| scholarly article | Q13442814 |
| P50 | author | John Anthony Hardy | Q6237755 |
| Noah Rosenberg | Q7045447 | ||
| Andrew Singleton | Q4758591 | ||
| Gonçalo Abecasis | Q16001382 | ||
| P2093 | author name string | Yun Li | |
| Paul Scheet | |||
| Lucy Huang | |||
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| Practical issues in imputation-based association mapping | Q33389849 | ||
| Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein | Q36719197 | ||
| HapMap tagSNP transferability in multiple populations: general guidelines | Q36774225 | ||
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| Testing untyped alleles (TUNA)-applications to genome-wide association studies | Q51933120 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | imputation | Q1660484 |
| P304 | page(s) | 235-250 | |
| P577 | publication date | 2009-02-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Genotype-imputation accuracy across worldwide human populations | |
| P478 | volume | 84 |
| Q30235548 | (Invited review) genetic research on alcohol use outcomes in African American populations: A review of the literature, associated challenges, and implications |
| Q34055667 | A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration |
| Q36154414 | A coalescent model for genotype imputation. |
| Q39681099 | A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples |
| Q21129496 | A flexible and accurate genotype imputation method for the next generation of genome-wide association studies |
| Q37422525 | A generic coalescent-based framework for the selection of a reference panel for imputation |
| Q28740367 | A genome-wide association search for type 2 diabetes genes in African Americans |
| Q53700633 | A large electronic-health-record-based genome-wide study of serum lipids |
| Q47378436 | Accurate haplotype imputation with individualized ancestry-adjusted reference panels |
| Q28972496 | Analysis of genomic diversity in Mexican Mestizo populations to develop genomic medicine in Mexico |
| Q33890017 | Assessing accuracy of genotype imputation in American Indians |
| Q35546078 | Assessing the impact of non-differential genotyping errors on rare variant tests of association |
| Q34505607 | Assessment of genotype imputation performance using 1000 Genomes in African American studies |
| Q35266136 | Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study |
| Q36132246 | Choosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest Leaf |
| Q34257609 | Cigarette smoking and the natural history of age-related macular degeneration: the Beaver Dam Eye Study |
| Q33743947 | Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture |
| Q37400706 | Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians |
| Q34252123 | Common variants at 11p13 are associated with susceptibility to tuberculosis |
| Q24641881 | Common variants on chromosome 6p22.1 are associated with schizophrenia |
| Q37306979 | Comparing performance of modern genotype imputation methods in different ethnicities |
| Q36512658 | Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples |
| Q34188020 | DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation |
| Q28646494 | DISSCO: direct imputation of summary statistics allowing covariates |
| Q35023479 | Defining the contribution of CNTNAP2 to autism susceptibility |
| Q36413365 | Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm |
| Q44865342 | Effects of reduced panel, reference origin, and genetic relationship on imputation of genotypes in Hereford cattle |
| Q51533507 | Efficient genomewide selection of PCA-correlated tSNPs for genotype imputation |
| Q33881593 | Empirical evaluations of analytical issues arising from predicting HLA alleles using multiple SNPs |
| Q30432415 | Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium |
| Q34129907 | Estimation of linkage disequilibrium in four US pig breeds |
| Q64236266 | Evaluating the Accuracy of Imputation Methods in a Five-Way Admixed Population |
| Q90093635 | Evaluating the promise of inclusion of African ancestry populations in genomics |
| Q92643672 | Evaluating the quality of the 1000 genomes project data |
| Q34253087 | Evaluation of the imputation performance of the program IMPUTE in an admixed sample from Mexico City using several model designs |
| Q37058014 | Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations |
| Q35879023 | Evidence for negative selection of gene variants that increase dependence on dietary choline in a Gambian cohort |
| Q58896028 | Factors Affecting the Accuracy of Genotype Imputation in Populations from Several Maize Breeding Programs |
| Q43106766 | GStream: Improving SNP and CNV Coverage on Genome-Wide Association Studies |
| Q35760246 | Gene-centric analysis of serum cotinine levels in African and European American populations. |
| Q26782062 | Genetic Diversity and Societally Important Disparities |
| Q35119487 | Genetic analysis of a population heavy drinking phenotype identifies risk variants in whites |
| Q58802309 | Genetic and genomic stability across lymphoblastoid cell line expansions |
| Q30430672 | Genetic association for renal traits among participants of African ancestry reveals new loci for renal function |
| Q35162846 | Genetic markers associated with plasma protein C level in African Americans: the atherosclerosis risk in communities (ARIC) study |
| Q37101431 | Genetic predictors of 25-hydroxyvitamin D levels and risk of multiple sclerosis |
| Q34984016 | Genetic variability of smoking persistence in African Americans |
| Q36109132 | Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index |
| Q37850339 | Genetic variants in urinary bladder cancer: collective power of the "wimp SNPs". |
| Q37385311 | Genetic variation in the extended major histocompatibility complex and susceptibility to childhood acute lymphoblastic leukemia: a review of the evidence |
| Q34718106 | Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster |
| Q28924376 | Genome-wide association analysis identifies three psoriasis susceptibility loci |
| Q28943499 | Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals |
| Q33904445 | Genome-wide association of anthropometric traits in African- and African-derived populations |
| Q30417624 | Genome-wide association of body fat distribution in African ancestry populations suggests new loci |
| Q21092459 | Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution |
| Q28658449 | Genome-wide association studies and beyond |
| Q34817128 | Genome-wide association studies in diverse populations |
| Q35226441 | Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels |
| Q28943558 | Genome-wide association study of recurrent early-onset major depressive disorder |
| Q37395196 | Genome-wide comparisons of variation in linkage disequilibrium |
| Q37237867 | GenomeLaser: fast and accurate haplotyping from pedigree genotypes |
| Q35496707 | Genomic best linear unbiased prediction method including imprinting effects for genomic evaluation |
| Q39592661 | Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels |
| Q92875638 | Genotype Imputation in Genome-Wide Association Studies |
| Q24633967 | Genotype Imputation with Thousands of Genomes |
| Q34708954 | Genotype imputation accuracy in a F2 pig population using high density and low density SNP panels |
| Q34085266 | Genotype imputation accuracy with different reference panels in admixed populations |
| Q34285635 | Genotype imputation for African Americans using data from HapMap phase II versus 1000 genomes projects. |
| Q29614880 | Genotype imputation for genome-wide association studies |
| Q41630600 | Genotype imputation in a coalescent model with infinitely-many-sites mutation |
| Q38121526 | Genotype imputation in genome-wide association studies |
| Q88324448 | Genotype imputation performance of three reference panels using African ancestry individuals |
| Q37194736 | Genotype imputation reference panel selection using maximal phylogenetic diversity. |
| Q36695418 | Genotyping of geographically diverse Druze trios reveals substructure and a recent bottleneck. |
| Q35554981 | Haplotype phasing: existing methods and new developments |
| Q36599387 | Haplotype variation and genotype imputation in African populations. |
| Q30984376 | High-accuracy haplotype imputation using unphased genotype data as the references |
| Q27303686 | Identification of QTL for UV-protective eye area pigmentation in cattle by progeny phenotyping and genome-wide association analysis |
| Q35700710 | Impact of genetic similarity on imputation accuracy |
| Q30961835 | Improved ancestry estimation for both genotyping and sequencing data using projection procrustes analysis and genotype imputation |
| Q39732290 | Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). |
| Q40061670 | Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels. |
| Q40784947 | Imputation of genotypes in Danish purebred and two-way crossbred pigs using low-density panels |
| Q41071347 | Imputation of high-density genotypes in the Fleckvieh cattle population |
| Q35030986 | Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets |
| Q42682328 | Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure |
| Q38274665 | Imputation of rare variants in next-generation association studies |
| Q28386845 | Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort |
| Q33677649 | Imputation-Based Whole-Genome Sequence Association Study Rediscovered the Missing QTL for Lumbar Number in Sutai Pigs |
| Q29417086 | Imputation-based meta-analysis of severe malaria in three African populations |
| Q33782578 | Linkage disequilibrium matches forensic genetic records to disjoint genomic marker sets |
| Q34067045 | Lipids, lipid genes, and incident age-related macular degeneration: the three continent age-related macular degeneration consortium |
| Q34237589 | Low-pass genome-wide sequencing and variant inference using identity-by-descent in an isolated human population |
| Q24635938 | MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes |
| Q36472911 | MaCH‐Admix: Genotype Imputation for Admixed Populations |
| Q36421493 | Measurement by a Novel LC-MS/MS Methodology Reveals Similar Serum Concentrations of Vitamin D-Binding Protein in Blacks and Whites |
| Q29417150 | Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. |
| Q29417043 | Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. |
| Q28681049 | Methodological challenges of genome-wide association analysis in Africa |
| Q34596720 | Methods of tagSNP selection and other variables affecting imputation accuracy in swine. |
| Q34607788 | Multi-population classical HLA type imputation |
| Q28751388 | Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies |
| Q30831955 | On the performance of multiple imputation based on chained equations in tackling missing data of the African α3.7 -globin deletion in a malaria association study |
| Q35013642 | Performance of genotype imputation for low frequency and rare variants from the 1000 genomes |
| Q34115604 | Performance of genotype imputations using data from the 1000 Genomes Project |
| Q34293327 | Phasing of many thousands of genotyped samples |
| Q44112220 | Population-based case-control association studies |
| Q36557564 | Possible positive selection for an arsenic-protective haplotype in humans |
| Q35720540 | Practical consideration of genotype imputation: Sample size, window size, reference choice, and untyped rate |
| Q34030741 | Practical considerations for imputation of untyped markers in admixed populations |
| Q30793085 | Predicting HLA alleles from high-resolution SNP data in three Southeast Asian populations |
| Q28751338 | Public access to genome-wide data: five views on balancing research with privacy and protection |
| Q45798843 | Recapitulation of genome-wide association studies on pulse pressure and mean arterial pressure in the Korean population |
| Q31106426 | References for Haplotype Imputation in the Big Data Era. |
| Q35085784 | Retinal thickness measured by spectral-domain optical coherence tomography in eyes without retinal abnormalities: the Beaver Dam Eye Study |
| Q36700644 | Risk alleles in CFH and ARMS2 and the long-term natural history of age-related macular degeneration: the Beaver Dam Eye Study |
| Q31133047 | SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children |
| Q35063705 | SNP imputation bias reduces effect size determination |
| Q83622865 | SNP imputation in association studies |
| Q34184913 | Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins |
| Q40627550 | Serum calcium and incident type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) study |
| Q29416998 | Seven new loci associated with age-related macular degeneration |
| Q44438393 | Short communication: Genotype imputation within and across Nordic cattle breeds |
| Q24658199 | Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations |
| Q57483508 | Statistical Detection of Relatives Typed with Disjoint Forensic and Biomedical Loci |
| Q28081028 | Strategies for Imputing and Analyzing Rare Variants in Association Studies |
| Q34193497 | Sunlight exposure, pigmentation, and incident age-related macular degeneration |
| Q34349012 | The Generation R Study: design and cohort update 2010. |
| Q35625409 | The effect of reference panels and software tools on genotype imputation |
| Q36236745 | The genetics of human autoimmune disease: A perspective on progress in the field and future directions |
| Q28259199 | The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009 |
| Q36021736 | The origin, global distribution, and functional impact of the human 8p23 inversion polymorphism |
| Q37417890 | The relationship between imputation error and statistical power in genetic association studies in diverse populations |
| Q30439266 | The relationship of atherosclerosis to the 10-year cumulative incidence of age-related macular degeneration: the Beaver Dam studies |
| Q41217516 | Twins, tissue, and time: an assessment of SNPs and CNVs |
| Q33867211 | USING LINEAR PREDICTORS TO IMPUTE ALLELE FREQUENCIES FROM SUMMARY OR POOLED GENOTYPE DATA. |
| Q35792860 | Using imputed genotypes for relative risk estimation in case-parent studies |
| Q33603074 | Utilizing genotype imputation for the augmentation of sequence data |
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| Q49796871 | Validation of genotype imputation in Southeast Asian populations and the effect of single nucleotide polymorphism annotation on imputation outcome |
| Q38983449 | Validation of imputation between equine genotyping arrays. |
| Q30841937 | Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond |
| Q33717629 | WWOX gene is associated with HDL cholesterol and triglyceride levels. |
| Q42784270 | Windfalls and pitfalls: Applications of population genetics to the search for disease genes. |
| Q89480995 | scHaplotyper: haplotype construction and visualization for genetic diagnosis using single cell DNA sequencing data |
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