT-CELL TYPE ASSOCIATIONS

Li, Ang, Wray, Naomi and Zeng, Jian (2025). BENCHMARKING METHODS INTEGRATING GWAS AND SINGLE-CELL TRANSCRIPTOMIC DATA FOR MAPPING TRAIT-CELL TYPE ASSOCIATIONS. AMSTERDAM: ELSEVIER. doi: 10.1016/j.euroneuro.2025.08.394

BENCHMARKING METHODS INTEGRATING GWAS AND SINGLE-CELL TRANSCRIPTOMIC DATA FOR MAPPING TRAIT-CELL TYPE ASSOCIATIONS

2025

Conference Publication

Functional genomic investigation of the immune hypothesis of mental illness

McGrath, Isabelle, Wray, Naomi and Lynall, Mary-Ellen (2025). Functional genomic investigation of the immune hypothesis of mental illness. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.210

Functional genomic investigation of the immune hypothesis of mental illness

2025

Conference Publication

The genetic architecture of difficult-to-treat depression: a Pharmlines initiative cohort study

Walker, Alicia, Klont, Frank, Bos, Jens, van Loo, Hanna, Taquet, Maxime, Hak, Eelko and Wray, Naomi (2025). The genetic architecture of difficult-to-treat depression: a Pharmlines initiative cohort study. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.409

The genetic architecture of difficult-to-treat depression: a Pharmlines initiative cohort study

2025

Conference Publication

STAGE-RESOLVED SINGLE CELL MULTIOMIC ANNOTATIONS FROM HUMAN PREFRONTAL CORTEX REFINE SCHIZOPHRENIA HERITABILITY ESTIMATION AND POLYGENIC PREDICTION

Li, Ang, Shen, Xueyi, Lister, Ryan, Wray, Naomi, Voineagu, Irina and Zeng, Jian (2025). STAGE-RESOLVED SINGLE CELL MULTIOMIC ANNOTATIONS FROM HUMAN PREFRONTAL CORTEX REFINE SCHIZOPHRENIA HERITABILITY ESTIMATION AND POLYGENIC PREDICTION. AMSTERDAM: ELSEVIER. doi: 10.1016/j.euroneuro.2025.08.560

STAGE-RESOLVED SINGLE CELL MULTIOMIC ANNOTATIONS FROM HUMAN PREFRONTAL CORTEX REFINE SCHIZOPHRENIA HERITABILITY ESTIMATION AND POLYGENIC PREDICTION

2025

Conference Publication

Heterogeneity of major depressive disorder investigated through sustained fill of specific antidepressant scripts

Walker, Alicia, Mitchell, Brittany, Lin, Tian, Crouse, Jacob, Martin, Nick, Taquet, Maxime, Medland, Sarah E., Hickie, Ian and Wray, Naomi (2025). Heterogeneity of major depressive disorder investigated through sustained fill of specific antidepressant scripts. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.504

Heterogeneity of major depressive disorder investigated through sustained fill of specific antidepressant scripts

2025

Conference Publication

Towards improving reproducibility in psychiatric blood biomarker research: a framework for systematic identification and control of confounding factors

Albinana, Clara, Shin, Mirim, Crouse, Jacob J., Hickie, Ian B. and Wray, Naomi (2025). Towards improving reproducibility in psychiatric blood biomarker research: a framework for systematic identification and control of confounding factors. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.315

Towards improving reproducibility in psychiatric blood biomarker research: a framework for systematic identification and control of confounding factors

2025

Conference Publication

Biobank-scale proteomic estimates of circadian dysregulation increase risk of bipolar disorder, schizophrenia and depression

Albinana, Clara, Zeng, Yanni, Crouse, Jacob J., Hickie, Ian B., Gachon, Frederic and Wray, Naomi (2025). Biobank-scale proteomic estimates of circadian dysregulation increase risk of bipolar disorder, schizophrenia and depression. World Congress of Psychiatric Genetics (WCPG), Cancun, Mexico, 19-23 October 2025. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2025.08.177

Biobank-scale proteomic estimates of circadian dysregulation increase risk of bipolar disorder, schizophrenia and depression

2025

Journal Article

Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

van der Laan, Camiel M., Ip, Hill F., Schipper, Marijn, Hottenga, Jouke-Jan, St Pourcain, Beate, Zayats, Tetyana, Pool, René, Krapohl, Eva M. L., Brikell, Isabell, Soler Artigas, María, Cabana-Domínguez, Judit, Llonga, Natalia, Nolte, Ilja M., Bolhuis, Koen, Palviainen, Teemu, Zafarmand, Hadi, Gordon, Scott, Aliev, Fazil, Burt, S. Alexandra, Wang, Carol A., Saunders, Gretchen, Karhunen, Ville, Adkins, Daniel E., Border, Richard, Peterson, Roseann E., Prinz, Joseph A., Thiering, Elisabeth, Vilor-Tejedor, Natàlia, Ahluwalia, Tarunveer S. ... Boomsma, Dorret I. (2025). Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes. Nature Genetics, 57 (10), 1-1. doi: 10.1038/s41588-025-02383-z

Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

2025

Journal Article

Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

van der Laan, Camiel M., Ip, Hill F., Schipper, Marijn, Hottenga, Jouke-Jan, St Pourcain, Beate, Zayats, Tetyana, Pool, René, Krapohl, Eva M. L., Brikell, Isabell, Soler Artigas, María, Cabana-Domínguez, Judit, Nolte, Ilja M., Bolhuis, Koen, Palviainen, Teemu, Zafarmand, Hadi, Gordon, Scott, Aliev, Fazil, Burt, S. Alexandra, Wang, Carol A., Saunders, Gretchen, Karhunen, Ville, Adkins, Daniel E., Border, Richard, Peterson, Roseann E., Prinz, Joseph A., Thiering, Elisabeth, Vilor-Tejedor, Natàlia, Ahluwalia, Tarunveer S., Allegrini, Andrea ... Llonga, Natalia (2025). Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes. Nature Genetics, 57 (10), 2427-2435. doi: 10.1038/s41588-025-02295-y

Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

2025

Journal Article

A methylome-wide association study of major depression with out-of-sample case-control classification and trans-ancestry comparison

Shen, Xueyi, Barbu, Miruna, Caramaschi, Doretta, Arathimos, Ryan, Czamara, Darina, David, Friederike S., Dearman, Anna, Dilkes, Evelyn, Herrera-Rivero, Marisol, Huider, Floris, Kuhn, Luise, Lu, Kuan-Chen, Palviainen, Teemu, Schowe, Alicia M., Shireby, Gemma, Weihs, Antoine, Wong, Chloe C. Y., Davyson, Eleanor, Casey, Hannah, Adams, Mark J., Allgaier, Antje-Kathrin, Barber, Michael, Burrage, Joe, Caspi, Avshalom, Costeira, Ricardo, Dunn, Erin C., Feldmann, Lisa, Frank, Josef, Freisleder, Franz J. ... Mcintosh, Andrew M. (2025). A methylome-wide association study of major depression with out-of-sample case-control classification and trans-ancestry comparison. Nature Mental Health, 3 (10), 1152-1167. doi: 10.1038/s44220-025-00486-4

A methylome-wide association study of major depression with out-of-sample case-control classification and trans-ancestry comparison

2025

Journal Article

White blood cell proportions are associated with response to psychosocial therapy in young people at ultra-high risk for psychosis

Barker, Lauren F., McRae, Allan F., Yuen, Hok Pan, Henders, Anjali K., Wallace, Leanne M., Lin, Tian, Phassouliotis, Christina, Spark, Jessica, Kerr, Melissa, Byrne, Enda M., Amminger, G. Paul, Nelson, Barnaby, Wray, Naomi R. and McGorry, Patrick D. (2025). White blood cell proportions are associated with response to psychosocial therapy in young people at ultra-high risk for psychosis. Biological Psychiatry Global Open Science, 5 (5) 100546, 1-11. doi: 10.1016/j.bpsgos.2025.100546

White blood cell proportions are associated with response to psychosocial therapy in young people at ultra-high risk for psychosis

2025

Conference Publication

Mental Health and Sleep Correlates of Self-Reported Outdoor Daylight Exposure in Over 13,000 Adults With Depression

Crouse, Jacob, Park, Shin Ho, Mitchell, Brittany, Byrne, Enda, Medland, Sarah, Lin, Tian, Scott, Jan, de Haan, Zsofi, Tonini, Emiliana, Iorfino, Frank, Wray, Naomi, Martin, Nicholas and Hickie, Ian (2025). Mental Health and Sleep Correlates of Self-Reported Outdoor Daylight Exposure in Over 13,000 Adults With Depression. HOBOKEN: WILEY.

Mental Health and Sleep Correlates of Self-Reported Outdoor Daylight Exposure in Over 13,000 Adults With Depression

2025

Conference Publication

Distinct Clinical, Metabolic-Inflammatory-Genetic Characteristics and Treatment Responses of Atypical Depression

Shin, Mirim, Crouse, Jacob J., Lin, Tian, Byrne, Enda M., Mitchell, Brittany L., Lind, Penelope A., Parker, Richard, McKenna, Sarah, Tonini, Emiliana, Carpenter, Joanne S., Wray, Naomi, Medland, Sarah E., Martin, Nicholas G. and Hickie, Ian B. (2025). Distinct Clinical, Metabolic-Inflammatory-Genetic Characteristics and Treatment Responses of Atypical Depression. HOBOKEN: WILEY.

Distinct Clinical, Metabolic-Inflammatory-Genetic Characteristics and Treatment Responses of Atypical Depression

2025

Journal Article

Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking

He, Weixiong, van der Most, Peter J., Ong, Jue-Sheng, Hwang, Liang-Dar, Wu, Yeda, Magnø, Morten S., Vehof, Jelle, Krebs, Kristi, Mauring, Laura, Õunap, Katrin, Abner, Erik, Martin, Nicholas G., Plotnikov, Denis, Jiang, Chen, Melles, Ronald B., Gharahkhani, Puya, Snieder, Harold, Palumaa, Teele, Kaljurand, Kuldar, Guggenheim, Jeremy A., Mackey, David A., Engle, Elizabeth C., Choquet, Hélène, MacGregor, Stuart, Lifelines Cohort Study, Aguirre-Gamboa, Raul, Deelen, Patrick, Franke, Lude, Kuivenhoven, Jan A. ... Wray, Naomi (2025). Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking. Nature Communications, 16 (1) 7890, 1-14. doi: 10.1038/s41467-025-62456-9

Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking

2025

Journal Article

Insulin resistance as an early marker in youth with mood disorders

Shin, Mirim, Crouse, Jacob J., Weger, Meltem, McKenna, Sarah, Wray, Naomi R., Scott, Elizabeth M., Hickie, Ian B. and Gachon, Frédéric (2025). Insulin resistance as an early marker in youth with mood disorders. Nature Mental Health, 3 (9), 1-3. doi: 10.1038/s44220-025-00472-w

Insulin resistance as an early marker in youth with mood disorders

Current funding

  • 2026 - 2028
    Identification of causal variants for complex traits (ARC Discovery Project administered by the University of Melbourne)
    University of Melbourne
    Open grant
  • 2024 - 2029
    MELODY: Testing a causal model of sleep and circadian rhythm disturbance and youth-onset mood disorders
    University of Sydney
    Open grant
  • 2024 - 2029
    Accelerated drug discovery using population-wide screening of patient iPSC's for MND (MRFF 2023 SCT Grant administered by University of Melbourne)
    University of Melbourne
    Open grant
  • 2023 - 2027
    How does Epstein-Barr virus infection lead to multiple sclerosis?
    NHMRC MRFF CTAI and EPCDRI Multiple Sclerosis
    Open grant
  • 2023 - 2028
    Understanding the causal mechanisms of antidepressant exposure and response (a Wellcome Trust application submitted by King's College London)
    Kings College London
    Open grant
  • 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
  • 2023 - 2027
    Rhythms and blues: Personalising care for body clock dysfunction in mood disorders (NHMRC Synergy grant administered by University of Sydney)
    University of Sydney
    Open grant
  • 2022 - 2027
    Youth-GEMs: Gene Environment interactions in Mental health trajectories of Youth
    NHMRC European Union Collaborative Research Grants
    Open grant
  • 2022 - 2026
    Risk and Resilience in Developmental Diversity and Mental Health (NHMRC-EU grant administered by Murdoch Children's Research Institute)
    Murdoch Childrens Research Institute
    Open grant
  • 2022 - 2025
    MAGNET - A multi-arm, adaptive, group-sequential trial network to evaluate drug efficacy in patients with Amyotrophic Lateral Sclerosis (ALS) (FightMND grant administered by NeuRA)
    Neuroscience Research Australia
    Open grant
  • 2022 - 2025
    Preparing Australia for use of genomics in prevention of heart-disease: Focus on South Asian Australians
    NHMRC MRFF Genomics Health Futures Mission
    Open grant
  • 2022 - 2027
    The Australian Genetic Diversity Database: towards a more equitable future for genomic medicine in Australia (MRFF Genomics Health Futures Mission grant administered by UNSW)
    University of New South Wales
    Open grant
  • 2020 - 2025
    A novel biomarker for ALS
    Cure for MND Foundation - Impact Grants
    Open grant
  • 2020 - 2027
    Kids are not OK: Emergency Department management of acute mental health crises in children and young people (Monash administered MRFF Million Minds
    Monash University
    Open grant
  • 2020 - 2026
    Quantitative Genomics of Common Disease
    NHMRC Investigator Grants
    Open grant

Past funding

  • 2023
    Establishing an Australian pathway to accreditation and clinical reporting for Polygenic Risk Scores (Administered by University of Melbourne under the NHMRC Australian Genomics Grant GNT2000001)
    University of Melbourne
    Open grant
  • 2023 - 2024
    An Australian Sporadic ALS transcriptome resource
    Motor Neurone Disease Research Institute of Australia Inc Innovator Grant
    Open grant
  • 2022 - 2025
    A high-throughput system to identify ALS risk genes from genome-wide association studies
    Cure for MND Foundation - Impact Grants
    Open grant
  • 2021 - 2025
    Genomic risk prediction and risk-tailored screening and early detection for common cancers (MRFF Genomics Grant led by University of Sydney)
    University of Sydney
    Open grant
  • 2021 - 2024
    iPSC clinical trials - population wide screening of patient iPSC¿s to reassess high value drug targets for motor neuron disease (MRFF Stem Cell Therapies administered by University of Melbourne)
    University of Melbourne
    Open grant
  • 2021 - 2022
    Targeting NAT1 to improve metabolism and slow disease progression in MND
    Motor Neurone Disease Research Institute of Australia Inc Innovator Grant
    Open grant
  • 2021
    Transcriptomic and Functional Evaluation of Immune-Activated Monocytes in MND
    Motor Neurone Disease Research Institute of Australia Inc Linda Rynalski Bridge Funding Grant
    Open grant
  • 2020 - 2021
    Understanding influence of genetics on Brain Biomarkers
    Alto Neuroscience (Australia) Pty Ltd
    Open grant
  • 2020 - 2022
    ATHENA CV-19 Genomics Study
    Queensland Health
    Open grant
  • 2020 - 2021
    Transcriptomic and Functional Evaluation of Immune-Activated Monocytes in MND.
    Motor Neurone Disease Research Institute of Australia Inc
    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
  • 2020 - 2023
    Prediction of phenotype for multiple traits from multi-omic data (ARC Discovery Project administered by University of Melbourne)
    University of Melbourne
    Open grant
  • 2020 - 2025
    Sporadic ALS Australian Systems Genomics Consortium (SALSA-SGC)
    Cure for MND Foundation - Translational Research Grants
    Open grant
  • 2019 - 2024
    Postpartum Depression: Action Towards Causes and Treatment
    Research Donation Generic
    Open grant
  • 2019 - 2020
    Immunogenetics of motor neurone disease - a pilot study
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2019 - 2024
    ALS Trials Australia (ALSTA) to develop precision medicine (MRFF RCRDUN led by University of Sydney)
    University of Sydney
    Open grant
  • 2019 - 2021
    Identifying molecular pathways affected by the sporadic ALS risk factor, GGNBP2
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2018 - 2020
    Cell-free DNA profiling in cases and disease-mimics to develop a biomarker test for Amyotrophic Lateral Sclerosis
    Brain Foundation
    Open grant
  • 2018 - 2024
    Estimating the genetic and environmental architecture of psychiatric disorders (NIH Grant administered by the University of Colorado)
    University of Colorado
    Open grant
  • 2018 - 2023
    Motor Neurone Disease: Patient centred care for a progressive neurological disease - evidence driving policy (NHMRC Partnership Project administered by the University of Sydney)
    University of Sydney
    Open grant
  • 2018 - 2019
    Longitudinal assessment of behaviour and cognition in ALS through brief Online Carers' behavioural Questionnaire (OCQ)
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2018 - 2020
    BRAIN-MEND: Biological Resource Analysis to Identify New MEchanisms and phenotypes in Neurodegenerative Diseases (EU JPDN grant led by King's College London)
    Kings College London
    Open grant
  • 2018 - 2021
    BRAIN-MEND: Biological Resource Analysis to identify new mechanisms and phenotypes in Neurodegenerative Diseases (NHMRC component of EU JPND application)
    NHMRC Boosting Dementia Research Grants
    Open grant
  • 2017 - 2020
    CogChip: development of a targeted genotyping chip for executive function (ARC Linkage Project administered by Monash University)
    Monash University
    Open grant
  • 2017 - 2018
    GWAS data for SALSA-SGC
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2017 - 2018
    Cell-free DNA and ALS; insight into disease mechanisms and progression
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2017 - 2018
    Inclusion of an environmental questionnaire into SALSA online data collection
    The Halpin Trust
    Open grant
  • 2017
    Functional analysis of ALS candidate genes
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2017 - 2018
    New and innovative polygenic approach for understanding and modelling MNDs in zebrafish
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2017 - 2023
    Complex trait genomics
    NHMRC Program Grant
    Open grant
  • 2016 - 2017
    Identification of phenotypic modifiers in sporadic ALS through systems genomics (Motor Neuron Disease Research Institute of Australia Inc project administered by Macquarie University)
    Macquarie University
    Open grant
  • 2016
    Single Cell Transcriptomic Laboratory
    UQ Major Equipment and Infrastructure
    Open grant
  • 2016
    Using biomarkers to explore heterogeneity of motor neurone disease
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2015 - 2021
    Development and validation of systems genomics-based predictors for autism (Stage 1)
    CRC for Living with Autism Spectrum Disorders (Autism CRC Limited)
    Open grant
  • 2015 - 2019
    Sporadic ALS Australian Systems Genomics Consortium (SALSA-SGC)
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2015 - 2019
    1/2 A Large-Scale Schizophrenia Association Study in Sweden (NIH grant administered by the University of North Carolina at Chapel Hill)
    University of North Carolina
    Open grant
  • 2015 - 2016
    Gene discovery in motor neuron disease through systems genomics
    NHMRC Project Grant
    Open grant
  • 2015 - 2020
    Multivariate whole genome estimation and prediction analysis of genomics data applied to psychiatric disorders
    NHMRC Project Grant
    Open grant
  • 2015 - 2019
    NHMRC Research Fellowship: Using genomics to understand psychiatric disorders
    NHMRC Research Fellowship
    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 - 2015
    The role of altered neuromuscular signaling in ALS: factors that modify the course of MND
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2014
    Trans-ethnic and trans-omic statistical analyses to identify new ALS risk variants
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2014 - 2015
    Whole exome sequencing of sporadic MND
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2013 - 2015
    Estimation and partitioning of the still-missing heritability for complex disease
    NHMRC Project Grant
    Open grant
  • 2013 - 2015
    Statistical analyses of whole genome genotype data to better understand psychiatric disorders
    NHMRC Project Grant
    Open grant
  • 2012 - 2013
    Towards an etiological understanding of the comorbidity of psychiatric disorders (transfer in from QIMR)
    NHMRC Project Grant
    Open grant
  • 2011 - 2014
    Better Methods for Individual Risk Prediction of Complex Traits in Human Populations
    NHMRC Project Grant
    Open grant
  • 2011 - 2014
    NHMRC Research Fellowship (SRF A)
    NHMRC Research Fellowship
    Open grant
  • 2011 - 2014
    Dissecting the shared genetic architecture of psychiatric and psychological traits with application to prediction of genetic risk
    ARC Future Fellowships
    Open grant

Availability

Professor Naomi Wray is:
Not available for supervision

Supervision history

Current supervision

  • Doctor Philosophy

    Genetic architecture and evolution of complex traits across populations in humans

    Associate Advisor

    Other advisors: Professor Peter Visscher, Dr Fleur Garton, Dr Jian Zeng

  • Doctor Philosophy

    Understanding cellular and molecular heterogeneity in endometriosis using multi-omics data

    Associate Advisor

    Other advisors: Dr Sally Mortlock, Dr Allan McRae

  • Doctor Philosophy

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

    Associate Advisor

    Other advisors: Dr Enda Byrne

Completed supervision

Enquiries

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communications@uq.edu.au