Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?

por Amiet, Claire, Gourfinkel-An, Isabelle, Laurent, Claudine, Bodeau, Nicolas, Génin, Bérengère, Leguern, Eric, Tordjman, Sylvie, Cohen, David
Publicado 2013

Whole exome sequencing for determination of tumor mutation load in liquid biopsy from advanced cancer patients

por Koeppel, Florence, Blanchard, Steven, Jovelet, Cécile, Genin, Bérengère, Marcaillou, Charles, Martin, Emmanuel, Rouleau, Etienne, Solary, Eric, Soria, Jean-Charles, André, Fabrice, Lacroix, Ludovic
Publicado 2017

A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism

por Carayol, Jérôme, Schellenberg, Gerard D., Dombroski, Beth, Amiet, Claire, Génin, Bérengère, Fontaine, Karine, Rousseau, Francis, Vazart, Céline, Cohen, David, Frazier, Thomas W., Hardan, Antonio Y., Dawson, Geraldine, Rio Frio, Thomas
Publicado 2014