Honorary Professor Jake Gratten
Honorary Professor

Jake Gratten

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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

Biological Sciences Biomedical and Clinical Sciences Genetics Zoology

Qualifications

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

Search Professor Jake Gratten’s works on UQ eSpace

204 works between 2001 and 2024
All (204) Journal Article (191) Conference Publication (11) Other Outputs (2)

61 - 80 of 204 works

2017

Journal Article

Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort

Garton, Fleur C., Benyamin, Beben, Zhao, Qiongyi, Liu, Zhijun, Gratten, Jacob, Henders, Anjali K., Zhang, Zong-Hong, Edson, Janette, Furlong, Sarah, Morgan, Sarah, Heggie, Susan, Thorpe, Kathryn, Pfluger, Casey, Mather, Karen A., Sachdev, Perminder S., McRae, Allan F., Robinson, Matthew R., Shah, Sonia, Visscher, Peter M., Mangelsdorf, Marie, Henderson, Robert D., Wray, Naomi R. and McCombe, Pamela A. (2017). Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort. Molecular Genetics and Genomic Medicine, 5 (4), 418-428. doi: 10.1002/mgg3.302

Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort

2017

Journal Article

Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

Ji, Sun-Gou, Juran, Brian D., Mucha, Soeren, Folseraas, Trine, Jostins, Luke, Melum, Espen, Kumasaka, Natsuhiko, Atkinson, Elizabeth J., Schlicht, Erik M., Liu, Jimmy Z., Shah, Tejas, Gutierrez-Achury, Javier, Boberg, Kirsten M., Bergquist, Annika, Vermeire, Severine, Eksteen, Bertus, Durie, Peter R., Farkkila, Martti, Mueller, Tobias, Schramm, Christoph, Sterneck, Martina, Weismueller, Tobias J., Gotthardt, Daniel N., Ellinghaus, David, Braun, Felix, Teufel, Andreas, Laudes, Mattias, Lieb, Wolfgang, Jacobs, Gunnar ... Anderson, Carl A. (2017). Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease. Nature Genetics, 49 (2), 269-273. doi: 10.1038/ng.3745

Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

2017

Conference Publication

Evidence for genetic overlap between schizophrenia and maternal age at first birth

Mehta, Divya, Tropf, Felix, Gratten, Jacob, Bacanu, Silviu, Bakshi, Andrew, Mowry, Bryan, Kendler, Kenneth, Yang, Jian, Visscher, Peter, McGrath, John, Mills, Melinda, Wray, Naomi and Lee, Sang Hong (2017). Evidence for genetic overlap between schizophrenia and maternal age at first birth. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto, ON, Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2015.09.010

Evidence for genetic overlap between schizophrenia and maternal age at first birth

2017

Conference Publication

Genome-wide association study of schizophrenia in the Iban of Sarawak reveals genetic overlap with Han Chinese and, to a lesser extent, Europeans

Periyasamy, Sathish, Barrett, Robert, Yue, Weihua, Gratten, Jacob, Nertney, Deborah, McLean, Duncan, Smith, Heather, Filippich, Cheryl, Loa, Peter, Zhang, Dai, Yolken, Robert and Mowry, Bryan (2017). Genome-wide association study of schizophrenia in the Iban of Sarawak reveals genetic overlap with Han Chinese and, to a lesser extent, Europeans. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier .

Genome-wide association study of schizophrenia in the Iban of Sarawak reveals genetic overlap with Han Chinese and, to a lesser extent, Europeans

2016

Journal Article

Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence

Wang, Qin, Wurtz, Peter, Auro, Kirsi, Makinen, Ville-Petteri, Kangas, Antti J., Soininen, Pasi, Tiainen, Mika, Tynkkynen, Tuulia, Jokelainen, Jari, Santalahti, Kristiina, Salmi, Marko, Blankenberg, Stefan, Zeller, Tanja, Viikari, Jorma, Kahonen, Mika, Lehtimaki, Terho, Salomaa, Veikko, Perola, Markus, Jalkanen, Sirpa, Jarvelin, Marjo-Riitta, Raitakari, Olli T., Kettunen, Johannes, Lawlor, Debbie A. and Ala-Korpela, Mika (2016). Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence. Bmc Medicine, 14 205. doi: 10.1186/s12916-016-0733-0

Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence

2016

Journal Article

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (vol 48, pg 624, 2016)

Okbay, Aysu, Baselmans, Bart M. L., De Neve, Jan-Emmanuel, Turley, Patrick, Nivard, Michel G., Fontana, Mark Alan, Meddens, S. Fleur W., Linner, Richard Karlsson, Rietveld, Cornelius A., Derringer, Jaime, Gratten, Jacob, Lee, James J., Liu, Jimmy Z., de Vlaming, Ronald, Ahluwalia, Tarunveer S., Buchwald, Jadwiga, Cavadino, Alana, Frazier-Wood, Alexis C., Furlotte, Nicholas A., Garfield, Victoria, Geisel, Marie Henrike, Gonzalez, Juan R., Haitjema, Saskia, Karlsson, Robert, van der Laan, Sander W., Ladwig, Karl-Heinz, Lahti, Jari, van der Lee, Sven J., Lind, Penelope A. ... Cesarini, David (2016). Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (vol 48, pg 624, 2016). Nature Genetics, 48 (12), 1591-1591. doi: 10.1038/ng1216-1587b

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (vol 48, pg 624, 2016)

2016

Journal Article

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

Barban, Nicola, Jansen, Rick, de Vlaming, Ronald, Vaez, Ahmad, Mandemakers, Jornt J., Tropf, Felix C., Shen, Xia, Wilson, James F., Chasman, Daniel I., Nolte, Illa M., Tragante, Vinicius, van der Laan, Sander W., Perry, John R. B., Kong, Augustine, Ahluwalia, Tarunveer S., Albrecht, Eva, Yerges-Armstrong, Laura, Atzmon, Gil, Auro, Kirsi, Ayers, Kristin, Bakshi, Andrew, Ben-Avraham, Danny, Berger, Klaus, Bergman, Aviv, Bertram, Lars, Bielak, Lawrence F., Bjornsdottir, Gyda, Bonder, Marc Jan, Broer, Linda ... Mills, Melinda C. (2016). Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nature Genetics, 48 (12), 1462-1472. doi: 10.1038/ng.3698

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

2016

Journal Article

Genome-Wide Meta-Analysis of Sciatica in Finnish Population

Lemmela, Susanna, Solovieva, Svetlana, Shiri, Rahman, Benner, Christian, Heliovaara, Markku, Kettunen, Johannes, Anttila, Verneri, Ripatti, Samuli, Perola, Markus, Seppala, Ilkka, Juonala, Markus, Kahonen, Mika, Salomaa, Veikko, Viikari, Jorma, Raitakari, Olli T., Lehtimaki, Terho, Palotie, Aarno, Viikari-Juntura, Eira and Husgafvel-Pursiainen, Kirsti (2016). Genome-Wide Meta-Analysis of Sciatica in Finnish Population. Plos One, 11 (10) e0163877. doi: 10.1371/journal.pone.0163877

Genome-Wide Meta-Analysis of Sciatica in Finnish Population

2016

Journal Article

Genome-wide associations for birth weight and correlations with adult disease

Horikoshi, Momoko, Beaumont, Robin N., Day, Felix R., Warrington, Nicole M., Kooijman, Marjolein N., Fernandez-Tajes, Juan, Feenstra, Bjarke, van Zuydam, Natalie R., Gaulton, Kyle J., Grarup, Niels, Bradfield, Jonathan P., Strachan, David P., Li-Gao, Ruifang, Ahluwalia, Tarunveer S., Kreiner, Eskil, Rueedi, Rico, Lyytikainen, Leo-Pekka, Cousminer, Diana L., Wu, Ying, Thiering, Elisabeth, Wang, Carol A., Have, Christian T., Hottenga, Jouke-Jan, Vilor-Tejedor, Natalia, Joshi, Peter K., Boh, Eileen Tai Hui, Ntalla, Ioanna, Pitkanen, Niina, Mahajan, Anubha ... Freathy, Rachel M. (2016). Genome-wide associations for birth weight and correlations with adult disease. Nature, 538 (7624), 248-252. doi: 10.1038/nature19806

Genome-wide associations for birth weight and correlations with adult disease

2016

Journal Article

No association of coronary artery disease with X-chromosomal variants in comprehensive international meta-analysis

Loley, Christina, Alver, Maris, Assimes, Themistocles L., Bjonnes, Andrew, Goel, Anuj, Gustafsson, Stefan, Hernesniemi, Jussi, Hopewell, Jemma C., Kanoni, Stavroula, Kleber, Marcus E., Lau, King Wai, Lu, Yingchang, Lyytikainen, Leo-Pekka, Nelson, Christopher P., Nikpay, Majid, Qu, Liming, Salfati, Elias, Scholz, Markus, Tukiainen, Taru, Willenborg, Christina, Won, Hong-Hee, Zeng, Lingyao, Zhang, Weihua, Anand, Sonia S., Beutner, Frank, Bottinger, Erwin P., Clarke, Robert, Dedoussis, George, Do, Ron ... Koenig, Inke R. (2016). No association of coronary artery disease with X-chromosomal variants in comprehensive international meta-analysis. Scientific Reports, 6 35278. doi: 10.1038/srep35278

No association of coronary artery disease with X-chromosomal variants in comprehensive international meta-analysis

2016

Journal Article

Effects of hormonal contraception on systemic metabolism: cross-sectional and longitudinal evidence

Wang, Qin, Wurtz, Peter, Auro, Kirsi, Morin-Papunen, Laure, Kangas, Antti J., Soininen, Pasi, Tiainen, Mika, Tynkkynen, Tuulia, Joensuu, Anni, Havulinna, Aki S., Aalto, Kristiina, Salmi, Marko, Blankenberg, Stefan, Zeller, Tanja, Viikari, Jorma, Kahonen, Mika, Lehtimaki, Terho, Salomaa, Veikko, Jalkanen, Sirpa, Jarvelin, Marjo-Riitta, Perola, Markus, Raitakari, Olli T., Lawlor, Debbie A., Kettunen, Johannes and Ala-Korpela, Mika (2016). Effects of hormonal contraception on systemic metabolism: cross-sectional and longitudinal evidence. International Journal of Epidemiology, 45 (5), 1445-1457. doi: 10.1093/ije/dyw147

Effects of hormonal contraception on systemic metabolism: cross-sectional and longitudinal evidence

2016

Journal Article

Metabolic signatures of birthweight in 18 288 adolescents and adults

Wurtz, Peter, Wang, Qin, Niironen, Marjo, Tynkkynen, Tuulia, Tiainen, Mika, Drenos, Fotios, Kangas, Antti J., Soininen, Pasi, Skilton, Michael R., Heikkila, Kauko, Pouta, Anneli, Kahonen, Mika, Lehtimaki, Terho, Rose, Richard J., Kajantie, Eero, Perola, Markus, Kaprio, Jaakko, Eriksson, Johan G., Raitakari, Olli T., Lawlor, Debbie A., Smith, George Davey, Jarvelin, Marjo-Riitta, Ala-Korpela, Mika and Auro, Kirsi (2016). Metabolic signatures of birthweight in 18 288 adolescents and adults. International Journal of Epidemiology, 45 (5), 1539-1550. doi: 10.1093/ije/dyw255

Metabolic signatures of birthweight in 18 288 adolescents and adults

2016

Journal Article

Metabolic profiling of alcohol consumption in 9778 young adults

Wurtz, Peter, Cook, Sarah, Wang, Qin, Tiainen, Mika, Tynkkynen, Tuulia, Kangas, Antti J., Soininen, Pasi, Laitinen, Jaana, Viikari, Jorma, Kahonen, Mika, Lehtimaki, Terho, Perola, Markus, Blankenberg, Stefan, Zeller, Tanja, Mannisto, Satu, Salomaa, Veikko, Jarvelin, Marjo-Riitta, Raitakari, Olli T., Ala-Korpela, Mika and Leon, David A. (2016). Metabolic profiling of alcohol consumption in 9778 young adults. International Journal of Epidemiology, 45 (5), 1493-1506. doi: 10.1093/ije/dyw175

Metabolic profiling of alcohol consumption in 9778 young adults

2016

Journal Article

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative <i>GFI1B</i> Splice Variants in Human Hematopoiesis

Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J. A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tonu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena ... Sankaran, Vijay G. (2016). Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics, 99 (2), 481-488. doi: 10.1016/j.ajhg.2016.06.016

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative <i>GFI1B</i> Splice Variants in Human Hematopoiesis

2016

Journal Article

Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits

Pavlides, Jennifer M. Whitehead, Zhu, Zhihong, Gratten, Jacob, Mcrae, Allan F., Wray, Naomi R. and Yang, Jian (2016). Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits. Genome Medicine, 8 (1) 84, 84. doi: 10.1186/s13073-016-0338-4

Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits

2016

Journal Article

Genetic pleiotropy in complex traits and diseases: implications for genomic medicine

Gratten, Jacob and Visscher, Peter M. (2016). Genetic pleiotropy in complex traits and diseases: implications for genomic medicine. Genome Medicine, 8 (78) 78, 1-3. doi: 10.1186/s13073-016-0332-x

Genetic pleiotropy in complex traits and diseases: implications for genomic medicine

2016

Journal Article

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in <i>ANGPTL4</i> determining fasting TG levels

van Leeuwen, Elisabeth M., Sabo, Aniko, Bis, Joshua C., Huffman, Jennifer E., Manichaikul, Ani, Smith, Albert V., Feitosa, Mary F., Demissie, Serkalem, Joshi, Peter K., Duan, Qing, Marten, Jonathan, van Klinken, Jan B., Surakka, Ida, Nolte, Ilja M., Zhang, Weihua, Mbarek, Hamdi, Li-Gao, Ruifang, Trompet, Stella, Verweij, Niek, Evangelou, Evangelos, Lyytikainen, Leo-Pekka, Tayo, Bamidele O., Deelen, Joris, van der Most, Peter J., van der Laan, Sander W., Arking, Dan E., Morrison, Alanna, Dehghan, Abbas, Franco, Oscar H. ... van Duijn, Cornelia M. (2016). Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. Journal of Medical Genetics, 53 (7), 441-449. doi: 10.1136/jmedgenet-2015-103439

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in <i>ANGPTL4</i> determining fasting TG levels

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

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

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Okbay, Aysu, Baselmans, Bart M. L., De Neve, Jan-Emmanuel, Turley, Patrick, Nivard, Michel G., Fontana, Mark Alan, Meddens, S. Fleur W., Linner, Richard Karlsson, Rietveld, Cornelius A., Derringer, Jaime, Gratten, Jacob, Lee, James J., Liu, Jimmy Z., de Vlaming, Ronald, Ahluwalia, Tarunveer S., Buchwald, Jadwiga, Cavadino, Alana, Frazier-Wood, Alexis C., Furlotte, Nicholas A., Garfield, Victoria, Geisel, Marie Henrike, Gonzalez, Juan R., Haitjema, Saskia, Karlsson, Robert, van der Laan, Sander W., Ladwig, Karl-Heinz, Lahti, Jari, van der Lee, Sven J., Lind, Penelope A. ... Cesarini, David (2016). Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature Genetics, 48 (6), 624-633. doi: 10.1038/ng.3552

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

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

Availability

Honorary Professor Jake Gratten is:
Available for supervision

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

Available projects

  • 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

Enquiries

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