Home LiteratureArticle Details
PMID: 11496372 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Incorporating language phenotypes strengthens evidence of linkage to autism.

American journal of medical genetics ·Vol. 105 ·No. 6 ·2001-08-08 ·Pages 539-47

Bradford Y, Haines J, Hutcheson H, Gardiner M, Braun T, Sheffield V, Cassavant T, Huang W, Wang K, Vieland V, Folstein S, Santangelo S, Piven J

Abstract

We investigated the effect of incorporating information about proband and parental structural language phenotypes into linkage analyses in the two regions for which we found the highest signals in our first-stage affected sibling pair genome screen: chromosomes 13q and 7q. We were particularly interested in following up on our chromosome 7q finding in light of two prior reports of linkage of this region to developmental language disorder, since one of the diagnostic criteria for autism is absent or abnormal language development. We hypothesized that if the language phenotype were genetically relevant to linkage at the chromosome 7q locus, then incorporating parents phenotypes would increase the signal at that locus, and most of the signal would originate from the subset of families in which both probands had severe language delay. The results support these hypotheses. The linkage signals we obtained on chromosome 7q as well as at least one signal on chromosome 13q are mainly attributable to the subgroup of families in which both probands had language delay. This became apparent only when the parents' history of language-related difficulties was also incorporated into the analyses. Although based on our data, we were not able to distinguish between epistasis or heterogeneity models, we tentatively concluded that there may be more than one autism susceptibility locus related to language development.

MeSH Terms
Autistic Disorder/genetics,pathology Chromosome Mapping Chromosomes, Human, Pair 13/genetics Chromosomes, Human, Pair 7/genetics Family Health Female Humans Language Disorders/genetics,pathology Lod Score Male Microsatellite Repeats Phenotype
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Bradford Y
Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, USA.
Haines J
Hutcheson H
Gardiner M
Braun T
Sheffield V
Cassavant T
Huang W
Wang K
Vieland V
Folstein S
Santangelo S
Piven J
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
2001-08-08
Pages
539-47
Language
English
Region
United States
NLM ID
7708900
Subset
IM
Grants
NIMH NIH HHS · K02-MH01432 · United States
NIMH NIH HHS · K02-MH01568 · United States
NIMH NIH HHS · K21-MH01338 · United States
NIMH NIH HHS · MH52841 · United States
NIMH NIH HHS · MH55135 · United States
NIMH NIH HHS · MH55284 · United States
NINDS NIH HHS · NS38668 · United States
NIDCD NIH HHS · P01-DC3610 · United States
Corrections
ErratumIn
-
RepublishedIn
External Links
PubMed source
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]