(Q48401327)

English

Genetic variation in catechol-O-methyltransferase (COMT) and obesity in the prostate, lung, colorectal, and ovarian (PLCO) cancer screening trial

scientific article published on 12 May 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

Genetic variation in catechol-O-methyltransferase (COMT) and obesity in the prostate, lung, colorectal, and ovarian (PLCO) cancer screening trial (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

0 references

genetic variation

1 reference

based on heuristic

inferred from title

Andrew W Bergen

3

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

Richard B Hayes

7

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

Stephen Chanock

8

object named as

Stephen J Chanock

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

Nilanjan Chatterjee

5

object named as

Nilanjan Chatterjee

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

2

object named as

Lindsay M Morton

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

1

object named as

Sophia S Wang

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

author name string

Elizabeth Z Lan

4

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

Paul Kvale

6

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

Neil E Caporaso

9

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

publication date

12 May 2007

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

122

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

1

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

41-49

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

Methods for etiologic and early marker investigations in the PLCO trial.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-007-0374-7

21 January 2018

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol-O-methyltransferase (COMT): biochemistry, molecular biology, pharmacology, and clinical efficacy of the new selective COMT inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation of an excess of the high enzyme activity COMTval allele in heroin addicts in a family-based haplotype relative risk study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic aspects of obesity

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol-o-methyltransferase inhibition improves set-shifting performance and elevates stimulated dopamine release in the rat prefrontal cortex

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between the functional variant of the catechol-O-methyltransferase (COMT) gene and type 1 alcoholism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significant association of catechol-O-methyltransferase (COMT) haplotypes with nicotine dependence in male and female smokers of two ethnic populations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obesity is Associated with Genetic Variants That Alter Dopamine Availability

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic influence on smoking--a study of male twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dopaminergic genes and substance abuse.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Implications of CYP2A6 genetic variation for smoking behaviors and nicotine dependence.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obesity and cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Actual Causes of Death in the United States, 2000

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The influence of genotype and sex on behavioral sensitivity to nicotine in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and environmental contributions to smoking

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association study between high and low activity polymorphism of catechol-O-methyltransferase gene and alcoholism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DRD2 genetic variation in relation to smoking and obesity in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Etiology of obesity: genetic factors.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of association between the functional variant of the catechol-o-methyltransferase (COMT) gene and early-onset alcoholism associated with severe antisocial behavior.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct pharmacological regulation of evoked dopamine efflux in the amygdala and striatum of the rat in vivo.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of catechol-O-methyltransferase with smoking cessation in two independent studies of women

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic origins of anxiety in women: a role for a functional catechol-O-methyltransferase polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

COMT polymorphisms and anxiety-related personality traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Design of the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Candidate genes for alcohol dependence: a review of genetic evidence from human studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotyping alcoholism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol-O-methyl-transferase functional polymorphism and nicotine dependence: an evaluation of nonreplicated results

1 reference

https://pubmed.ncbi.nlm.nih.gov/17497175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-007-0374-7

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/17497175

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