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

1456 works between 1975 and 2024
All (1456) Journal Article (1351) Book Chapter (14) Conference Publication (90) Other Outputs (1)

41 - 60 of 1456 works

2023

Journal Article

Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring

Campos, Adrian I., Ingold, Nathan, Huang, Yunru, Mitchell, Brittany L., Kho, Pik-Fang, Han, Xikun, García-Marín, Luis M., Ong, Jue-Sheng, 23andMe Research Team, Law, Matthew H., Yokoyama, Jennifer S., Martin, Nicholas G., Dong, Xianjun, Cuellar-Partida, Gabriel, MacGregor, Stuart, Aslibekyan, Stella and Rentería, Miguel E. (2023). Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep, 46 (3) zsac308, 1-14. doi: 10.1093/sleep/zsac308

Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring

2023

Journal Article

Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity

Bakker, Mark K., Kanning, Jos P., Abraham, Gad, Martinsen, Amy E., Winsvold, Bendik S., Zwart, John-Anker, Bourcier, Romain, Sawada, Tomonobu, Koido, Masaru, Kamatani, Yoichiro, Morel, Sandrine, Amouyel, Philippe, Debette, Stéphanie, Bijlenga, Philippe, Berrandou, Takiy, Ganesh, Santhi K., Bouatia-Naji, Nabila, Jones, Gregory, Bown, Matthew, Rinkel, Gabriel J.E., Veldink, Jan H., Ruigrok, Ynte M., Hege Aamodt, Anne, Heidi Skogholt, Anne, Brumpton, Ben M., Willer, Cristen J., Sandset, Else C., Kristoffersen, Espen S., Ellekjær, Hanne ... International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group (2023). Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity. Stroke, 54 (3), 810-818. doi: 10.1161/STROKEAHA.122.040715

Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity

2023

Journal Article

Author Correction: 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 (2023). Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 55 (3), 520-520. doi: 10.1038/s41588-023-01336-8

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

2023

Journal Article

Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9

Weihs, Antoine, Chaker, Layal, Martin, Tiphaine Christiane, Braun, Kim V.E., Campbell, Purdey J, Cox, Simon R, Fornage, Myriam, Gieger, Christian, Grabe, Hans J, Grallert, Harald, Harris, Sarah E, Kühnel, Brigitte, Marioni, Riccardo E, Martin, Nicholas G, McCartney, Daniel L, McRae, Allan F, Meisinger, Christa, Meurs, Joyce van, Nano, Jana, Nauck, Matthias, Peters, Annette, Prokisch, Holger, Roden, Michael, Selvin, Elizabeth, Beekman, Marian, van Heemst, Diana, Slagboom, Eline P, Swenson, Brenton R, Tin, Adrienne ... Teumer, Alexander (2023). Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9. Thyroid (ja), 301-311. doi: 10.1089/thy.2022.0373

Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9

2023

Journal Article

Adolescent substance use and high school noncompletion: exploring the nature of the relationship using a discordant twin design

Davis, Christal N., Gizer, Ian R., Lynskey, Michael T., Statham, Dixie J., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2023). Adolescent substance use and high school noncompletion: exploring the nature of the relationship using a discordant twin design. Addiction, 118 (1), 167-176. doi: 10.1111/add.15996

Adolescent substance use and high school noncompletion: exploring the nature of the relationship using a discordant twin design

2023

Journal Article

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

Mathieson, Iain, Day, Felix R., Barban, Nicola, Tropf, Felix C., Brazel, David M., van Heemst, Diana, Vaez, Ahmad, van Zuydam, Natalie, Bitarello, Bárbara D., Gardner, Eugene J., Akimova, Evelina T., Azad, Ajuna, Bergmann, Sven, Bielak, Lawrence F., Boomsma, Dorret I., Bosak, Kristina, Brumat, Marco, Buring, Julie E., Cesarini, David, Chasman, Daniel I., Chavarro, Jorge E., Cocca, Massimiliano, Concas, Maria Pina, Davey Smith, George, Davies, Gail, Deary, Ian J., Esko, Tõnu, Faul, Jessica D., Franco, Oscar ... Perry, John R. B. (2023). Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nature Human Behaviour, 7 (5), 790-801. doi: 10.1038/s41562-023-01528-6

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

2022

Journal Article

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

Kanoni, Stavroula, Graham, Sarah E., Wang, Yuxuan, Surakka, Ida, Ramdas, Shweta, Zhu, Xiang, Clarke, Shoa L., Bhatti, Konain Fatima, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Zajac, Greg J. M., Wu, Kuan-Han H., Ntalla, Ioanna, Hui, Qin, Klarin, Derek, Hilliard, Austin T., Wang, Zeyuan, Xue, Chao, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma, Olafsson, Isleifur, Hwang, Mi Yeong, Han, Sohee, Akiyama, Masato, Sakaue, Saori ... Peloso, Gina M. (2022). Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biology, 23 (1) 268, 1-42. doi: 10.1186/s13059-022-02837-1

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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

Conference Publication

Exploring the relationship between acne and mental health

Mitchell, B., Saklatvala, J., Martin, N.G., Smith, C., Barker, J., Renteria, M. and Simpson, M. (2022). Exploring the relationship between acne and mental health. 51st Annual ESDR Meeting, Amsterdam, Netherlands, 28 September-1 October 2022. Oxford, United Kingdom: Elsevier. doi: 10.1016/j.jid.2022.09.318

Exploring the relationship between acne and mental health

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

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

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

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

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

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

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

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

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

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

  • Doctor Philosophy

    Genetic architecture of differences in symptomatology and treatment response in major depressive disorder

    Associate Advisor

    Other advisors: Honorary Professor Sarah Medland

  • Doctor Philosophy

    Genetic architecture of complex respiratory and sleep-related human traits

    Associate Advisor

  • Doctor Philosophy

    Statistical Genetic Approaches in Eye Diseases

    Associate Advisor

Completed supervision

Enquiries

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communications@uq.edu.au