Camille Charbonnier
Camille Charbonnier
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Zitiert von
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers
G Bougeard, M Renaux-Petel, JM Flaman, C Charbonnier, P Fermey, ...
Journal of Clinical Oncology 33 (21), 2345-2352, 2015
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification
G Nicolas, C Pottier, C Charbonnier, L Guyant-Maréchal, I Le Ber, ...
Brain 136 (11), 3395-3407, 2013
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ...
Molecular psychiatry 25 (8), 1859-1875, 2020
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls
C Bellenguez, C Charbonnier, B Grenier-Boley, O Quenez, K Le Guennec, ...
Neurobiology of aging 59, 220. e1-220. e9, 2017
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease
G Nicolas, C Charbonnier, D Wallon, O Quenez, C Bellenguez, ...
Molecular psychiatry 21 (6), 831-836, 2016
Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons
G Nicolas, D Wallon, C Charbonnier, O Quenez, S Rousseau, AC Richard, ...
European Journal of Human Genetics 24 (5), 710-716, 2016
Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers
G Nicolas, C Charbonnier, RR de Lemos, AC Richard, O Guillin, D Wallon, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 …, 2015
De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease
A Rovelet-Lecrux, C Charbonnier, D Wallon, G Nicolas, MNJ Seaman, ...
Molecular psychiatry 20 (9), 1046-1056, 2015
Seizures in dominantly inherited Alzheimer disease
A Zarea, C Charbonnier, A Rovelet-Lecrux, G Nicolas, S Rousseau, ...
Neurology 87 (9), 912-919, 2016
Weighted-LASSO for structured network inference from time course data
C Charbonnier, J Chiquet, C Ambroise
Statistical applications in genetics and molecular biology 9 (1), 2010
ABCA7 rare variants and Alzheimer disease risk
K Le Guennec, G Nicolas, O Quenez, C Charbonnier, D Wallon, ...
Neurology 86 (23), 2134-2137, 2016
17q21. 31 duplication causes prominent tau-related dementia with increased MAPT expression
K Le Guennec, O Quenez, G Nicolas, D Wallon, S Rousseau, AC Richard, ...
Molecular Psychiatry 22 (8), 1119-1125, 2017
SORL1 genetic variants and Alzheimer disease risk: a literature review and meta-analysis of sequencing data
D Campion, C Charbonnier, G Nicolas
Acta neuropathologica 138 (2), 173-186, 2019
New insights on the genetic etiology of Alzheimer’s and related dementia
C Bellenguez, F Küçükali, I Jansen, V Andrade, S Moreno-Grau, N Amin, ...
MedRxiv, 2020
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
I de Rojas, S Moreno-Grau, N Tesi, B Grenier-Boley, V Andrade, ...
Nature communications 12 (1), 1-16, 2021
Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype
L Grangeon, D Wallon, C Charbonnier, O Quenez, AC Richard, ...
Brain 142 (6), 1573-1586, 2019
From common to rare variants: the genetic component of Alzheimer disease
G Nicolas, C Charbonnier, D Campion
Human heredity 81 (3), 129-141, 2016
Sparsity with sign-coherent groups of variables via the cooperative-lasso
J Chiquet, Y Grandvalet, C Charbonnier
The Annals of Applied Statistics 6 (2), 795-830, 2012
Contribution of genotoxic anticancer treatments to the development of multiple primary tumours in the context of germline TP53 mutations
E Kasper, E Angot, E Colasse, L Nicol, JC Sabourin, S Adriouch, ...
European Journal of Cancer 101, 254-262, 2018
Prevalence of MRI-defined recent silent ischemia and associated bleeding risk with thrombolysis
M Tisserand, L Le Guennec, E Touzé, A Hess, C Charbonnier, ...
Neurology 76 (15), 1288-1295, 2011
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