Published in Am J Hum Genet on March 01, 1995
A new statistical method for haplotype reconstruction from population data. Am J Hum Genet (2001) 59.30
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. Am J Hum Genet (2007) 24.68
Estimating African American admixture proportions by use of population-specific alleles. Am J Hum Genet (1998) 22.90
Score tests for association between traits and haplotypes when linkage phase is ambiguous. Am J Hum Genet (2001) 22.07
Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. Am J Hum Genet (2005) 14.09
A comparison of phasing algorithms for trios and unrelated individuals. Am J Hum Genet (2006) 12.45
Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data. Am J Hum Genet (2000) 11.47
Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms. Am J Hum Genet (2001) 10.48
Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet (2002) 7.40
A fine-scale linkage-disequilibrium measure based on length of haplotype sharing. Am J Hum Genet (2006) 6.02
Reconstructing genetic ancestry blocks in admixed individuals. Am J Hum Genet (2006) 5.92
Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease. Genome Res (2001) 5.78
Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. Am J Hum Genet (2009) 5.65
Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. Am J Hum Genet (2000) 4.74
Skin pigmentation, biogeographical ancestry and admixture mapping. Hum Genet (2003) 4.67
Haplotype phasing: existing methods and new developments. Nat Rev Genet (2011) 4.66
Gametic phase estimation over large genomic regions using an adaptive window approach. Hum Genomics (2003) 4.63
GERBIL: Genotype resolution and block identification using likelihood. Proc Natl Acad Sci U S A (2004) 4.36
The accuracy of statistical methods for estimation of haplotype frequencies: an example from the CD4 locus. Am J Hum Genet (2000) 4.07
Incorporating genotypes of relatives into a test of linkage disequilibrium. Am J Hum Genet (1998) 3.83
Inference on haplotype effects in case-control studies using unphased genotype data. Am J Hum Genet (2003) 3.74
Missing data imputation and haplotype phase inference for genome-wide association studies. Hum Genet (2008) 3.65
A generic estimation of population subdivision using distances between alleles with special reference for microsatellite loci. Genetics (1996) 3.41
Haplotype block structure and its applications to association studies: power and study designs. Am J Hum Genet (2002) 2.88
Association testing by DNA pooling: an effective initial screen. Proc Natl Acad Sci U S A (2002) 2.79
Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans. Am J Hum Genet (2003) 2.71
Association of neuregulin 1 with schizophrenia confirmed in a Scottish population. Am J Hum Genet (2002) 2.64
Caution on pedigree haplotype inference with software that assumes linkage equilibrium. Am J Hum Genet (2002) 2.51
Comparisons of two methods for haplotype reconstruction and haplotype frequency estimation from population data. Am J Hum Genet (2001) 2.44
Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations. Am J Hum Genet (2000) 2.43
Diploid genome reconstruction of Ciona intestinalis and comparative analysis with Ciona savignyi. Genome Res (2007) 2.37
Significant admixture linkage disequilibrium across 30 cM around the FY locus in African Americans. Am J Hum Genet (2000) 2.32
Ancestral proportions and their association with skin pigmentation and bone mineral density in Puerto Rican women from New York city. Hum Genet (2004) 2.00
Methods to impute missing genotypes for population data. Hum Genet (2007) 1.98
APOBEC3G genetic variants and their influence on the progression to AIDS. J Virol (2004) 1.97
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet (1998) 1.89
Understanding the accuracy of statistical haplotype inference with sequence data of known phase. Genet Epidemiol (2007) 1.87
A comprehensive literature review of haplotyping software and methods for use with unrelated individuals. Hum Genomics (2005) 1.84
Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients. Am J Hum Genet (2007) 1.76
Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies. Genome Res (2004) 1.74
Extracellular superoxide dismutase haplotypes are associated with acute lung injury and mortality. Am J Respir Crit Care Med (2008) 1.73
Incorporating genotyping uncertainty in haplotype inference for single-nucleotide polymorphisms. Am J Hum Genet (2004) 1.66
HIBAG--HLA genotype imputation with attribute bagging. Pharmacogenomics J (2013) 1.66
Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects. Am J Hum Genet (2000) 1.65
Dimensional anxiety mediates linkage of GABRA2 haplotypes with alcoholism. Am J Med Genet B Neuropsychiatr Genet (2006) 1.64
Modulating influence on HIV/AIDS by interacting RANTES gene variants. Proc Natl Acad Sci U S A (2002) 1.61
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus. Am J Hum Genet (2002) 1.61
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease. Am J Hum Genet (1999) 1.46
Estimation of haplotype frequencies, linkage-disequilibrium measures, and combination of haplotype copies in each pool by use of pooled DNA data. Am J Hum Genet (2003) 1.42
A functional polymorphism in the promoter of the progesterone receptor gene associated with endometrial cancer risk. Proc Natl Acad Sci U S A (2002) 1.41
Linkage disequilibrium testing when linkage phase is unknown. Genetics (2004) 1.41
Brain derived neurotrophic factor (BDNF) gene variants and Alzheimer's disease, affective disorders, posttraumatic stress disorder, schizophrenia, and substance dependence. Am J Med Genet B Neuropsychiatr Genet (2006) 1.41
Allelic variation at alcohol metabolism genes ( ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian population. Hum Genet (2003) 1.39
Human genetics of plasma dopamine beta-hydroxylase activity: applications to research in psychiatry and neurology. Psychopharmacology (Berl) (2004) 1.32
Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA. Proc Natl Acad Sci U S A (2003) 1.27
Polymorphisms of CUL5 are associated with CD4+ T cell loss in HIV-1 infected individuals. PLoS Genet (2007) 1.23
Haplotype information and linkage disequilibrium mapping for single nucleotide polymorphisms. Genome Res (2003) 1.21
Association of galanin haplotypes with alcoholism and anxiety in two ethnically distinct populations. Mol Psychiatry (2006) 1.18
Effects of worldwide population subdivision on ALDH2 linkage disequilibrium. Genome Res (1999) 1.13
Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes. PLoS Genet (2006) 1.09
Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data. PLoS One (2009) 1.09
Association of slow N-acetyltransferase 2 profile and anti-TB drug-induced hepatotoxicity in patients from Southern Brazil. Eur J Clin Pharmacol (2008) 1.08
High diversity of alpha-globin haplotypes in a Senegalese population, including many previously unreported variants. Am J Hum Genet (1995) 1.08
Regulatory polymorphisms in the cyclophilin A gene, PPIA, accelerate progression to AIDS. PLoS Pathog (2007) 1.08
Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data. Annu Rev Stat Appl (2014) 1.08
Single-molecule analysis for molecular haplotyping. Hum Mutat (2004) 1.06
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. Am J Med Genet B Neuropsychiatr Genet (2009) 1.05
Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization. Mol Genet Metab (2008) 1.05
Bayesian quantitative trait locus mapping using inferred haplotypes. Genetics (2010) 1.05
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants. Genet Epidemiol (2013) 1.04
Haplotype-based methods for detecting uncommon causal variants with common SNPs. Genet Epidemiol (2012) 1.04
Regulatory polymorphisms in the interleukin-18 promoter are associated with hepatitis C virus clearance. J Infect Dis (2008) 1.03
On a randomization procedure in linkage analysis. Am J Hum Genet (1999) 1.03
Single nucleotide polymorphisms in ANKK1 and the dopamine D2 receptor gene affect cognitive outcome shortly after traumatic brain injury: a replication and extension study. Brain Inj (2008) 1.01
Human estrogen sulfotransferase (SULT1E1) pharmacogenomics: gene resequencing and functional genomics. Br J Pharmacol (2003) 1.00
ICAM gene cluster SNPs and prostate cancer risk in African Americans. Hum Genet (2006) 0.99
Influence of host genetics on the severity of coccidioidomycosis. Emerg Infect Dis (1999) 0.99
Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence. Alcohol Clin Exp Res (2010) 0.99
A coalescence-guided hierarchical Bayesian method for haplotype inference. Am J Hum Genet (2006) 0.98
Nonparametric disequilibrium mapping of functional sites using haplotypes of multiple tightly linked single-nucleotide polymorphism markers. Genetics (2003) 0.97
Distribution of genome-wide linkage disequilibrium based on microsatellite loci in the Samoan population. Hum Genomics (2004) 0.96
Associations between TCF7L2 polymorphisms and risk of breast cancer among Hispanic and non-Hispanic white women: the Breast Cancer Health Disparities Study. Breast Cancer Res Treat (2012) 0.95
Genotype determination for polymorphisms in linkage disequilibrium. BMC Bioinformatics (2009) 0.94
Inferring haplotypes at the NAT2 locus: the computational approach. BMC Genet (2005) 0.93
The heterogeneous HLA genetic makeup of the Swiss population. PLoS One (2012) 0.93
Analysis and exploration of the use of rule-based algorithms and consensus methods for the inferral of haplotypes. Genetics (2003) 0.93
Consistent effects of TSG101 genetic variability on multiple outcomes of exposure to human immunodeficiency virus type 1. J Virol (2006) 0.92
Simultaneous estimation of haplotype frequencies and quantitative trait parameters: applications to the test of association between phenotype and diplotype configuration. Genetics (2004) 0.92
Wide disparity in genetic admixture among Mexican Americans from San Antonio, TX. Ann Hum Genet (2011) 0.90
Simultaneous detection of linkage disequilibrium and genetic differentiation of subdivided populations. Genetics (2004) 0.88
Mitochondrial uncoupling protein gene cluster variation (UCP2-UCP3) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Atherosclerosis (2010) 0.88
Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes. Hum Genomics (2004) 0.87
Natriuretic peptide pharmacogenetics: membrane metallo-endopeptidase (MME): common gene sequence variation, functional characterization and degradation. J Mol Cell Cardiol (2010) 0.87
Contribution of regulatory and structural variations in APOE to predicting dyslipidemia. J Lipid Res (2005) 0.87
Influence of genetic, biological and pharmacological factors on warfarin dose in a Southern Brazilian population of European ancestry. Br J Clin Pharmacol (2011) 0.87
16(th) IHIW: global analysis of registry HLA haplotypes from 20 million individuals: report from the IHIW Registry Diversity Group. Int J Immunogenet (2012) 0.87
Polymorphisms in the brain-derived neurotrophic factor gene influence memory and processing speed one month after brain injury. J Neurotrauma (2012) 0.86
Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages. BMC Genet (2005) 0.85
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