Distinct Genetic Risk Based on Association of <i>MET</i> in Families With Co-occurring Autism and Gastrointestinal Conditions
Jerry L. Campbell(Grand Rapids Community College), Pat Levitt(University of Southern California), James M. Perrin(Harvard University), Margaret L. Bauman(Boston Children's Hospital), Harland S. Winter(Massachusetts General Hospital), James S. Sutcliffe(Vanderbilt University), Timothy Buie(Harvard University)
Cited by 145
Related Papers
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
|Cell|1991|2.1k
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
|Neuron|2015|1.5k
Consensus guidelines of ECCO/ESPGHAN on the medical management of pediatric Crohn's disease
|Journal of Crohn s and Colitis|2014|1.1k
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
|Nature Genetics|1997|875