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Honorary Professor Jake Gratten
Honorary Professor

Jake Gratten

Email: 

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

81 - 100 of 203 works

2016

Journal Article

International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents

Parmar, Priyakumari Ganesh, Taal, H. Rob, Timpson, Nicholas J., Thiering, Elisabeth, Lehtimaki, Terho, Marinelli, Marcella, Lind, Penelope A., Howe, Laura D., Verwoert, Germaine, Aalto, Ville, Uitterlinden, Andre G., Briollais, Laurent, Evans, Dave M., Wright, Margie J., Newnham, John P., Whitfield, John B., Lyytikainen, Leo-Pekka, Rivadeneira, Fernando, Boomsma, Dorrett I., Viikari, Jorma, Gillman, Matthew W., St Pourcain, Beate, Hottenga, Jouke-Jan, Montgomery, Grant W., Hofman, Albert, Kahonen, Mika, Martin, Nicholas G., Tobin, Martin D., Raitakari, Ollie ... Palmer, Lyle J. (2016). International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents. Circulation: Cardiovascular Genetics, 9 (3), 266-278. doi: 10.1161/CIRCGENETICS.115.001190

International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents

2016

Journal Article

Childhood Infections, Socioeconomic Status, and Adult Cardiometabolic Risk

Liu, Richard S., Burgner, David P., Sabin, Matthew A., Magnussen, Costan G., Cheung, Michael, Hutri-Kahonen, Nina, Kahonen, Mika, Lehtimaki, Terho, Jokinen, Eero, Laitinen, Tomi, Taittonen, Leena, Dwyer, Terence, Viikari, Jorma S. A., Kivimaki, Mika, Raitakari, Olli T. and Juonala, Markus (2016). Childhood Infections, Socioeconomic Status, and Adult Cardiometabolic Risk. Pediatrics, 137 (6) e20160236. doi: 10.1542/peds.2016-0236

Childhood Infections, Socioeconomic Status, and Adult Cardiometabolic Risk

2016

Journal Article

Genome-wide association study identifies 74 loci associated with educational attainment

Okbay, Aysu, Beauchamp, Jonathan P., Fontana, Mark Alan, Lee, James J., Pers, Tune H., Rietveld, Cornelius A., Turley, Patrick, Chen, Guo-Bo, Emilsson, Valur, Meddens, S. Fleur W., Oskarsson, Sven, Pickrell, Joseph K., Thom, Kevin, Timshel, Pascal, de Vlaming, Ronald, Abdellaoui, Abdel, Ahluwalia, Tarunveer S., Bacelis, Jonas, Baumbach, Clemens, Bjornsdottir, Gyda, Brandsma, Johannes H., Concas, Maria Pina, Derringer, Jaime, Furlotte, Nicholas A., Galesloot, Tessel E., Girotto, Giorgia, Gupta, Richa, Hall, Leanne M., Harris, Sarah E. ... Benjamin, Daniel J. (2016). Genome-wide association study identifies 74 loci associated with educational attainment. Nature, 533 (7604), 539-542. doi: 10.1038/nature17671

Genome-wide association study identifies 74 loci associated with educational attainment

2016

Journal Article

Childhood Psychosocial Factors and Coronary Artery Calcification in Adulthood The Cardiovascular Risk in Young Finns Study

Juonala, Markus, Pulkki-Raback, Laura, Elovainio, Marko, Hakulinen, Christian, Magnussen, Costan G., Sabin, Matthew A., Burgner, David P., Hare, David L., Hartiala, Olli, Ukkonen, Heikki, Saraste, Antti, Kajander, Sami, Hutri-Kahonen, Nina, Kahonen, Mika, Rinta-Kiikka, Irina, Laitinen, Tomi, Kainulainen, Sakari, Viikari, Jorma S. A. and Raitakari, Olli T. (2016). Childhood Psychosocial Factors and Coronary Artery Calcification in Adulthood The Cardiovascular Risk in Young Finns Study. Jama Pediatrics, 170 (5), 466-472. doi: 10.1001/jamapediatrics.2015.4121

Childhood Psychosocial Factors and Coronary Artery Calcification in Adulthood The Cardiovascular Risk in Young Finns Study

2016

Journal Article

Evidence for genetic overlap between schizophrenia and age at first birth in women

Mehta, Divya, Tropf, Felix C., Gratten, Jacob, Bakshi, Andrew, Zhu, Zhihong, Bacanu, Silviu-Alin, Hemani, Gibran, Magnusson, Patrik K. E., Barban, Nicola, Esko, Tonu, Metspalu, Andres, Snieder, Harold, Mowry, Bryan J., Kendler, Kenneth S., Yang, Jian, Visscher, Peter M., McGrath, John J., Mills, Melinda C., Wray, Naomi R. and Lee, S. Hong (2016). Evidence for genetic overlap between schizophrenia and age at first birth in women. Jama Psychiatry, 73 (5), 497-505. doi: 10.1001/jamapsychiatry.2016.0129

Evidence for genetic overlap between schizophrenia and age at first birth in women

2016

Journal Article

Small non-coding RNA expression from anterior cingulate cortex in schizophrenia shows sex specific regulation

Ragan, Chikako, Patel, Kalpana, Edson, Janette, Zhang, Zong-Hong, Gratten, Jacob and Mowry, Bryan (2016). Small non-coding RNA expression from anterior cingulate cortex in schizophrenia shows sex specific regulation. Schizophrenia Research, 183, 82-87. doi: 10.1016/j.schres.2016.11.024

Small non-coding RNA expression from anterior cingulate cortex in schizophrenia shows sex specific regulation

2016

Journal Article

Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses

Aho, Vilma, Ollila, Hanna M., Kronholm, Erkki, Bondia-Pons, Isabel, Soininen, Pasi, Kangas, Antti J., Hilvo, Mika, Seppala, Ilkka, Kettunen, Johannes, Oikonen, Mervi, Raitoharju, Emma, Hyotylainen, Tuulia, Kahonen, Mika, Viikari, Jorma S. A., Harma, Mikko, Sallinen, Mikael, Olkkonen, Vesa M., Alenius, Harri, Jauhiainen, Matti, Paunio, Tiina, Lehtimaki, Terho, Salomaa, Veikko, Oresic, Matej, Raitakari, Olli T., Ala-Korpela, Mika and Porkka-Heiskanen, Tarja (2016). Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses. Scientific Reports, 6 (1) 24828. doi: 10.1038/srep24828

Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses

2016

Journal Article

Longitudinal study of circulating oxidized LDL and HDL and fatty liver: the Cardiovascular Risk in Young Finns Study

Kaikkonen, Jari E., Kresanov, Petri, Ahotupa, Markku, Jula, Antti, Mikkila, Vera, Viikari, Jorma S. A., Juonala, Markus, Hutri-Kahonen, Nina, Kahonen, Mika, Lehtimaki, Terho, Kangas, Antti J., Soininen, Pasi, Ala-Korpela, Mika and Raitakari, Olli T. (2016). Longitudinal study of circulating oxidized LDL and HDL and fatty liver: the Cardiovascular Risk in Young Finns Study. Free Radical Research, 50 (4), 396-404. doi: 10.3109/10715762.2015.1133906

Longitudinal study of circulating oxidized LDL and HDL and fatty liver: the Cardiovascular Risk in Young Finns Study

2016

Journal Article

Continuous and Dichotomous Metabolic Syndrome Definitions in Youth Predict Adult Type 2 Diabetes and Carotid Artery Intima Media Thickness: The Cardiovascular Risk in Young Finns Study

Magnussen, Costan G., Cheriyan, Sanith, Sabin, Matthew A., Juonala, Markus, Koskinen, Juha, Thomson, Russell, Skilton, Michael R., Kahonen, Mika, Laitinen, Tomi, Taittonen, Leena, Hutri-Kahonen, Nina, Viikari, Jorma S. A. and Raitakari, Olli T. (2016). Continuous and Dichotomous Metabolic Syndrome Definitions in Youth Predict Adult Type 2 Diabetes and Carotid Artery Intima Media Thickness: The Cardiovascular Risk in Young Finns Study. Journal of Pediatrics, 171, 97-+. doi: 10.1016/j.jpeds.2015.10.093

Continuous and Dichotomous Metabolic Syndrome Definitions in Youth Predict Adult Type 2 Diabetes and Carotid Artery Intima Media Thickness: The Cardiovascular Risk in Young Finns Study

2016

Journal Article

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

Seppala, Ilkka, Kleber, Marcus E., Bevan, Steve, Lyytikainen, Leo-Pekka, Oksala, Niku, Hernesniemi, Jussi A., Makela, Kari-Matti, Rothwell, Peter M., Sudlow, Cathie, Dichgans, Martin, Mononen, Nina, Vlachopoulou, Efthymia, Sinisalo, Juha, Delgado, Graciela E., Laaksonen, Reijo, Koskinen, Tuomas, Scharnagl, Hubert, Kahonen, Mika, Markus, Hugh S., Marz, Winfried and Lehtimaki, Terho (2016). Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke. Scientific Reports, 6 23207. doi: 10.1038/srep23207

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

2016

Journal Article

Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase

Wurtz, Peter, Wang, Qin, Soininen, Pasi, Kangas, Antti J., Fatemifar, Ghazaleh, Tynkkynen, Tuulia, Tiainen, Mika, Perola, Markus, Tillin, Therese, Hughes, Alun D., Mantyselka, Pekka, Kahonen, Mika, Lehtimaki, Terho, Sattar, Naveed, Hingorani, Aroon D., Casas, Juan-Pablo, Salomaa, Veikko, Kivimaki, Mika, Jarvelin, Marjo-Riitta, Smith, George Davey, Vanhala, Mauno, Lawlor, Debbie A., Raitakari, Olli T., Chaturvedi, Nish, Kettunen, Johannes and Ala-Korpela, Mika (2016). Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase. Journal of the American College of Cardiology, 67 (10), 1200-1210. doi: 10.1016/j.jacc.2015.12.060

Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase

2016

Journal Article

Mapping and differential expression analysis from short-read RNA-Seq data in model organisms

Zhao, Qiong-Yi, Gratten, Jacob, Restaudi, Restuadi and Li, Xuan (2016). Mapping and differential expression analysis from short-read RNA-Seq data in model organisms. Quantitative Biology, 4 (1), 22-35. doi: 10.1007/s40484-016-0060-7

Mapping and differential expression analysis from short-read RNA-Seq data in model organisms

2016

Journal Article

Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2

Ware, Jennifer J., Chen, Xiangning, Vink, Jacqueline, Loukola, Anu, Minica, Camelia, Pool, Rene, Milaneschi, Yuri, Mangino, Massimo, Menni, Cristina, Chen, Jingchun, Peterson, Roseann E., Auro, Kirsi, Lyytikainen, Leo-Pekka, Wedenoja, Juho, Stiby, Alexander I., Hemani, Gibran, Willemsen, Gonneke, Hottenga, Jouke Jan, Korhonen, Tellervo, Heliovaara, Markku, Perola, Markus, Rose, Richard J., Paternoster, Lavinia, Timpson, Nic, Wassenaar, Catherine A., Zhu, Andy Z. X., Smith, George Davey, Raitakari, Olli T., Lehtimaki, Terho ... Munafo, Marcus R. (2016). Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2. Scientific Reports, 6 20092. doi: 10.1038/srep20092

Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2

2016

Journal Article

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

Lu, Yingchang, Day, Felix R., Gustafsson, Stefan, Buchkovich, Martin L., Na, Jianbo, Bataille, Veronique, Cousminer, Diana L., Dastani, Zari, Drong, Alexander W., Esko, Tonu, Evans, David M., Falchi, Mario, Feitosa, Mary F., Ferreira, Teresa, Hedman, Asa K., Haring, Robin, Hysi, Pirro G., Iles, Mark M., Justice, Anne E., Kanoni, Stavroula, Lagou, Vasiliki, Li, Rui, Li, Xin, Locke, Adam, Lu, Chen, Magi, Reedik, Perry, John R. B., Pers, Tune H., Qi, Qibin ... Loos, Ruth J. F. (2016). New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Nature Communications, 7 (1) 10495, 10495-10495. doi: 10.1038/ncomms10495

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

2016

Journal Article

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

Kilpelainen, Tuomas O., Carli, Jayne F. Martin, Skowronski, Alicja A., Sun, Qi, Kriebel, Jennifer, Feitosa, Mary F., Hedman, Asa K., Drong, Alexander W., Hayes, James E., Zhao, Jinghua, Pers, Tune H., Schick, Ursula, Grarup, Niels, Kutalik, Zoltan, Trompet, Stella, Mangino, Massimo, Kristiansson, Kati, Beekman, Marian, Lyytikainen, Leo-Pekka, Eriksson, Joel, Henneman, Peter, Lahti, Jari, Tanaka, Toshiko, Luan, Jian'an, Del Greco M, Fabiola, Pasko, Dorota, Renstrom, Frida, Willems, Sara M., Mahajan, Anubha ... Loos, Ruth J. F. (2016). Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Nature Communications, 7 10494. doi: 10.1038/ncomms10494

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

2016

Journal Article

The Combined Effect of Common Genetic Risk Variants on Circulating Lipoproteins Is Evident in Childhood: A Longitudinal Analysis of the Cardiovascular Risk in Young Finns Study

Buscot, Marie-jeanne, Magnussen, Costan G., Juonala, Markus, Pitkanen, Niina, Lehtimaki, Terho, Viikari, Jorma S. A., Kahonen, Mika, Hutri-Kahonen, Nina, Schork, Nicholas J., Raitakari, Olli T. and Thomson, Russell J. (2016). The Combined Effect of Common Genetic Risk Variants on Circulating Lipoproteins Is Evident in Childhood: A Longitudinal Analysis of the Cardiovascular Risk in Young Finns Study. Plos One, 11 (1) e0146081. doi: 10.1371/journal.pone.0146081

The Combined Effect of Common Genetic Risk Variants on Circulating Lipoproteins Is Evident in Childhood: A Longitudinal Analysis of the Cardiovascular Risk in Young Finns Study

2016

Journal Article

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

Felix, Janine F., Bradfield, Jonathan P., Monnereau, Claire, van der Valk, Ralf J. P., Stergiakouli, Evie, Chesi, Alessandra, Gaillard, Romy, Feenstra, Bjarke, Thiering, Elisabeth, Kreiner-Moller, Eskil, Mahajan, Anubha, Pitkanen, Niina, Joro, Raimo, Cavadino, Alana, Huikari, Ville, Franks, Steve, Groen-Blokhuis, Maria M., Cousminer, Diana L., Marsh, Julie A., Lehtimaki, Terho, Curtin, John A., Vioque, Jesus, Ahluwalia, Tarunveer S., Myhre, Ronny, Price, Thomas S., Vilor-Tejedor, Natalia, Yengo, Loic, Grarup, Niels, Ntalla, Ioanna ... Jaddoe, Vincent W. V. (2016). Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Human Molecular Genetics, 25 (2), 389-403. doi: 10.1093/hmg/ddv472

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

2015

Journal Article

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

Artigas, Maria Soler, Wain, Louise V., Miller, Suzanne, Kheirallah, Abdul Kader, Huffman, Jennifer E., Ntalla, Ioanna, Shrine, Nick, Obeidat, Ma'en, Trochet, Holly, McArdle, Wendy L., Alves, Alexessander Couto, Hui, Jennie, Zhao, Jing Hua, Joshi, Peter K., Teumer, Alexander, Albrecht, Eva, Imboden, Medea, Rawal, Rajesh, Lopez, Lorna M., Marten, Jonathan, Enroth, Stefan, Surakka, Ida, Polasek, Ozren, Lyytikainen, Leo-Pekka, Granell, Raquel, Hysi, Pirro G., Flexeder, Claudia, Mahajan, Anubha, Beilby, John ... Zeggini, Eleftheria (2015). Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Nature Communications, 6 (8658) 89658, 1-12. doi: 10.1038/ncomms9658

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

2015

Journal Article

Coronary heart disease risk factors, coronary artery calcification and epicardial fat volume in the Young Finns Study

Hartiala, Olli, Magnussen, Costan G., Bucci, Marco, Kajander, Sami, Knuuti, Juhani, Ukkonen, Heikki, Saraste, Antti, Rinta-Kiikka, Irina, Kainulainen, Sakari, Kahonen, Mika, Hutri-Kahonen, Nina, Laitinen, Tomi, Lehtimaki, Terho, Viikari, Jorma S. A., Hartiala, Jaakko, Juonala, Markus and Raitakari, Olli T. (2015). Coronary heart disease risk factors, coronary artery calcification and epicardial fat volume in the Young Finns Study. European Heart Journal-Cardiovascular Imaging, 16 (11), 1256-1263. doi: 10.1093/ehjci/jev085

Coronary heart disease risk factors, coronary artery calcification and epicardial fat volume in the Young Finns Study

2015

Journal Article

Increased Body Mass Index in Parent-Child Dyads Predicts the Offspring Risk of Meeting Bariatric Surgery Criteria

Juonala, Markus, Sabin, Matthew A., Burgner, David, Cheung, Michael, Kahonen, Mika, Hutri-Kahonen, Nina, Lehtimaki, Terho, Jokinen, Eero, Koskinen, Juha, Tossavainen, Paivi, Laitinen, Tomi, Viikari, Jorma S. A., Raitakari, Olli T. and Magnussen, Costan G. (2015). Increased Body Mass Index in Parent-Child Dyads Predicts the Offspring Risk of Meeting Bariatric Surgery Criteria. Journal of Clinical Endocrinology & Metabolism, 100 (11), 4257-4263. doi: 10.1210/jc.2015-2524

Increased Body Mass Index in Parent-Child Dyads Predicts the Offspring Risk of Meeting Bariatric Surgery Criteria

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

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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

Completed supervision

Media

Enquiries

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