(Q44436579)

3 December 2017

title

Further evidence for a modulation of Novelty Seeking by DRD4 exon III, 5-HTTLPR, and COMT val/met variants (English)

1 reference

3 December 2017

1

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3 December 2017

Lesch KP

2

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3 December 2017

Jatzke S

series ordinal

3

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3 December 2017

Paetzold F

series ordinal

4

1 reference

3 December 2017

Brocke B

series ordinal

5

1 reference

3 December 2017

language of work or name

English

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publication date

1 April 2003

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3 December 2017

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3 December 2017

volume

8

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3 December 2017

issue

4

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3 December 2017

page(s)

371-372

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Dopamine D4 receptor (D4DR) exon III polymorphism associated with the human personality trait of Novelty Seeking

3 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

Population and familial association between the D4 dopamine receptor gene and measures of Novelty Seeking

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

Dopamine D4 receptor gene: novelty or nonsense?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

Association between the dopamine D4 receptor (DRD4) exon III polymorphism and measures of Novelty Seeking in a German population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

No association between dopamine D4 receptor gene exon III and -521C/T polymorphism and novelty seeking.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

Association between tridimensional personality questionnaire (TPQ) traits and three functional polymorphisms: dopamine receptor D4 (DRD4), serotonin transporter promoter region (5-HTTLPR) and catechol O-methyltransferase (COMT)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

inferred from DOI database lookup

7 January 2021

based on heuristic

Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity val allele with adhd impulsive-hyperactive phenotype

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001253

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.MP.4001253

1 reference

3 December 2017

1 reference