A. D. de Septenville

发表

Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin.

L. Naccache, O. Colliot, F. Lamari, 2014, JAMA neurology.

Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers

B. Dubois, V. Meininger, A. Brice, 2015, Alzheimer's & dementia.

SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.

J. Hardy, R. Guerreiro, D. Campion, 2013, JAMA neurology.

Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

Posterior cortical atrophy as an extreme phenotype of GRN mutations.

B. Dubois, D. Grabli, F. Lamari, 2015, JAMA neurology.

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

A. Brice, P. Yu-Wai-Man, J. Pouget, 2015, Brain : a journal of neurology.

Reconstructing the evolutionary history of a B cell lineage with minimum spanning tree and genotype abundances

F. Davi, J. Bernardes, A. D. de Septenville, 2022, bioRxiv.

Immunoglobulin gene analysis in chronic lymphocytic leukemia in the era of next generation sequencing

K. Stamatopoulos, R. Rosenquist, A. Langerak, 2020, Leukemia.

Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.

E. Génin, A. Brice, P. Yu-Wai-Man, 2016, Brain : a journal of neurology.

ViCloD, an interactive web tool for visualizing B cell repertoires and analyzing intra-clonal diversities: application to human B-cell tumors

F. Davi, J. Bernardes, M. Armand, 2022, bioRxiv.

A multi-objective based clustering for inferring BCR clones from high-throughput B cell repertoire data

H. Ripoche, F. Davi, J. Bernardes, 2021, bioRxiv.

Automatic generation of ground truth data for the evaluation of clonal grouping methods in B-cell populations

Juliana S. Bernardes, Nika Abdollahi, Anne de Septenville, 2020, bioRxiv.

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

The helicases DinG, Rep and UvrD cooperate to promote replication across transcription units in vivo

B. Michel, E. Viguera, H. Boubakri, 2009, The EMBO journal.

Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

E. Génin, A. Brice, P. Yu-Wai-Man, 2015, Brain : a journal of neurology.

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.

E. Génin, A. Brice, P. Yu-Wai-Man, 2015, Brain : a journal of neurology.

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

ViCloD, an interactive web tool for visualizing B cell repertoires and analyzing intraclonal diversities: application to human B-cell tumors

F. Davi, J. Bernardes, M. Armand, 2023, bioRxiv.

Replication Fork Reversal after Replication–Transcription Collision

B. Michel, H. Boubakri, A. D. de Septenville, 2012, PLoS genetics.

Evidence of somatic hypermutation in the antigen binding sites of patients with CLL harboring IGHV genes with 100% germline identity

K. Stamatopoulos, F. Davi, Elisavet Georgiou, 2022, Frontiers in Oncology.

DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypes.

A. Bonnet, R. Levy, S. Rivaud-Pechoux, 2014, JAMA neurology.

Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin.

L. Naccache, O. Colliot, F. Lamari, 2014, JAMA neurology.

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

P. Yu-Wai-Man, J. Pouget, I. Le Ber, 2015, Brain : a journal of neurology.