Literature DB >> 7344182

Measuring the strength of associations between HLA antigens and diseases.

B O Bengtsson, G Thomson.   

Abstract

The strength of the population association between an antigen and a disease can be estimated not only by the relative risk value, but also by what variously has been called the population attributable risk and the etiologic fraction. This alternative measure has certain advantages if the association is due to linkage disequilibrium between the antigen allele and a "disease" allele at a closely linked "disease susceptibility" locus. In particular, it can then be used to determine which of many antigens associated with the same disease has the strongest association from a genetical point of view.

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Year:  1981        PMID: 7344182     DOI: 10.1111/j.1399-0039.1981.tb01404.x

Source DB:  PubMed          Journal:  Tissue Antigens        ISSN: 0001-2815


  67 in total

1.  Characterisation of patients with primary biliary cirrhosis responding to long term ursodeoxycholic acid treatment.

Authors:  M Leuschner; C F Dietrich; T You; C Seidl; J Raedle; G Herrmann; H Ackermann; U Leuschner
Journal:  Gut       Date:  2000-01       Impact factor: 23.059

2.  Balancing selection at closely linked, overdominant loci in a finite population.

Authors:  M Slatkin
Journal:  Genetics       Date:  2000-03       Impact factor: 4.562

3.  QTL fine mapping by measuring and testing for Hardy-Weinberg and linkage disequilibrium at a series of linked marker loci in extreme samples of populations.

Authors:  H W Deng; W M Chen; R R Recker
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

4.  Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan Jews.

Authors:  R Colombo
Journal:  Am J Hum Genet       Date:  2000-08       Impact factor: 11.025

5.  Disequilibrium mapping of a quantitative-trait locus in an expanding population.

Authors:  M Slatkin
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

6.  A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.

Authors:  Zanhua Yi; Nanibaa' Garrison; Orit Cohen-Barak; Tatiana M Karafet; Richard A King; Robert P Erickson; Michael F Hammer; Murray H Brilliant
Journal:  Am J Hum Genet       Date:  2002-12-05       Impact factor: 11.025

7.  Identifying the susceptibility gene(s) in a set of trait-linked genes using genotype data.

Authors:  Ao Yuan; Guanjie Chen; Yuanxiu Chen; Charles Rotimi; George E Bonney
Journal:  Genetics       Date:  2004-07       Impact factor: 4.562

8.  Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia.

Authors:  L U Dzhemileva; O L Posukh; N A Barashkov; S A Fedorova; F M Teryutin; V L Akhmetova; I M Khidiyatova; R I Khusainova; S L Lobov; E K Khusnutdinova
Journal:  Acta Naturae       Date:  2011-07       Impact factor: 1.845

9.  Signature of positive selection of PTK6 gene in East Asian populations: a cross talk for Helicobacter pylori invasion and gastric cancer endemicity.

Authors:  Pankaj Jha; Dongsheng Lu; Yuan Yuan; Shuhua Xu
Journal:  Mol Genet Genomics       Date:  2015-04-03       Impact factor: 3.291

10.  Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.

Authors:  Elena A Bliznetz; Svetlana M Tverskaya; Rena A Zinchenko; Anna V Abrukova; Ekaterina N Savaskina; Maxim V Nikulin; Alexander G Kirillov; Evgeny K Ginter; Alexander V Polyakov
Journal:  Eur J Hum Genet       Date:  2009-01-28       Impact factor: 4.246

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