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Caburet, Sandrine
69
results:
Search for persons
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Format
Online (69)
Mediatypes
Articles (Online) (26)
OpenAccess-fulltext (43)
Languages
english (61)
french (5)
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?
1
An exome‐wide exploration of cases of primary ovarian insuf..:
Alvarez‐Mora, Maria Isabel
;
Todeschini, Anne‐Laure
;
Caburet, Sandrine
...
Clinical Genetics. 98 (2020) 3 - p. 293-298 , 2020
Link:
https://doi.org/10.1111/..
?
2
A missense in HSF2BP causing primary ovarian insufficiency ..:
Felipe-Medina, Natalia
;
Caburet, Sandrine
;
Sánchez-Sáez, Fernando
...
eLife. 9 (2020) - p. , 2020
Link:
https://doi.org/10.7554/..
?
3
Conventional and unconventional interactions of the transcr..:
Penrad‐Mobayed, May
;
Perrin, Caroline
;
Herman, Laetitia
...
The FASEB Journal. 34 (2019) 1 - p. 571-587 , 2019
Link:
https://doi.org/10.1096/..
?
4
A truncating MEIOB mutation responsible for familial primar..:
Caburet, Sandrine
;
Todeschini, Anne-Laure
;
Petrillo, Cynthia
...
EBioMedicine. 42 (2019) - p. 524-531 , 2019
Link:
https://doi.org/10.1016/..
?
5
A homozygous FANCM mutation underlies a familial case of no..:
Fouquet, Baptiste
;
Pawlikowska, Patrycja
;
Caburet, Sandrine
...
eLife. 6 (2017) - p. , 2017
Link:
https://doi.org/10.7554/..
?
6
A novel variant of DHH in a familial case of 46,XY disorder..:
Paris, Francoise
;
Flatters, Delphine
;
Caburet, Sandrine
...
Clinical Endocrinology. 87 (2017) 5 - p. 539-544 , 2017
Link:
https://doi.org/10.1111/..
?
7
Natural and molecular history of prolactinoma: insights fro..:
Bernard, Valérie
;
Villa, Chiara
;
Auguste, Aurélie
...
Oncotarget. 9 (2017) 5 - p. 6144-6155 , 2017
Link:
https://doi.org/10.18632..
?
8
Combined comparative genomic hybridization and transcriptom..:
Caburet, Sandrine
;
Anttonen, Mikko
;
Todeschini, Anne-Laure
...
BMC Cancer. 15 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
9
Molecular analyses of juvenile granulosa cell tumors bearin..:
Auguste, Aurélie
;
Bessière, Laurianne
;
Todeschini, Anne-Laure
...
Human Molecular Genetics. 24 (2015) 23 - p. 6687-6698 , 2015
Link:
https://doi.org/10.1093/..
?
10
STAG3 is a strong candidate gene for male infertility:
Llano, Elena
;
Gomez-H, Laura
;
García-Tuñón, Ignacio
...
Human Molecular Genetics. 23 (2014) 13 - p. 3421-3431 , 2014
Link:
https://doi.org/10.1093/..
?
11
The transcription factor FOXL2: At the crossroads of ovaria..:
Caburet, Sandrine
;
Georges, Adrien
;
L'Hôte, David
...
Molecular and Cellular Endocrinology. 356 (2012) 1-2 - p. 55-64 , 2012
Link:
https://doi.org/10.1016/..
?
12
Genome-Wide Linkage in a Highly Consanguineous Pedigree Rev..:
Caburet, Sandrine
;
Zavadakova, Petra
;
Ben-Neriah, Ziva
...
PLoS ONE. 7 (2012) 3 - p. e33412 , 2012
Link:
https://doi.org/10.1371/..
?
13
Forkhead transcription factors: key players in health and d..:
Benayoun, Bérénice A.
;
Caburet, Sandrine
;
Veitia, Reiner A.
Trends in Genetics. 27 (2011) 6 - p. 224-232 , 2011
Link:
https://doi.org/10.1016/..
?
14
Transcription factor FOXL2 protects granulosa cells from st..:
Benayoun, Bérénice A.
;
Georges, Adrien B.
;
L'Hôte, David
...
Human Molecular Genetics. 20 (2011) 9 - p. 1673-1686 , 2011
Link:
https://doi.org/10.1093/..
?
15
Functional Exploration of the Adult Ovarian Granulosa Cell ..:
Benayoun, Bérénice A.
;
Caburet, Sandrine
;
Dipietromaria, Aurélie
...
PLoS ONE. 5 (2010) 1 - p. e8789 , 2010
Link:
https://doi.org/10.1371/..
1-15