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

1492 works between 1975 and 2025
All (1492) Journal Article (1374) Other Outputs (1) Conference Publication (103) Book Chapter (14)

561 - 580 of 1492 works

2014

Journal Article

Sex differences in magical ideation: A community-based twin study

Karcher, Nicole R., Slutske, Wendy S., Kerns, John G., Piasecki, Thomas M. and Martin, Nicholas G. (2014). Sex differences in magical ideation: A community-based twin study. Personality Disorders-Theory Research and Treatment, 5 (2), 212-219. doi: 10.1037/per0000040

Sex differences in magical ideation: A community-based twin study

2014

Journal Article

Genome-wide association study reveals two new risk loci for bipolar disorder

Muehleisen, Thomas W., Leber, Markus, Schulze, Thomas G., Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Forstner, Andreas J., Schumacher, Johannes, Breuer, Rene, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, Andre, Witt, Stephanie H., Reif, Andreas, Mueller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Priebe, Lutz, Czerski, Piotr M., Hauser, Joanna ... Cichon, Sven (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. Nature Communications, 5 (3339) 3339, 1-8. doi: 10.1038/ncomms4339

Genome-wide association study reveals two new risk loci for bipolar disorder

2014

Journal Article

ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins

De Alwis, Duneesha, Agrawal, Arpana, Reiersen, Angela M., Constantino, John N., Henders, Anjali, Martin, Nicholas G. and Lynskey, Michael T. (2014). ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins. Journal of Studies On Alcohol and Drugs, 75 (2), 211-221. doi: 10.15288/jsad.2014.75.211

ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins

2014

Journal Article

Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis

Fede, Giuseppe, Spadaro, Luisa, Tomaselli, Tania, Privitera, Graziella, Scicali, Roberto, Vasianopoulou, Panayota, Thalassinos, Evangelos, Martin, Nicholas, Thomas, Michael, Purrello, Francesco and Burroughs, Andrew Kenneth (2014). Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis. Clinical Gastroenterology and Hepatology, 12 (3), 504-512. doi: 10.1016/j.cgh.2013.08.028

Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis

2014

Journal Article

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

Ligthart, Lannie, Hottenga, Jouke-Jan, Lewis, Cathryn M., Farmer, Anne E., Craig, Ian W., Breen, Gerome, Willemsen, Gonneke, Vink, Jacqueline M., Middeldorp, Christel M., Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W., Martin, Nicholas G., Penninx, Brenda W. J. H., McGuffin, Peter, Boomsma, Dorret I. and Nyholt, Dale R. (2014). Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders. Human Genetics, 133 (2), 173-186. doi: 10.1007/s00439-013-1370-8

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

2014

Journal Article

Modeling of the hemodynamic responses in block design fMRI studies

Shan, Zuyao Y., Wright, Margaret J., Thompson, Paul M., McMahon, Katie L., Blokland, Gabriella G. A. M., de Zubicaray, Greig I., Martin, Nicholas G., Vinkhuyzen, Anna A. E. and Reutens, David C. (2014). Modeling of the hemodynamic responses in block design fMRI studies. Journal of Cerebral Blood Flow and Metabolism, 34 (2), 316-324. doi: 10.1038/jcbfm.2013.200

Modeling of the hemodynamic responses in block design fMRI studies

2014

Journal Article

Genetic effects on the cerebellar role in working memory: same brain, different genes?

Blokland, Gabriëlla A. M., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2014). Genetic effects on the cerebellar role in working memory: same brain, different genes?. NeuroImage, 86, 392-403. doi: 10.1016/j.neuroimage.2013.10.006

Genetic effects on the cerebellar role in working memory: same brain, different genes?

2014

Journal Article

Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences

Richmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2014). Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences. Addiction, 109 (2), 323-331. doi: 10.1111/add.12310

Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences

2014

Journal Article

Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013)

Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, Rene C., Nichols, Thomas E., Almasy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Pol, Hilleke E. Hulshoff, Bastin, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2014). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013). Neuroimage, 90, 470-471. doi: 10.1016/j.neuroimage.2013.12.053

Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013)

2014

Journal Article

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins

Hill, W. D., Davies, G., Van De Lagemaat, L. N., Christoforou, A., Marioni, R. E., Fernandes, C. P. D., Liewald, D. C., Croning, M. D. R., Payton, A., Craig, L. C. A., Whalley, L. J., Horan, M., Ollier, W., Hansell, N. K., Wright, M. J., Martin, N. G., Montgomery, G. W., Steen, V. M., Le Hellard, S., Espeseth, T., Lundervold, A. J., Reinvang, I., Starr, J. M., Pendleton, N., Grant, S. G. N., Bates, T. C. and Deary, I. J. (2014). Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins. Translational Psychiatry, 4 (1) e341, 1-8. doi: 10.1038/tp.2013.114

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins

2014

Journal Article

DNA modification study of major depressive disorder: beyond locus-by-locus comparisons

Oh, Gabriel, Wang, Sun-Chong, Pal, Mrinal, Chen, Zheng Fei, Khare, Tarang, Tochigi, Mamoru, Ng, Catherine, Yang, Yeqing A., Kwan, Andrew, Kaminsky, Zachary A., Mill, Jonathan, Gunasinghe, Cerisse, Tackett, Jennifer L., Gottesman, Irving I., Willemsen, Gonneke, de Geus, Eco J. C., Vink, Jacqueline M., Slagboom, P. Eline, Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Turecki, Gustavo, Martin, Nicholas G., Boomsma, Dorret I., McGuffin, Peter, Kustra, Rafal and Petronis, Art (2014). DNA modification study of major depressive disorder: beyond locus-by-locus comparisons. Biological Psychiatry, 77 (3), 246-255. doi: 10.1016/j.biopsych.2014.06.016

DNA modification study of major depressive disorder: beyond locus-by-locus comparisons

2014

Journal Article

Genetic predisposition to schizophrenia associated with increased use of cannabis

Power, R. A., Verweij, K. J. H., Zuhair, M., Montgomery, G. W., Henders, A. K., Heath, A. C., Madden, P. A. F., Medland, S. E., Wray, N. R. and Martin, N. G. (2014). Genetic predisposition to schizophrenia associated with increased use of cannabis. Molecular Psychiatry, 19 (11), 1201-1204. doi: 10.1038/mp.2014.51

Genetic predisposition to schizophrenia associated with increased use of cannabis

2014

Conference Publication

Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure

Warstadt, Nicholus M., Jahanshad, Neda, Dennis, Emily L., Kohannim, Omid, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Wright, Margaret J. and Thompson, Paul M. (2014). Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure. Biomedical Imaging ISBI, Beijing, China, 29 April - 2 May, 2014. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2014.6867881

Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure

2014

Journal Article

Sexual orientation, prejudice, and segregation

Plug, Erik, Webbink, Dinand and Martin, Nick (2014). Sexual orientation, prejudice, and segregation. Journal of Labor Economics, 32 (1), 123-159. doi: 10.1086/673315

Sexual orientation, prejudice, and segregation

2014

Journal Article

Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index

Hoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J.H., Teumer, A., Winkler, T. W., Tsernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Mace, A., Rueger, S., Bochud, P.-Y., Barcella, M., Dauvilliers, Y., Benyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S. ... Kutalik Z. (2014). Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index. PLoS Genetics, 10 (7) e1004508, 1-12. doi: 10.1371/journal.pgen.1004508

Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index

2014

Journal Article

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

Li, M., Luo, X-j, Rietschel, M., Lewis, C. M., Mattheisen, M., Mueller-Myhsok, B., Jamain, S., Leboyer, M., Landen, M., Thompson, P. M., Cichon, S., Noethen, M. M., Schulze, T. G., Sullivan, P. F., Bergen, S. E., Donohoe, G., Morris, D. W., Hargreaves, A., Gill, M., Corvin, A., Hultman, C., Toga, A. W., Shi, L., Lin, Q., Shi, H., Gan, L., Meyer-Lindenberg, A., Czamara, D., Henry, C. ... Su, B. (2014). Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4), 452-461. doi: 10.1038/mp.2013.37

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

2014

Journal Article

POT1 loss-of-function variants predispose to familial melanoma

Robles-Espinoza, Carla Daniela, Harland, Mark, Ramsay, Andrew J, Aoude, Lauren G, Quesada, Víctor, Ding, Zhihao, Pooley, Karen A, Pritchard, Antonia L, Tiffen, Jessamy C, Petljak, Mia, Palmer, Jane M, Symmons, Judith, Johansson, Peter, Stark, Mitchell S., Gartside, Michael G, Snowden, Helen, Montgomery, Grant W, Martin, Nicholas G, Liu, Jimmy Z, Choi, Jiyeon, Makowski, Matthew, Brown, Kevin M, Dunning, Alison M, Keane, Thomas M, Lopez-Otin, Carlos, Gruis, Nelleke A, Hayward, Nicholas K, Bishop, D Timothy, Newton-Bishop, Julia A and Adams, David J (2014). POT1 loss-of-function variants predispose to familial melanoma. Nature Genetics, 46 (5), 478-481. doi: 10.1038/ng.2947

POT1 loss-of-function variants predispose to familial melanoma

2014

Book Chapter

Direction of causation models

Gillespie, Nathan A. and Martin, Nicholas G. (2014). Direction of causation models. Wiley StatsRef: Statistics Reference Online. (pp. *-*) Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06685

Direction of causation models

2014

Journal Article

Heritability of head motion during resting state functional MRI in 462 healthy twins

Couvy-Duchesne, Baptiste, Blokland, Gabriëlla A.M., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L. and Wright, Margaret J. (2014). Heritability of head motion during resting state functional MRI in 462 healthy twins. Neuroimage, 102 (2), 424-434. doi: 10.1016/j.neuroimage.2014.08.010

Heritability of head motion during resting state functional MRI in 462 healthy twins

2014

Journal Article

Testing the role of circadian genes in conferring risk for psychiatric disorders

Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G. and Wray, Naomi R. (2014). Testing the role of circadian genes in conferring risk for psychiatric disorders. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 165 (3), 254-260. doi: 10.1002/ajmg.b.32230

Testing the role of circadian genes in conferring risk for psychiatric disorders

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

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