Browsing by Author Mellick, George

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Issue DateTitleAuthor(s)Citation
2002The Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patientsLe Couteur, David; Buchanan, Daniel D.; Chalk, J.B.; Mellick, George; Silburn, P.A.; Concord Clinical School: ANZAC Research InstituteThe Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patients, Neuroscience Letters, vol.327,(2),2002,pp 91-94
2014DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitroArmstrong, Nicola Joy; Brodaty, Henry; Coupland, Kirsten; Dobston-Stone, Carol; Halliday, Glenda; Hallupp, Marianne; Huang, Yue; Kim, Woojin S; Kwok, John; Mather, Karen A; Mellick, George; Sachdev, Perminder; Silburn, Peter A.; Mathematics & StatisticsDNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro, Movement Disorders, vol.29, 13, 2014,pp 1606-1614
2007A functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's diseaseRowe, Dominic; Sue, Carolyn; Chan, Daniel K. Y.; Halliday, Glenda M.; Mellick, George; Silburn, Peter; Sutherland, Greg; Northern Clinical School: Medicine; Northern Clinical School: MedicineA functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's disease, Neuroscience Letters (2005), vol.414,(2),2007,pp 170-173
2008Haplotype analysis of the IGF2-INS-TH gene cluster in Parkinson's diseaseRowe, Dominic; Double, Kay L.; Halliday, Glenda; Lee, Linda; Mellick, George; Newman, Jeremy; Silburn, Peter; Stevens, Julia; Sutherland, Greg; Northern Clinical School: MedicineHaplotype analysis of the IGF2-INS-TH gene cluster in Parkinson's disease, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol.147B, 4, 2008,pp 495-499
2011Knowing Me, Knowing You: Can a Knowledge of Risk Factors for Alzheimer's Disease Prove Useful in Understanding the Pathogenesis of Parkinson's Disease?Kril, Jillian; Sutherland, Greg; Mellick, George; Siebert, Gerhard; Central Clinical School: Medicine; School of Medical Sciences: PathologyKnowing Me, Knowing You: Can a Knowledge of Risk Factors for Alzheimer's Disease Prove Useful in Understanding the Pathogenesis of Parkinson's Disease?, Journal of Alzheimer's Disease, vol.25, 3, 2011,pp 395-415
2009Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian communityHalliday, Glenda; Jones, Michael; Manwaring, Neil; Mehta, Prachi; Mitchell, Ronald (Paul); Rowe, Dominic; Sue, Carolyn; Vandebona, Himesha; Wang, Jie Jin; Mellick, George; Silburn, P A; Medicine Faculty Office; Clinical Schools; Northern Clinical School: Kolling Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Northern Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Kolling Institute; Western Clinical School: Westmead Millennium InstituteMitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community, Movement Disorders, vol.24,(2),2009,pp 290-292
2007Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's diseaseHalliday, Glenda; Rowe, Dominic; Sue, Carolyn; Vandebona, Himesha; Garlepp, Michael; Horne, Malcolm; Huang, Yue; Kotschet, Katya; Kwok, John B.J.; Mastaglia, Frank; Mellick, George; Rubio, Justin P.; Silburn, Peter A.; Stevens, Julia; Venn, Alison; Medicine Faculty Office; Northern Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Molecular Medicine (Kolling I)Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease, Movement Disorders (2005), vol.22,(7),2007,pp 982-989
2011Variance of Gene Expression Identifies Altered Network Constraints in Neurological DiseaseSue, Carolyn; Mackay-Sim, Alan; Mar, Jessica; Matigian, Nicholas; McGrath, John; Mellick, George; Quackenbush, John; Silburn, Peter A.; Wells, Christine A.; Northern Clinical School: MedicineVariance of Gene Expression Identifies Altered Network Constraints in Neurological Disease, PLoS Genetics, vol.7, 8, 2011,pp 1-12