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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

203 works between 2001 and 2024

161 - 180 of 203 works

2012

Journal Article

The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants

Mowry, B. J. and Gratten, J. (2012). The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants. Molecular Psychiatry, 18 (1), 38-52. doi: 10.1038/mp.2012.34

The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants

2012

Journal Article

Parental Smoking in Childhood and Brachial Artery Flow-Mediated Dilatation in Young Adults The Cardiovascular Risk in Young Finns Study and the Childhood Determinants of Adult Health Study

Juonala, Markus, Magnussen, Costan G., Venn, Alison, Gall, Seana, Kahonen, Mika, Laitinen, Tomi, Taittonen, Leena, Lehtimaki, Terho, Jokinen, Eero, Sun, Cong, Viikari, Jorma S. A., Dwyer, Terence and Raitakari, Olli T. (2012). Parental Smoking in Childhood and Brachial Artery Flow-Mediated Dilatation in Young Adults The Cardiovascular Risk in Young Finns Study and the Childhood Determinants of Adult Health Study. Arteriosclerosis Thrombosis and Vascular Biology, 32 (4), 1024-1031. doi: 10.1161/ATVBAHA.111.243261

Parental Smoking in Childhood and Brachial Artery Flow-Mediated Dilatation in Young Adults The Cardiovascular Risk in Young Finns Study and the Childhood Determinants of Adult Health Study

2012

Journal Article

Genome-Wide Screen for Metabolic Syndrome Susceptibility Loci Reveals Strong Lipid Gene Contribution But No Evidence for Common Genetic Basis for Clustering of Metabolic Syndrome Traits

Kristiansson, Kati, Perola, Markus, Tikkanen, Emmi, Kettunen, Johannes, Surakka, Ida, Havulinna, Aki S., Stancakova, Alena, Barnes, Chris, Widen, Elisabeth, Kajantie, Eero, Eriksson, Johan G., Viikari, Jorma, Kahonen, Mika, Lehtimaki, Terho, Raitakari, Olli T., Hartikainen, Anna-Liisa, Ruokonen, Aimo, Pouta, Anneli, Jula, Antti, Kangas, Antti J., Soininen, Pasi, Ala-Korpela, Mika, Mannisto, Satu, Jousilahti, Pekka, Bonnycastle, Lori L., Jarvelin, Marjo-Riitta, Kuusisto, Johanna, Collins, Francis S., Laakso, Markku ... Salomaa, Veikko (2012). Genome-Wide Screen for Metabolic Syndrome Susceptibility Loci Reveals Strong Lipid Gene Contribution But No Evidence for Common Genetic Basis for Clustering of Metabolic Syndrome Traits. Circulation-Cardiovascular Genetics, 5 (2), 242-249. doi: 10.1161/CIRCGENETICS.111.961482

Genome-Wide Screen for Metabolic Syndrome Susceptibility Loci Reveals Strong Lipid Gene Contribution But No Evidence for Common Genetic Basis for Clustering of Metabolic Syndrome Traits

2012

Journal Article

Genome-wide association study identifies multiple loci influencing human serum metabolite levels

Kettunen, Johannes, Tukiainen, Taru, Sarin, Antti-Pekka, Ortega-Alonso, Alfredo, Tikkanen, Emmi, Lyytikainen, Leo-Pekka, Kangas, Antti J., Soininen, Pasi, Wuertz, Peter, Silander, Kaisa, Dick, Danielle M., Rose, Richard J., Savolainen, Markku J., Viikari, Jorma, Kahonen, Mika, Lehtimaki, Terho, Pietilainen, Kirsi H., Inouye, Michael, McCarthy, Mark I., Jula, Antti, Eriksson, Johan, Raitakari, Olli T., Salomaa, Veikko, Kaprio, Jaakko, Jarvelin, Marjo-Riitta, Peltonen, Leena, Perola, Markus, Freimer, Nelson B., Ala-Korpela, Mika ... Ripatti, Samuli (2012). Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Nature Genetics, 44 (3), 269-U65. doi: 10.1038/ng.1073

Genome-wide association study identifies multiple loci influencing human serum metabolite levels

2012

Journal Article

Supine and upright haemodynamic effects of sublingual nitroglycerin and inhaled salbutamol: a double-blind, placebo-controlled, randomized study

Tahvanainen, Anna M., Tikkakoski, Antti J., Leskinen, Miia H., Nordhausen, Klaus, Kahonen, Mika, Koobi, Tiit, Mustonen, Jukka T. and Porsti, Ilkka H. (2012). Supine and upright haemodynamic effects of sublingual nitroglycerin and inhaled salbutamol: a double-blind, placebo-controlled, randomized study. Journal of Hypertension, 30 (2), 297-306. doi: 10.1097/HJH.0b013e32834e4b26

Supine and upright haemodynamic effects of sublingual nitroglycerin and inhaled salbutamol: a double-blind, placebo-controlled, randomized study

2012

Journal Article

Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey - A Meta-Analysis of Three Independent Studies

Hernesniemi, Jussi A., Seppala, Ilkka, Lyytikainen, Leo-Pekka, Mononen, Nina, Oksala, Niku, Hutri-Kahonen, Nina, Juonala, Markus, Taittonen, Leena, Smith, Erin N., Schork, Nicholas J., Chen, Wei, Srinivasan, Sathanur R., Berenson, Gerald S., Murray, Sarah S., Laitinen, Tomi, Jula, Antti, Kettunen, Johannes, Ripatti, Samuli, Laaksonen, Reijo, Viikari, Jorma, Kahonen, Mika, Raitakari, Olli T. and Lehtimaki, Terho (2012). Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey - A Meta-Analysis of Three Independent Studies. Plos One, 7 (1) e28931. doi: 10.1371/journal.pone.0028931

Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey - A Meta-Analysis of Three Independent Studies

2011

Journal Article

Fetal Growth and Preterm Birth Influence Cardiovascular Risk Factors and Arterial Health in Young Adults The Cardiovascular Risk in Young Finns Study

Skilton, Michael R., Viikari, Jorma S. A., Juonala, Markus, Laitinen, Tomi, Lehtimaki, Terho, Taittonen, Leena, Kahonen, Mika, Celermajer, David S. and Raitakari, Olli T. (2011). Fetal Growth and Preterm Birth Influence Cardiovascular Risk Factors and Arterial Health in Young Adults The Cardiovascular Risk in Young Finns Study. Arteriosclerosis Thrombosis and Vascular Biology, 31 (12), 2975-2981. doi: 10.1161/ATVBAHA.111.234757

Fetal Growth and Preterm Birth Influence Cardiovascular Risk Factors and Arterial Health in Young Adults The Cardiovascular Risk in Young Finns Study

2011

Journal Article

Genetic Variants and Blood Pressure in a Population-Based Cohort The Cardiovascular Risk in Young Finns Study

Oikonen, Mervi, Tikkanen, Emmi, Juhola, Jonna, Tuovinen, Tarja, Seppala, Ilkka, Juonala, Markus, Taittonen, Leena, Mikkila, Vera, Kahonen, Mika, Ripatti, Samuli, Viikari, Jorma, Lehtimaki, Terho, Havulinna, Aki S., Kee, Frank, Newton-Cheh, Christopher, Peltonen, Leena, Schork, Nicholas J., Murray, Sarah S., Berenson, Gerald S., Chen, Wei, Srinivasan, Sathanur R., Salomaa, Veikko and Raitakari, Olli T. (2011). Genetic Variants and Blood Pressure in a Population-Based Cohort The Cardiovascular Risk in Young Finns Study. Hypertension, 58 (6), 1079-U228. doi: 10.1161/HYPERTENSIONAHA.111.179291

Genetic Variants and Blood Pressure in a Population-Based Cohort The Cardiovascular Risk in Young Finns Study

2011

Journal Article

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

Bis, Joshua C., Kavousi, Maryam, Franceschini, Nora, Isaacs, Aaron, Abecasis, Goncalo R., Schminke, Ulf, Post, Wendy S., Smith, Albert V., Cupples, L. Adrienne, Markus, Hugh S., Schmidt, Reinhold, Huffman, Jennifer E., Lehtimaki, Terho, Baumert, Jens, Muenzel, Thomas, Heckbert, Susan R., Dehghan, Abbas, North, Kari, Oostra, Ben, Bevan, Steve, Stoegerer, Eva-Maria, Hayward, Caroline, Raitakari, Olli, Meisinger, Christa, Schillert, Arne, Sanna, Serena, Voelzke, Henry, Cheng, Yu-Ching, Thorsson, Bolli ... O'Donnell, Christopher J. (2011). Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nature Genetics, 43 (10), 940-U40. doi: 10.1038/ng.920

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

2011

Journal Article

A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol

Surakka, Ida, Isaacs, Aaron, Karssen, Lennart C., Laurila, Pirkka-Pekka P., Middelberg, Rita P. S., Tikkanen, Emmi, Ried, Janina S., Lamina, Claudia, Mangino, Massimo, Igl, Wilmar, Hottenga, Jouke-Jan, Lagou, Vasiliki, van der Harst, Pim, Leach, Irene Mateo, Esko, Tonu, Kutalik, Zoltan, Wainwright, Nicholas W., Struchalin, Maksim V., Sarin, Antti-Pekka, Kangas, Antti J., Viikari, Jorma S., Perola, Markus, Rantanen, Taina, Petersen, Ann-Kristin, Soininen, Pasi, Johansson, Asa, Soranzo, Nicole, Heath, Andrew C., Papamarkou, Theodore ... Ripatti, Samuli (2011). A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genetics, 7 (10) e1002333, e1002333. doi: 10.1371/journal.pgen.1002333

A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol

2011

Journal Article

Characterisation of the transcriptome of a wild great tit Parus major population by next generation sequencing

Santure, Anna W., Gratten, Jake, Mossman, Jim A., Sheldon, Ben C. and Slate, Jon (2011). Characterisation of the transcriptome of a wild great tit Parus major population by next generation sequencing. BMC Genomics, 12 (15) 283, 283.1-283.18. doi: 10.1186/1471-2164-12-283

Characterisation of the transcriptome of a wild great tit Parus major population by next generation sequencing

2011

Journal Article

The <i>APOE</i> -219G/T and +113G/C polymorphisms affect insulin resistance among Turks

Komurcu-Bayrak, Evrim, Onat, Altan, Yuzbasiogullari, Berna, Mononen, Nina, Laaksonen, Reijo, Kahonen, Mika, Hergenc, Gulay, Lehtimaki, Terho and Erginel-Unaltuna, Nihan (2011). The APOE -219G/T and +113G/C polymorphisms affect insulin resistance among Turks. Metabolism-Clinical and Experimental, 60 (5), 655-663. doi: 10.1016/j.metabol.2010.06.016

The <i>APOE</i> -219G/T and +113G/C polymorphisms affect insulin resistance among Turks

2011

Journal Article

Conventional and Mendelian randomization analyses suggest no association between lipoprotein(a) and early atherosclerosis: the Young Finns Study

Kivimaeki, Mika, Magnussen, Costan G., Juonala, Markus, Kahonen, Mika, Kettunen, Johannes, Loo, Britt-Marie, Lehtimaki, Terho, Viikari, Jorma and Raitakari, Olli T. (2011). Conventional and Mendelian randomization analyses suggest no association between lipoprotein(a) and early atherosclerosis: the Young Finns Study. International Journal of Epidemiology, 40 (2), 470-478. doi: 10.1093/ije/dyq205

Conventional and Mendelian randomization analyses suggest no association between lipoprotein(a) and early atherosclerosis: the Young Finns Study

2011

Journal Article

Reduced systemic vascular resistance in healthy volunteers with presyncopal symptoms during a nitrate-stimulated tilt-table test

Tahvanainen, Anna, Koskela, Jenni, Leskinen, Miia, Ilveskoski, Erkki, Nordhausen, Klaus, Kahonen, Mika, Koobi, Tiit, Mustonen, Jukka and Porsti, Ilkka (2011). Reduced systemic vascular resistance in healthy volunteers with presyncopal symptoms during a nitrate-stimulated tilt-table test. British Journal of Clinical Pharmacology, 71 (1), 41-51. doi: 10.1111/j.1365-2125.2010.03794.x

Reduced systemic vascular resistance in healthy volunteers with presyncopal symptoms during a nitrate-stimulated tilt-table test

2010

Journal Article

Influence of Age on Associations Between Childhood Risk Factors and Carotid Intima-Media Thickness in Adulthood The Cardiovascular Risk in Young Finns Study, the Childhood Determinants of Adult Health Study, the Bogalusa Heart Study, and the Muscatine Study for the International Childhood Cardiovascular Cohort (i3C) Consortium

Juonala, Markus, Magnussen, Costan G., Venn, Alison, Dwyer, Terence, Burns, Trudy L., Davis, Patricia H., Chen, Wei, Srinivasan, Sathanur R., Daniels, Stephen R., Kahonen, Mika, Laitinen, Tomi, Taittonen, Leena, Berenson, Gerald S., Viikari, Jorma S. A. and Raitakari, Olli T. (2010). Influence of Age on Associations Between Childhood Risk Factors and Carotid Intima-Media Thickness in Adulthood The Cardiovascular Risk in Young Finns Study, the Childhood Determinants of Adult Health Study, the Bogalusa Heart Study, and the Muscatine Study for the International Childhood Cardiovascular Cohort (i3C) Consortium. Circulation, 122 (24), 2514-2520. doi: 10.1161/CIRCULATIONAHA.110.966465

Influence of Age on Associations Between Childhood Risk Factors and Carotid Intima-Media Thickness in Adulthood The Cardiovascular Risk in Young Finns Study, the Childhood Determinants of Adult Health Study, the Bogalusa Heart Study, and the Muscatine Study for the International Childhood Cardiovascular Cohort (i3C) Consortium

2010

Journal Article

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Heid, Iris M., Jackson, Anne U., Randall, Joshua C., Winkler, Thomas W., Qi, Lu, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Zillikens, M. Carola, Speliotes, Elizabeth K., Maegi, Reedik, Workalemahu, Tsegaselassie, White, Charles C., Bouatia-Naji, Nabila, Harris, Tamara B., Berndt, Sonja I., Ingelsson, Erik, Willer, Cristen J., Weedon, Michael N., Luan, Jianan, Vedantam, Sailaja, Esko, Tonu, Kilpelaeinen, Tuomas O., Kutalik, Zoltan, Li, Shengxu, Monda, Keri L., Dixon, Anna L., Holmes, Christopher C., Kaplan, Lee M., Liang, Liming ... Lindgren, Cecilia M. (2010). Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics, 42 (11), 949-962. doi: 10.1038/ng.685

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

2010

Journal Article

No evidence for warming climate theory of coat colour change in Soay sheep: A comment on Maloney et al.

Gratten, J., Wilson, A. J., McRae, A. F., Beraldi, D., Visscher, P. M., Pemberton, J. M. and Slate, J. (2010). No evidence for warming climate theory of coat colour change in Soay sheep: A comment on Maloney et al.. Biology Letters, 6 (5), 678-679. doi: 10.1098/rsbl.2010.0160

No evidence for warming climate theory of coat colour change in Soay sheep: A comment on Maloney et al.

2010

Journal Article

Longitudinal Genome-Wide Association of Cardiovascular Disease Risk Factors in the Bogalusa Heart Study

Smith, Erin N., Chen, Wei, Kahonen, Mika, Kettunen, Johannes, Lehtimaki, Terho, Peltonen, Leena, Raitakari, Olli T., Salem, Rany M., Schork, Nicholas J., Shaw, Marian, Srinivasan, Sathanur R., Topol, Eric J., Viikari, Jorma S., Berenson, Gerald S. and Murray, Sarah S. (2010). Longitudinal Genome-Wide Association of Cardiovascular Disease Risk Factors in the Bogalusa Heart Study. Plos Genetics, 6 (9) e1001094. doi: 10.1371/journal.pgen.1001094

Longitudinal Genome-Wide Association of Cardiovascular Disease Risk Factors in the Bogalusa Heart Study

2010

Journal Article

Mapping quantitative trait loci in a wild population using linkage and linkage disequilibrium analyses

Hernandez-Sanchez, J., Chatzipli, A., Beraldi, D., Gratten, J., Pilkington, J. G. and Pemberton, J. M. (2010). Mapping quantitative trait loci in a wild population using linkage and linkage disequilibrium analyses. Genetics Research, 92 (4), 273-281. doi: 10.1017/S0016672310000340

Mapping quantitative trait loci in a wild population using linkage and linkage disequilibrium analyses

2010

Journal Article

Childbearing, Child-Rearing, Cardiovascular Risk Factors, and Progression of Carotid Intima-Media Thickness The Cardiovascular Risk in Young Finns Study

Skilton, Michael R., Bonnet, Fabrice, Begg, Lisa M., Juonala, Markus, Kahonen, Mika, Lehtimaki, Terho, Viikari, Jorma S. A. and Raitakari, Olli T. (2010). Childbearing, Child-Rearing, Cardiovascular Risk Factors, and Progression of Carotid Intima-Media Thickness The Cardiovascular Risk in Young Finns Study. Stroke, 41 (7), 1332-1337. doi: 10.1161/STROKEAHA.110.579219

Childbearing, Child-Rearing, Cardiovascular Risk Factors, and Progression of Carotid Intima-Media Thickness The Cardiovascular Risk in Young Finns Study

Funding

Current funding

  • 2025 - 2029
    Centre of multiple sclerosis research translation (NHMRC CRE led by University of Tasmania)
    University of Tasmania
    Open grant
  • 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

Past funding

  • 2022 - 2024
    Understanding the pathophysiology of Parkinson's disease using cellular genomics
    NHMRC IDEAS Grants
    Open grant
  • 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.

  • 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

Completed supervision

Media

Enquiries

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