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Matt Farrer
Matt Farrer
University of Florida
Verified email at can.ubc.ca - Homepage
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Cited by
Year
α-Synuclein locus triplication causes Parkinson's disease
AB Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, ...
science 302 (5646), 841-841, 2003
51872003
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
A Zimprich, S Biskup, P Leitner, P Lichtner, M Farrer, S Lincoln, ...
Neuron 44 (4), 601-607, 2004
34092004
α-synuclein locus duplication as a cause of familial Parkinson's disease
MC Chartier-Harlin, J Kachergus, C Roumier, V Mouroux, X Douay, ...
The Lancet 364 (9440), 1167-1169, 2004
25012004
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
22402009
VPS35 mutations in Parkinson disease
C Vilariño-Güell, C Wider, OA Ross, JC Dachsel, JM Kachergus, ...
The American Journal of Human Genetics 89 (1), 162-167, 2011
10502011
Missing pieces in the Parkinson's disease puzzle
JA Obeso, MC Rodriguez-Oroz, CG Goetz, C Marin, JH Kordower, ...
Nature medicine 16 (6), 653-661, 2010
9782010
Genetics of Parkinson disease: paradigm shifts and future prospects
MJ Farrer
Nature Reviews Genetics 7 (4), 306-318, 2006
9562006
Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplications
M Farrer, J Kachergus, L Forno, S Lincoln, DS Wang, M Hulihan, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
8662004
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
7822009
Alpha‐synuclein p. H50Q, a novel pathogenic mutation for Parkinson's disease
S Appel‐Cresswell, C Vilarino‐Guell, M Encarnacion, H Sherman, I Yu, ...
Movement disorders 28 (6), 811-813, 2013
7662013
α-Synuclein shares physical and functional homology with 14-3-3 proteins
N Ostrerova, L Petrucelli, M Farrer, N Mehta, P Choi, J Hardy, B Wolozin
Journal of Neuroscience 19 (14), 5782-5791, 1999
7401999
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
7182010
Parkin protects against the toxicity associated with mutant α-synuclein: proteasome dysfunction selectively affects catecholaminergic neurons
L Petrucelli, C O'Farrell, PJ Lockhart, M Baptista, K Kehoe, L Vink, P Choi, ...
Neuron 36 (6), 1007-1019, 2002
7072002
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
J Kachergus, IF Mata, M Hulihan, JP Taylor, S Lincoln, J Aasly, JM Gibson, ...
The American Journal of Human Genetics 76 (4), 672-680, 2005
6312005
Lewy bodies and parkinsonism in families with parkin mutations
M Farrer, P Chan, R Chen, L Tan, S Lincoln, D Hernandez, L Forno, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
6182001
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699-705, 2011
6172011
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
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
6072006
High-resolution whole-genome association study of Parkinson disease
DM Maraganore, M De Andrade, TG Lesnick, KJ Strain, MJ Farrer, ...
The American Journal of Human Genetics 77 (5), 685-693, 2005
5992005
LRRK2 in Parkinson's disease: protein domains and functional insights
IF Mata, WJ Wedemeyer, MJ Farrer, JP Taylor, KA Gallo
Trends in neurosciences 29 (5), 286-293, 2006
5882006
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