Fabienne Wavrant‐De Vrièze

Support for association between ADHD and two candidate genes: <i>NET1</i> and <i>DRD1</i>

Aaron J. Bobb, Anjené Addington, Ellen Sidransky et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2005 · 221 citations

Mutations in the <i>HSP27</i> ( <i>HSPB1</i> ) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

Henry Houlden, Matilde Laurá, Fabienne Wavrant‐De Vrièze et al. · Neurology · 2008 · 180 citations

A Scan of Chromosome 10 Identifies a Novel Locus Showing Strong Association with Late-Onset Alzheimer Disease

Andrew Grupe, Yonghong Li, Charles M. Rowland et al. · The American Journal of Human Genetics · 2005 · 156 citations · Full text

Neurodegenerative Diseases, Alzheimer's Disease, Genetics +9

Low frequency of α‐synuclein mutations in familial Parkinson's disease

Matthew J. Farrer, Fabienne Wavrant‐De Vrièze, Richard Crook et al. · Annals of Neurology · 1998 · 135 citations

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression

Yonghong Li, Andrew Grupe, Charles M. Rowland et al. · Human Molecular Genetics · 2006 · 123 citations · Full text