Vincent Meyer

SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome

Naresh K. Hanchate, Paolo Giacobini, Pierre Lhuillier et al. · PLoS Genetics · 2012 · 210 citations · Full text

Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

Céline Bellenguez, Camille Charbonnier, Benjamin Grenier‐Boley et al. · Neurobiology of Aging · 2017 · 164 citations · Full text

Neurodegenerative Diseases, Alzheimer's Disease, Disease Risk +11

SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease

Gaël Nicolas, Camille Charbonnier, David Wallon et al. · Molecular Psychiatry · 2015 · 127 citations

Neurodegenerative Diseases, Alzheimer's Disease, Major Risk Factor +9

Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy

Estelle Colin, Jens Daniel, Alban Ziegler et al. · The American Journal of Human Genetics · 2016 · 119 citations · Full text

Molecular Neuroscience, Mendelian Disorder, Biallelic Variants +11

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression

Kilan Le Guennec, Olivier Quenez, Gaël Nicolas et al. · Molecular Psychiatry · 2016 · 97 citations

Neurodegenerative Diseases, Alzheimer's Disease, Increased Mapt Expression +7