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Paper Details

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
Am J Hum Genet
190
2016
ARID1B, Autism, CANX, CNV, CNVs, DISC1, DNase I, DNase I hypersensitive sites, DSCAM, MBD5, NR3C2, PIK3CA, PRKCA, Putative Noncoding Regulatory DNA, RBFOX1, SAE1, SCN2A, SNV, WNT7A, autism, copy-number variant, exon, gene, neurodevelopmental genes, putative regulatory regions, regulatory elements, simplex autism
Author NameAffiliation
Fereydoun HormozdiariUniversity of Washington School of Medicine
Michael H DuyzendUniversity of Washington School of Medicine
Carl BakerUniversity of Washington School of Medicine
Carl BakerUniversity of Washington School of Medicine
Michael C Zody
Michael C Zody
Richard SandstromUniversity of Washington School of Medicine
Richard SandstromUniversity of Washington School of Medicine
Joshua D SmithUniversity of Washington School of Medicine
Joshua D SmithUniversity of Washington School of Medicine
Michael J BamshadUniversity of Washington School of Medicine
Michael J BamshadUniversity of Washington School of Medicine
John A StamatoyannopoulosUniversity of Washington School of Medicine
John A StamatoyannopoulosUniversity of Washington School of Medicine
Deborah A NickersonUniversity of Washington School of Medicine
Deborah A NickersonUniversity of Washington School of Medicine
Andrew S McCallionMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Andrew S McCallionMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Robert B DarnellUSA Howard Hughes Medical Institute, University of Washington, USA Rockefeller University
Evan E EichlerUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute, University of Washington
Evan E EichlerUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute, University of Washington
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