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)

401 - 420 of 1475 works

2016

Journal Article

Identification of STOML2 as a putative novel asthma risk gene associated with IL6R

Revez, J. A., Matheson, M. C., Hui, J., Baltic, S., James, A., Upham, J. W., Dharmage, S., Thompson, P. J., Martin, N. G., Hopper, J. L. and Ferreira, M. A. R. (2016). Identification of STOML2 as a putative novel asthma risk gene associated with IL6R. Allergy, 71 (7), 1020-1030. doi: 10.1111/all.12869

Identification of STOML2 as a putative novel asthma risk gene associated with IL6R

2016

Journal Article

Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts

Jelenkovic, Aline, Sund, Reijo, Hur, Yoon-Mi, Yokoyama, Yoshie, Hjelmborg, Jacob V. B., Miller, Soren, Honda, Chika, Magnusson, Patrik K. E., Pedersen, Nancy L., Ooki, Syuichi, Aaltonen, Sari, Stazi, Maria A., Fagnani, Corrado, D'Ippolito, Cristina, Freitas, Duarte L., Maia, Jose Antonio, Ji, Fuling, Ning, Feng, Pang, Zengchang, Rebato, Esther, Busjahn, Andreas, Kandler, Christian, Saudino, Kimberly J., Jang, Kerry L., Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Gao, Wenjing, Yu, Canqing ... Silventoinen, Karri (2016). Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts. Scientific Reports, 6 (1) 28496. doi: 10.1038/srep28496

Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts

2016

Journal Article

Heritability and genetic correlation between the cerebral cortex and associated white matter connections

Shen, Kai-Kai, Dore, Vincent, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2016). Heritability and genetic correlation between the cerebral cortex and associated white matter connections. Human Brain Mapping, 37 (6), 2331-2347. doi: 10.1002/hbm.23177

Heritability and genetic correlation between the cerebral cortex and associated white matter connections

2016

Journal Article

Five endometrial cancer risk loci identified through genome-wide association analysis

Cheng, Timothy H. T., Thompson, Deborah J., O'Mara, Tracy A., Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Webb, Penelope M., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W., Nyholt, Dale R., Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Dennis, Joe, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander ... Spurdle, Amanda B. (2016). Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics, 48 (6), 667-674. doi: 10.1038/ng.3562

Five endometrial cancer risk loci identified through genome-wide association analysis

2016

Journal Article

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

Zhao, Huiying, Eising, Else, De Vries, Boukje, Vijfhuizen, Lisanne S., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Stam, Anine H., Arfan Ikram, M., Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Müller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromas, Arpo, Eriksson, Johan G., Boomsma, Dorret I., Van Duijn, Cornelia M., Zwart, John-Anker, Quaye, Lydia, Kubisch, Christian, Dichgans, Martin, Wessman, Maija, Stefansson, Kari, Chasman, Daniel I. ... Nyholt, Dale R. (2016). Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia, 36 (7), 648-657. doi: 10.1177/0333102415591497

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

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

Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci

Smith, D. J., Escott-Price, V., Davies, G., Bailey, M. E. S., Colodro-Conde, L., Ward, J., Vedernikov, A., Marioni, R., Cullen, B., Lyall, D., Hagenaars, S. P., Liewald, D. C. M., Luciano, M., Gale, C. R., Ritchie, S. J., Hayward, C., Nicholl, B., Bulik-Sullivan, B., Adams, M., Couvy-Duchesne, B., Graham, N., Mackay, D., Evans, J., Smith, B. H., Porteous, D. J., Medland, S. E., Martin, N. G., Holmans, P., McIntosh, A. M. ... O'Donovan, M. C. (2016). Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci. Molecular Psychiatry, 21 (6), 749-757. doi: 10.1038/mp.2016.49

Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci

2016

Journal Article

Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility

Mbarek, Hamdi, Steinberg, Stacy, Nyholt, Dale R., Gordon, Scott D., Miller, Michael B., McRae, Allan F, Hottenga, Jouke Jan, Day, Felix R., Willemsen, Gonneke, de Geus, Eco J., Davies, Gareth E, Martin, Hilary C, Penninx, Brenda W, Jansen, Rick, McAloney, Kerrie, Vink, Jacqueline M., Kaprio, Jaakko, Plomin, Robert, Spector, Tim D., Magnusson, Patrik K., Reversade, Bruno, Harris, R. Alan, Aagaard, Kjersti, Kristjansson, Ragnar P., Olafsson, Isleifur, Eyjolfsson, Gudmundur Ingi, Sigurdardottir, Olof, Iacono, William G., Lambalk, Cornelis B ... Boomsman, Dorret I. (2016). Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility. American Journal of Human Genetics, 98 (5), 898-908. doi: 10.1016/j.ajhg.2016.03.008

Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility

2016

Journal Article

Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits

van Beijsterveldt, C. E.M., Overbeek, L. I.H., Rozendaal, L., McMaster, M. T.B., Glasner, T. J., Bartels, M., Vink, J. M., Martin, N. G., Dolan, C. V. and Boomsma, D. I. (2016). Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits. Behavior Genetics, 46 (3), 304-314. doi: 10.1007/s10519-015-9745-3

Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits

2016

Journal Article

Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

Read, Jazlyn, Symmons, Judith, Palmer, Jane M., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2016). Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families. Familial Cancer, 15 (4), 651-663. doi: 10.1007/s10689-016-9907-3

Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

2016

Journal Article

Shared genetic control of expression and methylation in peripheral blood

Shakhbazov, Konstantin, Powell, Joseph E., Hemani, Gibran, Henders, Anjali K., Martin, Nicholas G., Visscher, Peter M., Montgomery, Grant W. and McRae, Allan F. (2016). Shared genetic control of expression and methylation in peripheral blood. BMC Genomics, 17 (1) 278, 278. doi: 10.1186/s12864-016-2498-4

Shared genetic control of expression and methylation in peripheral blood

2016

Journal Article

Common genetic variants influence whorls in fingerprint patterns

Ho, Yvonne Y. W., Evans, David M., Montgomery, Grant W., Henders, Anjali K., Kemp, John P., Timpson, Nicholas J., Pourcain, Beate St., Heath, Andrew C., Madden, Pamela A. F., Loesch, Danuta Z., McNevin, Dennis, Daniel, Runa, Davey-Smith, George, Martin, Nicholas G. and Medland, Sarah E. (2016). Common genetic variants influence whorls in fingerprint patterns. Journal of Investigative Dermatology, 136 (4), 859-862. doi: 10.1016/j.jid.2015.10.062

Common genetic variants influence whorls in fingerprint patterns

2016

Journal Article

Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project

Yokoyama, Yoshie, Jelenkovic, Aline, Sund, Reijo, Sung, Joohon, Hopper, John L., Ooki, Syuichi, Heikkila, Kauko, Aaltonen, Sari, Tarnoki, Adam D., Tarnoki, David L., Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Toos C. E. M., Saudino, Kimberly J., Cutler, Tessa L., Nelson, Tracy L., Whitfield, Keith E., Wardle, Jane, Llewellyn, Clare H., Fisher, Abigail, He, Mingguang, Ding, Xiaohu, Bjerregaard-Andersen, Morten, Beck-Nielsen, Henning, Sodemann, Morten, Song, Yun-Mi, Yang, Sarah, Lee, Kayoung, Jeong, Hoe-Uk ... Silventoinen, Karri (2016). Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project. Twin Research and Human Genetics, 19 (2), 112-124. doi: 10.1017/thg.2016.11

Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project

2016

Journal Article

The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume

Lupton, Michelle K., Strike, Lachlan, Hansell, Narelle K., Wen, Wei, Mather, Karen A., Armstrong, Nicola J., Thalamuthu, Anbupalam, McMahon, Katie L., de Zubicaray, Greig I., Assareh, Amelia A., Simmons, Andrew, Proitsi, Petroula, Powell, John F., Montgomery, Grant W., Hibar, Derrek P., Westman, Eric, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Velas, Bruno, Lovestone, Simon, Brodaty, Henry, Ames, David, Trollor, Julian N., Martin, Nicholas G., Thompson, Paul M., Sachdev, Perminder S. and Wright, Margaret J. (2016). The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume. Neurobiology of Aging, 40, 68-77. doi: 10.1016/j.neurobiolaging.2015.12.023

The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume

2016

Journal Article

Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures

Kapoor, M., Chou, Y-L, Edenberg, H. J., Foroud, T., Martin, N. G., Madden, P A F, Wang, J. C., Bertelsen, S., Wetherill, L., Brooks, A., Chan, G., Hesselbrock, V., Kuperman, S., Medland, S. E., Montgomery, G., Tischfield, J., Whitfield, J. B., Bierut, L. J., Heath, A. C., Bucholz, K. K., Goate, A. M. and Agrawal, A. (2016). Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures. Translational Psychiatry, 6 (3) e761, e761-e761. doi: 10.1038/tp.2016.27

Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures

2016

Journal Article

Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group

Schmaal, L., Hibar, D. P., Samann, P. G., Hall, G. B., Baune, B. T., Jahanshad, N., Cheung, J. W., van Erp, T. G. M., Bos, D., Ikram, M. A., Vernooij, M. W., Niessen, W. J., Tiemeier, H., Hofman, A., Wittfeld, K., Grabe, H. J., Janowitz, D., Bulow, R., Selonke, M., Volzke, H., Grotegerd, D., Dannlowski, U., Arolt, V., Opel, N., Heindel, W., Kugel, H., Hoehn, D., Czisch, M., Couvy-Duchesne, B. ... Veltman, D. J. (2016). Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group. Molecular Psychiatry, 22 (6), 900-909. doi: 10.1038/mp.2016.60

Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group

2016

Journal Article

Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?

Hines, Lindsey A., Morley, Katherine I., Strang, John, Agrawal, Arpana, Nelson, Elliot C., Statham, Dixie, Martin, Nicholas G. and Lynskey, Michael T. (2016). Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?. Drug and Alcohol Dependence, 160, 57-64. doi: 10.1016/j.drugalcdep.2015.12.032

Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?

2016

Journal Article

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

Schwantes-An, Tae-Hwi, Zhang, Juan, Chen, Li-Shiun, Hartz, Sarah M., Culverhouse, Robert C., Chen, Xiangning, Coon, Hilary, Frank, Josef, Kamens, Helen M., Konte, Bettina, Kovanen, Leena, Latvala, Antti, Legrand, Lisa N., Maher, Brion S., Melroy, Whitney E., Nelson, Elliot C., Reid, Mark W., Robinson, Jason D., Shen, Pei-Hong, Yang, Bao-Zhu, Andrews, Judy A., Aveyard, Paul, Beltcheva, Olga, Brown, Sandra A., Cannon, Dale S., Cichon, Sven, Corley, Robin P., Dahmen, Norbert, Degenhardt, Louisa ... Saccone, Nancy L. (2016). Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46 (2), 151-169. doi: 10.1007/s10519-015-9737-3

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

2016

Journal Article

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

Stringer, S., Minică, C. C., Verweij, K. J. H., Mbarek, H., Bernard, M., Derringer, J., van Eijk, K. R., Isen, J. D., Loukola, A., Maciejewsk, D. F., Mihailov, E., van der Most, P. J., Sánchez-Mora, C., Roos, L., Sherva, R., Walters, R., Ware, J. J., Abdellaoui, A., Bigdeli, T. B., Branje, S. J. T., Brown, S. A., Bruinenberg, M., Casas, M., Esko, T., Garcia-Martinez, I., Gordon, S. D., Harris, J. M., Hartman, C. A., Henders, A. K. ... Vink, J. M. (2016). Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Translational Psychiatry, 6 (3) e769, e769-e769. doi: 10.1038/tp.2016.36

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

2016

Journal Article

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population

Clarke, T-K, Lupton, M. K., Fernandez-Pujals, A. M., Starr, J., Davies, G., Cox, S., Pattie, A., Liewald, D. C., Hall, L. S., MacIntyre, D. J., Smith, B. H., Hocking, L. J., Padmanabhan, S., Thomson, P. A., Hayward, C., Hansell, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Porteous, D. J., Deary, I. J. and McIntosh, A. M. (2016). Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population. Molecular Psychiatry, 21 (3), 419-425. doi: 10.1038/mp.2015.12

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population

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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