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Author
Alexis Brice
also known as A BRICE, A Brice, A. (c) Brice
Université Claude Bernard Lyon 1 · Université Paris-Sud · Délégation Paris 5 · Boston University
About this author
Works
1,189
Cited by
116,457
h-index
154
i10
804
ORCID ↗
Top papers
Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren, et al.
·
2003
·
Science
↗ 2,770
Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion
Victoria Campuzano, Laura Montermini, María Dolores Moltó, et al.
·
1996
·
Science
↗ 2,766
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, et al.
·
2019
·
The Lancet Neurology
↗ 2,501
OA
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
E. Sidransky, Mike A. Nalls, Jan Aasly, et al.
·
2009
·
New England Journal of Medicine
↗ 2,104
OA
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Mike A. Nalls, 23andMe, GenePD, et al.
·
2014
·
Nature Genetics
↗ 1,956
OA
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
Daniel G. Healy, Mario Falchi, Sean S. O’Sullivan, et al.
·
2008
·
The Lancet Neurology
↗ 1,551
OA
Association between Early-Onset Parkinson's Disease and Mutations in the<i>Parkin</i>Gene
Christoph B. Lücking, Alexandra Dürr, Vincenzo Bonifati, et al.
·
2000
·
New England Journal of Medicine
↗ 1,422
OA
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
Anne Rovelet‐Lecrux, Didier Hannequin, Grégory Raux, et al.
·
2005
·
Nature Genetics
↗ 1,249
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie, Alan E. Renton, Kin Y. Mok, et al.
·
2012
·
The Lancet Neurology
↗ 1,215
OA
Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
Alexandra Dürr, Mireille Cossée, Yves Agid, et al.
·
1996
·
New England Journal of Medicine
↗ 1,067
OA
Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease
Pablo Ibáñez, A-M Bonnet, Béatrice Debarges, et al.
·
2004
·
The Lancet
↗ 1,045
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
Andrew Escayg, Bryan T. MacDonald, Miriam H. Meisler, et al.
·
2000
·
Nature Genetics
↗ 987