Y. Agid

A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

N. Abbas, C.B. Lücking, Sylvain Ricard et al. · Human Molecular Genetics · 1999 · 533 citations

Life Sciences, Genetics, Molecular Genetics +17

Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families

Alexandra Dürr, Olivier Didierjean, G. Imbert et al. · Human Molecular Genetics · 1997 · 256 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations

Olivier Dubourg, Alexandra Dürr, Giovanni Stévanin et al. · Annals of Neurology · 1995 · 83 citations

Life Sciences, Genetics, Neurology +16

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

Suzanne Lesage, Étienne Patin, Christel Condroyer et al. · Human Molecular Genetics · 2010 · 63 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)

E. Le Guern, F. Sturtz, Michel Gugenheim et al. · Cytogenetics and Cell Genetics · 2008 · 52 citations

Life Sciences, Genetics, Molecular Genetics +17