Literature DB >> 3369448

Segregation analysis with uncertain ascertainment: application to Fanconi anemia.

A Rogatko1, A D Auerbach.   

Abstract

A Bayesian solution for making inferences about segregation parameters with no information about the ascertainment is presented. Inferences about the segregation probability and the probability of being sporadic are made through the posterior marginal distribution of these parameters after integrating out the ascertainment probability, the nuisance parameter. The method was tested with real and simulated data and performed well. Original Fanconi anemia data, for which no information about the ascertainment was available, were then analyzed, with results that confirmed a monogenic autosomal recessive mode of inheritance.

Entities:  

Mesh:

Year:  1988        PMID: 3369448      PMCID: PMC1715212     

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


  13 in total

1.  Genetic tests under incomplete ascertainment.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1959-03       Impact factor: 11.025

2.  Formal genetics of Fanconi's anemia.

Authors:  T M Schroeder; D Tilgen; J Krüger; F Vogel
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

3.  Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens.

Authors:  A D Auerbach; S R Wolman
Journal:  Nature       Date:  1976-06-10       Impact factor: 49.962

4.  Genetic studies on cystic fibrosis in Hawaii.

Authors:  S W Wright; N E Morton
Journal:  Am J Hum Genet       Date:  1968-03       Impact factor: 11.025

5.  Fanconi anemia: prenatal diagnosis in 30 fetuses at risk.

Authors:  A D Auerbach; M Sagi; B Adler
Journal:  Pediatrics       Date:  1985-11       Impact factor: 7.124

6.  Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method.

Authors:  A D Auerbach; B Adler; R S Chaganti
Journal:  Pediatrics       Date:  1981-01       Impact factor: 7.124

7.  [Spontaneous chromosome aberrations in familial panmyelopathy].

Authors:  T M Schroeder; F Anschütz; A Knopp
Journal:  Humangenetik       Date:  1964

8.  Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects.

Authors:  G Fanconi
Journal:  Semin Hematol       Date:  1967-07       Impact factor: 3.851

9.  Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia.

Authors:  A D Auerbach; Z Min; R Ghosh; E Pergament; Y Verlinsky; H Nicolas; J Boué
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

10.  A Bayesian method for the estimation of penetrance: application to mandibulofacial and frontonasal dysostoses.

Authors:  A Rogatko; C A Pereira; O Frota-Pessoa
Journal:  Am J Med Genet       Date:  1986-06
View more
  4 in total

1.  A locus for Fanconi anemia on 16q determined by homozygosity mapping.

Authors:  M Gschwend; O Levran; L Kruglyak; K Ranade; P C Verlander; S Shen; S Faure; J Weissenbach; C Altay; E S Lander; A D Auerbach; D Botstein
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

2.  Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype.

Authors:  Viktoria N Evdokimova; Reagan K McLoughlin; Sharon L Wenger; Stephen G Grant
Journal:  Am J Med Genet A       Date:  2005-05-15       Impact factor: 2.802

3.  Body proportions in Fanconi anemia heterozygotes.

Authors:  S Mohan; P Lakshminarayanan; P Sowmya; M Venkatadesikalu; V Pushpa
Journal:  Indian J Pediatr       Date:  2000-11       Impact factor: 1.967

Review 4.  Homing endonucleases: from basics to therapeutic applications.

Authors:  Maria J Marcaida; Inés G Muñoz; Francisco J Blanco; Jesús Prieto; Guillermo Montoya
Journal:  Cell Mol Life Sci       Date:  2010-03       Impact factor: 9.261

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.