Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Jhih Rong Lin, Yingjie Zhao, M. Reza Jabalameli, Nha Nguyen, Joydeep Mitra, Ann Swillen, Jacob A.S. Vorstman, Eva W.C. Chow, Marianne van den Bree, Beverly S. Emanuel, Joris R. Vermeesch, Michael J. Owen, Nigel M. Williams, Anne S. Bassett, Donna M. McDonald-McGinn, Raquel E. Gur, Carrie E. Bearden, Bernice E. Morrow, Herbert M. Lachman, Zhengdong D. Zhang