Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 2
2002 3
2003 1
2005 1
2006 2
2007 1
2008 3
2009 4
2010 2
2011 1
2014 1
2024 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

19 results

Results by year

Filters applied: . Clear all
Page 1
MET and autism susceptibility: family and case-control studies.
Sousa I, Clark TG, Toma C, Kobayashi K, Choma M, Holt R, Sykes NH, Lamb JA, Bailey AJ, Battaglia A, Maestrini E, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC). Sousa I, et al. Eur J Hum Genet. 2009 Jun;17(6):749-58. doi: 10.1038/ejhg.2008.215. Epub 2008 Nov 12. Eur J Hum Genet. 2009. PMID: 19002214 Free PMC article.
A 15q13.3 microdeletion segregating with autism.
Pagnamenta AT, Wing K, Sadighi Akha E, Knight SJ, Bölte S, Schmötzer G, Duketis E, Poustka F, Klauck SM, Poustka A, Ragoussis J, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium. Pagnamenta AT, et al. Eur J Hum Genet. 2009 May;17(5):687-92. doi: 10.1038/ejhg.2008.228. Epub 2008 Dec 3. Eur J Hum Genet. 2009. PMID: 19050728 Free PMC article.
Analysis of X chromosome inactivation in autism spectrum disorders.
Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsäter H, Rastam M, Gillberg IC, Gillberg C, Moreno-De-Luca D, Carone S, Nummela I, Rossi M, Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC); Jarvela I, Maestrini E, Bourgeron T. Gong X, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):830-5. doi: 10.1002/ajmg.b.30688. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18361425 Free PMC article.
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.
Sousa I, Clark TG, Holt R, Pagnamenta AT, Mulder EJ, Minderaa RB, Bailey AJ, Battaglia A, Klauck SM, Poustka F, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC). Sousa I, et al. Mol Autism. 2010 Mar 25;1(1):7. doi: 10.1186/2040-2392-1-7. Mol Autism. 2010. PMID: 20678249 Free PMC article.
FOXP2 is not a major susceptibility gene for autism or specific language impairment.
Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium. Newbury DF, et al. Am J Hum Genet. 2002 May;70(5):1318-27. doi: 10.1086/339931. Epub 2002 Mar 13. Am J Hum Genet. 2002. PMID: 11894222 Free PMC article.
19 results