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
Fields of research
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
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
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
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
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
2024
Conference Publication
Investigation Of De Novo Mutations In Schizophrenia Affected Indian Families
Periyasamy, Sathish, Youssef, Pierre, Qiongyi, Zhao, John, Sujit, Smith, Heather, Gratten, Jacob, Thara, Rangaswamy and Mowry, Bryan (2024). Investigation Of De Novo Mutations In Schizophrenia Affected Indian Families. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.285
2024
Conference Publication
Spatial Transcriptomics Reveals Brain-wide Changes In Gene Expression Associated With Prophylactic Effects Of Nortriptyline In A Mouse Model Of Chronic Stress Exposure
Yang, Yuanhao, Tannenberg, Rudolph, Hafey, Katelyn, Zhou, Mei, Groves, Natalie, Jhaveri, Dhanisha and Gratten, Jacob (2024). Spatial Transcriptomics Reveals Brain-wide Changes In Gene Expression Associated With Prophylactic Effects Of Nortriptyline In A Mouse Model Of Chronic Stress Exposure. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.159
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
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
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
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
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
2024
Journal Article
A Proposed Pediatric Clinical Cardiovascular Health Reference Standard
Petito, Lucia C., Mccabe, Megan E., Pool, Lindsay R., Krefman, Amy E., Perak, Amanda M., Marino, Bradley S., Juonala, Markus, Kahonen, Mika, Lehtimaki, Terho, Bazzano, Lydia A., Liu, Lei, Pahkala, Katja, Laitinen, Tomi T., Raitakari, Olli T., Gooding, Holly C., Daniels, Stephen R., Skinner, Asheley C., Greenland, Philip, Davis, Matthew M., Wakschlag, Lauren S., Van Horn, Linda, Hou, Lifang, Lloyd-Jones, DonaldM., Labarthe, Darwin R. and Allen, Norrina B. (2024). A Proposed Pediatric Clinical Cardiovascular Health Reference Standard. American Journal of Preventive Medicine, 66 (2), 216-225. doi: 10.1016/j.amepre.2023.09.019
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
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
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
2023
Journal Article
Selection of cross-reactive T cells by commensal and food-derived yeasts drives cytotoxic T<sub>H</sub>1 cell responses in Crohn's disease
Martini, Gabriela Rios, Tikhonova, Ekaterina, Rosati, Elisa, Decelie, Meghan Bialt, Sievers, Laura Katharina, Tran, Florian, Lessing, Matthias, Bergfeld, Arne, Hinz, Sophia, Nikolaus, Susanna, Kuempers, Julia, Matysiak, Anna, Hofmann, Philipp, Saggau, Carina, Schneiders, Stephan, Kamps, Ann-Kristin, Jacobs, Gunnar, Lieb, Wolfgang, Maul, Jochen, Siegmund, Britta, Seegers, Barbara, Hinrichsen, Holger, Oberg, Hans-Heinrich, Wesch, Daniela, Bereswill, Stefan, Heimesaat, Markus M., Rupp, Jan, Kniemeyer, Olaf, Brakhage, Axel A. ... Bacher, Petra (2023). Selection of cross-reactive T cells by commensal and food-derived yeasts drives cytotoxic TH1 cell responses in Crohn's disease. Nature Medicine, 29 (10), 2602-2614. doi: 10.1038/s41591-023-02556-5
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
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
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
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
Funding
Current funding
Supervision
Availability
- Honorary Professor Jake Gratten is:
- Available for supervision
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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
-
Doctor Philosophy
Cellular genomics of Parkinson's disease
Principal Advisor
Other advisors: Dr Quan Nguyen, Dr Allan McRae, Dr Yuanhao Yang
-
Doctor Philosophy
Multiomics of common co-occurring conditions in autism spectrum disorder
Principal Advisor
Other advisors: Dr Allan McRae, Dr Yuanhao Yang
-
Doctor Philosophy
Using multi-omics approaches to characterise determinants of early growth trajectories and their consequences on later life health
Associate Advisor
Other advisors: Professor David Evans, Dr Nicole Warrington
Completed supervision
-
2022
Doctor Philosophy
Multi-omics data offer systemic insights into autism
Principal Advisor
Other advisors: Professor Naomi Wray, Professor Gerald Holtmann
-
2019
Doctor Philosophy
Systems Genomics of Parkinson's Disease
Principal Advisor
Other advisors: Professor Peter Visscher
-
2018
Master Philosophy
Integrating genome-wide association study data with gene expression to understand complex traits and common diseases
Principal Advisor
Other advisors: Dr Allan McRae, Professor Naomi Wray
-
2024
Doctor Philosophy
The Role of the Gut Microbiome in Psychiatric Illness: From Prenatal Risk Factors to Treatment Resistance
Associate Advisor
Other advisors: Professor Dan Siskind, Professor Darryl Eyles
-
2015
Doctor Philosophy
Analysis of non-coding RNA expression in schizophrenia brain
Associate Advisor
Other advisors: Professor Bryan Mowry
Media
Enquiries
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