This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Related articles in BJP
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by ASHERSON, P. J.
Right arrow Articles by CURRAN, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by ASHERSON, P. J.
Right arrow Articles by CURRAN, S.
The British Journal of Psychiatry (2001) 179: 122-128
© 2001 The Royal College of Psychiatrists

Approaches to gene mapping in complex disorders and their application in child psychiatry and psychology{dagger}

PHILIP J. ASHERSON, MRCPsych and SARAH CURRAN, MRCPsych

Social, Genetic and Developmental Psychiatry Research Centre, Institute of Psychiatry, London, UK

Correspondence: Philip J. Asherson, Social, Genetic and Developmental Psychiatry Research Centre, Institute of Psychiatry, De Crespigny Park, Denmark Hill, London SE5 8AF, UK

Declaration of interest None. Funding detailed in Acknowledgements.

{dagger} See editorial, pp. 93–94, this issue.

Background Twin studies demonstrate the importance of genes and environment in the aetiology of childhood psychiatric and neurodevelopmental disorders. Advances in molecular genetics enable the identification of genes involved in complex disorders and enable the study of molecular mechanisms and gene—environment interactions.

Aims To review the role of molecular genetics studies in childhood behavioural and developmental traits.

Method Molecular approaches to complex disorders are reviewed, with examples from autism, reading disability and attention-deficit hyperactivity disorder (ADHD).

Results The most robust finding in ADHD is the association of a variable number tandem repeat polymorphism in exon 3 of the DRD4 gene. Other replicated associations with ADHD are outlined in the text. In autism, there is a replicated linkage finding on chromosome 7. Linkage studies in reading disability have confirmed a locus on chromosome 6 and strongly suggest one on chromosome 15.

Conclusions In the next 5-10 years susceptibility genes for these disorders will be established. Describing their relationship to biological and behavioural function will be a far greater challenge.


Related articles in BJP:

Causal processes in development and psychopathology
RICHARD HARRINGTON
BJP 2001 179: 93-94. [Full Text]  



This article has been cited by other articles:


Home page
PediatricsHome page
C. P. Johnson, S. M. Myers, and and the Council on Children With Disabilities
Identification and Evaluation of Children With Autism Spectrum Disorders
Pediatrics, November 1, 2007; 120(5): 1183 - 1215.
[Abstract] [Full Text] [PDF]


Home page
Adv. Psychiatr. Treat.Home page
M. Zwi and A. York
Attention-deficit hyperactivity disorder in adults: validity unknown
Adv. Psychiatr. Treat., July 1, 2004; 10(4): 248 - 256.
[Abstract] [Full Text] [PDF]


Home page
PediatricsHome page
R. Muhle, S. V. Trentacoste, and I. Rapin
The Genetics of Autism
Pediatrics, May 1, 2004; 113(5): e472 - e486.
[Abstract] [Full Text] [PDF]


Home page
Br. J. PsychiatryHome page
R. HARRINGTON
Causal processes in development and psychopathology
The British Journal of Psychiatry, August 1, 2001; 179(2): 93 - 94.
[Full Text] [PDF]