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

1475 works between 1975 and 2025
All (1475) Journal Article (1364) Book Chapter (14) Conference Publication (96) Other Outputs (1)

861 - 880 of 1475 works

2010

Journal Article

Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings

Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2010). Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings. NeuroImage, 52 (2), 455-469. doi: 10.1016/j.neuroimage.2010.04.236

Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings

2010

Journal Article

Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling

Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2010). Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling. Twin Research And Human Genetics, 13 (4), 330-339. doi: 10.1375/twin.13.4.330

Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling

2010

Journal Article

Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins

Mosing, Miriam A., Pedersen, Nancy L., Martin, Nicholas G. and Wright, Margaret J. (2010). Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins. Twin Research And Human Genetics, 13 (4), 322-329. doi: 10.1375/twin.13.4.322

Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins

2010

Journal Article

Nicotine withdrawal symptoms in adolescent and adult twins

Pergadia, Michele L., Agrawal, Arpana, Heath, Andrew C., Martin, Nicholas G., Bucholz, Kathleen K. and Madden, Pamela A. F. (2010). Nicotine withdrawal symptoms in adolescent and adult twins. Twin Research And Human Genetics, 13 (4), 359-369. doi: 10.1375/twin.13.4.359

Nicotine withdrawal symptoms in adolescent and adult twins

2010

Journal Article

The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs

Slutske, Wendy S., Piasecki, Thomas M., Ellingson, Jarrod M. and Martin, Nicholas G. (2010). The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs. Twin Research and Human Genetics, 13 (4), 340-346. doi: 10.1375/twin.13.4.340

The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs

2010

Journal Article

Heritability of head size in Dutch and Australian twin families at ages 0-50 years

Smit, Dirk J. A., Luciano, Michelle, Bartels, Meike, van Beijsterveldt, Catharine E. M., Wright, Margaret J., Hansell, Narelle K., Brunner, Han G., Estourgie-van Burk, G. Frederiek, de Geus, Eco J. C., Martin, Nicholas G. and Boomsma, Dorret I. (2010). Heritability of head size in Dutch and Australian twin families at ages 0-50 years. Twin Research And Human Genetics, 13 (4), 370-380. doi: 10.1375/twin.13.4.370

Heritability of head size in Dutch and Australian twin families at ages 0-50 years

2010

Journal Article

A versatile gene-based test for genome-wide association studies

Liu, Jimmy Z., McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Wray, Naomi R., Brown, Kevin M., AMFS Investigators, Hayward, Nicholas K., Montgomery, Grant W., Visscher, Peter M., Martin, Nicholas G. and Macgregor, Stuart (2010). A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87 (1), 139-145. doi: 10.1016/j.ajhg.2010.06.009

A versatile gene-based test for genome-wide association studies

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

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

Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs

Hatemi, Peter K., Hibbing, John R., Medland, Sarah E., Keller, Matthew C., Alford, John R., Smith, Kevin B., Martin, Nicholas G. and Eaves, Lindon J. (2010). Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs. American Journal of Political Science, 54 (3), 798-814. doi: 10.1111/j.1540-5907.2010.00461.x

Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs

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

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

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

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

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

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

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

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

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Supervision history

Current supervision

Completed supervision

Enquiries

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