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Professor

Nick Martin

Email: 

Overview

Availability

Professor Nick Martin is:
Available for supervision

Qualifications

  • Bachelor (Honours), University of Adelaide
  • Doctor of Philosophy, University of Birmingham

Works

Search Professor Nick Martin’s works on UQ eSpace

1507 works between 1975 and 2025

1001 - 1020 of 1507 works

2009

Journal Article

Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011

Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

2009

Journal Article

Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families

Medland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M., Hay, David A., Levy, Florence, Van-Beijsterveldt, Catherina E.M., Willemsen, Gonneke, Townsend, Grant C., White, Vicki, Hewitt, Alex W., Mackey, David A., Bailey, J. Michael, Slutske, Wendy S., Nyholt, Dale R., Treloar, Susan A., Martin, Nicholas G. and Boomsma, Dorret I. (2009). Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families. Neuropsychologia, 47 (2), 330-337. doi: 10.1016/j.neuropsychologia.2008.09.005

Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families

2009

Journal Article

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Yurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, Dorret Boomsma, Iris M Heid, Peter P Pramstaller, Brenda W J H Penninx, A Cecile J W Janssens, James F Wilson, Tim Spector, Nicholas G Martin, Nancy L Pedersen, Kirsten Ohm Kyvik, Jaakko Kaprio, Albert Hofman, Nelson B Freimer, Marjo-Riitta Jarvelin, Ulf Gyllensten, Harry Campbell, Igor Rudan, Åsa Johansson, Fabio Marroni, Caroline Hayward, Veronique Vitart, Inger Jonasson, Cristian Pattaro, Alan Wright, Nick Hastie, Irene Pichler ... Jouke-Jan Hottenga (2009). Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics, 41 (1), 47-55. doi: 10.1038/ng.269

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

2009

Book Chapter

Genetic and Environmental Influences on Sexual Orientation

Khytam Dawood, J. Michael Bailey and Nicholas G. Martin (2009). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics. (pp. 269-279) edited by Kim, Yong-Kyu. United Sates: Springer New York. doi: 10.1007/978-0-387-76727-7_19

Genetic and Environmental Influences on Sexual Orientation

2009

Journal Article

Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders

Psychiatric GWAS Consortium Coordinating Committee, Martin, N., Wray, N., Mowry, B. and Holliday, E. (2009). Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders. American Journal of Psychiatry, 166 (5), 540-556. doi: 10.1176/appi.ajp.2008.08091354

Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders

2009

Journal Article

Accumulation of trauma over time and risk for depression in a twin sample

V. V. McCutcheon, A. C. Heath, E. C. Nelson, K. K. Bucholz, P. A. F. Madden and N. G. Martin (2009). Accumulation of trauma over time and risk for depression in a twin sample. Psychological Medicine, 39 (3), 431-441. doi: 10.1017/S0033291708003759

Accumulation of trauma over time and risk for depression in a twin sample

2009

Journal Article

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

Sullivan, P. F., de Geus, E. J. C., Willemsen, G., James, M. R., Smit, J. H., Zandbelt, T., Martin, N. G., Wray, N. R., Boomsma, D. I. and Penninx, B. W. J. H. (2009). Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Molecular Psychiatry, 14 (4), 359-375. doi: 10.1038/mp.2008.125

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

2009

Journal Article

Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction

Cornes, B., Lind, P. A., Medland, S. E., Montgomery, G. W ., Nyholt, D. R. and Martin, N. G . (2009). Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction. International Journal of Obesity, 33 (1), 75-79. doi: 10.1038/ijo.2008.223

Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction

2008

Journal Article

Autosomal linkage analysis for cannabis use behaviors in Australian adults

Agrawal, Arpana, Morley, Katherine I., Hansell, Narelle K., Pergadia, Michele L., Montgomery, Grant W., Statham, Dixie J., Todd, Richard D., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John, Martin, Nicholas G. and Lynskey, Michael T. (2008). Autosomal linkage analysis for cannabis use behaviors in Australian adults. Drug and Alcohol Dependence, 98 (3), 185-190. doi: 10.1016/j.drugalcdep.2008.05.009

Autosomal linkage analysis for cannabis use behaviors in Australian adults

2008

Journal Article

Meeting the challenges of neuroimaging genetics

De Zubicaray, Greig I., Chiang, Ming-Chang, McMahon, Katie L., Shattuck, David W., Toga, Arthur W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2008). Meeting the challenges of neuroimaging genetics. Brian Imaging and Behavior, 2 (4), 258-263. doi: 10.1007/s11682-008-9029-0

Meeting the challenges of neuroimaging genetics

2008

Journal Article

Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence

Middelberg, Rita P., Gordon, Scott D., Zhu, Gu, McRae, Allan, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2008). Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence. Twin Research and Human Genetics, 11 (6), 603-620. doi: 10.1375/twin.11.6.603

Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence

2008

Journal Article

Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins

Reiersen, Angela M., Constantino, John N., Grimmer, Marisa, Martin, Nicholas G. and Todd, Richard D. (2008). Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins. Twin Research and Human Genetics, 11 (6), 579-585. doi: 10.1375/twin.11.6.579

Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins

2008

Journal Article

Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language

Bates, Timothy C., Luciano, Michelle, Lind, Penelope A., Wright, Margaret J., Montgomery, Grant W. and Martin, Nicholas G. (2008). Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language. Intelligence, 36 (6), 689-693. doi: 10.1016/j.intell.2008.04.001

Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language

2008

Journal Article

Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts

Waldron, Mary, Heath, Andrew C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2008). Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts. Alcoholism-Clinical and Experimental Research, 32 (11), 1865-1874. doi: 10.1111/j.1530-0277.2008.00771.x

Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts

2008

Journal Article

Early cannabis use and DSM-IV nicotine dependence: A twin study

Agrawal, Arpana, Lynskey, Michael T., Pergadia, Michele L., Bucholz, Kathleen K., Heath, Andrew C., Martin, Nicholas G. and Madden, Pamela A. F. (2008). Early cannabis use and DSM-IV nicotine dependence: A twin study. Addiction, 103 (11), 1896-1904. doi: 10.1111/j.1360-0443.2008.02354.x

Early cannabis use and DSM-IV nicotine dependence: A twin study

2008

Journal Article

The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies

Byrne, Enda M., Mcrae, Allan F., Zhao, Zhen-Zhen, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies. European Journal of Human Genetics, 16 (11), 1396-1403. doi: 10.1038/ejhg.2008.117

The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies

2008

Journal Article

Susceptibility variants for male-pattern baldness on chromosome 20p11

Hillmer, Axel M., Brockschmidt, Felix F., Hanneken, Sandra, Eigelshoven, Sibylle, Steffens, Michael, Flaquer, Antonia, Herms, Stefan, Becker, Tim, Kortuem, Anne-Katrin, Nyholt, Dale R., Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Muehleisen, Thomas W., Alblas, Margrieta A., Moebus, Susanne, Joeckel, Karl-Heinz, Broecker-Preuss, Martina, Erbel, Raimund, Reinartz, Roman, Betz, Regina C., Cichon, Sven, Propping, Peter, Baur, Max P., Wienker, Thomas F., Kruse, Roland and Noethen, Markus M. (2008). Susceptibility variants for male-pattern baldness on chromosome 20p11. Nature Genetics, 40 (11), 1279-1281. doi: 10.1038/ng.228

Susceptibility variants for male-pattern baldness on chromosome 20p11

2008

Journal Article

Genetic factors predisposing to homosexuality may increase mating success in heterosexuals

Zietsch, Brendan P., Morley, Katherine I., Shekar, Sri N., Verweij, Karin J. H., Keller, Matthew C., Macgregor, Stuart, Wright, Margaret J., Bailey, J. Michael and Martin, Nicholas G. (2008). Genetic factors predisposing to homosexuality may increase mating success in heterosexuals. Evolution and Human Behavior, 29 (6), 424-433. doi: 10.1016/j.evolhumbehav.2009.07.002

Genetic factors predisposing to homosexuality may increase mating success in heterosexuals

2008

Journal Article

A high-density association screen of 155 ion transport genes for involvement with common migraine

Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Farkkila, Markus, Hamalainen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Goebel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W. M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M. J. M. ... Palotie, Aarno (2008). A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics, 17 (21), 3318-3331. doi: 10.1093/hmg/ddn227

A high-density association screen of 155 ion transport genes for involvement with common migraine

2008

Journal Article

Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning

Zhao, Zhen Zhen, Painter, Jodie N., Palmer, James S., Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Boomsma, Dorret I., Martin, Nicholas G., Duffy, David L. and Montgomery, Grant W. (2008). Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning. Human Reproduction, 23 (10), 2372-2379. doi: 10.1093/humrep/den268

Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning

Funding

Past funding

  • 2010 - 2012
    Identifying genes for cognition
    ARC Discovery Projects
    Open grant
  • 2008 - 2009
    Infrastructure for an integrated cognitive neurophysiological research facility: Mapping the neurobiology of memory and language
    ARC Linkage Infrastructure, Equipment and Facilities
    Open grant
  • 2008
    Molecular actions of alcohol and smoking on the drug reward pathway of the brain
    Alcohol and Health Research Grants Scheme (AHRGS)
    Open grant
  • 2006 - 2008
    Locating Genes For Cognitive Traits Using Linkage And Association Analyses
    ARC Discovery Projects
    Open grant
  • 2003 - 2006
    Structural And Diffusion Tensor Neuroimaging In Twins Concordant And Discordant For Psychosis
    NHMRC Project Grant
    Open grant
  • 1998
    An Investigation of the Genetic Basis of Human Stature Disorders
    Royal Children's Hospital Foundation
    Open grant
  • 1998 - 2000
    Genetic analysis of working memory in twins
    ARC Australian Research Council (Large grants)
    Open grant
  • 1997
    An examination of transmission ratio distortion at 5 autosomal trinucleotide repeat loci associated with inherited human neurological disorders
    University of Queensland New Staff Research Grant
    Open grant

Supervision

Availability

Professor Nick Martin is:
Available for supervision

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Supervision history

Current supervision

  • Doctor Philosophy

    Investigating Risk Factors and Early Stage Biomarkers in Cognitive Aging and Dementia

    Associate Advisor

    Other advisors: Dr David Ward

  • Doctor Philosophy

    Statistical Genetic Approaches in Eye Diseases

    Associate Advisor

  • Doctor Philosophy

    Elucidating the genetic architecture of neuropsychiatric phenotypes and other complex human traits

    Associate Advisor

    Other advisors: Associate Professor Miguel Rentería

  • Doctor Philosophy

    Elucidating the genetic architecture of neuropsychiatric phenotypes and other complex human traits

    Associate Advisor

    Other advisors: Associate Professor Miguel Rentería

  • Doctor Philosophy

    Elucidating the genetic architecture of neuropsychiatric phenotypes and other complex human traits

    Associate Advisor

    Other advisors: Associate Professor Miguel Rentería

  • Doctor Philosophy

    Genetic architecture of differences in symptomatology and treatment response in major depressive disorder

    Associate Advisor

    Other advisors: Associate Professor Miguel Rentería, Honorary Professor Sarah Medland

Completed supervision

Media

Enquiries

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communications@uq.edu.au