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Employment (1)

Institut du Thorax: Nantes, FR

2010-09-04 to present | bioinformatician (BiRD bioinformatics core facility)
Employment
Source: Self-asserted source
Eric Charpentier

Education and qualifications (1)

University of Nantes: Nantes, FR

2008-09-01 to 2010-09-03 | MSc bioinformatics
Education
Source: Self-asserted source
Eric Charpentier

Works (21)

Human genetic structure in Northwest France provides new insights into West European historical demography

Nature Communications
2024-08-07 | Journal article
DOI: 10.1038/s41467-024-51087-1
Part of ISSN: 2041-1723
Contributors: Isabel Alves; Joanna Giemza; Michael G. B. Blum; Carolina Bernhardsson; Stéphanie Chatel; Matilde Karakachoff; Aude Saint Pierre; Anthony Herzig; Robert Olaso; Martial Monteil et al.
Source: Self-asserted source
Eric Charpentier

Transcriptomic Analysis Reveals the Inability of Recombinant AAV8 to Activate Human Monocyte-Derived Dendritic Cells.

International journal of molecular sciences
2023-06 | Journal article
DOI: 10.3390/ijms241310447
PMID: 37445621
PMC: PMC10341499
Contributors: Masri S; Carré L; Jaulin N; Vandamme C; Couzinié C; Guy-Duché A; Dupont JB; Pereira A; Charpentier E; David L et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Genetic population structure across Brittany and the downstream Loire basin provides new insights on the demographic history of Western Europe

2022-02 | Preprint
DOI: 10.1101/2022.02.03.478491
PPR: PPR450320
Contributors: Alves I; Giemza J; Blum M; Bernhardsson C; Chatel S; Karakachoff M; Saint Pierre A; Herzig AF; Olaso R; Monteil M et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.

Nature genetics
2022-02 | Journal article
DOI: 10.1038/s41588-021-01007-6
PMID: 35210625
Contributors: Barc J; Tadros R; Glinge C; Chiang DY; Jouni M; Simonet F; Jurgens SJ; Baudic M; Nicastro M; Potet F et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

Clinical and Translational Medicine
2021-06 | Journal article
DOI: 10.1002/ctm2.413
Part of ISSN: 2001-1326
Part of ISSN: 2001-1326
Source: Self-asserted source
Eric Charpentier

3’ RNA sequencing for robust and low-cost gene expression profiling

2021-01 | Preprint
DOI: 10.21203/rs.3.pex-1336/v1
OTHER-ID:

PPR275255
Contributors: Charpentier E; Cornec M; Dumont S; Meistermann D; Bordron P; David L; Redon R; Bonnaud S; Bihouée A
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Induction of Human Trophoblast Stem Cells from Somatic Cells and Pluripotent Stem Cells.

Cell reports
2020-11 | Journal article
DOI: 10.1016/j.celrep.2020.108419
PMID: 33238118
Contributors: Castel G; Meistermann D; Bretin B; Firmin J; Blin J; Loubersac S; Bruneau A; Chevolleau S; Kilens S; Chariau C et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Generation of human induced trophoblast stem cells

2020-09 | Preprint
DOI: 10.1101/2020.09.15.298257
OTHER-ID:

PPR214584
Contributors: Castel G; Meistermann D; Bretin B; Firmin J; Blin J; Loubersac S; Bruneau A; Chevolleau S; Kilens S; Chariau C et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.

Circulation. Genomic and precision medicine
2019-10 | Journal article
DOI: 10.1161/circgen.119.002617
PMID: 32141789
Contributors: Thériault S; Dina C; Messika-Zeitoun D; Le Scouarnec S; Capoulade R; Gaudreault N; Rigade S; Li Z; Simonet F; Lamontagne M et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Genetic association analyses highlight IL6, ALPL, and NAV1 as three new susceptibility genes underlying calcific aortic valve stenosis

2019-01 | Other
DOI: 10.1101/515494
OTHER-ID:

PPR67154
Contributors: Thériault S; Dina C; Messika-Zeitoun D; Scouarnec SL; Capoulade R; Gaudreault N; Rigade S; Li Z; Simonet F; Lamontagne M et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Parallel derivation of isogenic human primed and naive induced pluripotent stem cells.

Nature communications
2018-01 | Journal article
DOI: 10.1038/s41467-017-02107-w
PMID: 29367672
PMC: PMC5783949
Contributors: Kilens S; Meistermann D; Moreno D; Chariau C; Gaignerie A; Reignier A; Lelièvre Y; Casanova M; Vallot C; Nedellec S et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

American journal of human genetics
2017-11 | Journal article
DOI: 10.1016/j.ajhg.2017.10.003
PMID: 29100089
PMC: PMC5673671
Contributors: Küry S; van Woerden GM; Besnard T; Proietti Onori M; Latypova X; Towne MC; Cho MT; Prescott TE; Ploeg MA; Sanders S et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

An intermediate level of CD161 expression defines a novel activated, inflammatory, and pathogenic subset of CD8+ T cells involved in multiple sclerosis.

Journal of autoimmunity
2017-10 | Journal article
DOI: 10.1016/j.jaut.2017.10.005
PMID: 29054368
Contributors: Nicol B; Salou M; Vogel I; Garcia A; Dugast E; Morille J; Kilens S; Charpentier E; Donnart A; Nedellec S et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Killer Immunoglobulin-Like Receptor Allele Determination Using Next-Generation Sequencing Technology.

Frontiers in Immunology
2017-05 | Journal article
DOI: 10.3389/fimmu.2017.00547
PMID: 28579987
PMC: PMC5437120
Contributors: Maniangou B; Legrand N; Alizadeh M; Guyet U; Willem C; David G; Charpentier E; Walencik A; Retière C; Gagne K
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Transient antibody targeting of CD45RC induces transplant tolerance and potent antigen-specific regulatory T cells.

JCI insight
2017-02 | Journal article
DOI: 10.1172/jci.insight.90088
PMID: 28194440
PMC: PMC5291739
Contributors: Picarda E; Bézie S; Boucault L; Autrusseau E; Kilens S; Meistermann D; Martinet B; Daguin V; Donnart A; Charpentier E et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Ex Vivo Expanded Human Non-Cytotoxic CD8+CD45RClow/- Tregs Efficiently Delay Skin Graft Rejection and GVHD in Humanized Mice.

Frontiers in Immunology
2017-01 | Journal article
DOI: 10.3389/fimmu.2017.02014
PMID: 29445370
PMC: PMC5797797
Contributors: Bézie S; Meistermann D; Boucault L; Kilens S; Zoppi J; Autrusseau E; Donnart A; Nerrière-Daguin V; Bellier-Waast F; Charpentier E et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability.

Human mutation
2016-02 | Journal article
DOI: 10.1002/humu.22952
PMID: 26751395
Contributors: Isidor B; Küry S; Rosenfeld JA; Besnard T; Schmitt S; Joss S; Davies SJ; Lebel RR; Henderson A; Schaaf CP et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.

International journal of cardiology
2016-01 | Journal article
DOI: 10.1016/j.ijcard.2016.01.052
PMID: 26820365
Contributors: Daumy X; Amarouch MY; Lindenbaum P; Bonnaud S; Charpentier E; Bianchi B; Nafzger S; Baron E; Fouchard S; Thollet A et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta.

Circulation. Cardiovascular genetics
2015-12 | Journal article
DOI: 10.1161/circgenetics.115.001213
PMID: 26643481
Contributors: Sanchez-Castro M; Eldjouzi H; Charpentier E; Busson PF; Hauet Q; Lindenbaum P; Delasalle-Guyomarch B; Baudry A; Pichon O; Pascal C et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Fine-scale human genetic structure in Western France.

European journal of human genetics : EJHG
2014-09 | Journal article
DOI: 10.1038/ejhg.2014.175
PMID: 25182131
PMC: PMC4795055
Contributors: Karakachoff M; Duforet-Frebourg N; Simonet F; Le Scouarnec S; Pellen N; Lecointe S; Charpentier E; Gros F; Cauchi S; Froguel P et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

Nature genetics
2013-07 | Journal article
DOI: 10.1038/ng.2712
PMID: 23872634
PMC: PMC3869788
Contributors: Bezzina CR; Barc J; Mizusawa Y; Remme CA; Gourraud JB; Simonet F; Verkerk AO; Schwartz PJ; Crotti L; Dagradi F et al.
Source: Self-asserted source
Eric Charpentier via Europe PubMed Central
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