Mirzaa, Ghayda M. http://orcid.org/0000-0003-2648-7657
Chong, Jessica X.
Piton, Amélie
Popp, Bernt
Foss, Kimberly
Guo, Hui
Harripaul, Ricardo
Xia, Kun
Scheck, Joshua
Aldinger, Kimberly A.
Sajan, Samin A.
Tang, Sha
Bonneau, Dominique
Beck, Anita
White, Janson
Mahida, Sonal
Harris, Jacqueline
Smith-Hicks, Constance
Hoyer, Juliane
Zweier, Christiane
Reis, André
Thiel, Christian T.
Jamra, Rami Abou
Zeid, Natasha
Yang, Amy
Farach, Laura S.
Walsh, Laurence
Payne, Katelyn
Rohena, Luis
Velinov, Milen
Ziegler, Alban
Schaefer, Elise
Gatinois, Vincent
Geneviève, David
Simon, Marleen E.H.
Kohler, Jennefer
Rotenberg, Joshua
Wheeler, Patricia
Larson, Austin
Ernst, Michelle E.
Akman, Cigdem I.
Westman, Rachel
Blanchet, Patricia
Schillaci, Lori-Anne
Vincent-Delorme, Catherine
Gripp, Karen W.
Mattioli, Francesca
Guyader, Gwenaël Le
Gerard, Bénédicte
Mathieu-Dramard, Michèle
Morin, Gilles
Sasanfar, Roksana
Ayub, Muhammad
Vasli, Nasim
Yang, Sandra
Person, Rick
Monaghan, Kristin G.
Nickerson, Deborah A.
van Binsbergen, Ellen
Enns, Gregory M.
Dries, Annika M.
Rowe, Leah J.
Tsai, Anne C.H.
Svihovec, Shayna
Friedman, Jennifer
Agha, Zehra
Qamar, Raheel
Rodan, Lance H.
Martinez-Agosto, Julian
Ockeloen, Charlotte W.
Vincent, Marie
Sunderland, William James
Bernstein, Jonathan A.
Eichler, Evan E.
Vincent, John B.
Bamshad, Michael J.
Funding for this research was provided by:
NARSAD New Investigator Award (UM1 HG006493, UM1 HG006493)
Peterborough K.M. Hunter Charitable Foundation Graduate Scholarship
the Agence de la Biomédecine and the CREGEMES, the Canadian Institutes of Health Research (31671114)
National Natural Science Foundation of China
National Institute of Neurological Disorders and Stroke (K08NS092898)
This article is maintained by: Elsevier
Article Title: De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0693-9
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics