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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.

High-dimensional multi-block analysis of factors associated with thrombin generation potential.

Lorenzo, H., Razzaq, M., Odeberg, J., Saracco, J., Tregouet, D.-A., Thiébaut, R. (2019)

IEEE 32nd International Symposium on Computer-Based Medical Systems (CBMS) 2019. DOI: 10.1109/CBMS.2019.00094

Bayesian Network Analysis of plasma microRNA sequencing data in patients with venous thrombosis.

Florian Thibord, Gaëlle Munsch, Claire Perret, Pierre Suchon, Maguelonne Roux, Manal Ibrahim-Kosta, Louisa Goumidi, Jean-François Deleuze, Pierre-Emmanuel Morange, David-Alexandre Trégouët on behalf of the GENMED consortium.

European Heart Journal Supplements, Oxford University Press (OUP), In press, Epub Ahead of print. inserm02310241

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.

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