Cited by 5Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Quo Vadis clinical genomics of ASD?

Tammimies, Kristiina, Falck-Ytter, Terje, Bölte, Sven·2016·Autism

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Crossref · 10.1177/1362361316635798

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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].”

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References 27 · Cited by 5

Authors
Tammimies, K., Falck-Ytter, T., & Bölte, S.
Venue
Autism
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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