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alexis brice
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Year
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
43032013
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
34202003
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
32161996
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
JC Lambert, S Heath, G Even, D Campion, K Sleegers, M Hiltunen, ...
Nature genetics 41 (10), 1094-1099, 2009
27672009
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
22182009
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
21692003
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
21432011
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
21312019
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
19802014
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
19112000
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
16392008
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
A Rovelet-Lecrux, D Hannequin, G Raux, NL Meur, A Laquerrière, A Vital, ...
Nature genetics 38 (1), 24-26, 2006
15352006
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
14962019
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
13282004
Parkinson's disease: from monogenic forms to genetic susceptibility factors
S Lesage, A Brice
Human molecular genetics 18 (R1), R48-R59, 2009
12872009
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
12852012
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
12852000
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
12261996
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
10951999
First genetic evidence of GABAA 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
10552001
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