Literature DB >> 3225821

A simple method for calculating risks before DNA analysis.

M Jeanpierre1.   

Abstract

Calculation of carrier risk of an X linked disease may be performed on a small computer after DNA analysis, but a method for rapid hand estimation of the risk is still useful for a quick check of the results and weighing the relative importance of each element of information, such as the determination of a haplotype. Each risk estimation is a function of a prior risk and the product of likelihood ratios and these terms are derived themselves from parameters such as fitness or the relative mutation rate in male and female gametes. Even if it is often difficult to have strong experimental estimation of these variables, the existence of a normal father or grandfather must be considered whenever male fitness is not null. The likelihood ratio for a woman for not being a carrier, when her father is not affected and her mother has herself a likelihood R for not having the mutated gene, may be expressed as the ratio 2R/(CmR + 1), with Cm being a function of male fitness and relative mutation rate. Cm represents the odds ratio for the mother of a carrier not to be a carrier, given that the father of the known carrier is not affected. This formula can be used recurrently and reduces to 2R/(R + 1) in lethal X linked disease. When likelihood ratios are expressed as an algebraic function, maximum values are easily determined, hence fixing the limits of DNA analysis.

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Year:  1988        PMID: 3225821      PMCID: PMC1051559          DOI: 10.1136/jmg.25.10.663

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  13 in total

1.  A simple combinatorial method for calculating genetic risks.

Authors:  U R Maag; R J Gold
Journal:  Clin Genet       Date:  1975 May-Jun       Impact factor: 4.438

2.  Formal genetics of muscular dystrophy.

Authors:  N E MORTON; C S CHUNG
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

3.  A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information.

Authors:  M Sarfarazi; H Williams
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

4.  Playing the odds.

Authors:  D L Simel
Journal:  Lancet       Date:  1985-02-09       Impact factor: 79.321

Review 5.  Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.

Authors:  A E Emery
Journal:  Br Med Bull       Date:  1980-05       Impact factor: 4.291

6.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

7.  Carrier detection in sex-linked muscular dystrophy.

Authors:  A E Emery
Journal:  J Genet Hum       Date:  1965-12

8.  Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy.

Authors:  A E Emery; S Holloway
Journal:  Hum Hered       Date:  1977       Impact factor: 0.444

9.  Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families.

Authors:  C R Müller; T Grimm
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

10.  DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.

Authors:  D F Andrews; P M Brasher; K E Manchester; M E Percy; A C Rusk; H C Soltan; D W Trueman
Journal:  Am J Med Genet       Date:  1986-10
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  1 in total

1.  Germinal mosaicism and risk calculation in X-linked diseases.

Authors:  M Jeanpierre
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

  1 in total

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