Literature DB >> 1550129

A multilocus extension of the affected-pedigree-member method of linkage analysis.

D E Weeks1, K Lange.   

Abstract

The affected-pedigree-member (APM) method of linkage analysis is designed to detect departures from independent segregation of disease and marker phenotypes. The underlying statistic of the APM method operates on the identity-by-state relations implied by the marker phenotypes of the affected within a pedigree. Here we generalize the APM statistic to multiple linked markers. This generalization relies on recursive computation of two-locus kinship coefficients by an algorithm of Thompson. The distributional properties of the extended APM statistic are investigated theoretically and by simulation in the context of one real and one artificial data set. In both examples, the multilocus statistic tends to reject, more strongly than the single-locus statistics do, the null hypothesis of independent segregation between the disease locus and the marker loci.

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Year:  1992        PMID: 1550129      PMCID: PMC1682645     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  23 in total

1.  Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

Authors:  M A Pericak-Vance; J L Bebout; P C Gaskell; L H Yamaoka; W Y Hung; M J Alberts; A P Walker; R J Bartlett; C A Haynes; K A Welsh
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

Review 2.  Linkage methods for identifying genetic risk factors.

Authors:  K Lange; D E Weeks
Journal:  World Rev Nutr Diet       Date:  1990       Impact factor: 0.575

3.  The affected sib-pair method using identity by state relations.

Authors:  K Lange
Journal:  Am J Hum Genet       Date:  1986-07       Impact factor: 11.025

4.  Two-locus and three-locus gene identity by descent in pedigrees.

Authors:  E A Thompson
Journal:  IMA J Math Appl Med Biol       Date:  1988

5.  Sibling Method for Detecting HLA-linked genes in disease.

Authors:  J R Green; J C Woodrow
Journal:  Tissue Antigens       Date:  1977-01

6.  A robust method for the detection of linkage in familial disease.

Authors:  P M Fishman; B Suarez; S E Hodge; T Reich
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025

7.  Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.

Authors:  A Goate; M C Chartier-Harlin; M Mullan; J Brown; F Crawford; L Fidani; L Giuffra; A Haynes; N Irving; L James
Journal:  Nature       Date:  1991-02-21       Impact factor: 49.962

8.  Computer-simulation methods in human linkage analysis.

Authors:  J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

9.  A simple method to detect linkage for rare recessive diseases: an application to juvenile diabetes.

Authors:  B K Suarez; S E Hodge
Journal:  Clin Genet       Date:  1979-02       Impact factor: 4.438

10.  Genetic epidemiology of bilateral breast cancer: a linkage analysis using the affected-pedigree-member method.

Authors:  R W Haile; A M Goldstein; D E Weeks; R S Sparkes; A Paganini-Hill
Journal:  Genet Epidemiol       Date:  1990       Impact factor: 2.135

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  15 in total

1.  Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene region.

Authors:  R Arngrímsson; C Hayward; S Nadaud; A Baldursdóttir; J J Walker; W A Liston; R I Bjarnadóttir; D J Brock; R T Geirsson; J M Connor; F Soubrier
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

2.  Combining information within and between pedigrees for mapping complex traits.

Authors:  J Teng; D Siegmund
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

3.  Association between high serum total IgE levels and D11S97 on chromosome 11q13 in Japanese subjects.

Authors:  N Hizawa; E Yamaguchi; K Furuya; N Ohnuma; N Kodama; J Kojima; M Ohe; Y Kawakami
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

4.  Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.

Authors:  L R Weitkamp; A J Moss; R A Lewis; W J Hall; J W MacCluer; P J Schwartz; E H Locati; D Tzivoni; G M Vincent; J L Robinson
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

5.  Association of two loci on chromosome 2q with nodal osteoarthritis.

Authors:  G D Wright; A E Hughes; M Regan; M Doherty
Journal:  Ann Rheum Dis       Date:  1996-05       Impact factor: 19.103

6.  Angiotensinogen gene and hypertension in Chinese.

Authors:  T Niu; X Xu; J Rogus; Y Zhou; C Chen; J Yang; Z Fang; C Schmitz; J Zhao; V S Rao; K Lindpaintner
Journal:  J Clin Invest       Date:  1998-01-01       Impact factor: 14.808

7.  A novel class of tests for the detection of mitochondrial DNA-mutation involvement in diseases.

Authors:  Fengzhu Sun; Jing Cui; Haralambos Gavras; Faina Schwartz
Journal:  Am J Hum Genet       Date:  2003-04-30       Impact factor: 11.025

Review 8.  The Evolving Genome Project: current and future impact.

Authors:  E P Hoffman
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

9.  Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene.

Authors:  W H Berrettini; T N Ferraro; L R Goldin; D E Weeks; S Detera-Wadleigh; J I Nurnberger; E S Gershon
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205

10.  Linkage of the angiotensinogen gene locus to human essential hypertension in African Caribbeans.

Authors:  M Caulfield; P Lavender; J Newell-Price; M Farrall; S Kamdar; H Daniel; M Lawson; P De Freitas; P Fogarty; A J Clark
Journal:  J Clin Invest       Date:  1995-08       Impact factor: 14.808

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