| Evidence for carrier-mediated transport of glutathione across the blood-brain barrier in the rat. R Kannan, JF Kuhlenkamp, E Jeandidier, H Trinh, M Ookhtens, ... The Journal of clinical investigation 85 (6), 2009-2013, 1990 | 218 | 1990 |
| Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich’s ataxia A Hick, M Wattenhofer-Donzé, S Chintawar, P Tropel, JP Simard, ... Disease models & mechanisms 6 (3), 608-621, 2013 | 167 | 2013 |
| A high frequency of Y chromosome deletions in males with nonidiopathic infertility C Krausz, L Quintana-Murci, S Barbaux, JP Siffroi, H Rouba, ... The Journal of Clinical Endocrinology & Metabolism 84 (10), 3606-3612, 1999 | 142 | 1999 |
| A translocation t (2; 8)(q12; p11) fuses FGFR1 to a novel partner gene, RANBP2/NUP358, in a myeloproliferative/myelodysplastic neoplasm C Gervais, L Dano, N Perrusson, C Helias, E Jeandidier, AC Galoisy, ... Leukemia 27 (5), 1186-1188, 2013 | 47 | 2013 |
| First description of the t (10; 11)(q22; q23)/MLL-TET1 translocation in a T-cell lymphoblastic lymphoma, with subsequent lineage switch to acute myelomonocytic myeloid leukemia A Ittel, E Jeandidier, C Helias, N Perrusson, C Humbrecht, B Lioure, ... Haematologica 98 (12), e166, 2013 | 40 | 2013 |
| Transmission of Induced Chromosomal Aberrations through Successive Mitotic Divisions in Human Lymphocytes after In Vitro and In Vivo Radiation A Kaddour, B Colicchio, D Buron, E El Maalouf, E Laplagne, C Borie, ... Scientific reports 7 (1), 3291, 2017 | 37 | 2017 |
| French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature I Luquet, F Mugneret, PD Athis, N Nadal, B Favre, C Abel, N Chelloug, ... Annales de genetique 45 (2), 77-88, 2002 | 37 | 2002 |
| Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata S Barbaux, E Vilain, O Raoul, S Gilgenkrantz, E Jeandidier, D Chadenas, ... Human molecular genetics 4 (9), 1565-1568, 1995 | 34 | 1995 |
| Isolation, culture and main characteristics of mouse fat‐storing cells: interaction with viruses W Chen, JL Gendrault, AM Steffan, E Jeandidier, A Kirn Hepatology 9 (3), 352-362, 1989 | 34 | 1989 |
| Genotoxic risk of ethyl‐paraben could be related to telomere shortening F Finot, A Kaddour, L Morat, I Mouche, N Zaguia, C Cuceu, D Souverville, ... Journal of Applied Toxicology 37 (6), 758-771, 2017 | 29 | 2017 |
| Telomere shortening: a new prognostic factor for cardiovascular disease post-radiation exposure R M'kacher, T Girinsky, B Colicchio, M Ricoul, A Dieterlen, E Jeandidier, ... Radiation protection dosimetry 164 (1-2), 134-137, 2015 | 29 | 2015 |
| Phenotype in X chromosome rearrangements: pitfalls of X inactivation study C Schluth, M Cossee, F Girard-Lemaire, N Carelle, H Dollfus, ... Pathologie Biologie 55 (1), 29-36, 2007 | 29 | 2007 |
| Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Francais de Cytogenetique … E Jeandidier, N Dastugue, F Mugneret, M Lafage-Pochitaloff, ... Cancer genetics and cytogenetics 166 (1), 1-11, 2006 | 29 | 2006 |
| Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics AD Polityko, E Goncharova, L Shamgina, N Drozdovskaja, L Podleschuk, ... Journal of Histochemistry & Cytochemistry 53 (3), 361-364, 2005 | 28 | 2005 |
| A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with at (7; 21) associated with 5q abnormalities and exhibiting similar clinical and … E Jeandidier, C Gervais, I Radford-Weiss, E Zink, C Gangneux, A Eischen, ... Cancer genetics 205 (7-8), 365-372, 2012 | 27 | 2012 |
| Telomere and centromere staining followed by M-FISH improves diagnosis of chromosomal instability and its clinical utility R M’kacher, B Colicchio, C Borie, S Junker, V Marquet, L Heidingsfelder, ... Genes 11 (5), 475, 2020 | 22 | 2020 |
| Independent mechanisms lead to genomic instability in Hodgkin lymphoma: Microsatellite or chromosomal instability C Cuceu, B Colicchio, E Jeandidier, S Junker, F Plassa, G Shim, J Mika, ... Cancers 10 (7), 233, 2018 | 21 | 2018 |
| ONSL and OSKM cocktails act synergistically in reprogramming human somatic cells into induced pluripotent stem cells L Jung, P Tropel, Y Moal, M Teletin, E Jeandidier, R Gayon, ... Molecular human reproduction 20 (6), 538-549, 2014 | 21 | 2014 |
| Two cousins with partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of the chromosome 12 C Lagier‐Tourenne, E Ginglinger, Y Alembik, A De Saint Martin, MO Peter, ... American Journal of Medical Genetics Part A 125 (1), 77-85, 2004 | 20 | 2004 |
| Intrachromosomal triplication for the distal part of chromosome 15q C Schluth, MG Mattei, C Mignon‐Ravix, S Salman, Y Alembik, J Willig, ... American Journal of Medical Genetics Part A 136 (2), 179-184, 2005 | 18 | 2005 |
