Author:
Frohlich Joel,Senturk Damla,Saravanapandian Vidya,Golshani Peyman,Reiter Lawrence T.,Sankar Raman,Thibert Ronald L.,DiStefano Charlotte,Huberty Scott,Cook Edwin H.,Jeste Shafali S.
Funder
National Institutes of Health
Dup15q Alliance
National Institute of General Medical Sciences
National Institute of Child Health and Human Development
National Institute of Mental Health
Publisher
Public Library of Science (PLoS)
Reference50 articles.
1. Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions;GB Schaefer;Genetics in Medicine,2013
2. Most genetic risk for autism resides with common variation;T Gaugler;Nature genetics,2014
3. Molecular diagnostic yield of chromosomal microarray analysis and whole-exome sequencing in children with autism spectrum disorder;K Tammimies;JAMA,2015
4. Electrophysiological biomarkers of diagnosis and outcome in neurodevelopmental disorders;SS Jeste;Curr Opin Neurol,2015
5. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication;EH Cook Jr;American journal of human genetics,1997
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