Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents. (Q33953785)

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English	Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents.	scientific article

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14 February 2020

Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents (English)

1 reference

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14 February 2020

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conduct disorder

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Vladislav V. Ruchkin

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14 February 2020

Elena Grigorenko

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Elena L Grigorenko

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14 February 2020

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Colin G DeYoung

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14 February 2020

Marya Getchell

2

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14 February 2020

Roman A Koposov

3

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14 February 2020

Carolyn M Yrigollen

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14 February 2020

Gerald J Haeffel

5

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14 February 2020

Britt af Klinteberg

6

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14 February 2020

Lars Oreland

7

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14 February 2020

Andrew J Pakstis

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14 February 2020

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1 February 2010

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14 February 2020

Psychiatric Genetics

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14 February 2020

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14 February 2020

1

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14 February 2020

20-24

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14 February 2020

Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

5 July 2018

Catechol-O-methyltransferase (COMT): a gene contributing to sex differences in brain function, and to sexual dimorphism in the predisposition to psychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

5 July 2018

Platelet MAO-B, personality, and psychopathology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

5 July 2018

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

5 July 2018

Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

5 July 2018

HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

5 July 2018

A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

29 October 2018

Impact of complex genetic variation in COMT on human brain function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

29 October 2018

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

29 October 2018

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

29 October 2018

Violence Exposure, Posttraumatic Stress, and Personality in Juvenile Delinquents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2895253

29 October 2018

The reliability, validity, and unique contributions of self-report by adolescents receiving treatment for attention-deficit/hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19997043

12 December 2020

based on heuristic

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Suicidal ideations and attempts in juvenile delinquents

1 reference

https://pubmed.ncbi.nlm.nih.gov/19997043

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19997043

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/YPG.0B013E32833511E4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19997043%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19997043%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

Europe PubMed Central

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14 February 2020

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