Concepedia

Author

Alexandra Dürr

InsermORCID

Also Known As

A Durr, A Dürr, A. Benomar, A. DURR, A. Destée, A. Durr, A. Dürr, A. Dürr, ALEXANDRA DÜRR, Alexandra Durr

858

Publications

59.1K

Citations

119

H-Index

254

Concepts

All Affiliations

InsermSorbonne UniversitéAssistance Publique – Hôpitaux de ParisPitié-Salpêtrière HospitalInstitut du Cerveau
AD

About

Alexandra Dürr is an author at Inserm specializing in medicine, neurology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

77

178

23.5K

2

Health Sciences

12

13

1.2K

3

Natural Sciences

6

6

1.6K

4

Engineering

1

1

46

5

Language Studies

1

1

67

Alexandra Dürr

×

390

Publications

49.3K

Citations

109

H-Index

YearCitations

Second consensus statement on the diagnosis of multiple system atrophy

S. Gilman, Gregor K. Wenning, Phillip A. Low,

Neurology

2008

3.1K

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

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

New England Journal of Medicine

2009

2.1K

Scale for the assessment and rating of ataxia

T. Schmitz-Hübsch, Sophie Tézenas du Montcel, L. Baliko,

Neurology

2006

1.9K

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

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

Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data

Sarah J. Tabrizi, Douglas R. Langbehn, Blair R. Leavitt,

The Lancet Neurology

2009

959

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

Georges Imbert, Frédéric Saudou, Gaël Yvert,

Nature Genetics

1996

846

Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data

Sarah J. Tabrizi, Rachael I. Scahill, Gail Owen,

The Lancet Neurology

2013

822

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

Gilles David, Nacer Abbas, Giovanni Stévanin,

Nature Genetics

1997

769

Page 1