alexis brice
alexis brice
Verified email at icm-institute.org
Title
Cited by
Cited by
Year
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
D Harold, R Abraham, P Hollingworth, R Sims, A Gerrish, ML Hamshere, ...
Nature genetics 41 (10), 1088, 2009
3074*2009
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
V Bonifati, P Rizzu, MJ Van Baren, O Schaap, GJ Breedveld, E Krieger, ...
science 299 (5604), 256-259, 2003
27482003
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion
V Campuzano, L Montermini, MD Molto, L Pianese, M Cossée, ...
Science 271 (5254), 1423-1427, 1996
26991996
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
25312013
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
S Jamain, H Quach, C Betancur, M Råstam, C Colineaux, IC Gillberg, ...
Nature genetics 34 (1), 27-29, 2003
18072003
Association between early-onset Parkinson's disease and mutations in the parkin gene
CB Lücking, A Dürr, V Bonifati, J Vaughan, G De Michele, T Gasser, ...
New England Journal of Medicine 342 (21), 1560-1567, 2000
16222000
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ...
Nature genetics 43 (5), 429-435, 2011
15462011
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
14252009
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
A Rovelet-Lecrux, D Hannequin, G Raux, N Le Meur, A Laquerrière, ...
Nature genetics 38 (1), 24-26, 2006
12552006
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
11912014
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ...
The Lancet Neurology 7 (7), 583-590, 2008
11582008
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+ 2
A Escayg, BT MacDonald, MH Meisler, S Baulac, G Huberfeld, ...
Nature genetics 24 (4), 343-345, 2000
10982000
Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease
P Ibanez, AM Bonnet, B Debarges, E Lohmann, F Tison, Y Agid, A Dürr, ...
The Lancet 364 (9440), 1169-1171, 2004
10522004
Clinical and genetic abnormalities in patients with Friedreich's ataxia
A Dürr, M Cossee, Y Agid, V Campuzano, C Mignard, C Penet, JL Mandel, ...
New England Journal of Medicine 335 (16), 1169-1175, 1996
10091996
Parkinson's disease: from monogenic forms to genetic susceptibility factors
S Lesage, A Brice
Human molecular genetics 18 (R1), R48-R59, 2009
9692009
First genetic evidence of GABA A receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene
S Baulac, G Huberfeld, I Gourfinkel-An, G Mitropoulou, A Beranger, ...
Nature genetics 28 (1), 46-48, 2001
9072001
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
8812012
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
G Imbert, F Saudou, G Yvert, D Devys, Y Trottier, JM Garnier, C Weber, ...
Nature genetics 14 (3), 285-291, 1996
8731996
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum
D Campion, C Dumanchin, D Hannequin, B Dubois, S Belliard, M Puel, ...
The American Journal of Human Genetics 65 (3), 664-670, 1999
8711999
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
G David, N Abbas, G Stevanin, A Dürr, G Yvert, G Cancel, C Weber, ...
Nature genetics 17 (1), 65-70, 1997
8351997
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