E. Becquet

No genetic association of the Ubiquitin Carboxy-terminal Hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease

Clotilde Lévecque, A. Destée, Vincent Mouroux et al. · Journal of Neural Transmission · 2001 · 44 citations

Neurodegenerative Diseases, Mendelian Disorder, Familial Parkinson +8

Neuropsychological abnormalities in first degree relatives of patients with familial Parkinson's disease

Kathy Dujardin, Alain Duhamel, E. Becquet et al. · Journal of Neurology Neurosurgery & Psychiatry · 1999 · 36 citations · Full text

Linkage exclusion in French families with probable Parkinson's disease

Matthew J. Farrer, Alain Dest�e, E. Becquet et al. · Movement Disorders · 2000 · 32 citations

Linkage Exclusion, Mendelian Disorder, French Families +11

No pathogenic mutations in the β-synuclein gene in Parkinson's disease

Sarah Lincoln, Richard Crook, Marie‐Christine Chartier‐Harlin et al. · Neuroscience Letters · 1999 · 26 citations

Neurodegenerative Diseases, Disease Mechanism, Degenerative Diseases +9

Genetic Analysis of Synphilin-1 in Familial Parkinson's Disease

Matthew J. Farrer, A. Destée, Clotilde Lévecque et al. · Neurobiology of Disease · 2001 · 18 citations · Full text

Genetic Analysis, Mendelian Disorder, Genetic Disorder +6