Literature DB >> 22009217

No significant association between Catechol-O-methyl transferase (COMT) -287A/G gene polymorphism and Tourette's syndrome in family-based association study in Chinese Han population.

Shiguo Liu1, Mingji Yi, Fengguang Qi, Yuping Sun, Fengyuan Che, Xu Ma.   

Abstract

To identify the association of Catechol-O-methyl transferase (COMT) -287A/G polymorphism with susceptibility to TS in Chinese Han population. We evaluated the genetic contribution of the COMT -287A/G polymorphism in 108 TS patients including all their parents in Chinese Han population using transmission disequilibrium test and haplotype relative risk design. Our results revealed that no significant association was found in COMT -287A/G genotypic and allelic frequencies with TS. Our results also suggested that there may be a lack of association between the TS and -287A/G polymorphism of COMT in Chinese Han population.

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Year:  2011        PMID: 22009217     DOI: 10.1007/s00787-011-0226-9

Source DB:  PubMed          Journal:  Eur Child Adolesc Psychiatry        ISSN: 1018-8827            Impact factor:   4.785


  17 in total

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2.  Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.

Authors:  M H Grossman; B S Emanuel; M L Budarf
Journal:  Genomics       Date:  1992-04       Impact factor: 5.736

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Journal:  J Psychosom Res       Date:  2006-09       Impact factor: 3.006

4.  Catechol-O-methyltransferase and Gilles de la Tourette syndrome.

Authors:  C L Barr; K G Wigg; P Sandor
Journal:  Mol Psychiatry       Date:  1999-09       Impact factor: 15.992

5.  Dopamine axon varicosities in the prelimbic division of the rat prefrontal cortex exhibit sparse immunoreactivity for the dopamine transporter.

Authors:  S R Sesack; V A Hawrylak; C Matus; M A Guido; A I Levey
Journal:  J Neurosci       Date:  1998-04-01       Impact factor: 6.167

6.  Relationship of birth weight to the phenotypic expression of Gilles de la Tourette's syndrome in monozygotic twins.

Authors:  T M Hyde; B A Aaronson; C Randolph; K C Rickler; D R Weinberger
Journal:  Neurology       Date:  1992-03       Impact factor: 9.910

7.  Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.

Authors:  Jingshan Chen; Barbara K Lipska; Nader Halim; Quang D Ma; Mitsuyuki Matsumoto; Samer Melhem; Bhaskar S Kolachana; Thomas M Hyde; Mary M Herman; Jose Apud; Michael F Egan; Joel E Kleinman; Daniel R Weinberger
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8.  A twin study of Tourette syndrome.

Authors:  R A Price; K K Kidd; D J Cohen; D L Pauls; J F Leckman
Journal:  Arch Gen Psychiatry       Date:  1985-08

9.  Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.

Authors:  Elizabeth Tunbridge; Philip W J Burnet; Monsheel S Sodhi; Paul J Harrison
Journal:  Synapse       Date:  2004-02       Impact factor: 2.562

10.  Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

Authors:  Raymond A Clarke; Zhi Ming Fang; Ashish D Diwan; Donald L Gilbert
Journal:  Case Rep Med       Date:  2009-12-22
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  1 in total

1.  Support of positive association in family-based genetic analysis between COL27A1 and Tourette syndrome.

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Journal:  Sci Rep       Date:  2015-08-03       Impact factor: 4.379

  1 in total

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