Rare Coding Variation Illuminates the Allelic Architecture, Risk Genes, Cellular Expression Patterns, and Phenotypic Context of Autism
Jack M. Fu,F. Kyle Satterstrom,Minshi Peng,Harrison Brand,Ryan L. Collins,Shan Dong,Lambertus Klei,Christine R. Stevens,Caroline Cusick,Mehrtash Babadi,Eric Banks,Brett Collins,Sheila Dodge,Stacey B. Gabriel,Laura Gauthier,Samuel K. Lee,Lindsay Liang,Alicia Ljungdahl,Behrang Mahjani,Laura Sloofman,Andrey Smirnov,Mafalda Barbosa,Alfredo Brusco,Brian H.Y. Chung,Michael L. Cuccaro,Enrico Domenici,Giovanni Battista Ferrero,Jay J. Gargus,Gail E. Herman,Irva Hertz-Picciotto,Patricia Maciel,Dara S. Manoach,Maria Rita Passos-Bueno,Antonio M. Persico,Alessandra Renieri,Flora Tassone,Elisabetta Trabetti,Gabriele Campos,Marcus C.Y. Chan,Chiara Fallerini,Elisa Giorgio, Ana Cristina Girard,Emily Hansen-Kiss,So Lun Lee,Carla Lintas,Yunin Ludena,Rachel Nguyen,Lisa Pavinato,Margaret Pericak-Vance,Isaac Pessah,Evelise Riberi,Rebecca Schmidt,Moyra Smith, Claudia I.C. Souza,Slavica Trajkova,Jaqueline Y.T. Wang,Mullin H.C. Yu,David J. Cutler,Silvia De Rubeis,Joseph D. Buxbaum,Mark J. Daly,Bernie Devlin,Kathryn Roeder,Stephan J. Sanders,Michael E. Talkowski medRxiv（2021）
Key words
Exome Sequencing
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