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George D. Mellick
George D. Mellick
Professor of Clinical Neuroscience
Verified email at griffith.edu.au - Homepage
Title
Cited by
Cited by
Year
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
16062019
Collaborative analysis of α-synuclein gene promoter variability and Parkinson disease
DM Maraganore, M De Andrade, A Elbaz, MJ Farrer, JP Ioannidis, ...
Jama 296 (6), 661-670, 2006
6102006
Prevalence of smell loss in Parkinson's disease–a multicenter study
A Haehner, S Boesveldt, HW Berendse, A Mackay-Sim, J Fleischmann, ...
Parkinsonism & related disorders 15 (7), 490-494, 2009
5332009
Anxiety disorders in Parkinson's disease: prevalence and risk factors
NNW Dissanayaka, A Sellbach, S Matheson, JD O'Sullivan, PA Silburn, ...
Movement Disorders 25 (7), 838-845, 2010
4602010
Parkinson's disease, pesticides, and glutathione transferase polymorphisms
A Menegon, PG Board, AC Blackburn, GD Mellick, DG Le Couteur
The Lancet 352 (9137), 1344-1346, 1998
4241998
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study
OA Ross, AI Soto-Ortolaza, MG Heckman, JO Aasly, N Abahuni, G Annesi, ...
The Lancet Neurology 10 (10), 898-908, 2011
3432011
UCHL1 is a Parkinson's disease susceptibility gene
DM Maraganore, TG Lesnick, A Elbaz, MC Chartier‐Harlin, T Gasser, ...
Annals of neurology 55 (4), 512-521, 2004
3332004
The Vps35 D620N mutation linked to Parkinson's disease disrupts the cargo sorting function of retromer
J Follett, SJ Norwood, NA Hamilton, M Mohan, O Kovtun, S Tay, Y Zhe, ...
Traffic 15 (2), 230-244, 2014
2502014
GSK3B polymorphisms alter transcription and splicing in Parkinson's disease
JBJ Kwok, M Hallupp, CT Loy, DKY Chan, J Woo, GD Mellick, ...
Annals of Neurology: Official Journal of the American Neurological …, 2005
2492005
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology
GR Wilson, JCH Sim, C McLean, M Giannandrea, CA Galea, JR Riseley, ...
The American Journal of Human Genetics 95 (6), 729-735, 2014
2412014
Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
Q Zhang, CL Vallerga, RM Walker, T Lin, AK Henders, GW Montgomery, ...
Genome medicine 11, 1-11, 2019
2382019
Disease-specific, neurosphere-derived cells as models for brain disorders
N Matigian, G Abrahamsen, R Sutharsan, AL Cook, AM Vitale, ...
Disease models & mechanisms 3 (11-12), 785-798, 2010
2222010
Imagining an interdisciplinary doctoral pedagogy
C Manathunga, P Lant, G Mellick
Teaching in Higher Education 11 (3), 365-379, 2006
2072006
Tau haplotypes regulate transcription and are associated with Parkinson's disease
JBJ Kwok, ET Teber, C Loy, M Hallupp, G Nicholson, GD Mellick, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
2012004
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population
M Saad, S Lesage, A Saint-Pierre, JC Corvol, D Zelenika, JC Lambert, ...
Human molecular genetics 20 (3), 615-627, 2011
1962011
Factors associated with depression in Parkinson's disease
NNW Dissanayaka, A Sellbach, PA Silburn, JD O'Sullivan, R Marsh, ...
Journal of affective disorders 132 (1-2), 82-88, 2011
1802011
Large-scale replication and heterogeneity in Parkinson disease genetic loci
M Sharma, JPA Ioannidis, JO Aasly, G Annesi, A Brice, ...
Neurology 79 (7), 659-667, 2012
1582012
Variance of gene expression identifies altered network constraints in neurological disease
JC Mar, NA Matigian, A Mackay-Sim, GD Mellick, CM Sue, PA Silburn, ...
PLoS genetics 7 (8), e1002207, 2011
1582011
Heterozygous PINK1 p. G411S increases risk of Parkinson’s disease via a dominant-negative mechanism
A Puschmann, FC Fiesel, TR Caulfield, R Hudec, M Ando, D Truban, ...
Brain 140 (1), 98-117, 2017
1392017
Variations in the monoamine oxidase B lpar; MAOB) gene are associated with Parkinson's disease
GD Mellick, DD Buchanan, SJ McCann, KM James, AG Johnson, ...
Movement disorders: official journal of the Movement Disorder Society 14 (2 …, 1999
1231999
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