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Items: 1 to 20 of 79

1.

Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study.

Cho SC, Yoo HJ, Park M, Cho IH, Kim BN, Kim JW, Shin MS, Park TW, Son JW, Chung US, Kim HW, Yang YH, Kang JO, Yang SY, Kim SA.

Psychiatry Investig. 2011 Mar;8(1):61-6. doi: 10.4306/pi.2011.8.1.61. Epub 2011 Feb 25.

2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
3.

Role of metabotropic glutamate receptor 7 in autism spectrum disorders: a pilot study.

Yang Y, Pan C.

Life Sci. 2013 Feb 7;92(2):149-53. doi: 10.1016/j.lfs.2012.11.010. Epub 2012 Nov 28.

PMID:
23201551
4.

Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios.

Cho IH, Yoo HJ, Park M, Lee YS, Kim SA.

Brain Res. 2007 Mar 30;1139:34-41. Epub 2007 Jan 8.

PMID:
17280648
5.

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
6.

Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample.

Kantojärvi K, Onkamo P, Vanhala R, Alen R, Hedman M, Sajantila A, Nieminen-von Wendt T, Järvelä I.

Psychiatr Genet. 2010 Jun;20(3):102-8. doi: 10.1097/YPG.0b013e32833a2080.

PMID:
20410850
7.

Genome-wide association study of autistic-like traits in a general population study of young adults.

Jones RM, Cadby G, Melton PE, Abraham LJ, Whitehouse AJ, Moses EK.

Front Hum Neurosci. 2013 Oct 11;7:658. doi: 10.3389/fnhum.2013.00658. eCollection 2013.

8.

Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.

Liu X, Shimada T, Otowa T, Wu YY, Kawamura Y, Tochigi M, Iwata Y, Umekage T, Toyota T, Maekawa M, Iwayama Y, Suzuki K, Kakiuchi C, Kuwabara H, Kano Y, Nishida H, Sugiyama T, Kato N, Chen CH, Mori N, Yamada K, Yoshikawa T, Kasai K, Tokunaga K, Sasaki T, Gau SS.

Autism Res. 2016 Mar;9(3):340-9. doi: 10.1002/aur.1536. Epub 2015 Aug 28.

PMID:
26314684
9.

Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage.

Spence SJ, Cantor RM, Chung L, Kim S, Geschwind DH, Alarcón M.

Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):591-8.

10.

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
11.

Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean.

Yoo HJ, Lee SK, Park M, Cho IH, Hyun SH, Lee JC, Yang SY, Kim SA.

Neurosci Res. 2009 Mar;63(3):172-6. doi: 10.1016/j.neures.2008.11.007. Epub 2008 Nov 30.

PMID:
19100789
12.

A common variant in DRD3 receptor is associated with autism spectrum disorder.

de Krom M, Staal WG, Ophoff RA, Hendriks J, Buitelaar J, Franke B, de Jonge MV, Bolton P, Collier D, Curran S, van Engeland H, van Ree JM.

Biol Psychiatry. 2009 Apr 1;65(7):625-30. doi: 10.1016/j.biopsych.2008.09.035. Epub 2008 Dec 5.

PMID:
19058789
13.

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.

Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.

Neurosci Lett. 2008 Aug 15;441(1):56-60. doi: 10.1016/j.neulet.2008.06.022. Epub 2008 Jun 13.

PMID:
18597938
14.

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.

Chung RH, Ma D, Wang K, Hedges DJ, Jaworski JM, Gilbert JR, Cuccaro ML, Wright HH, Abramson RK, Konidari I, Whitehead PL, Schellenberg GD, Hakonarson H, Haines JL, Pericak-Vance MA, Martin ER.

Mol Autism. 2011 Nov 4;2(1):18. doi: 10.1186/2040-2392-2-18.

15.

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
16.

Family-based association study between GRIK2 polymorphisms and autism spectrum disorders in the Korean trios.

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

Neurosci Res. 2007 Jul;58(3):332-5. Epub 2007 Mar 13.

PMID:
17428563
17.

Association with tryptophan hydroxylase 2 gene polymorphisms and autism spectrum disorders in Korean families.

Yang SY, Yoo HJ, Cho IH, Park M, Kim SA.

Neurosci Res. 2012 Aug;73(4):333-6. doi: 10.1016/j.neures.2012.05.012. Epub 2012 Jun 12.

PMID:
22698779
18.

Examination of association to autism of common genetic variationin genes related to dopamine.

Anderson BM, Schnetz-Boutaud N, Bartlett J, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.

Autism Res. 2008 Dec;1(6):364-9. doi: 10.1002/aur.55.

19.

Clinic attenders with autism or attention-deficit/hyperactivity disorder: cognitive profile at school age and its relationship to preschool indicators of language delay.

Hagberg BS, Miniscalco C, Gillberg C.

Res Dev Disabil. 2010 Jan-Feb;31(1):1-8. doi: 10.1016/j.ridd.2009.07.012. Epub 2009 Aug 26.

PMID:
19713073
20.

No association between common variants in glyoxalase 1 and autism spectrum disorders.

Rehnström K, Ylisaukko-Oja T, Vanhala R, von Wendt L, Peltonen L, Hovatta I.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):124-7.

PMID:
17722011
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