Marie‐Christine Chartier‐Harlin

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

Alison Goate, Marie‐Christine Chartier‐Harlin, Jeremy Brown et al. · Nature · 1991 · 4.6K citations

Life Sciences, Genetics, Molecular Genetics +16

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

Marie‐Christine Chartier‐Harlin, Jennifer M. Kachergus, Christophe Roumier et al. · The Lancet · 2004 · 2K citations

Life Sciences, Genetics, Neuroscience +14

Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene

Marie‐Christine Chartier‐Harlin, Fiona Crawford, Henry Houlden et al. · Nature · 1991 · 1.2K citations

Life Sciences, Genetics, Molecular Genetics +16

Apolipoprotein E, ɛ4 allele as a major risk factor for sporadic early and late-onset forms of Alzheimer's disease: analysis of the 19q13.2 chromosomal region

Marie‐Christine Chartier‐Harlin, Matthew Parfitt, Sylvle Legrain et al. · Human Molecular Genetics · 1994 · 435 citations

Life Sciences, Genetics, Neurology +17

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

Owen A. Ross, Alexandra I. Soto‐Ortolaza, Michael G. Heckman et al. · The Lancet Neurology · 2011 · 344 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12