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Results: 1 to 20 of 195

1.

Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.

Campbell DB, Buie TM, Winter H, Bauman M, Sutcliffe JS, Perrin JM, Levitt P.

Pediatrics. 2009 Mar;123(3):1018-24. doi: 10.1542/peds.2008-0819. Erratum in: Pediatrics. 2009 Apr;123(4):1255.

PMID:
19255034
[PubMed - indexed for MEDLINE]
2.

Association of MET with social and communication phenotypes in individuals with autism spectrum disorder.

Campbell DB, Warren D, Sutcliffe JS, Lee EB, Levitt P.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):438-46. doi: 10.1002/ajmg.b.30998.

PMID:
19548256
[PubMed - indexed for MEDLINE]
3.

Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder.

Jackson PB, Boccuto L, Skinner C, Collins JS, Neri G, Gurrieri F, Schwartz CE.

Autism Res. 2009 Aug;2(4):232-6. doi: 10.1002/aur.87.

PMID:
19681062
[PubMed - indexed for MEDLINE]
4.

A genetic variant that disrupts MET transcription is associated with autism.

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P.

Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16834-9. Epub 2006 Oct 19.

PMID:
17053076
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.

Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P.

Autism Res. 2008 Jun;1(3):159-68. doi: 10.1002/aur.27.

PMID:
19360663
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Disruption of cerebral cortex MET signaling in autism spectrum disorder.

Campbell DB, D'Oronzio R, Garbett K, Ebert PJ, Mirnics K, Levitt P, Persico AM.

Ann Neurol. 2007 Sep;62(3):243-50.

PMID:
17696172
[PubMed - indexed for MEDLINE]
7.

Further evidence for the role of MET in autism susceptibility.

Thanseem I, Nakamura K, Miyachi T, Toyota T, Yamada S, Tsujii M, Tsuchiya KJ, Anitha A, Iwayama Y, Yamada K, Hattori E, Matsuzaki H, Matsumoto K, Iwata Y, Suzuki K, Suda S, Kawai M, Sugihara G, Takebayashi K, Takei N, Ichikawa H, Sugiyama T, Yoshikawa T, Mori N.

Neurosci Res. 2010 Oct;68(2):137-41. doi: 10.1016/j.neures.2010.06.014. Epub 2010 Jul 6.

PMID:
20615438
[PubMed - indexed for MEDLINE]
8.

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).

Eur J Hum Genet. 2009 Jun;17(6):749-58. doi: 10.1038/ejhg.2008.215. Epub 2008 Nov 12.

PMID:
19002214
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
[PubMed - indexed for MEDLINE]
10.

Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.

Plummer JT, Evgrafov OV, Bergman MY, Friez M, Haiman CA, Levitt P, Aldinger KA.

Transl Psychiatry. 2013 Oct 22;3:e316. doi: 10.1038/tp.2013.91.

PMID:
24150225
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

A surprising METamorphosis: autism genetics finds a common functional variant.

State MW.

Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16621-2. Epub 2006 Oct 30. No abstract available.

PMID:
17075042
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders.

Levitt P, Campbell DB.

J Clin Invest. 2009 Apr;119(4):747-54. doi: 10.1172/JCI37934. Epub 2009 Apr 1. Review.

PMID:
19339766
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Association of a MET genetic variant with autism-associated maternal autoantibodies to fetal brain proteins and cytokine expression.

Heuer L, Braunschweig D, Ashwood P, Van de Water J, Campbell DB.

Transl Psychiatry. 2011 Oct 18;1:e48. doi: 10.1038/tp.2011.48.

PMID:
22833194
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Possible association between the androgen receptor gene and autism spectrum disorder.

Henningsson S, Jonsson L, Ljunggren E, Westberg L, Gillberg C, Råstam M, Anckarsäter H, Nygren G, Landén M, Thuresson K, Betancur C, Leboyer M, Gillberg C, Eriksson E, Melke J.

Psychoneuroendocrinology. 2009 Jun;34(5):752-61. doi: 10.1016/j.psyneuen.2008.12.007. Epub 2009 Jan 23.

PMID:
19167832
[PubMed - indexed for MEDLINE]
15.

Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects.

Carayol J, Sacco R, Tores F, Rousseau F, Lewin P, Hager J, Persico AM.

Biol Psychiatry. 2011 Nov 1;70(9):880-7. doi: 10.1016/j.biopsych.2011.05.020. Epub 2011 Jul 14.

PMID:
21757185
[PubMed - indexed for MEDLINE]
16.

Autism risk gene MET variation and cortical thickness in typically developing children and adolescents.

Hedrick A, Lee Y, Wallace GL, Greenstein D, Clasen L, Giedd JN, Raznahan A.

Autism Res. 2012 Dec;5(6):434-9. doi: 10.1002/aur.1256. Epub 2012 Oct 24.

PMID:
23097380
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Macrophage migration inhibitory factor and autism spectrum disorders.

Grigorenko EL, Han SS, Yrigollen CM, Leng L, Mizue Y, Anderson GM, Mulder EJ, de Bildt A, Minderaa RB, Volkmar FR, Chang JT, Bucala R.

Pediatrics. 2008 Aug;122(2):e438-45. doi: 10.1542/peds.2007-3604.

PMID:
18676531
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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

Dutta S, Das S, Guhathakurta S, Sen B, Sinha S, Chatterjee A, Ghosh S, Ahmed S, Ghosh S, Usha R.

Cell Mol Neurobiol. 2007 Dec;27(8):1035-47. Epub 2007 Aug 22.

PMID:
17712621
[PubMed - indexed for MEDLINE]
19.

Reelin gene alleles and susceptibility to autism spectrum disorders.

Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson DR, Guidotti AR, Holden JJ.

Mol Psychiatry. 2002;7(9):1012-7.

PMID:
12399956
[PubMed - indexed for MEDLINE]
Free Article
20.

Family-based and population study of a functional promoter-region monoamine oxidase A polymorphism in autism: possible association with IQ.

Yirmiya N, Pilowsky T, Tidhar S, Nemanov L, Altmark L, Ebstein RP.

Am J Med Genet. 2002 Apr 8;114(3):284-7.

PMID:
11920849
[PubMed - indexed for MEDLINE]

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