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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

401 - 420 of 1507 works

2016

Journal Article

Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia

Lee, P. H., Baker, J. T., Holmes, A. J., Jahanshad, N., Ge, T., Jung, J. -Y., Cruz, Y., Manoach, D. S., Hibar, D. P., Faskowitz, J., McMahon, K. L., De Zubicaray, G. I., Martin, N. H., Wright, M. J., Ongur, D., Buckner, R., Roffman, J., Thompson, P. M. and Smoller, J. W. (2016). Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia. Molecular Psychiatry, 21 (12), 1680-1689. doi: 10.1038/mp.2016.164

Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia

2016

Journal Article

Shared genetic factors in the co-occurrence of depression and fatigue

Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Shared genetic factors in the co-occurrence of depression and fatigue. Twin Research and Human Genetics, 19 (6), 610-618. doi: 10.1017/thg.2016.79

Shared genetic factors in the co-occurrence of depression and fatigue

2016

Journal Article

Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis

Li, Ming, Huang, Liang, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Alkelai, Anna, Lerer, Bernard, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, MooDS Consortium, and The Swedish Bipolar Study Group, (2016). Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis. Molecular Neurobiology, 53 (10), 6608-6619. doi: 10.1007/s12035-015-9559-6

Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis

2016

Journal Article

Hans J. Eysenck and Raymond B. Cattell on intelligence and personality

Boyle, Gregory J., Stankov, Lazar, Martin, Nicholas G., Petrides, K. V., Eysenck, Michael W. and Ortet, Generos (2016). Hans J. Eysenck and Raymond B. Cattell on intelligence and personality. Personality and Individual Differences, 103, 40-47. doi: 10.1016/j.paid.2016.04.029

Hans J. Eysenck and Raymond B. Cattell on intelligence and personality

2016

Journal Article

4th Pediatric Allergy and Asthma Meeting (PAAM)

Yavuz, S. Tolga, Koc, Ozan, Gungor, Ali, Gok, Faysal, Hawley, Jessica, O’Brien, Christopher, Thomas, Matthew, Brodlie, Malcolm, Michaelis, Louise, Mota, Inês, Gaspar, Ângela, Piedade, Susana, Sampaio, Graça, Dias, José Geraldo, Paiva, Miguel, Morais‐Almeida, Mário, Madureira, Cristina, Lopes, Tânia, Lopes, Susana, Almeida, Filipa, Sequeira, Alexandra, Carvalho, Fernanda, Oliveira, José, Gay‐Crosier, Fabienne, Nenciu, Ioana‐Valentina, Nita, Andreia Florina, Ulmeanu, Alexandru, Oraseanu, Dumitru, Zapucioiu, Carmen ... Vaquero, Ibone (2016). 4th Pediatric Allergy and Asthma Meeting (PAAM). Clinical and Translational Allergy, 6 (S1), 1-60. doi: 10.1186/s13601-016-0117-8

4th Pediatric Allergy and Asthma Meeting (PAAM)

2016

Journal Article

Cannabis involvement and nonsuicidal self-injury: A discordant twin approach

Few, Lauren R., Grant, Julia D., Nelson, Elliot C., Trull, Timothy J., Grucza, Richard A., Bucholz, Kathleen K., Verweij, Karin J. H., Martin, Nicholas G., Statham, Dixie J., Madden, Pamela A. F., Heath, Andrew C., Lynskey, Michael T. and Agrawal, Arpana (2016). Cannabis involvement and nonsuicidal self-injury: A discordant twin approach. Journal of Studies on Alcohol and Drugs, 77 (6), 873-880. doi: 10.15288/jsad.2016.77.873

Cannabis involvement and nonsuicidal self-injury: A discordant twin approach

2016

Journal Article

Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis

Zhou, Yuan, Zhu, Gu, Charlesworth, Jac C., Simpson, Steve, Rubicz, Rohina, Göring, Harald H.H., Patsopoulos, Nikolaos A., Laverty, Caroline, Wu, Feitong, Henders, Anjali, Ellis, Jonathan J., Van Der Mei, Ingrid, Montgomery, Grant W., Blangero, John, Curran, Joanne E., Johnson, Matthew P., Martin, Nicholas G., Nyholt, Dale R. and Taylor, Bruce V. (2016). Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis. Multiple Sclerosis, 22 (13), 1655-1664. doi: 10.1177/1352458515626598

Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis

2016

Journal Article

Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal

Loehlin, John C., Hansell, Narelle K., Wright, Margaret J. and Martin, Nicholas G. (2016). Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal. Intelligence, 59, 24-31. doi: 10.1016/j.intell.2016.05.007

Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal

2016

Journal Article

Co-occurrence and symptomatology of fatigue and depression

Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Co-occurrence and symptomatology of fatigue and depression. Comprehensive Psychiatry, 71, 1-10. doi: 10.1016/j.comppsych.2016.08.004

Co-occurrence and symptomatology of fatigue and depression

2016

Journal Article

Is the association between sweet and bitter perception due to genetic variation?

Hwang, Liang-Dar, Breslin, Paul A. S., Reed, Danielle R., Zhu, Gu, Martin, Nicholas G. and Wright, Margaret J. (2016). Is the association between sweet and bitter perception due to genetic variation?. Chemical Senses, 41 (9), 737-744. doi: 10.1093/chemse/bjw083

Is the association between sweet and bitter perception due to genetic variation?

2016

Journal Article

Variation in latent classes of adult attention–deficit hyperactivity disorder by sex and environmental adversity

Ebejer, Jane L., Medland, Sarah E., van der Werf, Julius, Lynskey, Michael, Martin, Nicholas G. and Duffy, David L. (2016). Variation in latent classes of adult attention–deficit hyperactivity disorder by sex and environmental adversity. Journal of Attention Disorders, 20 (11), 934-945. doi: 10.1177/1087054713506261

Variation in latent classes of adult attention–deficit hyperactivity disorder by sex and environmental adversity

2016

Journal Article

Evidence for mitochondrial genetic control of autosomal gene expression

Kassam, Irfahan, Qi, Tuan, Lloyd-Jones, Luke, Holloway, Alexander, Bonder, Marc Jan, Henders, Anjali K., Martin, Nicholas G., Powell, Joseph E., Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and McRae, Allan F. (2016). Evidence for mitochondrial genetic control of autosomal gene expression. Human Molecular Genetics, 25 (24), 5332-5338. doi: 10.1093/hmg/ddw347

Evidence for mitochondrial genetic control of autosomal gene expression

2016

Journal Article

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Adams, Hieab H. H., Hibar, Derrek P., Chouraki, Vincent, Stein, Jason L., Nyquist, Paul A., Renteria, Miguel E., Trompet, Stella, Arias-Vasquez, Alejandro, Seshadri, Sudha, Desrivieres, Sylvane, Beecham, Ashley H., Jahanshad, Neda, Wittfeld, Katharina, Van der Lee, Sven J., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beiser, Alexa, Bernard, Manon, Bis, Joshua C., Blanken, Laura M. E., Blanton, SusanH., Bohlken, Marc M. ... Thompson, Paul M. (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12), 1569-1582. doi: 10.1038/nn.4398

Novel genetic loci underlying human intracranial volume identified through genome-wide association

2016

Journal Article

A genome-wide association meta-analysis of attention-deficit/hyperactivity disorder symptoms in population-based pediatric cohorts

Middeldorp, Christel M., Hammerschlag, Anke R., Ouwens, Klaasjan G., Groen-Blokhuis, Maria M., St Pourcain, Beate, Greven, Corina U., Pappa, Irene, Tiesler, Carla M. T., Ang, Wei, Nolte, Ilja M., Vilor-Tejedor, Natalia, Bacelis, Jonas, Ebejer, Jane L., Zhao, Huiying, Davies, Gareth E., Ehli, Erik A., Evans, David M., Fedko, Iryna O., Guxens, Monica, Hottenga, Jouke-Jan, Hudziak, James J., Jugessur, Astanand, Kemp, John P., Krapohl, Eva, Martin, Nicholas G., Murcia, Mario, Myhre, Ronny, Ormel, Johan, Ring, Susan M. ... Boomsma, Dorret I. (2016). A genome-wide association meta-analysis of attention-deficit/hyperactivity disorder symptoms in population-based pediatric cohorts. Journal of the American Academy of Child and Adolescent Psychiatry, 55 (10), 896-905.e6. doi: 10.1016/j.jaac.2016.05.025

A genome-wide association meta-analysis of attention-deficit/hyperactivity disorder symptoms in population-based pediatric cohorts

2016

Journal Article

Sweet taste perception is associated with body mass index at the phenotypic and genotypic level

Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, Breslin, Paul A. S., Reed, Danielle R., Macgregor, Stuart, Gharahkhani, Puya, Martin, Nicholas G. and Renteria, Miguel E. (2016). Sweet taste perception is associated with body mass index at the phenotypic and genotypic level. Twin Research and Human Genetics, 19 (5), 465-471. doi: 10.1017/thg.2016.60

Sweet taste perception is associated with body mass index at the phenotypic and genotypic level

2016

Journal Article

Genetic variants in RBFOX3 are associated with sleep latency

Amin, Najaf, Allebrandt, Karla V., van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G., Mbarek, Hamdi, Watson, Nathaniel F., Melville, Scott A., Del Greco, Fabiola M., Byrne, Enda M., Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S., Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A., Zgaga, Lina, Mihailov, Evelin, Stone, Katie L., Campbell, Harry, Brouwer, Rutger W. W., Demirkan, Ayse ... van Duijn, Cornelia M. (2016). Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics, 24 (10), 1488-1495. doi: 10.1038/ejhg.2016.31

Genetic variants in RBFOX3 are associated with sleep latency

2016

Journal Article

Meta-analysis of genome-wide association studies of anxiety disorders

Otowa, T., Hek, K., Lee, M., Byrne, E. M., Mirza, S. S., Nivard, M. G., Bigdeli, T., Aggen, S. H., Adkins, D., Wolen, A., Fanous, A., Keller, M. C., Castelao, E., Kutalik, Z., Der Auwera, S. V., Homuth, G., Nauck, M., Teumer, A., Milaneschi, Y., Hottenga, J. -J., Direk, N., Hofman, A., Uitterlinden, A., Mulder, C. L., Henders, A. K., Medland, S. E., Gordon, S., Heath, A. C., Madden, P. A. F. ... Hettema, J. M. (2016). Meta-analysis of genome-wide association studies of anxiety disorders. Molecular Psychiatry, 21 (10), 1391-1399. doi: 10.1038/mp.2015.197

Meta-analysis of genome-wide association studies of anxiety disorders

2016

Journal Article

Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis

Richmond-Rakerd, Leah S., Slutske, Wendy S., Lynskey, Michael T., Agrawal, Arpana, Madden, Pamela A. F., Bucholz, Kathleen K., Heath, Andrew C., Statham, Dixie J. and Martin, Nicholas G. (2016). Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis. Journal of Abnormal Psychology, 125 (7), 946-959. doi: 10.1037/abn0000191

Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis

2016

Journal Article

Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control

Ellingson, J. M., Richmond-Rakerd, L. S., Statham, D. J., Martin, N. G. and Slutske, W. S. (2016). Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control. Psychological Medicine, 46 (14), 2919-2930. doi: 10.1017/S0033291716001525

Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control

2016

Journal Article

Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins

Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Kirschbaum, Clemens, Frank, Josef, Hansell, Narelle K., Wright, Margaret J., McGrath, John J., Witt, Stephanie H., Rietschel, Marcella and Martin, Nicholas G. (2016). Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins. Twin Research and Human Genetics, 19 (5), 438-446. doi: 10.1017/thg.2016.50

Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins

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

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

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