Literature DB >> 22245443

A second look: no effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndrome.

Joel Stoddard, Yukari Takarae, Tony J Simon.   

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Year:  2012        PMID： 22245443      PMCID： PMC4331111          DOI： 10.1016/j.schres.2011.12.011

Source DB:  PubMed          Journal:  Schizophr Res        ISSN： 0920-9964            Impact factor:   4.939


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  10 in total

1.  COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.

Authors:  Vandana Shashi; Timothy D Howard; Matcheri S Keshavan; Jessica Kaczorowski; Margaret N Berry; Kelly Schoch; Edward J Spence; Thomas R Kwapil
Journal:  Psychiatry Res       Date:  2010-05-20       Impact factor: 3.222

2.  Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome.

Authors:  Anne S Bassett; Oana Caluseriu; Rosanna Weksberg; Donald A Young; Eva W C Chow
Journal:  Biol Psychiatry       Date:  2007-01-09       Impact factor: 13.382

3.  Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatology.

Authors:  Erik Boot; Jan Booij; Nico Abeling; Julia Meijer; Fabiana da Silva Alves; Janneke Zinkstok; Frank Baas; Don Linszen; Thérèse van Amelsvoort
Journal:  J Psychopharmacol       Date:  2011-03-29       Impact factor: 4.153

4.  High rates of schizophrenia in adults with velo-cardio-facial syndrome.

Authors:  K C Murphy; L A Jones; M J Owen
Journal:  Arch Gen Psychiatry       Date:  1999-10

5.  Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome.

Authors:  Joel Stoddard; Laurel Beckett; Tony J Simon
Journal:  J Neurodev Disord       Date:  2010-12-23       Impact factor: 4.025

6.  COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.

Authors:  Doron Gothelf; Stephan Eliez; Tracy Thompson; Christine Hinard; Lauren Penniman; Carl Feinstein; Hower Kwon; Shuting Jin; Booil Jo; Stylianos E Antonarakis; Michael A Morris; Allan L Reiss
Journal:  Nat Neurosci       Date:  2005-10-23       Impact factor: 24.884

7.  Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.

Authors:  Carrie E Bearden; Abbas F Jawad; David R Lynch; Set Sokol; Steven J Kanes; Donna M McDonald-McGinn; Sulagna C Saitta; Stacy E Harris; Edward Moss; Paul P Wang; Elaine Zackai; Beverly S Emanuel; Tony J Simon
Journal:  Am J Psychiatry       Date:  2004-09       Impact factor: 18.112

8.  No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.

Authors:  Bronwyn Glaser; Martin Debbane; Christine Hinard; Michael A Morris; Sophie P Dahoun; Stylianos E Antonarakis; Stephan Eliez
Journal:  Am J Psychiatry       Date:  2006-03       Impact factor: 18.112

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.  Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome.

Authors:  Yukari Takarae; Linda Schmidt; Flora Tassone; Tony J Simon
Journal:  Cogn Affect Behav Neurosci       Date:  2009-03       Impact factor: 3.282
  10 in total
  1 in total

1.  Mother-Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome.

Authors:  Omri Weisman; Ruth Feldman; Merav Burg-Malki; Miri Keren; Ronny Geva; Gil Diesendruck; Doron Gothelf
Journal:  J Autism Dev Disord       Date:  2015-08
  1 in total

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