Vincent Meyer
Commissariat à l'Énergie Atomique et aux Énergies Alternatives(FR)Centre National de Recherche en Génomique Humaine(FR)Direction de la Recherche Fondamentale(FR)CEA Paris-Saclay(FR)
Publications by Year
Research Areas
Alzheimer's disease research and treatments, Mitochondrial Function and Pathology, Genetic and phenotypic traits in livestock, Cellular transport and secretion, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome(2012)214 cited
- → Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls(2017)168 cited
- → SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease(2015)133 cited
- → Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy(2016)120 cited
- → 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression(2016)97 cited
- → Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons(2015)96 cited