Literature DB >> 1708492

Etiology of autism: genetic influences.

S E Folstein1, J Piven.   

Abstract

In summary, there are a few specific genetic conditions that can be associated with autism. Among cases of unknown etiology, there is ample evidence for a higher genetic liability to autism in siblings of autistic probands than expected from the population prevalence. It appears likely that both parents and siblings have a higher liability for social and cognitive deficits that are milder but conceptually similar to those found in autism. Others factors may alter this underlying genetic liability such as sex, IQ, and prenatal and perinatal injury. In the future, genetic analyses and genetic linkage studies will need to consider using a broader definition of the autism phenotype to include not only autism but severe cognitive and social deficits. The exact genetic mechanisms and genes involved are the subject of current investigations by several research groups. Investigations in this area are likely to continue to provide important information about the causes of autism.

Entities:  

Mesh:

Year:  1991        PMID: 1708492

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  34 in total

Review 1.  Genetic studies of autism: from the 1970s into the millennium.

Authors:  M Rutter
Journal:  J Abnorm Child Psychol       Date:  2000-02

2.  Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families.

Authors:  Molly Losh; Debra Childress; Kristen Lam; Joseph Piven
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2008-06-05       Impact factor: 3.568

Review 3.  Early pharmacological treatment of autism: a rationale for developmental treatment.

Authors:  Terrence C Bethea; Linmarie Sikich
Journal:  Biol Psychiatry       Date:  2007-02-15       Impact factor: 13.382

4.  Abnormalities of cholesterol metabolism in autism spectrum disorders.

Authors:  Elaine Tierney; Irena Bukelis; Richard E Thompson; Khalid Ahmed; Alka Aneja; Lisa Kratz; Richard I Kelley
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2006-09-05       Impact factor: 3.568

5.  Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders.

Authors:  MarcosRobertoHigino Estécio; Agnes Cristina Fett-Conte; Marileila Varella-Garcia; Cíntia Fridman; Ana Elizabete Silva
Journal:  J Autism Dev Disord       Date:  2002-02

Review 6.  Etiology of infantile autism: a review of recent advances in genetic and neurobiological research.

Authors:  G Trottier; L Srivastava; C D Walker
Journal:  J Psychiatry Neurosci       Date:  1999-03       Impact factor: 6.186

7.  Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder.

Authors:  P Baker; J Piven; S Schwartz; S Patil
Journal:  J Autism Dev Disord       Date:  1994-08

8.  Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder.

Authors:  Shruti Dutta; Subha Das; Subhrangshu Guhathakurta; Barsha Sen; Swagata Sinha; Anindita Chatterjee; Sagarmoy Ghosh; Shabina Ahmed; Saurabh Ghosh; Rajamma Usha
Journal:  Cell Mol Neurobiol       Date:  2007-08-22       Impact factor: 5.046

9.  Association study with two markers of a human homeogene in infantile autism.

Authors:  E Petit; J Hérault; J Martineau; A Perrot; C Barthélémy; L Hameury; D Sauvage; G Lelord; J P Müh
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

10.  Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.

Authors:  J Hallmayer; E Pintado; L Lotspeich; D Spiker; W McMahon; P B Petersen; P Nicholas; C Pingree; H C Kraemer; D L Wong
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.