Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
University of Washington · University of Oxford · +5 more institutions
Indexed incrossrefpubmed
Abstract
No abstract available for this paper.
Citation impact
1,216
total citations
- FWCI
- 74.41
- Percentile
- 100%
- References
- 54
Citations per year
Authors
16- BJBrian J. O’RoakCorresponding
University of Washington
- PDPelagia Deriziotis
University of Oxford, Centre for Human Genetics, Max Planck Society, Max Planck Institute for Psycholinguistics
- CLCholi Lee
University of Washington
- LVLaura Vives
University of Washington
- JJJerrod J. Schwartz
University of Washington
Topics & keywords
Topics
Keywords
- Biology
- Exome sequencing
- Genetics
- Missense mutation
- Exome
- Proband
- Locus (genetics)
- Autism
UN Sustainable Development Goals
- Good health and well-being
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