(Q46940916)

26 December 2017

title

Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS. (English)

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26 December 2017

10

Abraham Weizman

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26 December 2017

author name string

Elena Michaelovsky

1

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26 December 2017

Doron Gothelf

2

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26 December 2017

Michael Korostishevsky

3

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26 December 2017

Amos Frisch

4

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26 December 2017

Merav Burg

5

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26 December 2017

Miri Carmel

6

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26 December 2017

Tamar Steinberg

7

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26 December 2017

Dov Inbar

8

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26 December 2017

Alan Apter

9

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26 December 2017

publication date

22 October 2007

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26 December 2017

The International Journal of Neuropsychopharmacology

published in

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26 December 2017

volume

11

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26 December 2017

page(s)

351-363

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26 December 2017

issue

3

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26 December 2017

Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

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Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

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Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome.

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7 January 2021

A highly significant association between a COMT haplotype and schizophrenia.

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

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism

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7 January 2021

Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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

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7 January 2021

Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.

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7 January 2021

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7 January 2021

COMT genetic variation confers risk for psychotic and affective disorders: a case control study

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.

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7 January 2021

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

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https://api.crossref.org/works/10.1017%2FS1461145707008085

7 January 2021

Prevalence and parental origin in Tetralogy of Fallot associated with chromosome 22q11 microdeletion.

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7 January 2021

Catechol O-methyltransferase val158met genotype and neural mechanisms related to affective arousal and regulation.

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7 January 2021

Chromosomal microdeletions: dissecting del22q11 syndrome

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7 January 2021

Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature

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7 January 2021

10.1017/S1461145707008085

Identifiers

DOI

0 references

PubMed ID

17949513

1 reference

26 December 2017