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

1503 works between 1975 and 2025
All (1503) Journal Article (1363) Book Chapter (14) Conference Publication (96) Other Outputs (30)

221 - 240 of 1503 works

2019

Journal Article

Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults

Chang, Lun-Hsien, Whitfield, John B., Liu, Mengzhen, Medland, Sarah E., Hickie, Ian B., Martin, Nicholas G., Verhulst, Brad, Heath, Andrew C., Madden, Pamela A., Statham, Dixie J., Gillespie, Nathan A. and GSCAN Consortium (2019). Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults. Drug and Alcohol Dependence, 205 107704, 107704. doi: 10.1016/j.drugalcdep.2019.107704

Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults

2019

Journal Article

The Nigerian Twin and Sibling Registry: An Update

Hur, Yoon-Mi, Jeong, Hoe-Uk, Kang, Man Chull, Ajose, Frances, Kim, Jong Woo, Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Martin, Nicholas G., De Geus, Eco J., Boomsma, Dorret I., Davies, Gareth E. and Bates, Timothy (2019). The Nigerian Twin and Sibling Registry: An Update. Twin Research and Human Genetics, 22 (6), 637-640. doi: 10.1017/thg.2019.110

The Nigerian Twin and Sibling Registry: An Update

2019

Journal Article

Novel genetic loci affecting facial shape variation in humans

Xiong, Ziyi, Dankova, Gabriela, Howe, Laurence J., Lee, Myoung Keun, Hysi, Pirro G., de Jong, Markus A., Zhu, Gu, Adhikari, Kaustubh, Li, Dan, Li, Yi, Pan, Bo, Feingold, Eleanor, Marazita, Mary L., Shaffer, John R., McAloney, Kerrie, Xu, Shu-Hua, Jin, Li, Wang, Sijia, de Vrij, Femke Ms, Lendemeijer, Bas, Richmond, Stephen, Zhurov, Alexei, Lewis, Sarah, Sharp, Gemma C., Paternoster, Lavinia, Thompson, Holly, Gonzalez-Jose, Rolando, Bortolini, Maria Catira, Canizales-Quinteros, Samuel ... Kayser, Manfred (2019). Novel genetic loci affecting facial shape variation in humans. eLife, 8 e49898. doi: 10.7554/eLife.49898

Novel genetic loci affecting facial shape variation in humans

2019

Journal Article

The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese

Ye, Lin, Zhu, Gu, Martin, Nick and Liu, Yangyang (2019). The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese. Journal of Early Adolescence, 39 (9), 1337-1342. doi: 10.1177/0272431618824710

The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese

2019

Journal Article

Associations of autozygosity with a broad range of human phenotypes

Clark, David W., Okada, Yukinori, Moore, Kristjan H. S., Mason, Dan, Pirastu, Nicola, Gandin, Ilaria, Mattsson, Hannele, Barnes, Catriona L. K., Lin, Kuang, Zhao, Jing Hua, Deelen, Patrick, Rohde, Rebecca, Schurmann, Claudia, Guo, Xiuqing, Giulianini, Franco, Zhang, Weihua, Medina-Gomez, Carolina, Karlsson, Robert, Bao, Yanchun, Bartz, Traci M., Baumbach, Clemens, Biino, Ginevra, Bixley, Matthew J., Brumat, Marco, Chai, Jin-Fang, Corre, Tanguy, Cousminer, Diana L., Dekker, Annelot M., Eccles, David A. ... Wilson, James F. (2019). Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10 (1) 4957, 4957. doi: 10.1038/s41467-019-12283-6

Associations of autozygosity with a broad range of human phenotypes

2019

Journal Article

Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

Van Der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, De Geus, Eco J. C. ... Andreassen, Ole A. (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry, 77 (4), 1-11. doi: 10.1001/jamapsychiatry.2019.3779

Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

2019

Journal Article

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A. ... Morton, C. C. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

2019

Journal Article

Genetic architecture of subcortical brain structures in 38,851 individuals

Satizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E. ... Ikram, M. Arfan (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11), 1624-1636. doi: 10.1038/s41588-019-0511-y

Genetic architecture of subcortical brain structures in 38,851 individuals

2019

Other Outputs

Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank (n=408,317)

Campos, Adrián I., García-Marín, Luis M., Byrne, Enda M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2019). Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank (n=408,317). doi: 10.1101/808691

Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank (n=408,317)

2019

Journal Article

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

Nievergelt, Caroline M., Maihofer, Adam X., Klengel, Torsten, Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Dalvie, Shareefa, Duncan, Laramie E., Gelernter, Joel, Levey, Daniel F., Logue, Mark W., Polimanti, Renato, Provost, Allison C., Ratanatharathorn, Andrew, Stein, Murray B., Torres, Katy, Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Søren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Babić, Dragan, Bækvad-Hansen, Marie, Baker, Dewleen G. ... Koenen, Karestan C. (2019). International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications, 10 (1) 4558, 4558. doi: 10.1038/s41467-019-12576-w

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

2019

Journal Article

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

Tin, Adrienne, Marten, Jonathan, Halperin Kuhns, Victoria L., Li, Yong, Wuttke, Matthias, Kirsten, Holger, Sieber, Karsten B., Qiu, Chengxiang, Gorski, Mathias, Yu, Zhi, Giri, Ayush, Sveinbjornsson, Gardar, Li, Man, Chu, Audrey Y., Hoppmann, Anselm, O’Connor, Luke J., Prins, Bram, Nutile, Teresa, Noce, Damia, Akiyama, Masato, Cocca, Massimiliano, Ghasemi, Sahar, van der Most, Peter J., Horn, Katrin, Xu, Yizhe, Fuchsberger, Christian, Sedaghat, Sanaz, Afaq, Saima, Amin, Najaf ... Köttgen, Anna (2019). Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nature Genetics, 51 (10), 1459-1474. doi: 10.1038/s41588-019-0504-x

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

2019

Conference Publication

Anorexia nervosa genome-wide association study identifies eight loci and implicates psychiatric and metabolic origins

Hubel, C., Watson, H. J., Yilmaz, Z., Landen, M., Martin, N. G., Mortensen, P., Sullivan, P. F., Breen, G. and Bulik, C. M. (2019). Anorexia nervosa genome-wide association study identifies eight loci and implicates psychiatric and metabolic origins. 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg Sweden, Jun 15-18, 2019. LONDON: NATURE PUBLISHING GROUP.

Anorexia nervosa genome-wide association study identifies eight loci and implicates psychiatric and metabolic origins

2019

Journal Article

White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group

van Velzen, Laura S., Kelly, Sinead, Isaev, Dmitry, Aleman, Andre, Aftanas, Lyubomir I., Bauer, Jochen, Baune, Bernhard T., Brak, Ivan V., Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Danilenko, Konstantin V., Dannlowski, Udo, Enneking, Verena, Filimonova, Elena, Förster, Katharina, Frodl, Thomas, Gotlib, Ian H., Groenewold, Nynke A., Grotegerd, Dominik, Harris, Mathew A., Hatton, Sean N., Hawkins, Emma L., Hickie, Ian B., Ho, Tiffany C., Jansen, Andreas, Kircher, Tilo, Klimes-Dougan, Bonnie ... Schmaal, Lianne (2019). White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group. Molecular Psychiatry, 25 (7), 1511-1525. doi: 10.1038/s41380-019-0477-2

White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group

2019

Other Outputs

Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

Munn-Chernoff, Melissa A., Johnson, Emma C., Chou, Yi-Ling, Coleman, Jonathan R.I., Thornton, Laura M., Walters, Raymond K., Yilmaz, Zeynep, Baker, Jessica H., Hübel, Christopher, Gordon, Scott, Medland, Sarah E., Watson, Hunna J., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Adan, Roger A.H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Perica, Vesna Boraska ... Agrawal, Arpana (2019). Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies. doi: 10.1101/741512

Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

2019

Journal Article

Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium

Van der Spek, Ashley, Broer, Linda, Draisma, Harmen H. M., Pool, René, Albrecht, Eva, Beekman, Marian, Mangino, Massimo, Raag, Mait, Nyholt, Dale R., Dharuri, Harish K., Codd, Veryan, Amin, Najaf, de Geus, Eco J. C., Deelen, Joris, Demirkan, Ayse, Yet, Idil, Fischer, Krista, Haller, Toomas, Henders, Anjali K., Isaacs, Aaron, Medland, Sarah E., Montgomery, Grant W., Mooijaart, Simon P., Strauch, Konstantin, Suchiman, H. Eka D., Vaarhorst, Anika A. M., van Heemst, Diana, Wang-Sattler, Rui, Whitfield, John B. ... Gieger, Christian (2019). Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium. Scientific Reports, 9 (1) 11623, 11623. doi: 10.1038/s41598-019-47282-6

Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium

2019

Journal Article

Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated With depression

Glanville, Kylie P., Coleman, Jonathan R. I., Hanscombe, Ken B., Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L., Breen, Gerome, Air, Tracy M., Andlauer, Till F. M., Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Buttenschøn, Henriette N., Colodro-Conde, Lucía, Dannlowski, Udo, Direk, Nese, Dunn, Erin C., Forstner, Andreas J., de Geus, Eco J. C., Grabe, Hans J., Hamilton, Steven P., Jones, Ian, Jones, Lisa A., Knowles, James A., Kutalik, Zoltán, Levinson, Douglas F., Lewis, Glyn, Lind, Penelope A. ... Børglum, Anders D. (2019). Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated With depression. Biological Psychiatry, 87 (5), 419-430. doi: 10.1016/j.biopsych.2019.06.031

Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated With depression

2019

Journal Article

A behavior genetic analysis of the relationship between humor styles and depression

Kfrerer, Marisa L., Martin, Nicholas G. and Schermer, Julie Aitken (2019). A behavior genetic analysis of the relationship between humor styles and depression. Humor, 32 (3), 417-431. doi: 10.1515/humor-2017-0098

A behavior genetic analysis of the relationship between humor styles and depression

2019

Journal Article

Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array

Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Hur, Yoon-Mi, Martin, Nicholas G., De Geus, Eco J.C., Boomsma, Dorret I. and Davies, Gareth E. (2019). Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array. Twin Research and Human Genetics, 22 (4), 210-219. doi: 10.1017/thg.2019.41

Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array

2019

Journal Article

New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

Evangelou, Evangelos, Gao, He, Chu, Congying, Ntritsos, Georgios, Blakeley, Paul, Butts, Andrew R., Pazoki, Raha, Suzuki, Hideaki, Koskeridis, Fotios, Yiorkas, Andrianos M., Karaman, Ibrahim, Elliott, Joshua, Luo, Qiang, Aeschbacher, Stefanie, Bartz, Traci M., Baumeister, Sebastian E., Braund, Peter S., Brown, Michael R., Brody, Jennifer A., Clarke, Toni-Kim, Dimou, Niki, Faul, Jessica D., Homuth, Georg, Jackson, Anne U., Kentistou, Katherine A., Joshi, Peter K., Lemaitre, Rozenn N., Lind, Penelope A., Lyytikäinen, Leo-Pekka ... Elliott, Paul (2019). New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. Nature Human Behaviour, 3 (9), 950-961. doi: 10.1038/s41562-019-0653-z

New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

2019

Journal Article

Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins

Gillespie, Nathan A., Bates, Timothy C., Hickie, Ian B., Medland, Sarah E., Verhulst, Brad, Kirkpatrick, Robert M., Kendler, Kenneth S., Martin, Nicholas G. and Benotsch, Eric G. (2019). Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins. Addiction, 114 (12) add.14750, 2229-2240. doi: 10.1111/add.14750

Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins

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

    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

  • 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

Completed supervision

Enquiries

For media enquiries about Professor Nick Martin's areas of expertise, story ideas and help finding experts, contact our Media team:

communications@uq.edu.au