ADHD: strategies to unravel its genetic architecture.
Publication year
2005Author(s)
Source
Journal of Neural Transmission-Supplement, 2005, 69, (2005), pp. 1-17ISSN
Publication type
Article / Letter to editor
Display more detailsDisplay less details
Organization
Psychiatry
Journal title
Journal of Neural Transmission-Supplement
Volume
vol. 2005
Issue
iss. 69
Page start
p. 1
Page end
p. 17
Subject
110 003 Autism & depression; 110 012 Social cognition of verbal communication; DCN 1: Perception and Action; DCN 3: Neuroinformatics; EBP 1: Determinants in Health and Disease; NCEBP 9: Mental health; UMCN 3.2: Cognitive neurosciences; 110 003 Autism & depressionsAbstract
Attention deficit/hyperactivity disorder (ADHD) is a common and impairing neuropsychiatric disorder with onset at preschool age and strong persistence over time. Its validity as a psychiatric disorder has been established according to Robins and Guze criteria. Genetic factors predominate in the etiology of ADHD. This paper summarizes the current status of genetic research into ADHD, and describes eight factors that complicate research into genetically complex disorders as ADHD. These factors are that multiple genes of small main effects are involved rather than main genes, the relevant phenotype is unknown, presence of clinical heterogeneity, presence of genetic heterogeneity, gene-environment correlation, gene-environment interaction, importance of endophenotypes, and importance of developmental factors. The further unraveling of the genetic architecture of ADHD will depend to a large extent on how well these complicating factors are handled or even used.
This item appears in the following Collection(s)
- Academic publications [246425]
- Electronic publications [134061]
- Faculty of Medical Sciences [93307]
- Open Access publications [107607]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.