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Finding genes underlying risk of complex disease by linkage disequilibrium mapping
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Finding genes underlying risk of complex disease by linkage disequilibrium mapping
(English)
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stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
main subject
disequilibrium
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inferred from title
linkage disequilibrium
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inferred from title
author
Andrew G. Clark
object named as
Andrew G Clark
series ordinal
1
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ORCID Public Data File 2021
publication date
1 June 2003
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stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
published in
Current Opinion in Genetics & Development
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stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
volume
13
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stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
page(s)
296-302
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stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
cites work
The future of genetic studies of complex human diseases
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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland
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Patterns of linkage disequilibrium in the human genome
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Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism
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DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.
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A comparison of linkage disequilibrium measures for fine-scale mapping
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Linkage disequilibrium in the human genome
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The structure of haplotype blocks in the human genome
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A first-generation linkage disequilibrium map of human chromosome 22
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Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms
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Linkage disequilibrium and the search for complex disease genes
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Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations
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Sequence variations in the public human genome data reflect a bottlenecked population history
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Linkage disequilibrium in humans: models and data
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MULTIFACTORIAL GENETICSUNDERSTANDING QUANTITATIVE GENETIC VARIATION
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Searching for genetic determinants in the new millennium
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Linkage disequilibrium and the mapping of complex human traits.
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Linkage disequilibrium: what history has to tell us.
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The sampling theory of selectively neutral alleles
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On the allelic spectrum of human disease
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Are rare variants responsible for susceptibility to complex diseases?
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The allelic architecture of human disease genes: common disease-common variant... or not?
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Optimality, mutation and the evolution of ageing
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A polygenic basis for late-onset disease
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Complex signatures of natural selection at the Duffy blood group locus
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Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance
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Adaptive protein evolution at the Adh locus in Drosophila
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Interrogating a high-density SNP map for signatures of natural selection
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Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
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7 January 2021
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7 January 2021
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7 January 2021
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Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels
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Haplotype tagging for the identification of common disease genes
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7 January 2021
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A New Statistical Method for Haplotype Reconstruction from Population Data
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Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms
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Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms
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Inference of haplotypes from samples of diploid populations: complexity and algorithms
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High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools
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A comprehensive review of genetic association studies
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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
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Identifiers
DOI
10.1016/S0959-437X(03)00056-X
1 reference
stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
PubMed ID
12787793
1 reference
stated in
Europe PubMed Central
PubMed ID
12787793
retrieved
6 August 2017
ResearchGate publication ID
10724104
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