Jean‐Charles Lambert

Author

Also Known As

A Social, A. Ramirez, Alfredo Ramirez, Alison Goate, Amy Gerrish, Benoît Marin, Béatrice Lannes, C Tzourio, Carlos Cruchaga, Carole Dufouil

518

Publications

40.1K

Citations

H-Index

198

Concepts

All Affiliations

Inserm Institut Pasteur de Lille Université de Lille Centre Hospitalier Universitaire de Lille Centre National de la Recherche Scientifique

About

Jean‐Charles Lambert is an author at Inserm specializing in medicine, genetics, and alzheimer's disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	41	72	6.8K
2	Health Sciences	10	10	679
3	Engineering	7	7	256
4	Natural Sciences	4	4	172
5	Language Studies	2	2	47

Jean‐Charles Lambert

169

Publications

14.5K

Citations

H-Index

Page 1

	Year	Citations
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease Valentina Escott‐Price, Céline Bellenguez, Li‐San Wang, PLoS ONE	2014	1.4K
APOE and Alzheimer disease: a major gene with semi-dominant inheritance Emmanuelle Génin, Didier Hannequin, David Wallon, Molecular Psychiatry Alzheimer's DiseaseDementiaGeneticsDegenerative PathologyNeurochemical Biomarkers	2011	684
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease Laurie Robak, Iris E. Jansen, Jeroen van Rooij, Brain GeneticsGenetic EpidemiologyVariant BurdenDisease Gene IdentificationGenome-wide Association Study	2017	440
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy Suzanne Lesage, Valérie Drouet, Elisa Majounie, The American Journal of Human Genetics Cell AutophagyMitophagyMitochondrial FunctionGeneticsAutophagy	2016	427
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease Alexandria Beilina, Iakov N. Rudenko, Alice Kaganovich, Proceedings of the National Academy of Sciences	2014	362
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study Isabelle Le Ber, Agnès Camuzat, Didier Hannequin, Brain Corticobasal DegenerationGeneticsBrain Perfusion ProfilesGenetic EpidemiologyClinical Genetics	2008	344
A Polymorphism in CALHM1 Influences Ca2+ Homeostasis, Aβ Levels, and Alzheimer's Disease Risk Ute Dreses‐Werringloer, Jean‐Charles Lambert, Valérie Vingtdeux, Cell Alzheimer's DiseaseDisease RiskAβ LevelsGeneticsPhysiology	2008	320
A novel Alzheimer disease locus located near the gene encoding tau protein Gyungah Jun, Carla A. Ibrahim‐Verbaas, Maria Vronskaya, Molecular Psychiatry Alzheimer's DiseaseMolecular NeuroscienceGeneticsDegenerative PathologyProtein Misfolding	2015	301
High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease Cyril Pottier, Didier Hannequin, Sophie Coutant, Molecular Psychiatry Neurodegenerative DiseasesAlzheimer's DiseaseGeneticsDegenerative PathologyPathogenic Sorl1 Mutations	2012	300
Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease Jan P. Dumanski, Jean‐Charles Lambert, Chiara Rasi, The American Journal of Human Genetics Sporadic Alzheimer DiseaseAgingCytogeneticsGeneticsGenetic Epidemiology	2016	252

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