Quo Vadis clinical genomics of ASD?
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Today, up to 15% of autism variants can be linked to genetic determinants, with future projections that as much as 50% of genetic etiologies are discoverable using sequencing approaches.
“Today, up to 15% of autism variants can be linked to genetic determinants, with future projections that as much as to 50% of genetic etiologies are discoverable using sequencing approaches [26].”
From The contribution of environmental exposure to the etiology of autism spectrum disorder (2019) · cites this paper as [26]
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References 27 · Cited by 5
- Authors
- Tammimies, K., Falck-Ytter, T., & Bölte, S.
- Venue
- Autism
- Publisher
- SAGE Publications
- Published
- 2016-02-19
- Volume
- 20
- Issue
- 3
- Pages
- 259-261
- ISSN
- 1362-3613 (ISSN-L)
- 1461-7005
- OpenAlex
- W2283023194
- Cited by
- 5
- References
- 27
- Citations by year
- 2024: 1 · 2021: 1 · 2018: 1 · 2017: 2
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Autism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- autism spectrum disorder, clinical genomics, genetic diagnosis, precision medicine
- MeSH terms
- Autism Spectrum Disorder, Humans, Genomics
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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