(Q57234027)

1

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Joel S Bader

2

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Shaun Purcell

3

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Pak Sham

European Journal of Human Genetics

5

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publication date

February 2002

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published in

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volume

10

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page(s)

125-132

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issue

2

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200771

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cites work

The future of genetic studies of complex human diseases

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Extent and distribution of linkage disequilibrium in three genomic regions

21 January 2018

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

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A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies

21 January 2018

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DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children.

21 January 2018

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DNA pooling and dense marker maps: a systematic search for genes for cognitive ability.

21 January 2018

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A novel locus for Leber congenital amaurosis on chromosome 14q24.

21 January 2018

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Linkage disequilibrium mapping of the gene for Margarita Island ectodermal dysplasia (ED4) to 11q23.

21 January 2018

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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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Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

21 January 2018

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Accuracy and sensitivity of DNA pooling with microsatellite repeats using capillary electrophoresis.

21 January 2018

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Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects

21 January 2018

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Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

21 January 2018

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Accounting for unmeasured population substructure in case-control studies of genetic association using a novel latent-class model

21 January 2018

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

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Variations on a theme: cataloging human DNA sequence variation

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inferred from DOI database lookup

7 January 2021

based on heuristic

Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200771

inferred from DOI database lookup

7 January 2021

based on heuristic

Efficient SNP-based tests of association for quantitative phenotypes using pooled DNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200771