Professor

Nick Martin

Email: 

Availability

Professor Nick Martin is:
Available for supervision

Fields of research

Clinical sciences Genetics Psychology

Qualifications

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

Search Professor Nick Martin’s works on UQ eSpace

1507 works between 1975 and 2025
All (1507) Journal Article (1367) Book Chapter (14) Conference Publication (96) Other Outputs (30)

901 - 920 of 1507 works

2010

Journal Article

IRF4 variants have age-specific effects on nevus count and predispose to melanoma

Duffy, David L., Iles, Mark M., Glass, Dan, Zhu, Gu, Barrett, Jennifer H., Hoiom, Veronica, Zhao, Zhen Z., Sturm, Richard A., Soranzo, Nicole, Hammond, Chris, Kvaskoff, Marina, Whiteman, David C., Mangino, Massimo, Hansson, Johan, Newton-Bishop, Julia A., Bataille, Veronique, Hayward, Nicholas K., Martin, Nicholas G., Bishop, D. Timothy, Spector, Timothy D. and Montgomery, Grant W. (2010). IRF4 variants have age-specific effects on nevus count and predispose to melanoma. American Journal of Human Genetics, 87 (1), 6-16. doi: 10.1016/j.ajhg.2010.05.017

IRF4 variants have age-specific effects on nevus count and predispose to melanoma

2010

Journal Article

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

Macgregor, Stuart, Hewitt, Alex W., Hysi, Pirro G., Ruddle, Jonathan B., Medland, Sarah E., Henders, Anjali K., Gordon, Scott D., Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G., Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L., Craig, Jamie E., Montgomery, Grant W., Tran-Viet, Khanh-Nhat, Brown, Nadean L., Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J. and Mackey, David A. (2010). Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Human Molecular Genetics, 19 (13) ddq144, 2716-2724. doi: 10.1093/hmg/ddq144

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

2010

Journal Article

Common SNPs explain a large proportion of the heritability for human height

Yang, Jian, Benyamin, Beben, McEvoy, Brian P., Gordon, Scott, Henders, Anjali K., Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Goddard, Michael E. and Visscher, Peter M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature Genetics, 42 (7), 565-569. doi: 10.1038/ng.608

Common SNPs explain a large proportion of the heritability for human height

2010

Journal Article

Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes

Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2010). Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes. Environmental Health Perspectives, 118 (6), 776-782. doi: 10.1289/ehp.0901541

Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes

2010

Journal Article

The reliability and validity of the family history method for assessing pathological gambling and gambling involvement

Ellingson, Jarrod M., Slutske, Wendy S. and Martin, Nicholas G. (2010). The reliability and validity of the family history method for assessing pathological gambling and gambling involvement. Psychology of Addictive Behaviors, 24 (2), 292-299. doi: 10.1037/a0018126

The reliability and validity of the family history method for assessing pathological gambling and gambling involvement

2010

Journal Article

A genetic basis for social trust?

Sturgis, Patrick, Read, Sanna, Hatemi, Peter K., Zhu, Gu, Trull, Tim, Wright, Margaret J. and Martin, Nicholas G. (2010). A genetic basis for social trust?. Political Behavior, 32 (2), 205-230. doi: 10.1007/s11109-009-9101-5

A genetic basis for social trust?

2010

Journal Article

Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

Lind, Penelope A., Luciano, Michelle, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2010). Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics, 18 (6), 668-673. doi: 10.1038/ejhg.2009.237

Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

2010

Journal Article

Genetic and environmental influences on disordered gambling in men and women

Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2010). Genetic and environmental influences on disordered gambling in men and women. Archives of General Psychiatry, 67 (6), 624-630. doi: 10.1001/archgenpsychiatry.2010.51

Genetic and environmental influences on disordered gambling in men and women

2010

Journal Article

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

Painter, Jodie N., Willemsen, Gonneke, Nyholt, Dale, Hoekstra, Chantal, Duffy, David L., Henders, Anjali K., Wallace, Leanne, Healey, Sue, Cannon-Albright, Lisa A., Skolnick, Mark, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2010). A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Human Reproduction, 25 (6), 1569-1580. doi: 10.1093/humrep/deq084

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

2010

Journal Article

Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond. Christopher J., Macgregor, Stuart, Craig, Jamie E. and Mackey, David A. (2010). Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genetics, 6 (5) e1000947, e1000947.1-e1000947.10. doi: 10.1371/journal.pgen.1000947

Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

2010

Journal Article

Digital quantification of human eye color highlights genetic association of three new loci

Liu, Fan, Wollstein, Andreas, Hysi, Pirro G., Ankra-Badu, Georgina A., Spector, Timothy D., Park, Daniel, Zhu, Gu, Larsson, Mats, Duffy, David L., Montgomery, Grant W., Mackey, David A., Walsh, Susan, Lao, Oscar, Hofman, Albert, Rivadeneira, Fernando, Vingerling, Johannes R., Uitterlinden, Andrew G., Martin, Nicholas G., Hammond, Christopher J. and Kayser, Manfred (2010). Digital quantification of human eye color highlights genetic association of three new loci. PLoS Genetics, 6 (5) e1000934, e1000934-1-e1000934-15. doi: 10.1371/journal.pgen.1000934

Digital quantification of human eye color highlights genetic association of three new loci

2010

Journal Article

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

Thorgeirsson, Thorgeir E., Gudbjartsson, Daniel F., Surakka, Ida, Vink, Jacqueline M., Amin, Najaf, Geller, Frank, Sulem, Patrick, Rafnar, Thorunn, Esko, Tōnu, Walter, Stefan, Gieger, Christian, Rawal, Rajesh, Mangino, Massimo, Prokopenko, Inga, Mägi, Reedik, Keskitalo, Kaisu, Gudjonsdottir, Iris H., Gretarsdottir, Solveig, Stefansson, Hreinn, Thompson, John R., Aulchenko, Yurii S., Nelis, Mari, Aben, Katja K., den Heijer, Martin, Dirksen, Asger, Ashraf, Haseem, Soranzo, Nicole, Valdes, Ana M., Steves, Claire ... Stefansson, Kari (2010). Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, 42 (5), 448-454. doi: 10.1038/ng.573

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

2010

Journal Article

A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure

Medland, Sarah E., Zayats,Tetyana, Glaser, Beate, Nyholt, Dale R., Gordon,Scott D., Wright, Margaret J., Montgomery, Grant W., Campbell, Megan J., Henders, Anjali K., Timpson, Nicholas J., Peltonen, Leena, Wolke, Dieter, Ring, Susan M., Deloukas, Panos, Martin, Nicholas G., Smith, George Davey and Evans, David M. (2010). A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. American Journal of Human Genetics, 86 (4), 519-525. doi: 10.1016/j.ajhg.2010.02.017

A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure

2010

Journal Article

A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures

Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2010). A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures. Twin Research and Human Genetics, 13 (2), 121-130. doi: 10.1375/twin.13.2.121

A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures

2010

Conference Publication

Genome Wide Analysis Identifies Putative Loci Associated With Interpupillary Distance

Staffieri, S. E., Ruddle, J. B., Hewitt, A. W., Kearns, L. S., Sanfilippo, P. G., MacGregor, S., Martin, N. G., Young, T. L., Hammond, C. J. and Mackey, D. A. (2010). Genome Wide Analysis Identifies Putative Loci Associated With Interpupillary Distance. ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.

Genome Wide Analysis Identifies Putative Loci Associated With Interpupillary Distance

2010

Journal Article

Genome-wide association study of height and body mass index in Australian twin families

Liu, Jimmy Z., Medland, Sarah E., Wright, Margaret J., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Duncan, Alexis, Montgomery, Grant W., Martin, Nicholas G. and McRae, Allan F. (2010). Genome-wide association study of height and body mass index in Australian twin families. Twin Research And Human Genetics, 13 (2), 179-193. doi: 10.1375/twin.13.2.179

Genome-wide association study of height and body mass index in Australian twin families

2010

Conference Publication

Up to What Age is a Cyclopleged Refraction Required? Results From the Twins Eye Study Tasmania(TEST)

Kearns, L. S., Hewitt, A. W., Ruddle, J. B., Bigault, O., Staffieri, S. E., Sanfillipo, P., Martin, N. G., Hammond, C. J., Young, T. L. and Mackey, D. A. (2010). Up to What Age is a Cyclopleged Refraction Required? Results From the Twins Eye Study Tasmania(TEST). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.

Up to What Age is a Cyclopleged Refraction Required? Results From the Twins Eye Study Tasmania(TEST)

2010

Journal Article

Characterization of the methylation patterns of MS4A2 in atopic cases and controls

M. A. R. Ferreira, N. A. Oates, J. van Vliet, Z. Z. Zhao, M. Ehrich, N. G. Martin, G. W. Montgomery, E. Whitelaw and D. L. Duffy (2010). Characterization of the methylation patterns of MS4A2 in atopic cases and controls. ALLERGY, 65 (3), 333-337. doi: 10.1111/j.1398-9995.2009.02135.x

Characterization of the methylation patterns of MS4A2 in atopic cases and controls

2010

Journal Article

Common genetic contributions to alcohol and cannabis use and dependence symptomatology

Sartor, Carolyn E., Grant, Julia D., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C., Agrawal, Arpana, Whitfield, John B., Statham, Dixie J., Martin, Nicholas G. and Lynkey, Michael T. (2010). Common genetic contributions to alcohol and cannabis use and dependence symptomatology. Alcoholism: Clinical and Experimental Research, 34 (3), 545-554. doi: 10.1111/j.1530-0277.2009.01120.x

Common genetic contributions to alcohol and cannabis use and dependence symptomatology

2010

Journal Article

Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies

Verweij, Karin J. H., Zietsch, Brendan P., Lynskey, Michael T., Medland, Sarah E., Neale, Michael C., Martin, Nicholas G., Boomsma, Dorret I. and Vink, Jacqueline M. (2010). Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies. Addiction, 105 (3), 417-430. doi: 10.1111/j.1360-0443.2009.02831.x

Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies

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

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

Enquiries

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