Association of ADHD with genetic variants in the 5′-region of the dopamine transporter gene: Evidence for allelic heterogeneity-Reference-Cited by-同舟云学术

Association of ADHD with genetic variants in the 5′-region of the dopamine transporter gene: Evidence for allelic heterogeneity

Published:2008-12-05 Issue:8 Volume:147B Page:1519-1523
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Brookes K.J.,Xu X.,Anney R.,Franke B.,Zhou K.,Chen Wai,Banaschewski T.,Buitelaar J.,Ebstein R.,Eisenberg J.,Gill M.,Miranda A.,Oades R.D.,Roeyers H.,Rothenberger A.,Sergeant J.,Sonuga-Barke E.,Steinhausen H.-C.,Taylor E.,Faraone S.V.,Asherson P.

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference25 articles.

1. Attention-deficit hyperactivity, disorder in the post-genomic era;Asherson;Eur Child Adolesc Psychiatry,2004

2. Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD;Asherson;Am J Psychiatry,2007

3. Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder;Barr;Biol Psychiatry,2001

4. A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy;Brookes;Arch Gen Psychiatry,2006

Cited by 33 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Gene Interaction of Dopaminergic Synaptic Pathway Genes in Attention-Deficit Hyperactivity Disorder: a Case-Control Study in Chinese Children;Molecular Neurobiology;2023-08-14

2. Correlation research of susceptibility single nucleotide polymorphisms and the severity of clinical symptoms in attention deficit hyperactivity disorder;Frontiers in Psychiatry;2022-09-23

3. Genetics and pharmacogenetics of attention deficit hyperactivity disorder in childhood and adulthood;Personalized Psychiatry;2020

4. Association analyses reveal gender-specific associations of DAT1 40-bp VNTR and -839C/T polymorphisms with obsessive–compulsive disorder and obsessive–compulsive symptoms;Molecular Biology Reports;2019-07-19

5. Presence of recombination hotspots throughout SLC6A3;PLOS ONE;2019-06-11