Concepedia

Author

Alexis Brice

InsermORCID

Also Known As

A BRICE, A Brice, A. (c) Brice, A. BRICE, A. Brice, A. Brice*, ALEXIS BRICE, Aaron D. Gitler, Agnès Camuzat, Alberto Benussi

1.2K

Publications

115.3K

Citations

154

H-Index

225

Concepts

All Affiliations

InsermSorbonne UniversitéPitié-Salpêtrière HospitalAssistance Publique – Hôpitaux de ParisCentre National de la Recherche Scientifique
AB

About

Alexis Brice is an author at Inserm specializing in medicine, genetics, and neurology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

98

313

40.9K

2

Natural Sciences

16

16

2.4K

3

Health Sciences

13

13

1.9K

4

Arts

1

1

12

5

Engineering

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45

Alexis Brice

×

649

Publications

78.8K

Citations

138

H-Index

YearCitations

Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren,

Science

2003

2.8K

Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

Victoria Campuzano, Laura Montermini, María Dolores Moltó,

Science

1996

2.7K

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

E. Sidransky, Mike A. Nalls, Jan Aasly,

New England Journal of Medicine

2009

2.1K

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,

The Lancet Neurology

2008

1.5K

Association between Early-Onset Parkinson's Disease and Mutations in the<i>Parkin</i>Gene

Christoph B. Lücking, Alexandra Dürr, Vincenzo Bonifati,

New England Journal of Medicine

2000

1.4K

Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease

Valentina Escott‐Price, Céline Bellenguez, Li‐San Wang,

PLoS ONE

2014

1.4K

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

Anne Rovelet‐Lecrux, Didier Hannequin, Grégory Raux,

Nature Genetics

2005

1.2K

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,

The Lancet Neurology

2012

1.2K

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia

Alexandra Dürr, Mireille Cossée, Yves Agid,

New England Journal of Medicine

1996

1.1K

Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease

Pablo Ibáñez, A-M Bonnet, Béatrice Debarges,

The Lancet

2004

1K

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