Literature DB >> 6576632

Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium.

A Chakravarti.   

Abstract

A marker locus closely linked to a disease locus is often useful for genetic counseling provided that a counselee is heterozygous at both disease and marker loci. Furthermore, the linkage phase of these genes in the counselee must be known. When the linkage between the disease and marker loci is very close, one often finds linkage disequilibrium between the loci. To evaluate the effect of such nonrandom associations on the utility of linked marker genes for genetic counseling, the proportion of informative families is studied for X-linked recessive and autosomal dominant diseases. This proportion is higher for X-linked genes than for autosomal genes, if other factors are the same. In general, codominant markers are more useful than dominant markers. Also, under appropriate conditions, the proportion of informative families is higher when linkage disequilibrium is present. The results obtained in this paper are useful for evaluating the utility of polymorphic restriction endonuclease cleavage sites as markers in genetic counseling.

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Year:  1983        PMID: 6576632      PMCID: PMC1685725     

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


  26 in total

1.  Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.

Authors:  G Filippi; A Rinaldi; R Palmarino; E Seravalli; M Siniscalco
Journal:  Genetics       Date:  1977-05       Impact factor: 4.562

2.  Heterogeneity of DNA fragments associated with the sickle-globin gene.

Authors:  J Feldenzer; J G Mears; A L Burns; C Natta; A Bank
Journal:  J Clin Invest       Date:  1979-09       Impact factor: 14.808

3.  Use of genetic linkage for the detection of female carriers of hemophilia.

Authors:  P R McCurdy
Journal:  N Engl J Med       Date:  1971-07-22       Impact factor: 91.245

4.  Antenatal diagnosis of sickle-cell anaemia by D.N.A. analysis of amniotic-fluid cells.

Authors:  Y W Kan; A M Dozy
Journal:  Lancet       Date:  1978-10-28       Impact factor: 79.321

5.  Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

Authors:  G I Bell; J H Karam; W J Rutter
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

6.  Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

Authors:  S H Orkin; H H Kazazian; S E Antonarakis; S C Goff; C D Boehm; J P Sexton; P G Waber; P J Giardina
Journal:  Nature       Date:  1982-04-15       Impact factor: 49.962

7.  The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease.

Authors:  U Francke; J Felsenstein; S M Gartler; B R Migeon; J Dancis; J E Seegmiller; F Bakay; W L Nyhan
Journal:  Am J Hum Genet       Date:  1976-03       Impact factor: 11.025

8.  Prenatal diagnosis by linkage: hemophilia A and polymorphic glucose-6-phosphate deydrogenase.

Authors:  C J Edgell; H N Kirkman; E Clemons; P D Buchanan; C H Miller
Journal:  Am J Hum Genet       Date:  1978-01       Impact factor: 11.025

9.  Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites.

Authors:  H H Kazazian; J A Phillips; C D Boehm; T A Vik; M J Mahoney; A K Ritchey
Journal:  Blood       Date:  1980-11       Impact factor: 22.113

10.  The use of genetic linkage in counselling families with dystrophia myotonica.

Authors:  S L Gibson; M A Ferguson-Smith
Journal:  Clin Genet       Date:  1980-06       Impact factor: 4.438

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  7 in total

1.  The use of multiple restriction fragment length polymorphisms in prenatal risk estimation. I. X-linked diseases.

Authors:  A G Clark
Journal:  Am J Hum Genet       Date:  1985-01       Impact factor: 11.025

2.  A strategy for using multiple linked markers for genetic counseling.

Authors:  A Chakravarti; K H Buetow
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

3.  2013 William Allan Award: My multifactorial journey.

Authors:  Aravinda Chakravarti
Journal:  Am J Hum Genet       Date:  2014-03-06       Impact factor: 11.025

4.  DNA polymorphism and clinical genetics.

Authors:  R Chakraborty
Journal:  Indian J Pediatr       Date:  1986 Nov-Dec       Impact factor: 1.967

5.  Considerations in using linkage analysis as a presymptomatic test for Huntington's disease.

Authors:  L A Farrer; R H Myers; L A Cupples; P M Conneally
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

6.  Estimation of the marker gene frequency and linkage disequilibrium from conditional marker data.

Authors:  A Chakravarti; C C Li; K H Buetow
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

7.  Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland.

Authors:  J M Connor; A F Pettigrew; I M Hann; C D Forbes; G D Lowe; N A Affara
Journal:  J Med Genet       Date:  1985-12       Impact factor: 6.318

  7 in total

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