Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants
56 auth. Lucilla Pizzo, Matthew Jensen, Andrew Polyak, J. Rosenfeld, Katrin Mannik, Arjun Krishnan, E. McCready, Olivier Pichon, C. Le Caignec, Anke Van Dijck, K. Pope, E. Voorhoeve, J. Yoon, P. Stankiewicz, S. Cheung, ... D. Pazuchanics, Emily Huber, Vijay Kumar, Rachel L. Kember, F. Mari, Aurora Curró, L. Castiglia, O. Galesi, E. Avola, T. Mattina, M. Fichera, Luana Mandarà, M. Vincent, M. Nizon, S. Mercier, C. Bénéteau, S. Blesson, D. Martin‐Coignard, Anne-Laure Mosca-Boidron, J. Caberg, M. Bucan, S. Zeesman, M. Nowaczyk, M. Lefebvre, L. Faivre, P. Callier, C. Skinner, B. Keren, Charles Perrine, P. Prontera, N. Marle, A. Renieri, A. Reymond, R. Kooy, B. Isidor, C. Schwartz, C. Romano, E. Sistermans, D. Amor, J. Andrieux, S. Girirajan