Browsing by Author Montgomery, Grant W.

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Issue DateTitleAuthor(s)Citation
2013Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma riskCust, Anne; Mann, Graham; Amos, Christopher; Barrett, Jennifer H.; Chen, Wei; et al, Various; Iles, Mark; Law, Matthew; Lee, Jeffrey; Liu, Hongliang; Liu, Zhensheng; Montgomery, Grant W.; Taylor, John C.; Wang, Li-E; School of Public Health: Public Health; Western Clinical School: Westmead Millennium InstituteAssociation between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk, Carcinogenesis, vol.34, 4, 2013,pp 885-892
2006Butyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity.Whitfield, John; Martin, Nicholas G.; Montgomery, Grant W.; O'Connor, Daniel T.; Slagboom, P. Eline; Taylor, Palmer; Valle, Anne; Zhu, Gu; Central Clinical School: MedicineButyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity., Clinical Chemistry (Washington, DC): international journal of molecular diagnostics and laboratory medicine, vol.52,(6),2006,pp 1014-1020
2010Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal ThicknessHealey, Paul; Mitchell, Paul (Ronald); Burdon, Kathryn P; Craig, Jamie; Dimasi, David P; Hammond, Christopher J; Hansell, Narelle K; Hewitt, Alex; Hysi, Pirro; Li, Yi Ju; Lu, Yi; MacGregor, Stuart; Mackay, David A.; Martin, Nicholas G.; Montgomery, Grant W.; Ruddle, Jonathan; Spector, Tim; Toh, Tze'Yo; Young, Terri; Western Clinical School: Clinical Ophthal & Eye Health; Western Clinical School: Westmead Millennium InstituteCommon Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness, PLoS Genetics, vol.6, 5,pp e1000947 - 1-e1000947 - 10
2008Common sequence variants on 20q11.22 confer melanoma susceptibilityArmstrong, Bruce; Holland, Elizabeth; Kefford, Richard (Rick); Mann, Graham; Schmid, Helen; Brown, Kevin M; Campbell, M; Craig, David W; et al, Various; Henders, Anjali; Homer, Nils; Iyadurai, Kelly; MacGregor, Stuart; Montgomery, Grant W.; Stark, Mitchell; Thomas, Shane; Zhao, Zhen Zhen; School of Public Health: Public Health; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead)Common sequence variants on 20q11.22 confer melanoma susceptibility, Nature Genetics, vol.40, 7, 2008,pp 838-840
2007Evidence of genetic effects on blood lead concentrationWhitfield, John; Duffy, David L; Dy, Veronica; Ferreira, Manuel A R; Heath, Andrew C.; Heijmans, Bas T; Martin, Nicholas G.; McQuilty, Robert; Montgomery, Grant W.; Neale, Michael C.; Zhu, Gu; Central Clinical School: MedicineEvidence of genetic effects on blood lead concentration, Environmental Health Perspectives, vol.115,(8),2007,pp 1224-1230
2014Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancerClarke, Christine; Jane, Carpenter; Anton-Culver, Hoda; Chang-Claude, Jenny; Eccles, Diana; et al, Various; fasching, Peter A.; Goodfellow, Paul; Kristensen, Vessela Nedelcheva; Martin, Nicholas G.; Miron, Penelope; Montgomery, Grant W.; Purrington, Kristen S; Slager, Susan; Tapper, William J; Yannoukakos, Drakoulis; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium InstituteGenome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer, Carcinogenesis, vol.35, 5, 2014,pp 1012-1019
2011Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3Armstrong, Bruce; Cust, Anne; Holland, Elizabeth; Kefford, Richard (Rick); Mann, Graham; Schmid, Helen; Duffy, David L; et al, various; Henders, Anjali; Liu, Jimmy; MacGregor, Stuart; Montgomery, Grant W.; Nyholt, Dale; Painter, Jodie; Stark, Mitchell; Zhang, Mingfeng; Zhao, Zhen Zhen; School of Public Health: Public Health; School of Public Health: Public Health; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead)Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3, Nature Genetics, vol.43, 11, 2011,pp 1114-1119
2013A Genome-Wide Association Study of Sleep Habits and InsomniaHickie, Ian; Byrne, Edna; Gehrman, Philip; Heath, Andrew C.; Henders, Anjali; Madden, Pamela A.F.; Martin, Nicholas G.; Medland, Sarah E; Montgomery, Grant W.; Nyholt, Dale; van Duijn, Cornelia M.; Wray, Naomi; School of Medical Sciences: Brain & Mind Research InstituteA Genome-Wide Association Study of Sleep Habits and Insomnia, American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, vol.162B, 5, 2013,pp 439-451
2017Genome-wide association study of working memory brain activationHickie, Ian; Blokland, Gabriella; de Zubicaray, Greig; Hansell, Narelle K; Martin, N. G.; McMahon, Katie; Montgomery, Grant W.; Thompson, Paul; Wallace, Angus; Wright, Margie J.; Central Clinical School: PsychiatryGenome-wide association study of working memory brain activation, International Journal of Psychophysiology, vol.115, N/A, 2017,pp 98-111
2014Testing the role of circadian genes in conferring risk for psychiatric disordersHickie, Ian; Byrne, Enda; Heath, Andrew C.; Madden, Pamela A.F.; Martin, Nicholas; Montgomery, Grant W.; Pergadia, Michele; Wray, Naomi; School of Medical Sciences: Brain & Mind Research InstituteTesting the role of circadian genes in conferring risk for psychiatric disorders, American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, vol.165, 3, 2014,pp 254-260