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Sandrine Caburet
Sandrine Caburet
Université Paris Diderot
Verified email at ijm.fr
Title
Cited by
Cited by
Year
Forkhead transcription factors: key players in health and disease
BA Benayoun, S Caburet, RA Veitia
Trends in Genetics 27 (6), 224-232, 2011
3562011
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
3072014
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
2422004
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
1742005
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
1152004
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
1072010
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
1062011
Mechanisms of Mendelian dominance
RA Veitia, S Caburet, JA Birchler
Clinical Genetics 93 (3), 419-428, 2018
862018
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
862012
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
852014
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
822010
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
702016
A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency
B Fouquet, P Pawlikowska, S Caburet, C Guigon, M Mäkinen, L Tanner, ...
Elife 6, e30490, 2017
682017
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
682008
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
602015
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand …
S Caburet, AL Todeschini, C Petrillo, E Martini, ND Farran, B Legois, ...
EBioMedicine 42, 524-531, 2019
532019
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
522012
Coding repeats and evolutionary “agility”
S Caburet, J Cocquet, D Vaiman, RA Veitia
Bioessays 27 (6), 581-587, 2005
482005
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
472017
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, 1-11, 2015
402015
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