Sandrine Caburet

Years Active: 2017-2020
Publications (10 Years): 3

Universite de Paris

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Universite de Paris Sep 01 2006

France

Assistant Professor, Genomics :: UFR Sciences du Vivant

Publications

Natalia Felipe-Medina, Sandrine Caburet, Fernando Sánchez-Sáez, Yazmine B Condezo, Dirk G de Rooij, Laura Gómez-H, Rodrigo García-Valiente, Anne Laure Todeschini, Paloma Duque, Manuel Adolfo Sánchez-Martin, Stavit A Shalev, Elena Llano, Reiner A Veitia, Alberto M Pendas
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1. eLife 9 (2020)
Sandrine Caburet, Abdelkader Heddar, Elodie Dardillac, Héléne Creux, Marie Lambert, Sébastien Messiaen, Sophie Tourpin, Gabriel Livera, Bernard S Lopez, Abdelkader Heddar
Homozygous hypomorphic BRCA2 variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait. Journal of medical genetics (2020)
Baptiste Fouquet, Patrycja Pawlikowska, Sandrine Caburet, Celine Guigon, Marika Mäkinen, Laura Tanner, Marja Hietala, Kaja Urbanska, Laura Bellutti, Bérangère Legois, Bettina Bessieres, Alain Gougeon, Alexandra Benachi, Gabriel Livera, Filippo Rosselli, Reiner A Veitia, Abdelkader Heddar
A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency. eLife 6 (2017)

Sandrine Caburet.css-eqlu8i{font-size:small;padding-left:4px;}