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Honorary Professor Jake Gratten
Honorary Professor

Jake Gratten

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Overview

Background

Dr Gratten completed his undergraduate studies and PhD at The University of Queensland, before undertaking postdoctoral training in evolutionary and quantitative genetics at the University of Sheffield. He then returned to Australia and shifted research focus to psychiatric and neurological genetics, taking up a position as research fellow at the Queensland Brain Institute. In 2013, he was recruited to UQ's Centre for Neurogenetics and Statistical Genomics, and in 2017 was awarded an NHMRC Career Development Fellowship (Level 2). He established the Cognitive Health Genomics group at Mater Research Institute in 2018, with the goal to improve understanding of the etiology of psychiatric and neurological disorders through analysis and integration of whole genome datasets. He has received >$5M in research funding from the NHMRC, Autism Cooperative Research Centre and both Australian (BICARE) and international (Brain & Behavior Research Foundation) philanthropic funders.

Availability

Honorary Professor Jake Gratten is:
Available for supervision

Qualifications

  • Bachelor of Science, The University of Queensland
  • Bachelor (Honours) of Science, The University of Queensland
  • Doctor of Philosophy, The University of Queensland

Works

Search Professor Jake Gratten’s works on UQ eSpace

148 works between 2001 and 2024

1 - 20 of 148 works

Featured

2016

Journal Article

Rare variants are common in schizophrenia

Gratten, Jacob (2016). Rare variants are common in schizophrenia. Nature Neuroscience, 19 (11), 1426-1428. doi: 10.1038/nn.4422

Rare variants are common in schizophrenia

Featured

2016

Journal Article

Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations

Gratten, Jacob, Wray, Naomi R., Peyrot, Wouter J., McGrath, John J., Visscher, Peter M. and Goddard, Michael E. (2016). Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations. Nature Genetics, 48 (7), 718-+. doi: 10.1038/ng.3577

Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations

Featured

2013

Journal Article

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

Gratten, Jacob, Visscher, Peter M., Mowry, Bryan J. and Wray, Naomi R. (2013). Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nature Genetics, 45 (3), 234-238. doi: 10.1038/ng.2555

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

2024

Journal Article

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura T., Andlauer, Till F. M., von Scheidt, Moritz, Ruderfer, Douglas M., Ripke, Stephan, McQuillin, Andrew, Stahl, Eli A., Domenici, Enrico, Adolfsson, Rolf, Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Bene, Judit, Bergen, Sarah E., Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Blackwood, Douglas H. R., Borglum, Anders D., Bramon, Elvira, Bruggeman, Richard ... Ziller, Michael J. (2024). Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications , 15 (1) 5534. doi: 10.1038/s41467-024-49338-2

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

2024

Journal Article

Absence of association between maternal adverse events and long-term gut microbiome outcomes in the Australian Autism Biobank

Vasileva, Svetlina, Yap, Chloe X., Whitehouse, Andrew J. O., Gratten, Jacob and Eyles, Darryl (2024). Absence of association between maternal adverse events and long-term gut microbiome outcomes in the Australian Autism Biobank. Brain, Behavior, and Immunity - Health, 39 100814. doi: 10.1016/j.bbih.2024.100814

Absence of association between maternal adverse events and long-term gut microbiome outcomes in the Australian Autism Biobank

2024

Journal Article

Association of number of siblings with preclinical markers of cardiovascular disease. the cardiovascular risk in Young Finns study

Pihlman, Jukka, Magnussen, Costan G., Laitinen, Tomi T., Ruohonen, Saku, Pahkala, Katja, Jokinen, Eero, Laitinen, Tomi P., Hutri-Kahonen, Nina, Tossavainen, Paivi, Taittonen, Leena, Kahonen, Mika, Viikari, Jorma SA., Raitakari, Olli T., Juonala, Markus and Nuotio, Joel (2024). Association of number of siblings with preclinical markers of cardiovascular disease. the cardiovascular risk in Young Finns study. International Journal of Cardiology Cardiovascular Risk and Prevention, 20 200227. doi: 10.1016/j.ijcrp.2023.200227

Association of number of siblings with preclinical markers of cardiovascular disease. the cardiovascular risk in Young Finns study

2024

Journal Article

Connecting clinical and genetic heterogeneity in ADHD

Yap, Chloe X. and Gratten, Jacob (2024). Connecting clinical and genetic heterogeneity in ADHD. Nature Genetics, 56 (2), 195-196. doi: 10.1038/s41588-024-01652-7

Connecting clinical and genetic heterogeneity in ADHD

2024

Journal Article

Connecting clinical and genetic heterogeneity in ADHD

Yap, Chloe X. and Gratten, Jacob (2024). Connecting clinical and genetic heterogeneity in ADHD. Nature Genetics, 56 (2), 195-196. doi: 10.1038/s41588-024-01652-7

Connecting clinical and genetic heterogeneity in ADHD

2024

Journal Article

Associations of the Gut Microbiome With Treatment Resistance in Schizophrenia

Vasileva, Svetlina S., Yang, Yuanhao, Baker, Andrea, Siskind, Dan, Gratten, Jacob and Eyles, Darryl (2024). Associations of the Gut Microbiome With Treatment Resistance in Schizophrenia. JAMA Psychiatry, 81 (3), 292-302. doi: 10.1001/jamapsychiatry.2023.5371

Associations of the Gut Microbiome With Treatment Resistance in Schizophrenia

2024

Journal Article

Erratum: Autism-related dietary preferences mediate autism-gut microbiome associations (Cell (2021) 184(24) (5916–5931.e17), (S0092867421012319), (10.1016/j.cell.2021.10.015))

Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Wood, David L.A., Krause, Lutz, Tyson, Gene W., Restuadi, Restuadi, Wallace, Leanne, McLaren, Tiana, Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Frenk, Mira Levis, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Holtmann, Gerald, Strike, Lachlan T., de Zubicaray, Greig I. ... Gratten, Jacob (2024). Erratum: Autism-related dietary preferences mediate autism-gut microbiome associations (Cell (2021) 184(24) (5916–5931.e17), (S0092867421012319), (10.1016/j.cell.2021.10.015)). Cell, 187 (2), 495-510. doi: 10.1016/j.cell.2023.12.001

Erratum: Autism-related dietary preferences mediate autism-gut microbiome associations (Cell (2021) 184(24) (5916–5931.e17), (S0092867421012319), (10.1016/j.cell.2021.10.015))

2024

Other Outputs

TRS-BIOME

Eyles, Darryl, Vasileva, Svetlina, Siskind, Dan, Alexander, Suzy, Gratten, Jake, Ko, Pauline and Vasileva, Svetlina (2024). TRS-BIOME. The University of Queensland. (Dataset) doi: 10.48610/23fd2eb

TRS-BIOME

2023

Journal Article

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

Kavousi, Maryam, Bos, Maxime M., Barnes, Hanna J., Cardenas, Christian L. Lino, Wong, Doris, Lu, Haojie, Hodonsky, Chani J., Landsmeer, Lennart P. L., Turner, Adam W., Kho, Minjung, Hasbani, Natalie R., de Vries, Paul S., Bowden, Donald W., Chopade, Sandesh, Deelen, Joris, Benavente, Ernest Diez, Guo, Xiuqing, Hofer, Edith, Hwang, Shih-Jen, Lutz, Sharon M., Lyytikaeinen, Leo-Pekka, Slenders, Lotte, Smith, Albert V., Stanislawski, Maggie A., van Setten, Jessica, Wong, Quenna, Yanek, Lisa R., Becker, Diane M., Beekman, Marian ... Miller, Clint L. (2023). Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. Nature Genetics, 55 (10), 1651-1664. doi: 10.1038/s41588-023-01518-4

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

2023

Journal Article

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Maury, Eduardo A., Sherman, Maxwell A., Genovese, Giulio, Gilgenast, Thomas G., Kamath, Tushar, Burris, S. J., Rajarajan, Prashanth, Flaherty, Erin, Akbarian, Schahram, Chess, Andrew, McCarroll, Steven A., Loh, Po-Ru, Phillips-Cremins, Jennifer E., Brennand, Kristen J., Macosko, Evan Z., Walters, James T.R., O'Donovan, Michael, Sullivan, Patrick, Marshall, Christian R., Merico, Daniele, Thiruvahindrapuram, Bhooma, Wang, Zhouzhi, Scherer, Stephen W., Howrigan, Daniel P, Ripke, Stephan, Bulik-Sullivan, Brendan, Farh, Kai-How, Fromer, Menachem, Goldstein, Jacqueline I. ... Walsh, Christopher A. (2023). Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions. Cell Genomics, 3 (8) 100356, 1-21. doi: 10.1016/j.xgen.2023.100356

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

2023

Journal Article

Genetic insights into resting heart rate and its role in cardiovascular disease

van de Vegte, Yordi, Eppinga, Ruben P., van der Ende, M. Yldau, Hagemeijer, Yanick, Mahendran, Yuvaraj V., Salfati, Elias Y., Smith, Albert E., Tan, Vanessa, Arking, Dan V., Ntalla, Ioanna, Appel, Emil A., Schurmann, Claudia, Brody, Jennifer, Rueedi, Rico, Polasek, Ozren, Sveinbjornsson, Gardar, Lecoeur, Cecile, Ladenvall, Claes, Zhao, Jing Hua, Isaacs, Aaron, Wang, Lihua, Luan, Jian'an, Hwang, Shih-Jen, Mononen, Nina U., Auro, Kirsi F., Jackson, Anne, Bielak, Lawrence, Zeng, Linyao, Shah, Nabi ... van der Harst, Pim (2023). Genetic insights into resting heart rate and its role in cardiovascular disease. Nature Communications, 14 (1) 4646, 1-21. doi: 10.1038/s41467-023-39521-2

Genetic insights into resting heart rate and its role in cardiovascular disease

2023

Journal Article

Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: a general population study

Saarinen, Aino, Hietala, Jarmo, Lyytikainen, Leo-Pekka, Mishra, Binisha Hamal, Sormunen, Elina, Kahonen, Mika, Rovio, Suvi, Viikari, Jorma, Raitakari, Olli, Lehtimaki, Terho and Keltikangas-Jarvinen, Liisa (2023). Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: a general population study. Psychiatry Research, 326 115355, 1-9. doi: 10.1016/j.psychres.2023.115355

Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: a general population study

2023

Journal Article

Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

Hsu, Yu-Han H., Pintacuda, Greta, Liu, Ruize, Nacu, Eugeniu, Kim, April, Tsafou, Kalliopi, Petrossian, Natalie, Crotty, William, Suh, Jung Min, Riseman, Jackson, Martin, Jacqueline M., Biagini, Julia C., Mena, Daya, Ching, Joshua K.T., Malolepsza, Edyta, Li, Taibo, Singh, Tarjinder, Ge, Tian, Egri, Shawn B., Tanenbaum, Benjamin, Stanclift, Caroline R., Apffel, Annie M., Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T.R., Farh, Kai-How, Holmans, Peter A., Lee, Phil ... Lage, Kasper (2023). Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia. iScience, 26 (5) 106701, 1-28. doi: 10.1016/j.isci.2023.106701

Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

2023

Journal Article

Interactions between the lipidome and genetic and environmental factors in autism

Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Giles, Corey, Huynh, Kevin, Nguyen, Anh, Wallace, Leanne, McLaren, Tiana, Yang, Yuanhao, Hernandez, Leanna M., Gandal, Michael J., Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Levis Frenk, Mira, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Strike, Lachlan T. ... The Busselton Health Study Investigators (2023). Interactions between the lipidome and genetic and environmental factors in autism. Nature Medicine, 29 (4), 936-949. doi: 10.1038/s41591-023-02271-1

Interactions between the lipidome and genetic and environmental factors in autism

2023

Journal Article

The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders

Yang, Yuanhao, Zhou, Yuan, Nyholt, Dale R., Yap, Chloe X., Tannenberg, Rudolph K., Wang, Ying, Wu, Yang, Zhu, Zhihong, Taylor, Bruce V. and Gratten, Jacob (2023). The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders. Cell Genomics, 3 (2) 100249, 100249. doi: 10.1016/j.xgen.2022.100249

The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders

2022

Journal Article

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Trubetskoy, Vassily, Pardiñas, Antonio F, Qi, Ting, Panagiotaropoulou, Georgia, Awasthi, Swapnil, Bigdeli, Tim B, Bryois, Julien, Chen, Chia-Yen, Dennison, Charlotte A, Hall, Lynsey S, Lam, Max, Watanabe, Kyoko, Frei, Oleksandr, Ge, Tian, Harwood, Janet C, Koopmans, Frank, Magnusson, Sigurdur, Richards, Alexander L, Sidorenko, Julia, Wu, Yang, Zeng, Jian, Grove, Jakob, Kim, Minsoo, Li, Zhiqiang, Voloudakis, Georgios, Zhang, Wen, Adams, Mark, Agartz, Ingrid, Atkinson, Elizabeth G ... Schizophrenia Working Group of the Psychiatric Genomics Consortium (2022). Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature, 604 (7906), 502-508. doi: 10.1038/s41586-022-04434-5

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

2022

Journal Article

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

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

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

Funding

Current funding

  • 2023 - 2027
    Unravelling the interplay between EBV genomics and host T cell immune regulation in multiple sclerosis (Ex-led UTas MRFF MS grant)
    University of Tasmania
    Open grant
  • 2023 - 2027
    Towards improved clinical outcomes for common brain disorders using large-scale statistical genomics
    NHMRC Investigator Grants
    Open grant
  • 2022 - 2024
    Understanding the pathophysiology of Parkinson's disease using cellular genomics
    NHMRC IDEAS Grants
    Open grant

Past funding

  • 2020 - 2021
    Vitamin D in autism; preventative mechanisms
    Child Development Grant
    Open grant
  • 2018 - 2020
    Investigating the molecular signature of ASD through integrative genomics (NHMRC Project Grant administered by UNSW)
    University of New South Wales
    Open grant
  • 2017 - 2020
    Understanding the etiology of psychiatric disorders through whole genome analyses
    NHMRC Career Development Fellowship
    Open grant
  • 2016 - 2018
    Genomic Analysis of Sex Differences in Prevalence of Psychiatric Disorders (2015 NARSAD Young Investigator Grant)
    Brain and Behavior Research Foundation
    Open grant
  • 2016 - 2019
    Genetic analysis of the relationship between parental age and risk of psychiatric disorders
    NHMRC Project Grant
    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 - 2020
    Multivariate whole genome estimation and prediction analysis of genomics data applied to psychiatric disorders
    NHMRC Project Grant
    Open grant
  • 2014 - 2018
    Genetic analysis of de novo and inherited exome variation in schizophrenia
    NHMRC Project Grant
    Open grant

Supervision

Availability

Honorary Professor Jake Gratten is:
Available for supervision

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

Available projects

  • Cellular genomics of Parkinson's disease

    We are seeking a highly motivated PhD candidate with a background and interest in human genomics, statistics and neurodegenerative disease to join the Cognitive Health Genomics group at the Mater Research Institute, UQ. The successful candidate would work on an NHMRC-funded study to identify selectively vulnerable neuronal and/or glial cell types across the spatial and temporal course of Parkinson’s disease using single cell approaches.

    Project description

    Parkinson’s disease (PD) is a complex neurodegenerative condition affecting 1% of Australians aged ≥60-years. There is no cure, and the number of affected individuals is rising steeply as populations age. Understanding the genetic basis of PD is critical to developing new therapeutics to counter the growing disease burden. Large-scale genome-wide association studies (GWAS) of PD have identified nearly 100 risk loci, but interpretation of these findings remains challenging; we do not yet know the identity of most PD risk genes, nor the specific cell types in which they act, nor when they act during the course of disease, which hampers efforts to identify targets for interventions. We will address these challenges by using single nucleus RNA-seq to identify cell types involved in the onset and progression of Lewy body pathology in PD-related brain regions.

    Requirements

    • Bachelor’s degree with first class honours, or Masters, in statistics, mathematics, bioinformatics, human genetics, animal breeding, or an equivalent field.
    • Prior research experience in human genomics or animal breeding, including a familiarity with high-throughput genomic data and working in a high-performance computing environment.
    • Skills in the R statistical computing language and/or python, C++ or an equivalent computing language.
    • High degree of motivation and organisation, and an ability to work both independently and as part of a team.
    • (Co-)authorship on at least one peer-reviewed publication (for International applicants)
    • Excellent written and oral communications skills in English.

    For further information please contact Dr Jake Gratten, jacob.gratten@mater.uq.edu.au, +61-7-34437585.

Supervision history

Current supervision

Completed supervision

Media

Enquiries

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