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Attention Deficit Hyperactivity Disorder: Fine Mapping Supports Linkage to 5p13, 6q12, 16p13, and 17p11

Authors :
Sandra K. Loo
Janeen Ishii
James J. McGough
Matthew N. Ogdie
James T. McCracken
Stanley F. Nelson
Clyde Francks
May Yang
Simon E. Fisher
Susan L. Smalley
Rita M. Cantor
Source :
Ogdie, Matthew N; Fisher, Simon E; Yang, May; Ishii, Janeen; Francks, Clyde; Loo, Sandra K; et al.(2004). Attention deficit hyperactivity disorder: Fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. American Journal of Human Genetics, 75(4), 661-668. UCLA: Retrieved from: http://www.escholarship.org/uc/item/5x93x5rq, American Journal of Human Genetics
Publication Year :
2004
Publisher :
Elsevier BV, 2004.

Abstract

We completed fine mapping of nine positional candidate regions for attention-deficit/hyperactivity disorder (ADHD) in an extended population sample of 308 affected sibling pairs (ASPs), constituting the largest linkage sample of families with ADHD published to date. The candidate chromosomal regions were selected from all three published genomewide scans for ADHD, and fine mapping was done to comprehensively validate these positional candidate regions in our sample. Multipoint maximum LOD score (MLS) analysis yielded significant evidence of linkage on 6q12 (MLS 3.30; empiric P=.024) and 17p11 (MLS 3.63; empiric P=.015), as well as suggestive evidence on 5p13 (MLS 2.55; empiric P=.091). In conjunction with the previously reported significant linkage on the basis of fine mapping 16p13 in the same sample as this report, the analyses presented here indicate that four chromosomal regions--5p13, 6q12, 16p13, and 17p11--are likely to harbor susceptibility genes for ADHD. The refinement of linkage within each of these regions lays the foundation for subsequent investigations using association methods to detect risk genes of moderate effect size.

Details

ISSN :
00029297
Volume :
75
Issue :
4
Database :
OpenAIRE
Journal :
The American Journal of Human Genetics
Accession number :
edsair.doi.dedup.....684138b79bc8e3a2335049b588125b61
Full Text :
https://doi.org/10.1086/424387