Literature DB >> 3169523

Segregation and linkage analysis of nine Utah breast cancer pedigrees.

D T Bishop1, L Cannon-Albright, T McLellan, E J Gardner, M H Skolnick.   

Abstract

The analysis of nine Utah families that were ascertained for clusters of breast cancer cases is reported. Segregation analysis of an inherited susceptibility to breast cancer shows two distinct maximum likelihood solutions that have almost equal likelihood. One model indicates that most females had zero risk for breast cancer, but 10% of the female population had risks much greater than the Utah age-specific incidence rates. The other model indicates that most females have a risk defined by the Utah rates for breast cancer, but a rare dominant gene is segregating for increased susceptibility to breast cancer. Our analysis shows that linkage results under the two models are consistent in sign but not in magnitude. No evidence for linkage was found with the 14 marker loci examined. In addition to demonstrating distortion of linkage results from ignoring sporadic cases, this analysis shows the inherent difficulty of obtaining parameter estimates for segregation analysis when families are ascertained from a cluster of cases.

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Year:  1988        PMID: 3169523     DOI: 10.1002/gepi.1370050303

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  16 in total

1.  Segregation analyses of 1,476 population-based Australian families affected by prostate cancer.

Authors:  J Cui; M P Staples; J L Hopper; D R English; M R McCredie; G G Giles
Journal:  Am J Hum Genet       Date:  2001-04-11       Impact factor: 11.025

2.  Linkage strategies for genetically complex traits. II. The power of affected relative pairs.

Authors:  N Risch
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

3.  Linkage of familial breast cancer to chromosome 17q21 may not be restricted to early-onset disease.

Authors:  P Margaritte; C Bonaiti-Pellie; M C King; F Clerget-Darpoux
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

4.  Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13.

Authors:  D F Easton; L Steele; P Fields; W Ormiston; D Averill; P A Daly; R McManus; S L Neuhausen; D Ford; R Wooster; L A Cannon-Albright; M R Stratton; D E Goldgar
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

5.  Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype.

Authors:  J Gudmundsson; G Johannesdottir; A Arason; J T Bergthorsson; S Ingvarsson; V Egilsson; R B Barkardottir
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

6.  The calculation of breast cancer risk for women with a first degree family history of ovarian cancer.

Authors:  E B Claus; N Risch; W D Thompson
Journal:  Breast Cancer Res Treat       Date:  1993-11       Impact factor: 4.872

7.  Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.

Authors:  P Devilee; R S Cornelis; A Bootsma; A Bardoel; M van Vliet; I van Leeuwen; F J Cleton; A de Klein; D Lindhout; H F Vasen
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

8.  Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.

Authors:  D F Easton; D T Bishop; D Ford; G P Crockford
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

9.  Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast/ovarian cancer relationship.

Authors:  J M Schildkraut; N Risch; W D Thompson
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

10.  Estimating the power of linkage analysis in hereditary breast cancer.

Authors:  S A Narod; C Amos
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

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