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Items: 1 to 20 of 240

1.

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
2.

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
3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
4.

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
5.

Serotonin transporter intron 2 polymorphism associated with rigid-compulsive behaviors in Dutch individuals with pervasive developmental disorder.

Mulder EJ, Anderson GM, Kema IP, Brugman AM, Ketelaars CE, de Bildt A, van Lang ND, den Boer JA, Minderaa RB.

Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):93-6.

PMID:
15635668
6.

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.

PMID:
20615438
7.

Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skills.

Yirmiya N, Rosenberg C, Levi S, Salomon S, Shulman C, Nemanov L, Dina C, Ebstein RP.

Mol Psychiatry. 2006 May;11(5):488-94.

PMID:
16520824
8.

Role of the serotonin transporter gene in the behavioral expression of autism.

Tordjman S, Gutknecht L, Carlier M, Spitz E, Antoine C, Slama F, Carsalade V, Cohen DJ, Ferrari P, Roubertoux PL, Anderson GM.

Mol Psychiatry. 2001 Jul;6(4):434-9.

9.

HLA-DR4 as a risk allele for autism acting in mothers of probands possibly during pregnancy.

Johnson WG, Buyske S, Mars AE, Sreenath M, Stenroos ES, Williams TA, Stein R, Lambert GH.

Arch Pediatr Adolesc Med. 2009 Jun;163(6):542-6. doi: 10.1001/archpediatrics.2009.74.

PMID:
19487610
10.

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.

Kaufmann WE, Cortell R, Kau AS, Bukelis I, Tierney E, Gray RM, Cox C, Capone GT, Stanard P.

Am J Med Genet A. 2004 Sep 1;129A(3):225-34.

PMID:
15326621
11.

Quantifying the phenotype in autism spectrum disorders.

Lord C, Leventhal BL, Cook EH Jr.

Am J Med Genet. 2001 Jan 8;105(1):36-8.

PMID:
11424991
12.

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.

13.

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.

Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):628-36. doi: 10.1002/ajmg.b.30655.

PMID:
18205172
14.

Heterogeneous association between engrailed-2 and autism in the CPEA network.

Brune CW, Korvatska E, Allen-Brady K, Cook EH Jr, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):187-93.

PMID:
17948868
15.

Family-based studies indicate association of Engrailed 2 gene with autism in an Indian population.

Sen B, Singh AS, Sinha S, Chatterjee A, Ahmed S, Ghosh S, Usha R.

Genes Brain Behav. 2010 Mar 1;9(2):248-55. doi: 10.1111/j.1601-183X.2009.00556.x.

16.

Copy number and sequence variants implicate APBA2 as an autism candidate gene.

Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.

Autism Res. 2009 Dec;2(6):359-64. doi: 10.1002/aur.107.

PMID:
20029827
17.

Autism spectrum disorder in the second year: stability and change in syndrome expression.

Chawarska K, Klin A, Paul R, Volkmar F.

J Child Psychol Psychiatry. 2007 Feb;48(2):128-38.

PMID:
17300551
18.

Autism spectrum disorder: interaction of air pollution with the MET receptor tyrosine kinase gene.

Volk HE, Kerin T, Lurmann F, Hertz-Picciotto I, McConnell R, Campbell DB.

Epidemiology. 2014 Jan;25(1):44-7. doi: 10.1097/EDE.0000000000000030.

19.

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.

Am J Hum Genet. 2005 Aug;77(2):265-79.

20.

Domains of social communication handicap in autism spectrum disorder.

Robertson JM, Tanguay PE, L'Ecuyer S, Sims A, Waltrip C.

J Am Acad Child Adolesc Psychiatry. 1999 Jun;38(6):738-45.

PMID:
10361793

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