Chen CH - Search Results

1

Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of autism.

Gau SS, Liao HM, Hong CC, Chien WH, Chen CH. Gau SS, et al. Among authors: chen ch. Am J Med Genet B Neuropsychiatr Genet. 2012 Sep;159B(6):710-7. doi: 10.1002/ajmg.b.32074. Epub 2012 Jul 9. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22778016

2

Mutation analysis of the human dystrobrevin-binding protein 1 gene in schizophrenic patients.

Liao HM, Chen CH. Liao HM, et al. Among authors: chen ch. Schizophr Res. 2004 Nov 1;71(1):185-9. doi: 10.1016/j.schres.2003.11.002. Schizophr Res. 2004. PMID: 15374586

3

Identification of molecular variants at the promoter region of the human alpha 7 neuronal nicotinic acetylcholine receptor subunit gene but lack of association with schizophrenia.

Li CH, Liao HM, Chen CH. Li CH, et al. Among authors: chen ch. Neurosci Lett. 2004 Nov 30;372(1-2):1-5. doi: 10.1016/j.neulet.2004.07.013. Neurosci Lett. 2004. PMID: 15531077

4

Mutation analysis of DARPP-32 as a candidate gene for schizophrenia.

Li CH, Liao HM, Hung TW, Chen CH. Li CH, et al. Among authors: chen ch. Schizophr Res. 2006 Oct;87(1-3):1-5. doi: 10.1016/j.schres.2006.04.003. Epub 2006 Jun 5. Schizophr Res. 2006. PMID: 16750903

5

Mutation analysis of adenosine A2a receptor gene and interaction study with dopamine D2 receptor gene in schizophrenia.

Luu SU, Liao HM, Hung TW, Liu BY, Cheng MC, Liao DL, Chen SJ, Chen CH. Luu SU, et al. Among authors: chen ch, chen sj. Psychiatr Genet. 2008 Feb;18(1):43. doi: 10.1097/YPG.0b013e3281b1173c. Psychiatr Genet. 2008. PMID: 18197085 No abstract available.

6

Lack of evidence to support the glyoxalase 1 gene (GLO1) as a risk gene of autism in Han Chinese patients from Taiwan.

Wu YY, Chien WH, Huang YS, Gau SS, Chen CH. Wu YY, et al. Among authors: chen ch. Prog Neuropsychopharmacol Biol Psychiatry. 2008 Oct 1;32(7):1740-4. doi: 10.1016/j.pnpbp.2008.07.019. Epub 2008 Aug 5. Prog Neuropsychopharmacol Biol Psychiatry. 2008. PMID: 18721844

7

Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan.

Chien WH, Wu YY, Gau SS, Huang YS, Soong WT, Chiu YN, Chen CH. Chien WH, et al. Among authors: chen ch. Prog Neuropsychopharmacol Biol Psychiatry. 2010 Feb 1;34(1):189-92. doi: 10.1016/j.pnpbp.2009.11.004. Epub 2009 Nov 10. Prog Neuropsychopharmacol Biol Psychiatry. 2010. PMID: 19913066

8

Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome.

Liao HM, Niu DM, Chen YJ, Fang JS, Chen SJ, Chen CH. Liao HM, et al. Among authors: chen yj, chen ch, chen sj. J Hum Genet. 2011 Jan;56(1):8-11. doi: 10.1038/jhg.2010.121. Epub 2010 Sep 30. J Hum Genet. 2011. PMID: 20882036

9

Association study of the CNS patterning genes and autism in Han Chinese in Taiwan.

Chien YL, Wu YY, Chiu YN, Liu SK, Tsai WC, Lin PI, Chen CH, Gau SS, Chien WH. Chien YL, et al. Among authors: chen ch. Prog Neuropsychopharmacol Biol Psychiatry. 2011 Aug 1;35(6):1512-7. doi: 10.1016/j.pnpbp.2011.04.010. Epub 2011 May 5. Prog Neuropsychopharmacol Biol Psychiatry. 2011. PMID: 21575668

10

Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1;q21.3) in a family co-segregating with mental retardation, language delay, and microcephaly.

Liao HM, Fang JS, Chen YJ, Wu KL, Lee KF, Chen CH. Liao HM, et al. Among authors: chen yj, chen ch. BMC Med Genet. 2011 May 20;12:70. doi: 10.1186/1471-2350-12-70. BMC Med Genet. 2011. PMID: 21595979 Free PMC article.

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