| Forkhead transcription factors: key players in health and disease BA Benayoun, S Caburet, RA Veitia Trends in Genetics 27 (6), 224-232, 2011 | 242 | 2011 |
| Eucaryotic genome evolution through the spontaneous duplication of large chromosomal segments R Koszul, S Caburet, B Dujon, G Fischer The EMBO journal 23 (1), 234-243, 2004 | 218 | 2004 |
| Mutant cohesin in premature ovarian failure S Caburet, VA Arboleda, E Llano, PA Overbeek, JL Barbero, K Oka, ... New England Journal of Medicine 370 (10), 943-949, 2014 | 198 | 2014 |
| Human ribosomal RNA gene arrays display a broad range of palindromic structures S Caburet, C Conti, C Schurra, R Lebofsky, SJ Edelstein, A Bensimon Genome research 15 (8), 1079-1085, 2005 | 135 | 2005 |
| A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation S Caburet, A Demarez, L Moumne, M Fellous, E De Baere, RA Veitia Journal of medical genetics 41 (12), 932-936, 2004 | 110 | 2004 |
| Generic binding sites, generic DNA‐binding domains: where does specific promoter recognition come from? AB Georges, BA Benayoun, S Caburet, RA Veitia The FASEB Journal 24 (2), 346-356, 2010 | 97 | 2010 |
| Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase BA Benayoun, AB Georges, D l'Hôte, N Andersson, A Dipietromaria, ... Human molecular genetics 20 (9), 1673-1686, 2011 | 84 | 2011 |
| Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p. Cys134Trp (c. 402C> G) BA Benayoun, S Caburet, A Dipietromaria, A Georges, B d'Haene, ... PloS one 5 (1), e8789, 2010 | 73 | 2010 |
| The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology S Caburet, A Georges, D L’Hôte, AL Todeschini, BA Benayoun, RA Veitia Molecular and cellular endocrinology 356 (1-2), 55-64, 2012 | 72 | 2012 |
| The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles BA Benayoun, S Caburet, A Dipietromaria, M Bailly-Bechet, F Batista, ... Human molecular genetics 17 (20), 3118-3127, 2008 | 63 | 2008 |
| STAG3 is a strong candidate gene for male infertility E Llano, L Gomez-H, I García-Tuñón, M Sánchez-Martín, S Caburet, ... Human molecular genetics 23 (13), 3421-3431, 2014 | 54 | 2014 |
| Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial premature ovarian failure S Caburet, P Zavadakova, Z Ben-Neriah, K Bouhali, A Dipietromaria, ... PLoS One 7 (3), e33412, 2012 | 43 | 2012 |
| Coding repeats and evolutionary “agility” S Caburet, J Cocquet, D Vaiman, RA Veitia Bioessays 27 (6), 581-587, 2005 | 42 | 2005 |
| A non‐sense MCM9 mutation in a familial case of primary ovarian insufficiency F Fauchereau, S Shalev, E Chervinsky, R Beck‐Fruchter, B Legois, ... Clinical Genetics 89 (5), 603-607, 2016 | 39 | 2016 |
| Combing the genome for genomic instability S Caburet, C Conti, A Bensimon TRENDS in Biotechnology 20 (8), 344-350, 2002 | 36 | 2002 |
| Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes S Caburet, M Anttonen, AL Todeschini, L Unkila-Kallio, D Mestivier, ... BMC cancer 15 (1), 1-11, 2015 | 30 | 2015 |
| Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads A Auguste, L Bessière, AL Todeschini, S Caburet, S Sarnacki, J Prat, ... Human molecular genetics 24 (23), 6687-6698, 2015 | 29 | 2015 |
| Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction. E De Baere, S Copelli, S Caburet, P Laissue, D Beysen, S Christin-Maitre, ... Pediatric endocrinology reviews: PER 2 (4), 653-660, 2005 | 29 | 2005 |
| Molecular combing C Conti, S Caburet, C Schurra, A Bensimon Current protocols in Cytometry 16 (1), 8.10. 1-8.10. 23, 2001 | 29 | 2001 |
| The genetic make‐up of ovarian development and function: the focus on the transcription factor FOXL2 M Elzaiat, AL Todeschini, S Caburet, RA Veitia Clinical genetics 91 (2), 173-182, 2017 | 28 | 2017 |
VEITIA Reiner A.Professor, Université de Paris. Head François Jacob Institute, CEA. Editor In Chief Clinical GenetEmail verificata su ijm.fr
