| Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ... Nature genetics 45 (9), 1044-1049, 2013 | 538 | 2013 |
| De novo mutations in protein kinase genes CAMK2A and CAMK2B cause intellectual disability S Küry, GM van Woerden, T Besnard, MP Onori, X Latypova, MC Towne, ... The American Journal of Human Genetics 101 (5), 768-788, 2017 | 144 | 2017 |
| Parallel derivation of isogenic human primed and naive induced pluripotent stem cells S Kilens, D Meistermann, D Moreno, C Chariau, A Gaignerie, A Reignier, ... Nature communications 9 (1), 360, 2018 | 134 | 2018 |
| Induction of human trophoblast stem cells from somatic cells and pluripotent stem cells G Castel, D Meistermann, B Bretin, J Firmin, J Blin, S Loubersac, ... Cell Reports 33 (8), 2020 | 125 | 2020 |
| Ex Vivo Expanded Human Non-Cytotoxic CD8+CD45RClow/− Tregs Efficiently Delay Skin Graft Rejection and GVHD in Humanized Mice S Bézie, D Meistermann, L Boucault, S Kilens, J Zoppi, E Autrusseau, ... Frontiers in immunology 8, 2014, 2018 | 75 | 2018 |
| Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ... Nature genetics 54 (3), 232-239, 2022 | 64 | 2022 |
| Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I X Daumy, MY Amarouch, P Lindenbaum, S Bonnaud, E Charpentier, ... International journal of cardiology 207, 349-358, 2016 | 60 | 2016 |
| Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis S Thériault, C Dina, D Messika-Zeitoun, S Le Scouarnec, R Capoulade, ... Circulation: Genomic and Precision Medicine 12 (10), e002617, 2019 | 54 | 2019 |
| De Novo Truncating Mutations in the Kinetochore‐Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability B Isidor, S Küry, JA Rosenfeld, T Besnard, S Schmitt, S Joss, SJ Davies, ... Human Mutation 37 (4), 354-358, 2016 | 51 | 2016 |
| Transient antibody targeting of CD45RC induces transplant tolerance and potent antigen-specific regulatory T cells E Picarda, S Bézie, L Boucault, E Autrusseau, S Kilens, D Meistermann, ... JCI insight 2 (3), 2017 | 50 | 2017 |
| Fine-scale human genetic structure in Western France M Karakachoff, N Duforet-Frebourg, F Simonet, S Le Scouarnec, N Pellen, ... European Journal of Human Genetics 23 (6), 831-836, 2015 | 47 | 2015 |
| 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 M Sanchez-Castro, H Eldjouzi, E Charpentier, PF Busson, Q Hauet, ... Circulation: Cardiovascular Genetics 9 (1), 86-94, 2016 | 41 | 2016 |
| An intermediate level of CD161 expression defines a novel activated, inflammatory, and pathogenic subset of CD8+ T cells involved in multiple sclerosis B Nicol, M Salou, I Vogel, A Garcia, E Dugast, J Morille, S Kilens, ... Journal of Autoimmunity 88, 61-74, 2018 | 32 | 2018 |
| Killer immunoglobulin-like receptor allele determination using next-generation sequencing technology B Maniangou, N Legrand, M Alizadeh, U Guyet, C Willem, G David, ... Frontiers in immunology 8, 547, 2017 | 28 | 2017 |
| 3’RNA sequencing for robust and low-cost gene expression profiling E Charpentier, M Cornec, S Dumont, D Meistermann, P Bordron, L David, ... | 12 | 2021 |
| Genetic population structure across Brittany and the downstream Loire basin provides new insights on the demographic history of Western Europe I Alves, J Giemza, M Blum, C Bernhardsson, S Chatel, M Karakachoff, ... bioRxiv, 2022.02. 03.478491, 2022 | 6 | 2022 |
| A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype ZR Al Sayed, M Jouni, J Gourraud, N Belbachir, J Barc, A Girardeau, ... Clinical and Translational Medicine 11 (6), 2021 | 6 | 2021 |
| Genetic association analyses highlight IL6, ALPL, and NAV1 as three new susceptibility genes underlying calcific aortic valve stenosis S Thériault, C Dina, D Messika-Zeitoun, S Le Scouarnec, R Capoulade, ... bioRxiv, 515494, 2019 | 4 | 2019 |
| Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ... Nature Genetics 45 (11), 1409-1409, 2013 | 4 | 2013 |
| Generation of human induced trophoblast stem cells G Castel, D Meistermann, B Bretin, J Firmin, J Blin, S Loubersac, ... bioRxiv, 2020.09. 15.298257, 2020 | 2 | 2020 |
Dimitri MeistermannHelsinki Institute of Life Science (HiLIFE)Verified email at helsinki.fi
