Sandrine Caburet

4PUBLICATIONS
9CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Obstetrics and gynaecology
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Publications (4)

|Apr 17, 2025
Reclassifying NOBOX variants in primary ovarian insufficiency cases with a corrected gene model and a novel quantitative framework.

Reiner A Veitia, Jamie D Cowles, Sandrine Caburet

|Jun 03, 2020
Homozygous hypomorphic BRCA2 variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait.

Sandrine Caburet, Abdelkader Heddar, Elodie Dardillac

|Dec 13, 2017
A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.

Baptiste Fouquet, Patrycja Pawlikowska, Sandrine Caburet

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