Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. uri icon

authors

  • Fu, Jack M
  • Hao, Stephanie P
  • Stevens, Christine R
  • Cusick, Caroline
  • Babadi, Mehrtash
  • Banks, Eric
  • Collins, Brett
  • Dodge, Sheila
  • Gabriel, Stacey B
  • Gauthier, Laura
  • Lee, Samuel K
  • Satterstrom, F Kyle
  • Liang, Lindsay
  • Ljungdahl, Alicia
  • Mahjani, Behrang
  • Sloofman, Laura
  • Smirnov, Andrey N
  • Barbosa, Mafalda
  • Betancur, Catalina
  • Brusco, Alfredo
  • Chung, Brian H Y
  • Cook, Edwin H
  • Peng, Minshi
  • Cuccaro, Michael L
  • Domenici, Enrico
  • Ferrero, Giovanni Battista
  • Gargus, J Jay
  • Herman, Gail E
  • Hertz-Picciotto, Irva
  • Maciel, Patricia
  • Manoach, Dara S
  • Passos-Bueno, Maria Rita
  • Persico, Antonio M
  • Brand, Harrison
  • Renieri, Alessandra
  • Sutcliffe, James S
  • Tassone, Flora
  • Trabetti, Elisabetta
  • Campos, Gabriele
  • Cardaropoli, Simona
  • Carli, Diana
  • Chan, Marcus C Y
  • Fallerini, Chiara
  • Giorgio, Elisa
  • Collins, Ryan L
  • Girardi, Ana Cristina
  • Hansen-Kiss, Emily
  • Lee, So Lun
  • Lintas, Carla
  • Ludena, Yunin
  • Nguyen, Rachel
  • Pavinato, Lisa
  • Pericak-Vance, Margaret
  • Pessah, Isaac N
  • Schmidt, Rebecca J
  • Dong, Shan
  • Smith, Moyra
  • Costa, Claudia I S
  • Trajkova, Slavica
  • Wang, Jaqueline Y T
  • Yu, Mullin H C
  • Cutler, David J
  • De Rubeis, Silvia
  • Wamsley, Brie
  • Buxbaum, Joseph D
  • Daly, Mark J
  • Devlin, Bernie
  • Roeder, Kathryn
  • Sanders, Stephan J
  • Talkowski, Michael E
  • Klei, Lambertus
  • Wang, Lily

publication date

  • January 1, 2022