Refined Mapping of a Quantitative Trait Locus on Chromosome 1 Responsible for Mouse Embryonic Death

by Vatin, Magalie, Burgio, Gaetan, Renault, Gilles, Laissue, Paul, Firlej, Virginie, Mondon, Françoise, Montagutelli, Xavier, Vaiman, Daniel, Serres, Catherine, Ziyyat, Ahmed
Published 2012

Exome Sequencing Is an Efficient Tool for Variant Late-Infantile Neuronal Ceroid Lipofuscinosis Molecular Diagnosis

by Patiño, Liliana Catherine, Battu, Rajani, Ortega-Recalde, Oscar, Nallathambi, Jeyabalan, Anandula, Venkata Ramana, Renukaradhya, Umashankar, Laissue, Paul
Published 2014

Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure

by Caburet, Sandrine, Zavadakova, Petra, Ben-Neriah, Ziva, Bouhali, Kamal, Dipietromaria, Aurélie, Charon, Céline, Besse, Céline, Laissue, Paul, Chalifa-Caspi, Vered, Christin-Maitre, Sophie, Vaiman, Daniel, Levi, Giovanni, Veitia, Reiner A., Fellous, Marc
Published 2012

Whole-Exome Sequencing Enables Rapid Determination of Xeroderma Pigmentosum Molecular Etiology

by Ortega-Recalde, Oscar, Vergara, Jéssica Inés, Fonseca, Dora Janeth, Ríos, Xiomara, Mosquera, Hernando, Bermúdez, Olga María, Medina, Claudia Liliana, Vargas, Clara Inés, Pallares, Argemiro Enrique, Restrepo, Carlos Martín, Laissue, Paul
Published 2013

Success stories in genomic medicine from resource-limited countries

by Mitropoulos, Konstantinos, Al Jaibeji, Hayat, Forero, Diego A., Laissue, Paul, Wonkam, Ambroise, Lopez-Correa, Catalina, Mohamed, Zahurin, Chantratita, Wasun, Lee, Ming Ta Michael, Llerena, Adrian, Brand, Angela, Ali, Bassam R., Patrinos, George P.
Published 2015

Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

by Ducat, Aurélien, Doridot, Ludivine, Calicchio, Rosamaria, Méhats, Celine, Vilotte, Jean-Luc, Castille, Johann, Barbaux, Sandrine, Couderc, Betty, Jacques, Sébastien, Letourneur, Franck, Buffat, Christophe, Le Grand, Fabien, Laissue, Paul, Miralles, Francisco, Vaiman, Daniel
Published 2016

Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

by Laissue, Paul, Lakhal, Besma, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Gris, Jean-Christophe, Cocquet, Julie, Vaiman, Daniel
Published 2016