(Q22337300)

Dimensions Publication ID

Dimensions

1051065086

ABO blood groups and secretor character in duodenal ulcer; population and sibship studies.

7 February 2023

language of work or name

English

0 references

publication date

15 June 2000

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published in

Nature

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volume

405

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issue

6788

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page(s)

847-856

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cites work

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Use of siblings as controls in case-control association studies.

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A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

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Genetic association mapping based on discordant sib pairs: the discordant-alleles test

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The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling

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Use of parents, sibs, and unrelated controls for detection of associations between genetic markers and disease

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A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus

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Extreme discordant sib pairs for mapping quantitative trait loci in humans

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Locating human quantitative trait loci: guidelines for the selection of sibling pairs for genotyping

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Mapping Genes through the Use of Linkage Disequilibrium Generated by Genetic Drift: ‘Drift Mapping’ in Small Populations with No Demographic Expansion

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The future of genetic studies of complex human diseases

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Variations on a theme: cataloging human DNA sequence variation

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Prospects for whole-genome linkage disequilibrium mapping of common disease genes

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Demographic history and linkage disequilibrium in human populations

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Allelic association between marker loci

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Population choice in mapping genes for complex diseases

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Power of association and linkage tests when the disease alleles are unobserved

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DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene

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Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: studies of the HLA class II loci

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Association mapping of disease loci, by use of a pooled DNA genomic screen

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

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Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

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A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

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Tests and estimates of allelic association in complex inheritance

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Use of unlinked genetic markers to detect population stratification in association studies.

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Genomic control for association studies

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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7 January 2021

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium

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7 January 2021

DQB1*0602 and DQA1*0102 (DQ1) are better markers than DR2 for narcolepsy in Caucasian and black Americans.

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7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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