den Hoed, Joery
de Boer, Elke
Voisin, Norine
Dingemans, Alexander J.M.
Guex, Nicolas
Wiel, Laurens
Nellaker, Christoffer
Amudhavalli, Shivarajan M.
Banka, Siddharth
Bena, Frederique S.
Ben-Zeev, Bruria
Bonagura, Vincent R.
Bruel, Ange-Line
Brunet, Theresa
Brunner, Han G.
Chew, Hui B.
Chrast, Jacqueline
Cimbalistienė, Loreta
Coon, Hilary
Délot, Emmanuèlle C.
Démurger, Florence
Denommé-Pichon, Anne-Sophie
Depienne, Christel
Donnai, Dian
Dyment, David A.
Elpeleg, Orly
Faivre, Laurence
Gilissen, Christian
Granger, Leslie
Haber, Benjamin
Hachiya, Yasuo
Abedi, Yasmin Hamzavi
Hanebeck, Jennifer
Hehir-Kwa, Jayne Y.
Horist, Brooke
Itai, Toshiyuki
Jackson, Adam
Jewell, Rosalyn
Jones, Kelly L.
Joss, Shelagh
Kashii, Hirofumi
Kato, Mitsuhiro
Kattentidt-Mouravieva, Anja A.
Kok, Fernando
Kotzaeridou, Urania
Krishnamurthy, Vidya
Kučinskas, Vaidutis
Kuechler, Alma
Lavillaureix, Alinoë
Liu, Pengfei
Manwaring, Linda
Matsumoto, Naomichi
Mazel, Benoît
McWalter, Kirsty
Meiner, Vardiella
Mikati, Mohamad A.
Miyatake, Satoko
Mizuguchi, Takeshi
Moey, Lip H.
Mohammed, Shehla
Mor-Shaked, Hagar
Mountford, Hayley
Newbury-Ecob, Ruth
Odent, Sylvie
Orec, Laura
Osmond, Matthew
Palculict, Timothy B.
Parker, Michael
Petersen, Andrea K.
Pfundt, Rolph
Preikšaitienė, Eglė
Radtke, Kelly
Ranza, Emmanuelle
Rosenfeld, Jill A.
Santiago-Sim, Teresa
Schwager, Caitlin
Sinnema, Margje
Snijders Blok, Lot
Spillmann, Rebecca C.
Stegmann, Alexander P.A.
Thiffault, Isabelle
Tran, Linh
Vaknin-Dembinsky, Adi
Vedovato-dos-Santos, Juliana H.
Schrier Vergano, Samantha A.
Vilain, Eric
Vitobello, Antonio
Wagner, Matias
Waheeb, Androu
Willing, Marcia
Zuccarelli, Britton
Kini, Usha
Newbury, Dianne F.
Kleefstra, Tjitske
Reymond, Alexandre
Fisher, Simon E.
Vissers, Lisenka E.L.M.
Funding for this research was provided by:
Max-Planck-Gesellschaft
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
This article is maintained by: Elsevier
Article Title: Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2021.01.007
Content Type: article
Copyright: © 2021 American Society of Human Genetics.