| scholarly article | Q13442814 |
| P50 | author | David Altshuler | Q5230746 |
| David Reich | Q5238967 | ||
| Stacey Gabriel | Q32649203 | ||
| Stephen F Schaffner | Q37366508 | ||
| Mark Joseph Daly | Q39071290 | ||
| P2093 | author name string | Catherine Foo | |
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| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1576-1583 | |
| P577 | publication date | 2005-11-01 | |
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| Q33321249 | Parallel selection on TRPV6 in human populations |
| Q24645332 | Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions |
| Q33290652 | Patterns of population differentiation of candidate genes for cardiovascular disease |
| Q42028641 | Patterns of variation in DNA segments upstream of transcription start sites |
| Q40016140 | Perfect simulation from nonneutral population genetic models: variable population size and population subdivision |
| Q35540760 | Permutation-based variance component test in generalized linear mixed model with application to multilocus genetic association study |
| Q38754834 | PhredEM: a phred-score-informed genotype-calling approach for next-generation sequencing studies |
| Q28647065 | Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models |
| Q35001618 | Population differentiation as an indicator of recent positive selection in humans: an empirical evaluation |
| Q34407779 | Population genetic analysis of the uncoupling proteins supports a role for UCP3 in human cold resistance |
| Q33736564 | Population genetic inference from genomic sequence variation |
| Q34734445 | Population genetic simulations of complex phenotypes with implications for rare variant association tests |
| Q28082728 | Population genetic studies in the genomic sequencing era |
| Q34961094 | Population genomic analysis of ALMS1 in humans reveals a surprisingly complex evolutionary history |
| Q21145248 | Population structure and eigenanalysis |
| Q39802425 | Positive selection on mitochondrial M7 lineages among the Gelong people in Hainan |
| Q90467268 | Positive selection on schizophrenia-associated ST8SIA2 gene in post-glacial Asia |
| Q34384481 | Positive selection on the osteoarthritis-risk and decreased-height associated variants at the GDF5 gene in East Asians |
| Q21145263 | Possible ancestral structure in human populations |
| Q37129418 | Power of deep, all-exon resequencing for discovery of human trait genes |
| Q47791475 | Powerful Genetic Association Analysis for Common or Rare Variants with High-Dimensional Structured Traits. |
| Q49822312 | Powerful and robust cross-phenotype association test for case-parent trios. |
| Q39528269 | Prioritizing individual genetic variants after kernel machine testing using variable selection. |
| Q51959007 | QMSim: a large-scale genome simulator for livestock. |
| Q33915788 | QTLMAS 2010: simulated dataset |
| Q24655574 | Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering |
| Q41812992 | Rapidly Registering Identity-by-Descent Across Ancestral Recombination Graphs. |
| Q36063830 | Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level |
| Q39345468 | Rare variant association test in family-based sequencing studies |
| Q37484322 | Rare variant association testing by adaptive combination of P-values |
| Q40133735 | Rare variant testing across methods and thresholds using the multi-kernel sequence kernel association test (MK-SKAT). |
| Q35133493 | Rare variants detection with kernel machine learning based on likelihood ratio test |
| Q31094385 | Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples |
| Q33954046 | Rare-variant association testing for sequencing data with the sequence kernel association test |
| Q46655315 | Rare-variant association tests in longitudinal studies, with an application to the Multi-Ethnic Study of Atherosclerosis (MESA). |
| Q51556717 | Re-examining Dis/Similarity-Based Tests for Rare-Variant Association with Case-Control Samples. |
| Q41667582 | Recent explosive human population growth has resulted in an excess of rare genetic variants |
| Q46848051 | Recombination networks as genetic markers in a human variation study of the Old World |
| Q46523768 | Recombination rates in admixed individuals identified by ancestry-based inference |
| Q39496810 | Refining the Use of Linkage Disequilibrium as a Robust Signature of Selective Sweeps |
| Q57278407 | Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution |
| Q41963101 | Replication of genetic associations as pseudoreplication due to shared genealogy |
| Q53392505 | Reproducible simulations of realistic samples for next-generation sequencing studies using Variant Simulation Tools. |
| Q36702004 | Reproduction and immunity-driven natural selection in the human WFDC locus |
| Q34400818 | Resurrecting surviving Neandertal lineages from modern human genomes |
| Q90573058 | Retrospective Association Analysis of Longitudinal Binary Traits Identifies Important Loci and Pathways in Cocaine Use |
| Q30992447 | Reveel: large-scale population genotyping using low-coverage sequencing data |
| Q35748549 | Robust and Powerful Affected Sibpair Test for Rare Variant Association |
| Q40235180 | Sampling ARG of multiple populations under complex configurations of subdivision and admixture |
| Q24676642 | Scan of human genome reveals no new Loci under ancient balancing selection |
| Q36017094 | Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets |
| Q37318455 | Scanning for genomic regions subject to selective sweeps using SNP-MaP strategy. |
| Q50631433 | Searching for signals of evolutionary selection in 168 genes related to immune function. |
| Q37076975 | Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants |
| Q34462822 | Selection and reduced population size cannot explain higher amounts of Neandertal ancestry in East Asian than in European human populations |
| Q42684890 | SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure |
| Q40377156 | SeqSIMLA2_exact: simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence |
| Q34778042 | SeqSIMLA: a sequence and phenotype simulation tool for complex disease studies |
| Q35982039 | Sequence Kernel Association Analysis of Rare Variant Set Based on the Marginal Regression Model for Binary Traits |
| Q36494204 | Sequence Kernel Association Test of Multiple Continuous Phenotypes |
| Q36909285 | Sequence kernel association tests for the combined effect of rare and common variants |
| Q33559782 | Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels |
| Q42854796 | Sequence-level population simulations over large genomic regions |
| Q50707628 | SequenceLDhot: detecting recombination hotspots. |
| Q24630443 | Shared and unique components of human population structure and genome-wide signals of positive selection in South Asia |
| Q24651949 | Signals of recent positive selection in a worldwide sample of human populations |
| Q34153592 | Signatures of positive selection apparent in a small sample of human exomes |
| Q33862553 | Similarity in recombination rate estimates highly correlates with genetic differentiation in humans |
| Q35898620 | Similarity-based multimarker association tests for continuous traits. |
| Q31125474 | Simulating association studies: a data-based resampling method for candidate regions or whole genome scans |
| Q34590469 | Simulating gene trees under the multispecies coalescent and time-dependent migration |
| Q33546641 | Simulating gene-environment interactions in complex human diseases |
| Q37480771 | Simulation of genomes: a review. |
| Q33354962 | Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies |
| Q35862959 | Small Sample Kernel Association Tests for Human Genetic and Microbiome Association Studies |
| Q24678953 | Statistical evaluation of alternative models of human evolution |
| Q35919633 | Strong Selection at MHC in Mexicans since Admixture |
| Q34569870 | Sum of parts is greater than the whole: inference of common genetic history of populations |
| Q36202029 | Systematic underestimation of the age of selected alleles |
| Q24678506 | TLR4 polymorphisms, infectious diseases, and evolutionary pressure during migration of modern humans |
| Q31115682 | Tag SNP selection for candidate gene association studies using HapMap and gene resequencing data |
| Q36010533 | Testing Rare-Variant Association without Calling Genotypes Allows for Systematic Differences in Sequencing between Cases and Controls |
| Q50968371 | Testing the effect of rare compound-heterozygous and recessive mutations in case--parent sequencing studies. |
| Q37025075 | The Complex Admixture History and Recent Southern Origins of Siberian Populations |
| Q21090229 | The case for selection at CCR5-Delta32 |
| Q37636303 | The deleterious mutation load is insensitive to recent population history |
| Q30577440 | The effect of genomic inversions on estimation of population genetic parameters from SNP data |
| Q33895392 | The effect of recent admixture on inference of ancient human population history |
| Q47335562 | The effective size of the Icelandic population and the prospects for LD mapping: inference from unphased microsatellite markers |
| Q30853607 | The effects of demography and long-term selection on the accuracy of genomic prediction with sequence data |
| Q35514258 | The genetic legacy of the expansion of Turkic-speaking nomads across Eurasia |
| Q60046260 | The impact of a fine-scale population stratification on rare variant association test results |
| Q37628796 | The impact of accelerating faster than exponential population growth on genetic variation |
| Q46816983 | The impact of natural selection on an ABCC11 SNP determining earwax type. |
| Q36935092 | The impact of natural selection on health and disease: uses of the population genetics approach in humans |
| Q42118230 | The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent |
| Q41809234 | The promise and limitations of population exomics for human evolution studies |
| Q21145001 | The role of geography in human adaptation |
| Q36993031 | The signature of long-standing balancing selection at the human defensin beta-1 promoter. |
| Q24599166 | The timing of pigmentation lightening in Europeans |
| Q42135854 | The value of statistical or bioinformatics annotation for rare variant association with quantitative trait |
| Q42369086 | To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests |
| Q46650409 | Tracing genetic history of modern humans using X-chromosome lineages |
| Q26828744 | Two-phase and family-based designs for next-generation sequencing studies |
| Q38606760 | Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-Analysis of Noncoding Variation in Metabochip Data |
| Q43731365 | Using maximal segmental score in genome-wide association studies |
| Q34000914 | Utilizing population controls in rare-variant case-parent association tests |
| Q53093415 | Variants in SNAP25 are targets of natural selection and influence verbal performances in women. |
| Q28603568 | Whole-genome sequence analyses of Western Central African Pygmy hunter-gatherers reveal a complex demographic history and identify candidate genes under positive natural selection |
| Q35927954 | Widely distributed noncoding purifying selection in the human genome |
| Q37119639 | Widespread balancing selection and pathogen-driven selection at blood group antigen genes |
| Q91639265 | metaFARVAT: An Efficient Tool for Meta-Analysis of Family-Based, Case-Control, and Population-Based Rare Variant Association Studies |
| Q51927442 | msHOT: modifying Hudson's ms simulator to incorporate crossover and gene conversion hotspots. |
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