
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
2019
Journal Article
Parkinson's disease age at onset genome-wide association study: defining heritability, genetic loci, and α-synuclein mechanisms
Blauwendraat, Cornelis, Heilbron, Karl, Vallerga, Costanza L., Bandres-Ciga, Sara, von Coelln, Rainer, Pihlstrøm, Lasse, Simón-Sánchez, Javier, Schulte, Claudia, Sharma, Manu, Krohn, Lynne, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Noyce, Alastair J., Tan, Manuela, Gibbs, J. Raphael, Hernandez, Dena G., Scholz, Sonja W., Jankovic, Joseph, Shulman, Lisa M., Lesage, Suzanne, Corvol, Jean-Christophe, Brice, Alexis, van Hilten, Jacobus J., Marinus, Johan, Eerola-Rautio, Johanna, Tienari, Pentti, Majamaa, Kari, Toft, Mathias ... Singleton, Andrew B. (2019). Parkinson's disease age at onset genome-wide association study: defining heritability, genetic loci, and α-synuclein mechanisms. Movement Disorders, 34 (6) mds.27659, 866-875. doi: 10.1002/mds.27659
2019
Journal Article
Examining the impact of imputation errors on fine-mapping using DNA methylation QTL as a model trait
Chundru, V. Kartik, Marioni, Riccardo E., Prendergast, James G. D., Vallerga, Costanza L., Lin, Tian, Berveridge, Allan J., SGPD Consortium, Gratten, Jacob, Hume, David A., Deary, Ian J., Wray, Naomi R., Visscher, Peter M. and McRae, Allan F. (2019). Examining the impact of imputation errors on fine-mapping using DNA methylation QTL as a model trait. Genetics, 212 (3), 577-586. doi: 10.1534/genetics.118.301861
2019
Journal Article
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability
Reynolds, Regina H., Botia, Juan, Nalls, Mike A., Hardy, John, Taliun, Sarah A. Gagliano, Ryten, Mina, Noyce, Alastair J., Nicolas, Aude, Cookson, Mark R., Bandres-Ciga, Sara, Gibbs, J. Raphael, Hernandez, Dena G., Singleton, Andrew B., Reed, Xylena, Leonard, Hampton, Blauwendraat, Cornelis, Faghri, Faraz, Bras, Jose, Guerreiro, Rita, Tucci, Arianna, Kia, Demis A., Houlden, Henry, Plun-Favreau, Helene, Mok, Kin Y., Wood, Nicholas W., Lovering, Ruth, R'Bibo, Lea, Rizig, Mie, Chelban, Viorica ... Pearson, John (2019). Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability. Npj Parkinsons Disease, 5 (1) 6, 6. doi: 10.1038/s41531-019-0076-6
2019
Journal Article
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Karlsson Linnér, Richard, Biroli, Pietro, Kong, Edward, Meddens, S. Fleur W., Wedow, Robbee, Fontana, Mark Alan, Lebreton, Maël, Tino, Stephen P., Abdellaoui, Abdel, Hammerschlag, Anke R., Nivard, Michel G., Okbay, Aysu, Rietveld, Cornelius A., Timshel, Pascal N., Trzaskowski, Maciej, Vlaming, Ronald de, Zünd, Christian L., Bao, Yanchun, Buzdugan, Laura, Caplin, Ann H., Chen, Chia-Yen, Eibich, Peter, Fontanillas, Pierre, Gonzalez, Juan R., Joshi, Peter K., Karhunen, Ville, Kleinman, Aaron, Levin, Remy Z., Lill, Christina M. ... Beauchamp, Jonathan P. (2019). Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Nature Genetics, 51 (2), 245-257. doi: 10.1038/s41588-018-0309-3
2019
Conference Publication
First genome-wide association study of schizophrenia in an Indian population reveals a novel susceptibility locus
Periyasamy, Sathish, John, Sujit, Padmavati, Raman, Rajendren, Preeti, Thirunavukkarasu, Priyadarshini, Gratten, Jacob, Holliday, Elizabeth, Bakshi, Andrew, Jorde, Lynn, Brown, Matthew, Wray, Naomi, Suetani, Rachel, Giacomotto, Jean, Thara, Rangaswamy and Mowry, Bryan (2019). First genome-wide association study of schizophrenia in an Indian population reveals a novel susceptibility locus. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October 2018. Amsterdam, The Netherlands: Elsevier . doi: 10.1016/j.euroneuro.2018.08.017
2019
Conference Publication
Connecting comorbidities with brain-gut-microbiome stress axis biology in autism spectrum disorder
Yap, Chloe, Wray, Naomi, Brix, Susanne and Gratten, Jacob (2019). Connecting comorbidities with brain-gut-microbiome stress axis biology in autism spectrum disorder. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, California, 26-31 October 2019 . Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2019.08.215
2019
Conference Publication
Common genetic variation explains a high proportion of the elevated risk of psychiatric disorders in children of younger mothers
Gratten, Jacob, Yang, Yuanhao, Trzaskowski, Maciej, Kemper, Kathryn, Yengo, Loic, Zheng, Zhili, Zhang, Futao, Zhu, Zhihong, Mcrae, Allan, Yang, Jian, Wray, Naomi and Visscher, Peter (2019). Common genetic variation explains a high proportion of the elevated risk of psychiatric disorders in children of younger mothers. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October, 2018. Amsterdam, Netherlands: Elsevier BV. doi: 10.1016/j.euroneuro.2018.08.167
2019
Journal Article
The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: the Vitality 90+study
Ozsait-Selcuk, B., Komurcu-Bayrak, E., Jylha, M., Luukkaala, T., Perola, M., Kristiansson, K., Mononen, N., Hurme, M., Kahonen, M., Goebeler, S., Laaksonen, R., Hervonen, A., Erginel-Unaltuna, N., Karhunen, P. J. and Lehtimaki, T. (2019). The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: the Vitality 90+study. Annals of Human Genetics, 83 (1), 34-45. doi: 10.1111/ahg.12282
2018
Journal Article
Imprint of assortative mating on the human genome
Yengo, Loic, Robinson, Matthew R., Keller, Matthew C., Kemper, Kathryn E., Yang, Yuanhao, Trzaskowski, Maciej, Gratten, Jacob, Turley, Patrick, Cesarini, David, Benjamin, Daniel J., Wray, Naomi R., Goddard, Michael E., Yang, Jian and Visscher, Peter M. (2018). Imprint of assortative mating on the human genome. Nature Human Behaviour, 2 (12), 948-954. doi: 10.1038/s41562-018-0476-3
2018
Other Outputs
The genetic relationship between female reproductive traits and six psychiatric disorders
Ni, Guiyan, Amare, Azmeraw, Zhou, Xuan, Mills, Natalie, Gratten, Jacob and Lee, Sang Hong (2018). The genetic relationship between female reproductive traits and six psychiatric disorders. doi: 10.1101/433946
2018
Journal Article
Study protocol for the Australian autism biobank: an international resource to advance autism discovery research
Alvares, Gail A., Dawson, Paul A., Dissanayake, Cheryl, Eapen, Valsamma, Gratten, Jacob, Grove, Rachel, Henders, Anjali, Heussler, Helen, Lawson, Lauren, Masi, Anne, Raymond, Emma, Rose, Felicity, Wallace, Leanne, Wray, Naomi R. and Whitehouse, Andrew J. O. (2018). Study protocol for the Australian autism biobank: an international resource to advance autism discovery research. BMC Pediatrics, 18 (1) 284, 284. doi: 10.1186/s12887-018-1255-z
2018
Journal Article
Salbutamol-induced Decrease in Augmentation Index is Related to the Parallel Increase in Heart Rate
Tikkakoski, Antti J., Kangas, Pauliina, Suojanen, Lauri, Tahvanainen, Anna M., Eraranta, Arttu, Kahonen, Mika A. P., Sipila, Kalle, Mustonen, Jukka T. and Porsti, Ilkka H. (2018). Salbutamol-induced Decrease in Augmentation Index is Related to the Parallel Increase in Heart Rate. Basic & Clinical Pharmacology & Toxicology, 123 (2), 161-173. doi: 10.1111/bcpt.12988
2018
Journal Article
Age at first birth in women is genetically associated with increased risk of schizophrenia
Ni, Guiyan, Gratten, Jacob, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Wray, Naomi R. and Lee, Sang Hong (2018). Age at first birth in women is genetically associated with increased risk of schizophrenia. Scientific Reports, 8 (1) 10168, 10168. doi: 10.1038/s41598-018-28160-z
2018
Journal Article
Serum proteomic profiling to identify biomarkers of premature carotid atherosclerosis
Bhosale, Santosh D., Moulder, Robert, Venalainen, Mikko S., Koskinen, Juhani S., Pitkanen, Niina, Juonala, Markus T., Kahonen, Mika A. P., Lehtimaki, Terho J., Viikari, Jorma S. A., Elo, Laura L., Goodlett, David R., Lahesmaa, Riitta and Raitakari, Olli T. (2018). Serum proteomic profiling to identify biomarkers of premature carotid atherosclerosis. Scientific Reports, 8 (1) 9209. doi: 10.1038/s41598-018-27265-9
2018
Journal Article
Trans-eQTLs identified in whole blood have limited influence on complex disease biology
Yap, Chloe X., Lloyd-Jones, Luke, Holloway, Alexander, Smartt, Peter, Wray, Naomi R., Gratten, Jacob and Powell, Joseph E. (2018). Trans-eQTLs identified in whole blood have limited influence on complex disease biology. European Journal of Human Genetics, 26 (9), 1-8. doi: 10.1038/s41431-018-0174-7
2018
Journal Article
Sizing up whole-genome sequencing studies of common diseases
Wray, Naomi R. and Gratten, Jacob (2018). Sizing up whole-genome sequencing studies of common diseases. Nature Genetics, 50 (5), 635-637. doi: 10.1038/s41588-018-0113-0
2018
Conference Publication
Critical Periods in Cardiovascular Health Across the Life Course: A Pooled Cohort Analysis
Allen, Norrina B., Krefman, Amy, Labarthe, Darwin, Greenland, Philip, Juonala, Markus, Kahonen, Mika, Day, S. Rena, Lehtimaki, Terho, Van Horn, Linda, Bazzano, Lydia, Liu, Lei, Alonso, Camilo F., Webber, Larry S., Pahkala, Katja, Laitinen, Tomi, Raitakari, Olli and Lloyd-Jones, Donald (2018). Critical Periods in Cardiovascular Health Across the Life Course: A Pooled Cohort Analysis. Scientific Sessions of the American-Heart-Association on Epidemiology and Prevention/Lifestyle and Cardiometabolic Health, New Orleans La, Mar 20-23, 2018. PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS.
2018
Journal Article
Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis
McKeown, Nicola M., Dashti, Hassan S., Ma, Jiantao, Haslam, Danielle E., Kiefte-de Jong, Jessica C., Smith, Caren E., Tanaka, Toshiko, Graff, Mariaelisa, Lemaitre, Rozenn N., Rybin, Denis, Sonestedt, Emily, Frazier-Wood, Alexis C., Mook-Kanamori, Dennis O., Li, Yanping, Wang, Carol A., Leermakers, Elisabeth T. M., Mikkila, Vera, Young, Kristin L., Mukamal, Kenneth J., Cupples, L. Adrienne, Schulz, Christina-Alexandra, Chen, Tzu-An, Li-Gao, Ruifang, Huang, Tao, Oddy, Wendy H., Raitakari, Olli, Rice, Kenneth, Meigs, James B., Ericson, Ulrika ... Herman, Mark A. (2018). Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis. Diabetologia, 61 (2), 317-330. doi: 10.1007/s00125-017-4475-0
2017
Journal Article
Gene networks associated with non-syndromic intellectual disability
Lee, Soohyun, Rudd, Stephen, Gratten, Jacob, Visscher, Peter M., Prins, Johannes B. and Dawson, Paul A. (2017). Gene networks associated with non-syndromic intellectual disability. Journal of Neurogenetics, 32 (1), 6-14. doi: 10.1080/01677063.2017.1404058
2017
Journal Article
Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese
Gratten, Jacob, Zhao, Qiongyi, Benyamin, Beben, Garton, Fleur, He, Ji, Leo, Paul J., Mangelsdorf, Marie, Anderson, Lisa, Zhang, Zong-Hong, Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Edson, Janette, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K., Jin, Zi-Bing, Li, Zhongshan, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, Mowry, Bryan J., Ran, Shu, Reutens, David C., Song, Sharon, Tan, Li-Jun, Tang, Lu, Wallace, Robyn H. ... Fan, Dongsheng (2017). Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese. Genome Medicine, 9 (97) 97, 97. doi: 10.1186/s13073-017-0487-0
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.
-
Understanding mechanisms underlying multiple sclerosis using large-scale multi-omics
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 improve understanding of the pathophysiology of multiple sclerosis by integrating large-scale multi-omics data using cutting-edge statistical methods.
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.
- Excellent written and oral communications skills in English.
For further information please contact Prof Jake Gratten, jacob.gratten@mater.uq.edu.au.
Supervision history
Current supervision
-
Doctor Philosophy
Multiomics of common co-occurring conditions in autism spectrum disorder
Principal Advisor
Other advisors: Dr Allan McRae, Dr Yuanhao Yang
-
Doctor Philosophy
Cellular genomics of Parkinson's disease
Principal Advisor
Other advisors: Dr Quan Nguyen, 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
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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
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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
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