Sandrine Caburet
机构: Université Paris Diderot
每年引用次数
引用次数
引用: 2,736
H-指数: 27
I10-指数 : 36
出版物: 49
Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction.
Elfride De Baere , Silvia Copelli , Sandrine Caburet , Paul Laissue
Pediatric endocrinology reviews 2 ( 4) 653 -660
20
2005
Compositional Biases and Polyalanine Runs in Humans
Julie Cocquet , Elfride De Baere , Sandrine Caburet , Reiner A Veitia
Genetics 165 ( 3) 1613 -1617
20
2003
A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations.
Francoise Paris , Delphine Flatters , Sandrine Caburet , Bérangère Legois
Clinical Endocrinology 87 ( 5) 539 -544
11
2017
The post-translational modification profile of the forkhead transcription factor FOXL2 suggests the existence of parallel processive/concerted modification pathways.
Bérénice A Benayoun , Jana Auer , Sandrine Caburet , Reiner A Veitia
Proteomics 8 ( 15) 3118 -3123
16
2008
Combing the genome for genomic instability
Aaron Bensimon , Sandrine Caburet , Chiara Conti
Trends in Biotechnology 20 ( 8) 344 -350
34
2002
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1.
Pendás AM. Felipe-Medina N , Caburet S , Sánchez-Sáez F , Condezo YB
eLife 9
25
2020
Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes
Sandrine Caburet , Mikko Anttonen , Anne-Laure Todeschini , Leila Unkila-Kallio
BMC Cancer 15 ( 1) 251 -251
25
2015
Targeting the molecular mechanism of DNA replication.
Chiara Conti , Sandrine Caburet , Aaron Bensimon
Drug Discovery Today 6 ( 15) 786 -792
4
2001
Extensive sequence turnover of the signal peptides of members of the GDF/BMP family: exploring their evolutionary landscape.
Reiner A Veitia , Sandrine Caburet ,
Biology Direct 4 ( 1) 22 -22
5
2009
Eucaryotic genome evolution through the spontaneous duplication of large chromosomal segments.
Romain Koszul , Sandrine Caburet , Bernard Dujon , Gilles Fischer
The EMBO Journal 23 ( 1) 234 -243
237
2004
The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology
Sandrine Caburet , Adrien Georges , David L’Hôte , Anne-Laure Todeschini
Molecular and Cellular Endocrinology 356 ( 1) 55 -64
55
2012
Forkhead transcription factors: key players in health and disease
Bérénice A Benayoun , Sandrine Caburet , Reiner A Veitia ,
Trends in Genetics 27 ( 6) 224 -232
186
2011
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
Sandrine Caburet , Anne-Laure Todeschini , Cynthia Petrillo , Emmanuelle Martini
EBioMedicine 42 524 -531
23
2019
An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes.
Maria Isabel Alvarez‐Mora , Anne‐Laure Todeschini , Sandrine Caburet , Lilach Peled Perets
Clinical Genetics 98 ( 3) 293 -298
2
2020
Conventional and unconventional interactions of the transcription factor FOXL2 uncovered by a proteome‐wide analysis
May Penrad‐Mobayed , Caroline Perrin , Laetitia Herman , Anne‐Laure Todeschini
The FASEB Journal 34 ( 1) 571 -587
3
2020
A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency
Baptiste Fouquet , Patrycja Pawlikowska , Sandrine Caburet , Celine Guigon
eLife 6
32
2017
Mutant Cohesin in Premature Ovarian Failure
Sandrine Caburet , Valerie A Arboleda , Elena Llano , Paul A Overbeek
The New England Journal of Medicine 370 ( 10) 943 -949
278
2014
Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?
Adrien B. Georges , Berenice A. Benayoun , Sandrine Caburet , Reiner A. Veitia
The FASEB Journal 24 ( 2) 346 -356
102
2010
Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)
Berenice A Benayoun , Sandrine Caburet , Aurélie Dipietromaria , Adrien Georges
PLoS ONE 5 ( 1) e8789
62
2010
A homozygous hypomorphic BRCA2 variant causes primary ovarian insufficiency without cancer or Fanconi anemia traits
Sandrine Caburet , Abdelkader Heddar , Elodie Dardillac , Helene Creux
bioRxiv 751644
3
2019