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

authors

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

publication date

  • March 3, 2023