Unknown

Dataset Information

0

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.


ABSTRACT: Attention-deficit/hyperactivity disorder (ADHD) is the most commonly diagnosed behavioral disorder in childhood and likely represents an extreme of normal behavior. ADHD significantly impacts learning in school-age children and leads to impaired functioning throughout the life span. There is strong evidence for a genetic etiology of the disorder, although putative alleles, principally in dopamine-related pathways suggested by candidate-gene studies, have very small effect sizes. We use affected-sib-pair analysis in 203 families to localize the first major susceptibility locus for ADHD to a 12-cM region on chromosome 16p13 (maximum LOD score 4.2; P=.000005), building upon an earlier genomewide scan of this disorder. The region overlaps that highlighted in three genome scans for autism, a disorder in which inattention and hyperactivity are common, and physically maps to a 7-Mb region on 16p13. These findings suggest that variations in a gene on 16p13 may contribute to common deficits found in both ADHD and autism.

SUBMITTER: Smalley SL 

PROVIDER: S-EPMC378550 | biostudies-literature | 2002 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.

Smalley Susan L SL   Kustanovich Vlad V   Minassian Sonia L SL   Stone Jennifer L JL   Ogdie Matthew N MN   McGough James J JJ   McCracken James T JT   MacPhie I Laurence IL   Francks Clyde C   Fisher Simon E SE   Cantor Rita M RM   Monaco Anthony P AP   Nelson Stanley F SF  

American journal of human genetics 20020814 4


Attention-deficit/hyperactivity disorder (ADHD) is the most commonly diagnosed behavioral disorder in childhood and likely represents an extreme of normal behavior. ADHD significantly impacts learning in school-age children and leads to impaired functioning throughout the life span. There is strong evidence for a genetic etiology of the disorder, although putative alleles, principally in dopamine-related pathways suggested by candidate-gene studies, have very small effect sizes. We use affected-  ...[more]

Similar Datasets

| S-EPMC1182053 | biostudies-literature
| S-EPMC4511106 | biostudies-literature
| S-EPMC8649805 | biostudies-literature
| S-EPMC2839489 | biostudies-literature
| S-EPMC7880081 | biostudies-literature
| S-EPMC3441928 | biostudies-literature
| S-EPMC4440572 | biostudies-other
| S-EPMC5750043 | biostudies-literature
| S-EPMC5507945 | biostudies-literature
| S-EPMC5836146 | biostudies-literature