Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Neuron2015Vol. 87(6), pp. 1215–1233
Citations Over TimeTop 1% of 2015 papers
Stephan Sanders, Xin He, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Kaitlin E. Samocha, A. Ercüment Çiçek, Michael T. Murtha, Vanessa H. Bal, Somer Bishop, Shan Dong, Arthur P. Goldberg, Jinlu Cai, John F. Keaney, Lambertus Klei, Jeffrey D. Mandell, Daniel Moreno‐De‐Luca, Christopher S. Poultney, Elise Robinson, Louw Smith, Tor Solli-Nowlan, Mack Y. Su, Nicole A. Teran, Michael F. Walker, Donna M. Werling, Arthur L. Beaudet, Rita M. Cantor, Éric Fombonne, Daniel H. Geschwind, Dorothy E. Grice, Catherine Lord, Jennifer K. Lowe, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Michael E. Talkowski, James S. Sutcliffe, Christopher A. Walsh, Timothy W. Yu, David H. Ledbetter, Christa Lese Martin, Edwin H. Cook, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Matthew W. State
Related Papers
- → Trio-whole exome sequencing reveals the importance of de novo variants in children with intellectual disability and developmental delay(2024)13 cited
- → Exome sequencing and the genetics of intellectual disability(2011)78 cited
- → SETD5 gene variant associated with mild intellectual disability - a case report(2017)19 cited
- → Estimation of association of CNTN6 copy number variation with idiopathic intellectual disability(2016)2 cited
- → WDR13: A Novel Gene Implicated in Non-Syndromic Intellectual Disability(2021)