Publications

A Novel Rare c.-39C>T Mutation in the PROS1 5'UTR Causing PS Deficiency by Creating a New Upstream Translation Initiation Codons.

Labrouche-Colomer  S, Soukarieh O,  Proust C, Mouton C, Huguenin Y, Roux M , Besse C, Boland A, Olaso R , Constans J,  Deleuze JF , Morange PE , Jaspard-Vinassa B , Trégouët DA.

Clin Sci (Lond)  2020 May 19;CS20200403. doi: 10.1042/CS20200403. Online ahead of print [PMID: 32426810].

Associations of autozygosity with a broad range of human phenotypes.

Clark et al.

Nat Commun. 2019 Oct 31;10(1):4957. doi: 10.1038/s41467-019-12283-6. PMID: 31673082.

Unification of miRNA and isomiR research: the mirGFF3 format and the mirtop API

Desvignes T,  Loher P, Eilbeck K,  Ma J,  Urgese G, Fromm B, Sydes J,  Aparicio-Puerta E,  Barrera V,  Espín R, Thibord F,  Bofill-De Ros X, Londin E, Telonis AG, Ficarra E,  Friedländer MR, Postlethwait JH, Rigoutsos I, Hackenberg M, Vlachos IS,  Halushka MK , Pantano L

Bioinformatics, btz675, https://doi.org/10.1093/bioinformatics/btz675.

Evaluation of six blood-based age prediction models using DNA methylation analysis by pyrosequencing.

Daunay A, Baudrin LG, Deleuze JF, How-Kit A

Sci Rep. 2019 Jun 20;9(1):8862. doi: 10.1038/s41598-019-45197-w.

cephinsermuniversiteBordeauxceacng