The DOI matches its Crossref record.
Genetics of autism
Abstract
Recent clinical and family studies of autism and fragile X syndrome are reviewed in the context of determining the mode of transmission of autism. Current data are not compatible with simple Mendelian transmission models. Other processes such as genetic anticipation and imprinting may be involved.
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The presence of affected father-son pairs is not compatible with simple X-linked transmission.
“As underscored by Todd and Hudziak (28) the presence of affected father–son pairs is not compatible with simple X-linked transmission.”
From Gene × Environment Interactions in Autism Spectrum Disorders: Role of Epigenetic Mechanisms (2014) · cites this paper as [28]
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Gene × Environment Interactions in Autism Spectrum Disorders: Role of Epigenetic Mechanisms
Tordjman, S., Somogyi, E., Coulon, N., Kermarrec, S., Cohen, D., Bronsard, G., Bonnot, O., Weismann-Arcache, C., Botbol, M., Lauth, B., et al. (2014) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2014.00053 · Cited by 283
Metadata
- Authors
- Todd, R. D., & Hudziak, J. J.
- Affiliations
- Washington University in St. Louis (US)
- University of Vermont (US)
- Corresponding author
- Hudziak, James J.
- ORCID
- Hudziak, James J.
- Venue
- Current Opinion in Psychiatry
- Published
- 1993-08
- Volume
- 6
- Issue
- 4
- Pages
- 486-488
- ISSN
- 0951-7367 (ISSN-L)
- OpenAlex
- W2026375163
- Cited by
- 6
- References
- 0
- Citations by year
- 2017: 1 · 2014: 1
- FWCI
- 0.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Opinion in Psychiatry (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
- Keywords
- autism spectrum disorder, fragile X syndrome, mode of inheritance, genetic anticipation, genomic imprinting, Mendelian inheritance, family studies, medical genetics
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