ORCID Profile
0000-0002-9087-526X
Current Organisation
University of California, San Diego
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Publisher: Springer Science and Business Media LLC
Date: 30-09-2015
DOI: 10.1038/NATURE15394
Publisher: Springer Science and Business Media LLC
Date: 11-12-1994
DOI: 10.1038/NATURE15393
Publisher: Elsevier BV
Date: 03-2014
Publisher: Springer Science and Business Media LLC
Date: 14-02-2010
DOI: 10.1038/NG.534
Publisher: Springer Science and Business Media LLC
Date: 12-06-2011
DOI: 10.1038/NG.862
Publisher: American Psychiatric Association Publishing
Date: 05-2009
Publisher: Springer Science and Business Media LLC
Date: 31-10-2012
DOI: 10.1038/NATURE11632
Publisher: American Association for the Advancement of Science (AAAS)
Date: 20-04-2018
Abstract: About one-quarter of genetic variants that are associated with autism spectrum disorder (ASD) are due to de novo mutations in protein-coding genes. Brandler et al. wanted to determine whether changes in noncoding regions of the genome are associated with autism. They applied whole-genome sequencing to ∼2600 families with at least one affected child. Children with ASD had inherited structural variants in noncoding regions from their father. Regulatory regions of some specific genes were disrupted among multiple families, supporting the idea that a component of autism risk involves inherited noncoding variation. Science , this issue p. 327
Location: United States of America
Location: United States of America
No related grants have been discovered for Jonathan Sebat.