Published in Am J Hum Genet on November 13, 2000
Linkage disequilibrium in humans: models and data. Am J Hum Genet (2001) 14.97
Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers. Am J Hum Genet (2005) 6.12
Runs of homozygosity in European populations. Am J Hum Genet (2008) 5.34
A dynamic programming algorithm for haplotype block partitioning. Proc Natl Acad Sci U S A (2002) 5.12
Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis. Am J Hum Genet (2004) 3.83
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Extensive and breed-specific linkage disequilibrium in Canis familiaris. Genome Res (2004) 2.85
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Linkage disequilibrium in domestic sheep. Genetics (2002) 2.29
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Genetic association analysis using data from triads and unrelated subjects. Am J Hum Genet (2005) 2.06
Hierarchical modeling of linkage disequilibrium: genetic structure and spatial relations. Am J Hum Genet (2003) 2.05
Sequence variation and linkage disequilibrium in the human T-cell receptor beta (TCRB) locus. Am J Hum Genet (2001) 1.91
Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion. Am J Hum Genet (2001) 1.80
A comparison of linkage disequilibrium patterns and estimated population recombination rates across multiple populations. Am J Hum Genet (2005) 1.75
Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs. BMC Genomics (2005) 1.68
The power to detect linkage disequilibrium with quantitative traits in selected samples. Am J Hum Genet (2001) 1.64
Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci U S A (2002) 1.60
Application of coalescent methods to reveal fine-scale rate variation and recombination hotspots. Genetics (2004) 1.59
Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome. Am J Hum Genet (2003) 1.58
Power calculations for genetic association studies using estimated probability distributions. Am J Hum Genet (2002) 1.53
Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations. Am J Hum Genet (2001) 1.43
Multilocus LD measure and tagging SNP selection with generalized mutual information. Genet Epidemiol (2005) 1.33
Integration of association statistics over genomic regions using Bayesian adaptive regression splines. Hum Genomics (2003) 1.28
Allele frequency matching between SNPs reveals an excess of linkage disequilibrium in genic regions of the human genome. PLoS Genet (2006) 1.27
Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites. Am J Hum Genet (2004) 1.26
Haplotype and linkage disequilibrium architecture for human cancer-associated genes. Genome Res (2002) 1.26
Randomly distributed crossovers may generate block-like patterns of linkage disequilibrium: an act of genetic drift. Hum Genet (2003) 1.23
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Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11. Genomics (2004) 1.17
Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps. Proc Natl Acad Sci U S A (2004) 1.16
SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex. Immunogenetics (2004) 1.15
Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes. Hum Genet (2005) 1.13
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program. Genome Res (2003) 1.13
The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activity. Am J Hum Genet (2003) 1.11
Comparison of population-based association study methods correcting for population stratification. PLoS One (2008) 1.11
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes. BMC Med Genet (2004) 1.10
Linkage disequilibrium in Angus, Charolais, and Crossbred beef cattle. Front Genet (2012) 1.07
Two critical genes (HLA-DRB1 and ABCF1)in the HLA region are associated with the susceptibility to autoimmune pancreatitis. Immunogenetics (2006) 1.00
Modulation of DNA damage/DNA repair capacity by XPC polymorphisms. DNA Repair (Amst) (2007) 0.99
Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy. Am J Hum Genet (2002) 0.98
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Linkage disequilibrium between microsatellite markers in the Swedish Sami relative to a worldwide selection of populations. Hum Genet (2004) 0.95
Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype. Neurogenetics (2004) 0.93
Linkage disequilibrium between STRPs and SNPs across the human genome. Am J Hum Genet (2008) 0.91
Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma. Respir Res (2001) 0.89
Genomic Diversity in Pig (Sus scrofa) and its Comparison with Human and other Livestock. Curr Genomics (2011) 0.89
Single nucleotide polymorphisms and disease gene mapping. Arthritis Res (2002) 0.86
Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes. BMC Genet (2004) 0.86
Common 5' beta-globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism. Hum Genet (2003) 0.86
Haplotype block partitioning as a tool for dimensionality reduction in SNP association studies. BMC Genomics (2008) 0.85
Characterisation of the genomic architecture of human chromosome 17q and evaluation of different methods for haplotype block definition. BMC Genet (2005) 0.84
Protein kinase C/zeta (PRKCZ) gene is associated with type 2 diabetes in Han population of North China and analysis of its haplotypes. World J Gastroenterol (2003) 0.83
HLA Class I and II profiles in São Miguel Island (Azores): genetic diversity and linkage disequilibrium. BMC Res Notes (2010) 0.83
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Identification and prioritization of NUAK1 and PPP1CC as positional candidate loci for skeletal muscle strength phenotypes. Physiol Genomics (2011) 0.81
Linkage disequilibrium and diversity for three genomic regions in Azoreans and mainland Portuguese. Genet Mol Biol (2009) 0.81
Evaluation of microsatellite markers in association studies: a search for an immune-related susceptibility gene in sarcoidosis. Immunogenetics (2005) 0.81
Mapping of susceptibility and protective loci for acute GVHD in unrelated HLA-matched bone marrow transplantation donors and recipients using 155 microsatellite markers on chromosome 22. Immunogenetics (2007) 0.80
Genetic mapping of high caries experience on human chromosome 13. BMC Med Genet (2013) 0.78
Association between evolutionary history of angiotensinogen haplotypes and plasma levels. Hum Genet (2004) 0.77
Association between HLA-B*46 allele and Graves disease in Asian populations: a meta-analysis. Int J Med Sci (2013) 0.77
Imputing Phenotypes for Genome-wide Association Studies. Am J Hum Genet (2016) 0.77
Environmental Association Analyses Identify Candidates for Abiotic Stress Tolerance in Glycine soja, the Wild Progenitor of Cultivated Soybeans. G3 (Bethesda) (2016) 0.76
Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages. Am J Hum Genet (2015) 0.75
Genetic Structure of and Evidence for Admixture between Western and Korean Native Pig Breeds Revealed by Single Nucleotide Polymorphisms. Asian-Australas J Anim Sci (2014) 0.75
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Using local multiplicity to improve effect estimation from a hypothesis-generating pharmacogenetics study. Pharmacogenomics J (2015) 0.75
Combined effects of multiple linked loci on pairwise sibling tests. Int J Legal Med (2016) 0.75
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