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Items: 1 to 20 of 99

1.

No association between the EN2 gene and autistic disorder.

Zhong H, Serajee FJ, Nabi R, Huq AH.

J Med Genet. 2003 Jan;40(1):e4. No abstract available.

2.

Association of the homeobox transcription factor gene ENGRAILED 2 with autistic disorder in Chinese children.

Yang P, Lung FW, Jong YJ, Hsieh HY, Liang CL, Juo SH.

Neuropsychobiology. 2008;57(1-2):3-8. doi: 10.1159/000123115.

PMID:
18424904
3.

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.

Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH.

Mol Psychiatry. 2004 May;9(5):474-84.

PMID:
15024396
4.

The WNT2 gene polymorphism associated with speech delay inherent to autism.

Lin PI, Chien YL, Wu YY, Chen CH, Gau SS, Huang YS, Liu SK, Tsai WC, Chiu YN.

Res Dev Disabil. 2012 Sep-Oct;33(5):1533-40. doi: 10.1016/j.ridd.2012.03.004.

PMID:
22522212
5.

Association of the ENGRAILED 2 (EN2) gene with autism in Chinese Han population.

Wang L, Jia M, Yue W, Tang F, Qu M, Ruan Y, Lu T, Zhang H, Yan H, Liu J, Guo Y, Zhang J, Yang X, Zhang D.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):434-8.

PMID:
17948901
6.

No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.

Nabi R, Zhong H, Serajee FJ, Huq AH.

Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):98-101.

PMID:
12707945
7.

Back to where it all started: monoamines and behavior--from drug responses to genes.

Licinio J, Wong ML.

Mol Psychiatry. 2004 May;9(5):427. No abstract available.

PMID:
15118733
8.

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
9.

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.

10.

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.

11.

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
12.

Cerebellum development and schizophrenia: an association study of the human homeogene Engrailed 2.

Gourion D, Leroy S, Bourdel MC, Goldberger C, Poirier MF, Olié JP, Krebs MO.

Psychiatry Res. 2004 Apr 30;126(2):93-8.

PMID:
15123388
13.

A comparison between methods for linkage disequilibrium fine mapping of quantitative trait loci.

Abdallah JM, Mangin B, Goffinet B, Cierco-Ayrolles C, Pérez-Enciso M.

Genet Res. 2004 Feb;83(1):41-7.

PMID:
15125065
14.

Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.

Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM, Millonig JH.

Biol Psychiatry. 2009 Nov 15;66(10):911-7. doi: 10.1016/j.biopsych.2009.05.027.

15.

En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder.

Cheh MA, Millonig JH, Roselli LM, Ming X, Jacobsen E, Kamdar S, Wagner GC.

Brain Res. 2006 Oct 20;1116(1):166-76.

PMID:
16935268
16.

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.

McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):104-12.

PMID:
15108191
17.

Association study of the commonly recognized breakpoints in chromosome 15q11-q13 in Japanese autistic patients.

Kato C, Tochigi M, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, Sasaki T.

Psychiatr Genet. 2008 Jun;18(3):133-6. doi: 10.1097/YPG.0b013e3282fb0064.

PMID:
18496211
18.

Genetic mapping of the homeobox-containing gene Otx1 gene on mouse chromosome 11.

DeGregorio L, Manenti G, Simeone A, Dragani TA.

Mamm Genome. 1996 Mar;7(3):241. No abstract available.

PMID:
8833255
19.

Association of Reelin gene polymorphisms with autism.

Serajee FJ, Zhong H, Mahbubul Huq AH.

Genomics. 2006 Jan;87(1):75-83.

20.

No association between allelic variants of HOXA1/HOXB1 and autism.

Gallagher L, Hawi Z, Kearney G, Fitzgerald M, Gill M.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):64-7.

PMID:
14681917
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