Home LiteratureArticle Details
PMID: 10638369 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Linkage analysis in heterogeneous and complex traits.

European child & adolescent psychiatry ·Vol. 8 Suppl 3 ·1999-00-00 ·Pages 43-6

Ott J, Bhat A

Abstract

Linkage analysis is generally carried out under single-gene models, while complex traits are thought to be under the control of multiple interacting genes. Current issues related to linkage analysis for complex traits are discussed. It is argued that linkage analyses should be carried out for sub-phenotypes, in addition to classical "affected-unaffected" phenotypes. Correlations for phenotypes among family members are often computed on the basis of extreme phenotypes of a proband, which results in biased estimates. Methods for ascertainment corrections are recommended. A generalized version of heterogeneity analysis is introduced and are shown to provide an effective single-locus analysis for complex traits.

MeSH Terms
Adult Child Chromosome Mapping Dyslexia/diagnosis,genetics Genetic Heterogeneity Genetic Predisposition to Disease/genetics Genotype Humans Models, Genetic Phenotype
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ott J
Laboratory of Statistical Genetics, Rockefeller University, New York, NY 10021, USA. [email protected]
Bhat A
References (12)
12 references, click to expand
  1. Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats.
    Nat Genet. 1993 Apr;3(4):354-7 PMID: 7981757
  2. Neural network analysis of complex traits.
    Genet Epidemiol. 1997;14(6):1101-6 PMID: 9433631
  3. Polygenic trait analysis by neural network learning.
    Artif Intell Med. 1994 Feb;6(1):51-65 PMID: 8004147
  4. Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits.
    Am J Hum Genet. 1993 Nov;53(5):1127-36 PMID: 8213836
  5. Model misspecification and multipoint linkage analysis.
    Hum Hered. 1992;42(1):77-92 PMID: 1555848
  6. Statistical evaluation of multiple-locus linkage data in experimental species and its relevance to human studies: application to nonobese diabetic (NOD) mouse and human insulin-dependent diabetes mellitus (IDDM).
    Am J Hum Genet. 1993 Sep;53(3):702-14 PMID: 8352278
  7. Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I.
    Mayo Clin Proc. 1983 Jul;58(7):430-5 PMID: 6865476
  8. Effects of misspecifying genetic parameters in lod score analysis.
    Biometrics. 1986 Jun;42(2):393-9 PMID: 3741977
  9. Model-free linkage analysis using likelihoods.
    Am J Hum Genet. 1995 Sep;57(3):703-16 PMID: 7668300
  10. Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis.
    Genet Epidemiol. 1990;7(4):237-43 PMID: 2227370
  11. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.
    Am J Hum Genet. 1997 Jan;60(1):27-39 PMID: 8981944
  12. Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12.
    Am J Med Genet. 1997 May 31;74(3):247-53 PMID: 9184306
Article Info
Journal
European child & adolescent psychiatry
Abbr.
Eur Child Adolesc Psychiatry
ISSN
1018-8827
Published
1999-00-00
Pages
43-6
Language
English
Region
Germany
NLM ID
9212296
Subset
IM
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]