(Q46174524)

English

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

scientific article published on 23 October 2005

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scholarly article

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

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

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

1 reference

based on heuristic

inferred from title

Stilianos Antonarakis

10

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

12

object named as

Allan L Reiss

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

2

object named as

Stephan Eliez

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

author name string

Doron Gothelf

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Tracy Thompson

3

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Christine Hinard

4

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Lauren Penniman

5

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Carl Feinstein

6

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Hower Kwon

7

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Shuting Jin

8

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Booil Jo

9

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Michael A Morris

11

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

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publication date

23 October 2005

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Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/16234808

Nature Neuroscience

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Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/16234808

8

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

1500-1502

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

From neuropathology to neurodevelopment

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

A comprehensive analysis of 22q11 gene expression in the developing and adult brain

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 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://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

Catechol O -methyltransferase val 158 -met genotype and individual variation in the brain response to amphetamine

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

The principal features and mechanisms of dopamine modulation in the prefrontal cortex

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

Effect of catechol-O-methyltransferase val158met genotype on attentional control.

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

Longitudinal assessment of premorbid cognitive functioning in patients with schizophrenia through examination of standardized scholastic test performance.

1 reference

https://api.crossref.org/works/10.1038%2FNN1572

21 January 2018

Identifiers

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/16234808

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