Literature DB >> 1897524

Regressive logistic models for familial diseases: a formulation assuming an underlying liability model.

F M Demenais1.   

Abstract

Statistical models have been developed to delineate the major-gene and non-major-gene factors accounting for the familial aggregation of complex diseases. The mixed model assumes an underlying liability to the disease, to which a major gene, a multifactorial component, and random environment contribute independently. Affection is defined by a threshold on the liability scale. The regressive logistic models assume that the logarithm of the odds of being affected is a linear function of major genotype, phenotypes of antecedents and other covariates. An equivalence between these two approaches cannot be derived analytically. I propose a formulation of the regressive logistic models on the supposition of an underlying liability model of disease. Relatives are assumed to have correlated liabilities to the disease; affected persons have liabilities exceeding an estimable threshold. Under the assumption that the correlation structure of the relatives' liabilities follows a regressive model, the regression coefficients on antecedents are expressed in terms of the relevant familial correlations. A parsimonious parameterization is a consequence of the assumed liability model, and a one-to-one correspondence with the parameters of the mixed model can be established. The logits, derived under the class A regressive model and under the class D regressive model, can be extended to include a large variety of patterns of family dependence, as well as gene-environment interactions.

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Year:  1991        PMID: 1897524      PMCID: PMC1683192     

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


  9 in total

1.  Search for faster methods of fitting the regressive models to quantitative traits.

Authors:  F M Demenais; C Murigande; G E Bonney
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2.  Equivalence of the mixed and regressive models for genetic analysis. I. Continuous traits.

Authors:  F M Demenais; G E Bonney
Journal:  Genet Epidemiol       Date:  1989       Impact factor: 2.135

3.  Analysis of family resemblance. 3. Complex segregation of quantitative traits.

Authors:  N E Morton; C J MacLean
Journal:  Am J Hum Genet       Date:  1974-07       Impact factor: 11.025

4.  The use of multiple thresholds in determining the mode of transmission of semi-continuous traits.

Authors:  T Reich; J W James; C A Morris
Journal:  Ann Hum Genet       Date:  1972-11       Impact factor: 1.670

5.  A general model for the genetic analysis of pedigree data.

Authors:  R C Elston; J Stewart
Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

6.  A unified model for complex segregation analysis.

Authors:  J M Lalouel; D C Rao; N E Morton; R C Elston
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

7.  On the statistical determination of major gene mechanisms in continuous human traits: regressive models.

Authors:  G E Bonney
Journal:  Am J Med Genet       Date:  1984-08

8.  Complex segregation analysis with pointers.

Authors:  J M Lalouel; N E Morton
Journal:  Hum Hered       Date:  1981       Impact factor: 0.444

9.  A time-dependent logistic hazard function for modeling variable age of onset in analysis of familial diseases.

Authors:  L Abel; G E Bonney
Journal:  Genet Epidemiol       Date:  1990       Impact factor: 2.135

  9 in total
  11 in total

1.  Interactions between genetic and reproductive factors in breast cancer risk in a French family sample.

Authors:  N Andrieu; F Demenais
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

2.  Testing association between candidate-gene markers and phenotype in related individuals, by use of estimating equations.

Authors:  D A Trégouët; P Ducimetière; L Tiret
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

Review 3.  Clinical-pathological correlations of BAV and the attendant thoracic aortopathies. Part 2: Pluridisciplinary perspective on their genetic and molecular origins.

Authors:  Ares Pasipoularides
Journal:  J Mol Cell Cardiol       Date:  2019-06-06       Impact factor: 5.000

4.  An autologistic model for the genetic analysis of familial binary data.

Authors:  L Abel; J L Golmard; A Mallet
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

5.  Severe hepatic fibrosis in Schistosoma mansoni infection is controlled by a major locus that is closely linked to the interferon-gamma receptor gene.

Authors:  A J Dessein; D Hillaire; N E Elwali; S Marquet; Q Mohamed-Ali; A Mirghani; S Henri; A A Abdelhameed; O K Saeed; M M Magzoub; L Abel
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

6.  A parametric copula model for analysis of familial binary data.

Authors:  D A Trégou t; P Ducimetière; V Bocquet; S Visvikis; F Soubrier; L Tiret
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

7.  Evidence for a major gene controlling susceptibility to tegumentary leishmaniasis in a recently exposed Bolivian population.

Authors:  A Alcaïs; L Abel; C David; M E Torrez; P Flandre; J P Dedet
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

8.  Genetic segregation analysis of early-onset recurrent unipolar depression.

Authors:  M L Marazita; K Neiswanger; M Cooper; G S Zubenko; D E Giles; E Frank; D J Kupfer; B B Kaplan
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

9.  Evidence for a dominant major gene conferring predisposition to hepatitis C virus infection in endemic conditions.

Authors:  Cédric Laouénan; Sabine Plancoulaine; Mostafa Kamal Mohamed; Naglaa Arafa; Iman Bakr; Mohamed Abdel-Hamid; Claire Rekacewicz; Dorothée Obach; Arnaud Fontanet; Laurent Abel
Journal:  Hum Genet       Date:  2009-07-23       Impact factor: 4.132

10.  Using an age-at-onset phenotype with interval censoring to compare methods of segregation and linkage analysis in a candidate region for elevated systolic blood pressure.

Authors:  Karen A Kopciuk; Laurent Briollais; Florence Demenais; Shelley B Bull
Journal:  BMC Genet       Date:  2003-12-31       Impact factor: 2.797

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