The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Genetic Influences in Autism
Abstract
Autism represents a prototypical form of pervasive developmental disorder. In the majority of narrowly defined cases, there is no clearly identifiable aetiology. In this paper, the evidence for genetic influences that stems from twin, family, cytogenetic and molecular genetic studies is reviewed. It suggests that genetic factors play a predominant role in the origins of a more broadly defined phenotype, characterized by a combination of cognitive and social deficits. Genetic mechanisms that may account for the findings, including single gene, mixed and multifactorial models are evaluated and directions for future research are considered.
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Citations
Cites
Wing, L., & Gould, J. (1979) · Journal of Autism and Developmental Disorders · doi:10.1007/bf01531288 · Cited by 2,587
Asperger’s syndrome: a clinical account
Wing, L. (1981) · Psychological Medicine · doi:10.1017/s0033291700053332 · Cited by 1,913
INFANTILE AUTISM: A GENETIC STUDY OF 21 TWIN PAIRS
Folstein, S., & Rutter, M. (1977) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.1977.tb00443.x · Cited by 1,361
Self-citationHypoplasia of cerebellar vermal lobules VI and VII in autism
Courchesne, E., Yeung-Courchesne, R., Hesselink, J. R., & Jernigan, T. L. (1988) · New England Journal of Medicine · doi:10.1056/nejm198805263182102 · Cited by 1,058
Epidemiology of autistic conditions in young children: 1. Prevalence
Lotter, V. (1966) · Social Psychiatry · doi:10.1007/bf00584048 · Cited by 780
An analysis of autism in fifty males with the fragile X syndrome
Hagerman, R. J., Jackson, A. W., Levitas, A., Rimland, B., Braden, M., Opitz, J. M., & Reynolds, J. F. (1986) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320230128 · Cited by 238
Cited by
Baron-Cohen, S., Wheelwright, S., Skinner, R., Martin, J., & Clubley, E. (2001) · Journal of Autism and Developmental Disorders · doi:10.1023/a:1005653411471 · Cited by 6,450
Baron-Cohen, S., & Wheelwright, S. (2004) · Journal of Autism and Developmental Disorders · doi:10.1023/b:jadd.0000022607.19833.00 · Cited by 4,093
Autism as a strongly genetic disorder: evidence from a British twin study
Bailey, A., Le Couteur, A., Gottesman, I., Bolton, P., Simonoff, E., Yuzda, E., & Rutter, M. (1995) · Psychological Medicine · doi:10.1017/s0033291700028099 · Cited by 2,461
Self-citationBaron‐Cohen, S., Jolliffe, T., Mortimore, C., & Robertson, M. (1997) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.1997.tb01599.x · Cited by 1,970
A case-control family history study of autism
Bolton, P., Macdonald, H., Pickles, A., Rios, P., Goode, S., Crowson, M., Bailey, A., & Rutter, M. (1994) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.1994.tb02300.x · Cited by 1,094
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Metadata
- Authors
- Bolton, P., & Rutter, M.
- Venue
- International Review of Psychiatry
- Publisher
- Informa UK Limited
- Published
- 1990-01
- Volume
- 2
- Issue
- 1
- Pages
- 67-80
- ISSN
- 0954-0261 (ISSN-L)
- 1369-1627
- OpenAlex
- W2077285874
- Cited by
- 202
- References
- 6
- FWCI
- 26.30
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
