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)

61 - 80 of 1503 works

2022

Journal Article

Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts

Silventoinen, Karri, Piirtola, Maarit, Jelenkovic, Aline, Sund, Reijo, Tarnoki, Adam D., Tarnoki, David L., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Gatz, Margaret, Butler, David A., Lee, Jooyeon, Lee, Soo Ji, Sung, Joohon, Franz, Carol E., Kremen, William S., Lyons, Michael J., Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Tynelius, Per, Rasmussen, Finn, Martin, Nicholas G., Medland, Sarah E. ... Kaprio, Jaakko (2022). Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts. Scientific Reports, 12 (1) 13148, 1-9. doi: 10.1038/s41598-022-17536-x

Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts

2022

Journal Article

Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study

Gomez, Lina, Díaz-Torres, Santiago, Colodro-Conde, Lucía, Garcia-Marin, Luis M., Yap, Chloe X., Byrne, Enda M., Yengo, Loic, Lind, Penelope A., Wray, Naomi R., Medland, Sarah E., Hickie, Ian B., Lupton, Michelle K., Rentería, Miguel E., Martin, Nicholas G. and Campos, Adrian I. (2022). Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study. European Archives of Psychiatry and Clinical Neuroscience, 273 (6), 1359-1368. doi: 10.1007/s00406-022-01527-0

Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study

2022

Conference Publication

Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?

Hopkins, Kristen L., Lind, Penelope A., Mitchell, Brittany L., Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian B., Martin, Nicholas G. and Medland, Sarah E. (2022). Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.

Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?

2022

Journal Article

Discovery of 42 genome-wide significant loci associated with dyslexia

Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2022). Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11), 1621-1629. doi: 10.1038/s41588-022-01192-y

Discovery of 42 genome-wide significant loci associated with dyslexia

2022

Conference Publication

Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health Practice

Medland, Sarah E., Mitchell, Brittany, Campos, Adrian, Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian, Lind, Penelope A. and Martin, Nicholas G. (2022). Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health Practice. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.

Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health Practice

2022

Journal Article

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

Tielbeek, Jorim J., Uffelmann, Emil, Williams, Benjamin S., Colodro-Conde, Lucía, Gagnon, Éloi, Mallard, Travis T., Levitt, Brandt E., Jansen, Philip R., Johansson, Ada, Sallis, Hannah M., Pistis, Giorgio, Saunders, Gretchen R. B., Allegrini, Andrea G., Rimfeld, Kaili, Konte, Bettina, Klein, Marieke, Hartmann, Annette M., Salvatore, Jessica E., Nolte, Ilja M., Demontis, Ditte, Malmberg, Anni L. K., Burt, S. Alexandra, Savage, Jeanne E., Sugden, Karen, Poulton, Richie, Harris, Kathleen Mullan, Vrieze, Scott, McGue, Matt, Iacono, William G. ... Spit for Science Working Group (2022). Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis. Molecular Psychiatry, 27 (11), 4453-4463. doi: 10.1038/s41380-022-01793-3

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

2022

Journal Article

Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond

Gaddis, Nathan, Mathur, Ravi, Marks, Jesse, Zhou, Linran, Quach, Bryan, Waldrop, Alex, Levran, Orna, Agrawal, Arpana, Randesi, Matthew, Adelson, Miriam, Jeffries, Paul W., Martin, Nicholas G., Degenhardt, Louisa, Montgomery, Grant W., Wetherill, Leah, Lai, Dongbing, Bucholz, Kathleen, Foroud, Tatiana, Porjesz, Bernice, Runarsdottir, Valgerdur, Tyrfingsson, Thorarinn, Einarsson, Gudmundur, Gudbjartsson, Daniel F., Webb, Bradley Todd, Crist, Richard C., Kranzler, Henry R., Sherva, Richard, Zhou, Hang, Hulse, Gary ... Johnson, Eric Otto (2022). Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. Scientific Reports, 12 (1) 16873, 1-16. doi: 10.1038/s41598-022-21003-y

Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond

2022

Journal Article

Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use

Davis, Christal N., Gizer, Ian R., Colodro-Conde, Lucía, Statham, Dixie J., Martin, Nicholas G. and Slutske, Wendy S. (2022). Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use. Twin Research and Human Genetics, 25 (4-5) PII S1832427422000330, 187-195. doi: 10.1017/thg.2022.33

Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use

2022

Journal Article

Common genetic variation and age of onset of anorexia nervosa

Watson, Hunna J., Thornton, Laura M., Yilmaz, Zeynep, Baker, Jessica H., Coleman, Jonathan R.I., Adan, Roger A.H., Alfredsson, Lars, Andreassen, Ole A., Ask, Helga, Berrettini, Wade H., Boehnke, Michael, Boehm, Ilka, Boni, Claudette, Buehren, Katharina, Bulant, Josef, Burghardt, Roland, Chang, Xiao, Cichon, Sven, Cone, Roger D., Courtet, Philippe, Crow, Scott, Crowley, James J., Danner, Unna N., de Zwaan, Martina, Dedoussis, George, DeSocio, Janiece E., Dick, Danielle M., Dikeos, Dimitris, Dina, Christian ... Bulik, Cynthia M. (2022). Common genetic variation and age of onset of anorexia nervosa. Biological Psychiatry Global Open Science, 2 (4), 368-378. doi: 10.1016/j.bpsgos.2021.09.001

Common genetic variation and age of onset of anorexia nervosa

2022

Journal Article

Self-reported impact of developmental stuttering across the lifespan

Boyce, Jessica O., Jackson, Victoria E., van Reyk, Olivia, Parker, Richard, Vogel, Adam P., Eising, Else, Horton, Sarah E., Gillespie, Nathan A., Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Fisher, Simon E., Martin, Nicholas G., Reilly, Sheena, Bahlo, Melanie and Morgan, Angela T. (2022). Self-reported impact of developmental stuttering across the lifespan. Developmental Medicine and Child Neurology, 64 (10), 1297-1306. doi: 10.1111/dmcn.15211

Self-reported impact of developmental stuttering across the lifespan

2022

Conference Publication

Exploring the genome-wide genetic overlap between anxiety and fear disorders

ter Kuile, Abigail, Mitchell, Brittany, Peel, Alicia, Mundy, Jessica, Hubel, Christopher, Zvrskovec, Johan, Palmos, Alish, Coleman, Jonathan, Davies, Molly, Martin, Nick, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Adey, Brett N., Lee, Sang Hyuck, Furtjes, Anna E., Morneau-Vaillancourt, Genevieve, Purves, Kirstin, Skelton, Megan, Hotopf, Matthew, Smith, Daniel J., Veale, David, Armour, Cherie, McIntosh, Andrew, Walters, James T. R., Jones, Ian R., Hirsch, Colette R., Kalsi, Gursharan, Breen, Gerome and Eley, Thalia (2022). Exploring the genome-wide genetic overlap between anxiety and fear disorders. World Congress of Psychiatric Genetics (WCPG), Florence, Italy, 13-17 September 2022. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2022.07.014

Exploring the genome-wide genetic overlap between anxiety and fear disorders

2022

Journal Article

Author correction: 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., Agee, Michelle, Alipanahi, Babak ... the 23andMe Research Team (2022). Author correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 13 (1) 5543, 5543. doi: 10.1038/s41467-022-33222-y

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

2022

Journal Article

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Wang, Zhe, Emmerich, Andrew, Pillon, Nicolas J., Moore, Tim, Hemerich, Daiane, Cornelis, Marilyn C., Mazzaferro, Eugenia, Broos, Siacia, Ahluwalia, Tarunveer S., Bartz, Traci M., Bentley, Amy R., Bielak, Lawrence F., Chong, Mike, Chu, Audrey Y., Berry, Diane, Dorajoo, Rajkumar, Dueker, Nicole D., Kasbohm, Elisa, Feenstra, Bjarke, Feitosa, Mary F., Gieger, Christian, Graff, Mariaelisa, Hall, Leanne M., Haller, Toomas, Hartwig, Fernando P., Hillis, David A., Huikari, Ville, Heard-Costa, Nancy, Holzapfel, Christina ... Lifelines Cohort Study (2022). Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature Genetics, 54 (9), 1332-1344. doi: 10.1038/s41588-022-01165-1

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

2022

Journal Article

Phenome-wide screening of the putative causal determinants of depression using genetic data

Aman, Asma M., García-Marín, Luis M., Thorp, Jackson G., Campos, Adrian I., Cuellar-Partida, Gabriel, Martin, Nicholas G.. and Rentería, Miguel E. (2022). Phenome-wide screening of the putative causal determinants of depression using genetic data. Human Molecular Genetics, 31 (17), 2887-2898. doi: 10.1093/hmg/ddac081

Phenome-wide screening of the putative causal determinants of depression using genetic data

2022

Journal Article

Polygenic influences associated with adolescent cognitive skills

Mitchell, Brittany L., Hansell, Narelle K., McAloney, Kerrie, Martin, Nicholas G., Wright, Margaret J., Renteria, Miguel E. and Grasby, Katrina L. (2022). Polygenic influences associated with adolescent cognitive skills. Intelligence, 94 101680, 1-9. doi: 10.1016/j.intell.2022.101680

Polygenic influences associated with adolescent cognitive skills

2022

Journal Article

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L., Wang, Carol A., Truong, Dongnhu T., Allegrini, Andrea G., Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G., Gerritse, Margot L., Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R., Andlauer, Till F M, Bates, Timothy C., Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S. ... Fisher, Simon E. (2022). Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America, 119 (35) e2202764119, 1-12. doi: 10.1073/pnas.2202764119

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

2022

Journal Article

Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

Silventoinen, Karri, Li, Weilong, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Aaltonen, Sari, Piirtola, Maarit, Sugawara, Masumi, Tanaka, Mami, Matsumoto, Satoko, Baker, Laura A., Tuvblad, Catherine, Tynelius, Per, Rasmussen, Finn, Craig, Jeffrey M., Saffery, Richard, Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Catharina E. M., Martin, Nicholas G., Medland, Sarah E., Montgomery, Grant W., Lichtenstein, Paul, Krueger, Robert F., McGue, Matt, Pahlen, Shandell, Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O. ... Kaprio, Jaakko (2022). Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts. International Journal of Obesity, 46 (10), 1901-1909. doi: 10.1038/s41366-022-01202-3

Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

2022

Journal Article

Exploring the clinical and genetic associations of adult weight trajectories using electronic health records in a racially diverse biobank: a phenome-wide and polygenic risk study

Xu, Jiayi, Johnson, Jessica S., Signer, Rebecca, Eating Disorders Working Group of the Psychiatric Genomics Consortium, Birgegård, Andreas, Jordan, Jennifer, Kennedy, Martin A., Landén, Mikael, Maguire, Sarah L., Martin, Nicholas G., Mortensen, Preben Bo, Petersen, Liselotte V., Thornton, Laura M., Bulik, Cynthia M. and Huckins, Laura M. (2022). Exploring the clinical and genetic associations of adult weight trajectories using electronic health records in a racially diverse biobank: a phenome-wide and polygenic risk study. The Lancet Digital Health, 4 (8), e604-e614. doi: 10.1016/S2589-7500(22)00099-1

Exploring the clinical and genetic associations of adult weight trajectories using electronic health records in a racially diverse biobank: a phenome-wide and polygenic risk study

2022

Journal Article

Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants

Campos, Adrian I., Byrne, Enda M., Iorfino, Frank, Fabbri, Chiara, Hickie, Ian B., Lewis, Cathryn M., Wray, Naomi R., Medland, Sarah E., Rentería, Miguel E. and Martin, Nicholas G. (2022). Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 189 (6), 196-206. doi: 10.1002/ajmg.b.32913

Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants

2022

Journal Article

Co-inheritance of variation in all-cause mortality and biochemical risk factors

Whitfield, John B., Colodro-Conde, Lucía, Zhu, Gu, Timmers, Paul R. H. J., Joshi, Peter K., Montgomery, Grant W. and Martin, Nicholas G (2022). Co-inheritance of variation in all-cause mortality and biochemical risk factors. Twin Research and Human Genetics, 25 (3), 1-8. doi: 10.1017/thg.2022.25

Co-inheritance of variation in all-cause mortality and biochemical risk factors

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

    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

  • 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

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