Literature DB >> 3459355

Approximate confidence intervals for risk prediction in genetic counseling.

K Lange.   

Abstract

In current genetic counseling practice, a single risk estimate is often quoted to a family rather than a range of risks. Such point estimates are predicated on knowing basic parameters like recombination fractions exactly when, in fact, there may be considerable uncertainty about them. Using the large sample theory of statistics, it is possible to derive approximate risk intervals that incorporate known statistical imprecision. The necessary theory will be briefly discussed and illustrated by an application to family counseling for Duchenne muscular dystrophy in the presence of two flanking markers. Some of the problems of the theory will be mentioned. These include lack of adequate sample size to justify the conclusions of large sample theory, pronounced nonlinearity in the risk function, and failure to take into proper account genetic interference. Except in trivial cases, sophisticated computer software is needed to carry out the computations of risk intervals.

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Year:  1986        PMID: 3459355      PMCID: PMC1684836     

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


  7 in total

1.  Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods.

Authors:  K Lange; M Boehnke
Journal:  Hum Hered       Date:  1983       Impact factor: 0.444

2.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors:  D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

3.  The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.

Authors:  P S Harper; T O'Brien; J M Murray; K E Davies; P Pearson; R Williamson
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

4.  Multiexponential, multicompartmental, and noncompartmental modeling. II. Data analysis and statistical considerations.

Authors:  E M Landaw; J J DiStefano
Journal:  Am J Physiol       Date:  1984-05

5.  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

6.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

7.  Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.

Authors:  K E Davies; P L Pearson; P S Harper; J M Murray; T O'Brien; M Sarfarazi; R Williamson
Journal:  Nucleic Acids Res       Date:  1983-04-25       Impact factor: 16.971

  7 in total
  7 in total

1.  Variability of genotype-specific penetrance probabilities in the calculation of risk support intervals.

Authors:  S M Leal; J Ott
Journal:  Genet Epidemiol       Date:  1995       Impact factor: 2.135

2.  Determining informativity of marker typing for genetic counseling in a pedigree.

Authors:  L Sandkuyl; J Ott
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

3.  Risk calculations under heterogeneity.

Authors:  D E Weeks; J Ott
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

4.  Genetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree.

Authors:  G K Suthers; S R Wilson
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

5.  A likelihood approach to calculating risk support intervals.

Authors:  S M Leal; J Ott
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

6.  Prenatal prediction of spinal muscular atrophy.

Authors:  R J Daniels; G K Suthers; K E Morrison; N H Thomas; M J Francis; C G Mathew; S Loughlin; A Heiberg; D Wood; V Dubowitz
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

7.  X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

Authors:  R J Gibbons; G K Suthers; A O Wilkie; V J Buckle; D R Higgs
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

  7 in total

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