Suivre
William K. Scott
William K. Scott
Professor of Human Genetics, University of Miami
Adresse e-mail validée de med.miami.edu
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Année
Complement factor H variant increases the risk of age-related macular degeneration
JL Haines, MA Hauser, S Schmidt, WK Scott, LM Olson, P Gallins, ...
Science 308 (5720), 419-421, 2005
30252005
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
19972014
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
14252016
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
TH Hamza, CP Zabetian, A Tenesa, A Laederach, J Montimurro, ...
Nature genetics 42 (9), 781-785, 2010
8862010
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
8582013
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
JM Van Der Walt, KK Nicodemus, ER Martin, WK Scott, MA Nance, ...
The American Journal of Human Genetics 72 (4), 804-811, 2003
6522003
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
CM Lill, JT Roehr, MB McQueen, FK Kavvoura, S Bagade, BMM Schjeide, ...
PLoS genetics 8 (3), e1002548, 2012
6122012
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
W Chen, D Stambolian, AO Edwards, KE Branham, M Othman, ...
Proceedings of the National Academy of Sciences 107 (16), 7401-7406, 2010
6052010
Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
TL Edwards, WK Scott, C Almonte, A Burt, EH Powell, GW Beecham, ...
Annals of human genetics 74 (2), 97-109, 2010
5732010
Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of α-synuclein
G Wang, JM van der Walt, G Mayhew, YJ Li, S Züchner, WK Scott, ...
The American Journal of Human Genetics 82 (2), 283-289, 2008
5572008
Complete genomic screen in late-onset familial Alzheimer disease: evidence for a new locus on chromosome 12
MA Pericak-Vance, MP Bass, LH Yamaoka, PC Gaskell, WK Scott, ...
Jama 278 (15), 1237-1241, 1997
4661997
Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration
S Schmidt, MA Hauser, WK Scott, EA Postel, A Agarwal, P Gallins, ...
The American Journal of Human Genetics 78 (5), 852-864, 2006
4142006
Age at onset in two common neurodegenerative diseases is genetically controlled
YJ Li, WK Scott, DJ Hedges, F Zhang, PC Gaskell, MA Nance, RL Watts, ...
The American Journal of Human Genetics 70 (4), 985-993, 2002
3862002
Pesticide exposure and risk of Parkinson's disease: a family-based case-control study
DB Hancock, ER Martin, GM Mayhew, JM Stajich, R Jewett, MA Stacy, ...
BMC neurology 8, 1-12, 2008
3652008
Complete genomic screen in Parkinson disease: evidence for multiple genes
WK Scott, MA Nance, RL Watts, JP Hubble, WC Koller, K Lyons, R Pahwa, ...
Jama 286 (18), 2239-2244, 2001
3492001
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease
KY Hui, H Fernandez-Hernandez, J Hu, A Schaffner, N Pankratz, NY Hsu, ...
Science translational medicine 10 (423), eaai7795, 2018
3472018
Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2
N Pankratz, GW Beecham, AL DeStefano, TM Dawson, KF Doheny, ...
Annals of neurology 71 (3), 370-384, 2012
3372012
Analysis of European mitochondrial haplogroups with Alzheimer disease risk
JM van der Walt, YA Dementieva, ER Martin, WK Scott, KK Nicodemus, ...
Neuroscience letters 365 (1), 28-32, 2004
3272004
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease
YJ Li, SA Oliveira, P Xu, ER Martin, JE Stenger, CR Scherzer, MA Hauser, ...
Human molecular genetics 12 (24), 3259-3267, 2003
2992003
Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study
RN Alcalay, E Caccappolo, H Mejia-Santana, MX Tang, L Rosado, ...
Neurology 78 (18), 1434-1440, 2012
2962012
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