Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 212

Similar articles for PubMed (Select 16261168)

1.

Autism spectrum disorders associated with X chromosome markers in French-Canadian males.

Gauthier J, Joober R, Dubé MP, St-Onge J, Bonnel A, Gariépy D, Laurent S, Najafee R, Lacasse H, St-Charles L, Fombonne E, Mottron L, Rouleau GA.

Mol Psychiatry. 2006 Feb;11(2):206-13.

PMID:
16261168
2.

Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.

Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J.

BMC Med Genet. 2007 Dec 6;8:74.

3.

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.

Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T, Sinsheimer JS, Peltonen L, Järvelä I.

Am J Hum Genet. 2002 Oct;71(4):777-90. Epub 2002 Aug 21.

4.

Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.

Guhathakurta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Gangopadhyay PK, Usha R.

Brain Res. 2008 Nov 13;1240:12-21. doi: 10.1016/j.brainres.2008.08.063. Epub 2008 Sep 4.

PMID:
18804097
5.

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
6.

Association of the neuropilin-2 (NRP2) gene polymorphisms with autism in Chinese Han population.

Wu S, Yue W, Jia M, Ruan Y, Lu T, Gong X, Shuang M, Liu J, Yang X, Zhang D.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):492-5.

PMID:
17427189
7.

Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.

Conroy J, Cochrane L, Anney RJ, Sutcliffe JS, Carthy P, Dunlop A, Mullarkey M, O'hici B, Green AJ, Ennis S, Gill M, Gallagher L.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):535-44. doi: 10.1002/ajmg.b.30854.

PMID:
18846500
8.

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. Epub 2009 Nov 24.

PMID:
20050924
9.

Lack of association between autism and SLC25A12.

Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA.

Am J Psychiatry. 2006 May;163(5):929-31.

PMID:
16648338
10.

Evidence for multiple loci from a genome scan of autism kindreds.

Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM.

Mol Psychiatry. 2006 Nov;11(11):1049-60, 979. Epub 2006 Aug 1.

PMID:
16880825
11.

Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region.

Vincent JB, Melmer G, Bolton PF, Hodgkinson S, Holmes D, Curtis D, Gurling HM.

Psychiatr Genet. 2005 Jun;15(2):83-90.

PMID:
15900222
12.

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.

Martin I, Gauthier J, D'Amelio M, Védrine S, Vourc'h P, Rouleau GA, Persico AM, Andres CR.

Neurosci Res. 2007 Dec;59(4):426-30. Epub 2007 Aug 19.

PMID:
17897745
13.

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
14.

Chromosome 11-q24 region in Tourette syndrome: association and linkage disequilibrium study in the French Canadian population.

Díaz-Anzaldúa A, Rivière JB, Dubé MP, Joober R, Saint-Onge J, Dion Y, Lespérance P, Richer F, Chouinard S, Rouleau GA; Montreal Tourette Syndrome Study Group.

Am J Med Genet A. 2005 Oct 15;138A(3):225-8.

PMID:
16158425
15.

Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition.

Lerer E, Levi S, Salomon S, Darvasi A, Yirmiya N, Ebstein RP.

Mol Psychiatry. 2008 Oct;13(10):980-8. Epub 2007 Sep 25.

PMID:
17893705
16.

The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population.

Li H, Li Y, Shao J, Li R, Qin Y, Xie C, Zhao Z.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):194-200.

PMID:
17955477
17.

Association between PTGS2 polymorphism and autism spectrum disorders in Korean trios.

Yoo HJ, Cho IH, Park M, Cho E, Cho SC, Kim BN, Kim JW, Kim SA.

Neurosci Res. 2008 Sep;62(1):66-9. doi: 10.1016/j.neures.2008.05.008. Epub 2008 Jun 5.

PMID:
18579107
18.

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.

Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA, Dicicco-Bloom E, Brzustowicz LM, Millonig JH.

Am J Hum Genet. 2005 Nov;77(5):851-68. Epub 2005 Oct 5.

19.

Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios.

Kim SA, Kim JH, Park M, Cho IH, Yoo HJ.

Neuropsychobiology. 2006;54(3):160-5. Epub 2007 Jan 17.

PMID:
17230033
20.

Analysis of linkage and linkage disequilibrium for eight X-STR markers.

Tillmar AO, Mostad P, Egeland T, Lindblom B, Holmlund G, Montelius K.

Forensic Sci Int Genet. 2008 Dec;3(1):37-41. doi: 10.1016/j.fsigen.2008.09.006. Epub 2008 Oct 26.

PMID:
19083865
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk