Ruben Attali

Alban Ziegler 1 collaboration

Rémi Duclaux-Loras 1 collaboration

Céline Revenu 1 collaboration

Fabienne Charbit-Henrion 1 collaboration

Bernadette Begue 1 collaboration

Karine Duroure 1 collaboration

Linda Grimaud 1 collaboration

Anne Laure Guihot 1 collaboration

Valérie Desquiret-Dumas 1 collaboration

Mohammed Zarhrate 1 collaboration

Nicolas Cagnard 1 collaboration

Emmanuel Mas 1 collaboration

Anne Breton 1 collaboration

Thomas Edouard 1 collaboration

Clarisse Billon 1 collaboration

Michael Frank 1 collaboration

Estelle Colin 1 collaboration

Guy Lenaers 1 collaboration

Daniel Henrion 1 collaboration

Stanislas Lyonnet 1 collaboration

Laurence Faivre 1 collaboration

Yves Alembik 1 collaboration

Anaïs Philippe 1 collaboration

Bruno Moulin 1 collaboration

Eyal Reinstein 1 collaboration

Shay Tzur 1 collaboration

George McGillivray 1 collaboration

Susan M White 1 collaboration

Lyndon Gallacher 1 collaboration

Kerstin Kutsche 1 collaboration

Pauline Schneeberger 1 collaboration

Katta M Girisha 1 collaboration

Shalini S Nayak 1 collaboration

Lynn Pais 1 collaboration

Reza Maroofian 1 collaboration

Aboulfazl Rad 1 collaboration

Barbara Vona 1 collaboration

Ehsan Ghayoor Karimiani 1 collaboration

Caroline Lekszas 1 collaboration

Thomas Haaf 1 collaboration

Ludovic Martin 1 collaboration

Frank Ruemmele 1 collaboration

Dominique Bonneau 1 collaboration

Nadine Cerf-Bensussan 1 collaboration

Filippo Del Bene 1 collaboration

Marianna Parlato 1 collaboration

Sara M Fielder 1 collaboration

Jill A Rosenfeld 1 collaboration

Lindsay C Burrage 1 collaboration

Lisa Emrick 1 collaboration

Seema Lalani 1 collaboration

Joshua N Bembenek 1 collaboration

Hieu Hoang 1 collaboration

Dustin Baldridge 1 collaboration

Gary A Silverman 1 collaboration

None None 1 collaboration

Tim Schedl 1 collaboration

Stephen C Pak 1 collaboration

Affiliations

Publications (2)

Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation.

Functional analysis of a novel de novo variant in PPP5C associated with microcephaly, seizures, and developmental delay.

Réseau de co-auteurs