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A Comparison of Bayesian Methods for Haplotype Reconstruction from Population Genotype Data
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Sequence variation in the human angiotensin converting enzyme
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Complex promoter and coding region β 2 -adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness
inferredcites →https://doi.org/10.1086/319501openalex-snapshot
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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Haplotype Inference in Random Population Samples
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Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040591openalex-snapshot
Inference of haplotypes from PCR-amplified samples of diploid populations.
inferredcites →https://doi.org/10.1111/1467-9868.00254openalex-snapshot
Inference in Molecular Population Genetics
inferredcites →https://doi.org/10.1111/j.2517-6161.1974.tb00999.xopenalex-snapshot
Spatial Interaction and the Statistical Analysis of Lattice Systems
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Identification of the Cystic Fibrosis Gene: Genetic Analysis
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Identification of the cystic fibrosis gene.
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Therapy of CF-Patients with Amitriptyline and Placebo - a Randomised, Double-Blind, Placebo-Controlled Phase IIb Multicenter, Cohort-Study
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Update on Key Emerging Challenges in Cystic Fibrosis
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Phylogeography and Genetic Structure in the California Giant Salamander (Dicamptodon ensatus): Impacts of current and historic landscape features
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A new microendemic gecko from the small forest fragments of south-eastern Madagascar (Squamata, Gekkonidae, Paragehyra)
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inferred← citeshttps://doi.org/10.5324/fn.v43i0.5886zenodo-depositor-declared
Paralumbricillus gen. nov. and other new marine enchytraeids from the North Atlantic
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inferred← citeshttps://doi.org/10.1001/archgenpsychiatry.2009.120openalex-snapshot
Dopaminergic Haplotype as a Predictor of Spatial Inattention in Children With Attention-Deficit/Hyperactivity Disorder
inferred← citeshttps://doi.org/10.1001/archgenpsychiatry.2011.152openalex-snapshot
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Association and Expression Analyses With Single-Nucleotide Polymorphisms in TOMM40 in Alzheimer Disease
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Dementia Risk in Parkinson Disease
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Evolutionary modeling in haplotype analysis
inferred← citeshttps://doi.org/10.1002/9780470397428.ch17openalex-snapshot
Machine Learning for Computational Haplotype Analysis
inferred← citeshttps://doi.org/10.1002/9780470892107.ch36openalex-snapshot
Haplotype Inference Models and Algorithms
inferred← citeshttps://doi.org/10.1002/9781119125556.devpsy210openalex-snapshot
Molecular Genetics Methods for Developmental Scientists
inferred← citeshttps://doi.org/10.1002/9781119272182.ch16openalex-snapshot
Probabilistic Viral Quasispecies Assembly
inferred← citeshttps://doi.org/10.1002/9781119487845.ch21openalex-snapshot
Genome‐Wide Association Studies
inferred← citeshttps://doi.org/10.1002/9781119487845.ch3openalex-snapshot
Haplotype Estimation and Genotype Imputation
inferred← citeshttps://doi.org/10.1002/9783527619368.ch38openalex-snapshot
Association Studies of Complex Diseases
inferred← citeshttps://doi.org/10.1002/9783527847617.ch25openalex-snapshot
Determination and Typing of Other Polymorphic Systems
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Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease
inferred← citeshttps://doi.org/10.1002/ajh.21440openalex-snapshot
Genome‐wide association studies and the genetic dissection of complex traits
inferred← citeshttps://doi.org/10.1002/ajhb.22464openalex-snapshot
Polymorphism of LRP5, but not of TNFRSF11B, is associated with a decrease in bone mineral density in postmenopausal maya‐mestizo women
inferred← citeshttps://doi.org/10.1002/ajhb.22887openalex-snapshot
Population variation of LIN28B in the Mediterranean: Novel markers for microgeographic discrimination
inferred← citeshttps://doi.org/10.1002/ajmg.a.30826openalex-snapshot
Variations of theCFTR gene in the Hanoi-Vietnamese
inferred← citeshttps://doi.org/10.1002/ajmg.a.32504openalex-snapshot
Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation inTP53and neural tube defect risk in an Irish population
inferred← citeshttps://doi.org/10.1002/ajmg.b.30091openalex-snapshot
Allelic and haplotypic association of GABRA2 with alcohol dependence
inferred← citeshttps://doi.org/10.1002/ajmg.b.30151openalex-snapshot
Serotonin receptor 2C (HTR2C) and schizophrenia: Examination of possible medication and genetic influences on expression levels
inferred← citeshttps://doi.org/10.1002/ajmg.b.30324openalex-snapshot
Three major haplotypes of the β2 adrenergic receptor define psychological profile, blood pressure, and the risk for development of a common musculoskeletal pain disorder
inferred← citeshttps://doi.org/10.1002/ajmg.b.30332openalex-snapshot
Brain derived neurotrophic factor (BDNF) gene variants and Alzheimer's disease, affective disorders, posttraumatic stress disorder, schizophrenia, and substance dependence
inferred← citeshttps://doi.org/10.1002/ajmg.b.30336openalex-snapshot
Dimensional anxiety mediates linkage of GABRA2 haplotypes with alcoholism
inferred← citeshttps://doi.org/10.1002/ajmg.b.30338openalex-snapshot
BDNF gene variants and brain morphology in schizophrenia
inferred← citeshttps://doi.org/10.1002/ajmg.b.30378openalex-snapshot
Cannabis receptor haplotype associated with fewer cannabis dependence symptoms in adolescents
inferred← citeshttps://doi.org/10.1002/ajmg.b.30464openalex-snapshot
Association of the neuronal nicotinic receptor β2 subunit gene (CHRNB2) with subjective responses to alcohol and nicotine
inferred← citeshttps://doi.org/10.1002/ajmg.b.30485openalex-snapshot
Association studies testing for risk for late‐onset Alzheimer's disease with common variants in the β‐amyloid precursor protein (APP)
inferred← citeshttps://doi.org/10.1002/ajmg.b.30499openalex-snapshot
Identification of two risk haplotypes for schizophrenia and bipolar disorder in the synaptic vesicle monoamine transporter gene (SVMT)
inferred← citeshttps://doi.org/10.1002/ajmg.b.30507openalex-snapshot
Why do young women smoke? IV. Role of genetic variation in the dopamine transporter and lifetime traumatic experience
inferred← citeshttps://doi.org/10.1002/ajmg.b.30577openalex-snapshot
An association study of RGS4 polymorphisms with clinical phenotypes of schizophrenia in a Chinese population
inferred← citeshttps://doi.org/10.1002/ajmg.b.30589openalex-snapshot
ADH7 variation modulates extraversion and conscientiousness in substance‐dependent subjects
inferred← citeshttps://doi.org/10.1002/ajmg.b.30655openalex-snapshot
A DRD1 haplotype is associated with risk for autism spectrum disorders in male‐only affected sib‐pair families
inferred← citeshttps://doi.org/10.1002/ajmg.b.30674openalex-snapshot
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients
inferred← citeshttps://doi.org/10.1002/ajmg.b.30716openalex-snapshot
Catechol‐O‐methyltransferase (COMT) gene variants: Possible association of the Val158Met variant with opiate addiction in hispanic women
inferred← citeshttps://doi.org/10.1002/ajmg.b.30908openalex-snapshot
Impact of the dopamine receptor gene family on temperament traits in a population‐based birth cohort
inferred← citeshttps://doi.org/10.1002/ajmg.b.30950openalex-snapshot
Risk variants in the S100B gene predict elevated S100B serum concentrations in healthy individuals
inferred← citeshttps://doi.org/10.1002/ajmg.b.30955openalex-snapshot
Functional polymorphisms in the serotonin 1B receptor gene (HTR1B) predict self‐reported anger and hostility among young men
inferred← citeshttps://doi.org/10.1002/ajmg.b.30990openalex-snapshot
ADH1A variation predisposes to personality traits and substance dependence
inferred← citeshttps://doi.org/10.1002/ajmg.b.31059openalex-snapshot
Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims
inferred← citeshttps://doi.org/10.1002/ajmg.b.31243openalex-snapshot
ACRHR1haplotype moderates the effect of adverse childhood experiences on lifetime risk of major depressive episode in African‐American women
inferred← citeshttps://doi.org/10.1002/ajmg.b.32061openalex-snapshot
Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms
inferred← citeshttps://doi.org/10.1002/ajmg.b.32283openalex-snapshot
An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults
inferred← citeshttps://doi.org/10.1002/ajmg.b.32417openalex-snapshot
Longitudinal predictors of cannabis use and dependence in offspring from families at ultra high risk for alcohol dependence and in control families
inferred← citeshttps://doi.org/10.1002/ajpa.20653openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajpa.22010openalex-snapshot
Stability or variation? Patterns of lactase gene and its enhancer region distributions in Brazilian Amerindians
inferred← citeshttps://doi.org/10.1002/ajpa.22460openalex-snapshot
The evolutionary history ofSLC6A4and the role of plasticity inmacaca
inferred← citeshttps://doi.org/10.1002/ajpa.24483openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/art.20813openalex-snapshot
Accuracy of haplotype association studies is enhanced by increasing number of polymorphic loci examined: Comment on the article by Meulenbelt et al
inferred← citeshttps://doi.org/10.1002/art.21285openalex-snapshot
Correlation of rheumatoid arthritis severity with the genetic functional variants and circulating levels of macrophage migration inhibitory factor
inferred← citeshttps://doi.org/10.1002/art.21811openalex-snapshot
Vascular endothelial growth factor gene haplotypes in Kawasaki disease
inferred← citeshttps://doi.org/10.1002/art.21928openalex-snapshot
Association between the interleukin‐1 family gene cluster and psoriatic arthritis
inferred← citeshttps://doi.org/10.1002/art.22262openalex-snapshot
Genetic association between the PRKCH gene encoding protein kinase Cη isozyme and rheumatoid arthritis in the Japanese population
inferred← citeshttps://doi.org/10.1002/art.22570openalex-snapshot
Association of Anti–Cyclic citrullinated peptide antibody levels with PADI4 haplotypes in early rheumatoid arthritis and with shared epitope alleles in very late rheumatoid arthritis
inferred← citeshttps://doi.org/10.1002/art.22742openalex-snapshot
Evidence of potential interaction of chemokine genes in susceptibility to systemic sclerosis
inferred← citeshttps://doi.org/10.1002/art.23592openalex-snapshot
A broad analysis of IL1 polymorphism and rheumatoid arthritis
inferred← citeshttps://doi.org/10.1002/art.24268openalex-snapshot
Associations of 25 structural, degradative, and inflammatory candidate genes with lumbar disc desiccation, bulging, and height narrowing
inferred← citeshttps://doi.org/10.1002/art.33464openalex-snapshot
Association of single‐nucleotide polymorphisms in CCR6, TAGAP, and TNFAIP3 with rheumatoid arthritis in African Americans
inferred← citeshttps://doi.org/10.1002/bdra.20604openalex-snapshot
Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/bimj.200800215openalex-snapshot
Haplotype Inference for Population Data with Genotyping Errors
inferred← citeshttps://doi.org/10.1002/cncr.22582openalex-snapshot
Polymorphisms of the neuronal and inducible nitric oxide synthase genes and the risk of cutaneous melanoma
inferred← citeshttps://doi.org/10.1002/cncr.22794openalex-snapshot
X‐ray repair cross‐complementing group 1 (XRCC1) single‐nucleotide polymorphisms and the risk of salivary gland carcinomas
inferred← citeshttps://doi.org/10.1002/cncr.23453openalex-snapshot
The modifying effect of C‐reactive protein gene polymorphisms on the association between central obesity and endometrial cancer risk
inferred← citeshttps://doi.org/10.1002/cncr.24702openalex-snapshot
Protein phosphatase 2A subunit gene haplotypes and proliferative breast disease modify breast cancer risk
inferred← citeshttps://doi.org/10.1002/cncr.26669openalex-snapshot
Matrix metalloproteinase‐2 polymorphisms and clinical outcome of Chinese patients with nonsmall cell lung cancer treated with first‐line, platinum‐based chemotherapy
inferred← citeshttps://doi.org/10.1002/cpt.1463openalex-snapshot
Enantiospecific Pharmacogenomics of Fluvastatin
inferred← citeshttps://doi.org/10.1002/cpt.1928openalex-snapshot
UGT1A3 and Sex Are Major Determinants of Telmisartan Pharmacokinetics—A Comprehensive Pharmacogenomic Study
inferred← citeshttps://doi.org/10.1002/cpt.2053openalex-snapshot
Identification of Glycochenodeoxycholate 3‐O‐Glucuronide and Glycodeoxycholate 3‐O‐Glucuronide as Highly Sensitive and Specific OATP1B1 Biomarkers
inferred← citeshttps://doi.org/10.1002/cpt.2429openalex-snapshot
Performance of Plasma Coproporphyrin I and III as OATP1B1 Biomarkers in Humans
inferred← citeshttps://doi.org/10.1002/cpt.2674openalex-snapshot
Genomewide Association Study of Simvastatin Pharmacokinetics
inferred← citeshttps://doi.org/10.1002/cpt.891openalex-snapshot
Comprehensive Pharmacogenomic Study Reveals an Important Role of UGT1A3 in Montelukast Pharmacokinetics
inferred← citeshttps://doi.org/10.1002/cpt.892openalex-snapshot
Variants in theCYP2B63′UTR AlterIn VitroandIn VivoCYP2B6 Activity: Potential Role of MicroRNAs
inferred← citeshttps://doi.org/10.1002/dmrr.3676openalex-snapshot
Prevalence, clinical characteristics and HLA genotypes of idiopathic type 1 diabetes: A cross‐sectional study
inferred← citeshttps://doi.org/10.1002/dmrr.70103openalex-snapshot
The Role of HLA Class II Two‐Locus Haplotypes and Genotypes in Chinese With Type 1 Diabetes
inferred← citeshttps://doi.org/10.1002/dmrr.866openalex-snapshot
Association of glucose transporter 1 polymorphisms with type 2 diabetes in the Tunisian population
inferred← citeshttps://doi.org/10.1002/dmrr.882openalex-snapshot
Genetic variants in protein kinase C zeta gene and type 2 diabetes risk: a case‐control study of a Chinese Han population
inferred← citeshttps://doi.org/10.1002/ece3.10073openalex-snapshot
Population structure and phylogeography of three closely related tree peonies
inferred← citeshttps://doi.org/10.1002/ece3.1027openalex-snapshot
Genomic replacement of nativeCobitis lutheriwith introducedC. tetralineatathrough a hybrid swarm following the artificial connection of river systems
inferred← citeshttps://doi.org/10.1002/ece3.11204openalex-snapshot
Historical fragmentation and stepping‐stone gene flow led to population genetic differentiation in a coastal seabird
inferred← citeshttps://doi.org/10.1002/ece3.1137openalex-snapshot
Contrasting patterns of polymorphism and selection in bacterial‐sensing toll‐like receptor 4 in two house mouse subspecies
inferred← citeshttps://doi.org/10.1002/ece3.1865openalex-snapshot
Assessing models of speciation under different biogeographic scenarios; an empirical study using multi‐locus and RNA ‐seq analyses
inferred← citeshttps://doi.org/10.1002/ece3.2230openalex-snapshot
Late Pleistocene climate change promoted divergence betweenPicea asperataandP. crassifoliaon the Qinghai–Tibet Plateau through recent bottlenecks
inferred← citeshttps://doi.org/10.1002/ece3.2465openalex-snapshot
Cryptic diversity and multiple origins of the widespread mayfly species group Baetis rhodani (Ephemeroptera: Baetidae) on northwestern Mediterranean islands
inferred← citeshttps://doi.org/10.1002/ece3.2524openalex-snapshot
Population genetic isolation and limited connectivity in the purple finch (Haemorhous purpureus)
inferred← citeshttps://doi.org/10.1002/ece3.3503openalex-snapshot
Radiation of the polymorphic Little Devil poison frog ( Oophaga sylvatica ) in Ecuador
inferred← citeshttps://doi.org/10.1002/ece3.390openalex-snapshot
Historical demographic dynamics underlying local adaptation in the presence of gene flow
inferred← citeshttps://doi.org/10.1002/ece3.4368openalex-snapshot
Asymmetric hybridization in Cordulegaster (Odonata: Cordulegastridae): Secondary postglacial contact and the possible role of mechanical constraints
inferred← citeshttps://doi.org/10.1002/ece3.4419openalex-snapshot
No evidence for MHC ‐based mate choice in wild giant pandas
inferred← citeshttps://doi.org/10.1002/ece3.4830openalex-snapshot
Bidirectional mitochondrial introgression between Korean cobitid fish mediated by hybridogenetic hybrids
inferred← citeshttps://doi.org/10.1002/ece3.5113openalex-snapshot
Pleistocene climate change and phylogeographic structure of the Gymnocarpos przewalskii (Caryophyllaceae) in the northwest China: Evidence from plastid DNA, ITS sequences, and Microsatellite
inferred← citeshttps://doi.org/10.1002/ece3.5265openalex-snapshot
Is MHC diversity a better marker for conservation than neutral genetic diversity? A case study of two contrasting dolphin populations
inferred← citeshttps://doi.org/10.1002/ece3.5744openalex-snapshot
Genetic admixture despite ecological segregation in a North African sparrow hybrid zone (Aves, Passeriformes, Passer domesticus × Passer hispaniolensis)
inferred← citeshttps://doi.org/10.1002/ece3.6504openalex-snapshot
Hidden diversity in Antarctica: Molecular and morphological evidence of two different species within one of the most conspicuous ascidian species
inferred← citeshttps://doi.org/10.1002/ece3.6855openalex-snapshot
Genetic drift and bottleneck do not influence diversity in Toll‐like receptor genes at a small spatial scale in a Himalayan passerine
inferred← citeshttps://doi.org/10.1002/ece3.70331openalex-snapshot
The influence of the forest corridors to the north of the Andes on the diversification of the bright‐rumped Attila, Attila spadiceus (Passeriformes, Tyrannidae), during the climatic oscillations of the middle Pleistocene
inferred← citeshttps://doi.org/10.1002/ece3.734openalex-snapshot
Testing the genetic predictions of a biogeographical model in a dominant endemic Eastern Pacific coral (Porites panamensis) using a genetic seascape approach
inferred← citeshttps://doi.org/10.1002/ece3.73450openalex-snapshot
Contrasting Dispersal Patterns of Co‐Occurring Benthic Sister Sea Star Labidiaster Species (Asteroidea: Heliasteridae) in the Southern Ocean
inferred← citeshttps://doi.org/10.1002/ece3.7387openalex-snapshot
Migration‐tracking integrated phylogeography supports long‐distance dispersal‐driven divergence for a migratory bird species in the Japanese archipelago
inferred← citeshttps://doi.org/10.1002/ece3.7479openalex-snapshot
Color vision and niche partitioning in a diverse neotropical primate community in lowland Amazonian Ecuador
inferred← citeshttps://doi.org/10.1002/ece3.768openalex-snapshot
Coalescent analyses show isolation without migration in two closely related tropical orioles: the case of Icterus graduacauda and I cterus chrysater
inferred← citeshttps://doi.org/10.1002/ece3.7805openalex-snapshot
Southern introgression increases adaptive immune gene variability in northern range margin populations of Fire‐bellied toad
inferred← citeshttps://doi.org/10.1002/ece3.828openalex-snapshot
Nucleotide diversity of vernalization and flowering‐time‐related genes in a germplasm collection of meadow fescue ( F estuca pratensis H uds. syn. L olium pratense ( H uds.) D arbysh.)
inferred← citeshttps://doi.org/10.1002/ece3.8635openalex-snapshot
Quaternary geomorphological and climatic changes associated with the diversification of Iberian freshwater fishes: The case of the genus Cobitis (Cypriniformes, Cobitidae)
inferred← citeshttps://doi.org/10.1002/ece3.886openalex-snapshot
Deceptive single‐locus taxonomy and phylogeography: Wolbachia‐associated divergence in mitochondrial DNA is not reflected in morphology and nuclear markers in a butterfly species
inferred← citeshttps://doi.org/10.1002/ece3.92openalex-snapshot
Increased divergence but reduced variation on the Z chromosome relative to autosomes in Ficedula flycatchers: differential introgression or the faster‐Z effect?
inferred← citeshttps://doi.org/10.1002/ece3.9404openalex-snapshot
Molecular phylogeny and taxonomy of the genus Nectogale (Mammalia: Eulipotyphla: Soricidae)
inferred← citeshttps://doi.org/10.1002/ece3.9545openalex-snapshot
Phylogeography of the endangered “eyed” turtles (genus Sacalia) and the discovery of a lineage derived from natural interspecific hybridization
inferred← citeshttps://doi.org/10.1002/elps.201000536openalex-snapshot
Haplotyping of putative microRNA‐binding sites in the SNAP‐25 gene
inferred← citeshttps://doi.org/10.1002/elps.201100128openalex-snapshot
Confirmation that SNPs in the high mobility group‐A2 gene (HMGA2) are associated with adult height in the Japanese population; wide‐ranging population survey of height‐related SNPs in HMGA2
inferred← citeshttps://doi.org/10.1002/elps.201200260openalex-snapshot
Genetic and expression analysis of SNP s in the human deoxyribonuclease II: SNP s in the promoter region reduce its in vivo activity through decreased promoter activity
inferred← citeshttps://doi.org/10.1002/em.21896openalex-snapshot
Genetic variation in arsenic (+3 oxidation state) methyltransferase (AS3MT), arsenic metabolism and risk of basal cell carcinoma in a E uropean population
inferred← citeshttps://doi.org/10.1002/em.22104openalex-snapshot
Associations between arsenic (+3 oxidation state) methyltransferase (AS3MT) and N‐6 adenine‐specific DNA methyltransferase 1 (N6AMT1) polymorphisms, arsenic metabolism, and cancer risk in a chilean population
inferred← citeshttps://doi.org/10.1002/gcc.20436openalex-snapshot
Association of human leukocyte antigen ancestral haplotype 8.1 with adverse outcome of non‐Hodgkin's lymphoma
inferred← citeshttps://doi.org/10.1002/gcc.20912openalex-snapshot
A putative “hepitype” in the ATM gene associated with chronic lymphocytic leukemia risk
inferred← citeshttps://doi.org/10.1002/gepi.20024openalex-snapshot
Algorithms for inferring haplotypes
inferred← citeshttps://doi.org/10.1002/gepi.20056openalex-snapshot
Characterization of multilocus linkage disequilibrium
inferred← citeshttps://doi.org/10.1002/gepi.20061openalex-snapshot
Accounting for haplotype uncertainty in matched association studies: A comparison of simple and flexible techniques
inferred← citeshttps://doi.org/10.1002/gepi.20072openalex-snapshot
Bayesian modelling of multivariate quantitative traits using seemingly unrelated regressions
inferred← citeshttps://doi.org/10.1002/gepi.20076openalex-snapshot
Characterizing allelic associations from unphased diploid data by graphical modeling
inferred← citeshttps://doi.org/10.1002/gepi.20080openalex-snapshot
Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes
inferred← citeshttps://doi.org/10.1002/gepi.20111openalex-snapshot
Haplotypes and haplotype-tagging single-nucleotide polymorphism: Presentation Group 8 of Genetic Analysis Workshop 14
inferred← citeshttps://doi.org/10.1002/gepi.20131openalex-snapshot
Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database
inferred← citeshttps://doi.org/10.1002/gepi.20134openalex-snapshot
Fine mapping of disease genes via haplotype clustering
inferred← citeshttps://doi.org/10.1002/gepi.20140openalex-snapshot
A Bayesian toolkit for genetic association studies
inferred← citeshttps://doi.org/10.1002/gepi.20142openalex-snapshot
Estimation and testing of genotype and haplotype effects in case‐control studies: comparison of weighted regression and multiple imputation procedures
inferred← citeshttps://doi.org/10.1002/gepi.20154openalex-snapshot
A comparison of several methods for haplotype frequency estimation and haplotype reconstruction for tightly linked markers from general pedigrees
inferred← citeshttps://doi.org/10.1002/gepi.20161openalex-snapshot
Simple estimates of haplotype relative risks in case‐control data
inferred← citeshttps://doi.org/10.1002/gepi.20185openalex-snapshot
Understanding the accuracy of statistical haplotype inference with sequence data of known phase
inferred← citeshttps://doi.org/10.1002/gepi.20210openalex-snapshot
A variant of the myosin light chain kinase gene is associated with severe asthma in African Americans
inferred← citeshttps://doi.org/10.1002/gepi.20215openalex-snapshot
Haplotype uncertainty in association studies
inferred← citeshttps://doi.org/10.1002/gepi.20216openalex-snapshot
Efficient multilocus association testing for whole genome association studies using localized haplotype clustering
inferred← citeshttps://doi.org/10.1002/gepi.20253openalex-snapshot
Haplotype inference using a Bayesian Hidden Markov model
inferred← citeshttps://doi.org/10.1002/gepi.20273openalex-snapshot
Accounting for haplotype phase uncertainty in linkage disequilibrium estimation
inferred← citeshttps://doi.org/10.1002/gepi.20322openalex-snapshot
Inference from genome‐wide association studies using a novel Markov model
inferred← citeshttps://doi.org/10.1002/gepi.20353openalex-snapshot
Bayesian variable and model selection methods for genetic association studies
inferred← citeshttps://doi.org/10.1002/gepi.20523openalex-snapshot
Genotype‐based association mapping of complex diseases: gene‐environment interactions with multiple genetic markers and measurement error in environmental exposures
inferred← citeshttps://doi.org/10.1002/gepi.20638openalex-snapshot
On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium
inferred← citeshttps://doi.org/10.1002/gepi.21623openalex-snapshot
Accurate Imputation of Rare and Common Variants in a Founder Population From a Small Number of Sequenced Individuals
inferred← citeshttps://doi.org/10.1002/gepi.21730openalex-snapshot
BRCA1 Polymorphisms and Breast Cancer Epidemiology in the Western New York Exposures and Breast Cancer (WEB) Study
inferred← citeshttps://doi.org/10.1002/gepi.22060openalex-snapshot
An efficient study design to test parent‐of‐origin effects in family trios
inferred← citeshttps://doi.org/10.1002/hbm.23161openalex-snapshot
Modulative effects of COMT haplotype on age-related associations with brain morphology
inferred← citeshttps://doi.org/10.1002/hed.20699openalex-snapshot
Fas single nucleotide polymorphisms and risk of thyroid and salivary gland carcinomas: A case‐control analysis
inferred← citeshttps://doi.org/10.1002/hep.20150openalex-snapshot
From genotypes to haplotypes in hepatobiliary diseases: One plus one equals (sometimes) more than two
inferred← citeshttps://doi.org/10.1002/hep.20322openalex-snapshot
Haplotype-tagging RANTES gene variants influence response to antiviral therapy in chronic hepatitis C†
inferred← citeshttps://doi.org/10.1002/hep.21636openalex-snapshot
Myxovirus-1 and protein kinase haplotypes and fibrosis in chronic hepatitis C virus
inferred← citeshttps://doi.org/10.1002/humu.20100openalex-snapshot
High-Density SNP genotyping defines 17 distinct haplotypes of the TNF block in the Caucasian population: Implications for haplotype tagging
inferred← citeshttps://doi.org/10.1002/humu.20199openalex-snapshot
Assessment of multiple displacement amplification for polymorphism discovery and haplotype determination at a highly polymorphic locus,MC1R
inferred← citeshttps://doi.org/10.1002/humu.20203openalex-snapshot
Worldwide haplotype diversity and coding sequence variation at human bitter taste receptor loci
inferred← citeshttps://doi.org/10.1002/humu.20226openalex-snapshot
Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint
inferred← citeshttps://doi.org/10.1002/humu.20364openalex-snapshot
Common variations in theIL4Rgene affect splicing and influence natural expression of the soluble isoform
inferred← citeshttps://doi.org/10.1002/humu.20462openalex-snapshot
Genetic variants inMGMTand risk of lung cancer in Southeastern Chinese: a haplotype-based analysis
inferred← citeshttps://doi.org/10.1002/humu.20667openalex-snapshot
CYBB, an NADPH-oxidase gene: restricted diversity in humans and evidence for differential long-term purifying selection on transmembrane and cytosolic domains
inferred← citeshttps://doi.org/10.1002/humu.20775openalex-snapshot
An unusual haplotype structure on human chromosome 8p23 derived from the inversion polymorphism
inferred← citeshttps://doi.org/10.1002/humu.21029openalex-snapshot
Three common polymorphisms in theCYBAgene form a haplotype associated with decreased ROS generation
inferred← citeshttps://doi.org/10.1002/humu.21109openalex-snapshot
A common variant inMTHFD1Lis associated with neural tube defects and mRNA splicing efficiency
inferred← citeshttps://doi.org/10.1002/humu.21122openalex-snapshot
Deep sequencing to reveal new variants in pooled DNA samples
inferred← citeshttps://doi.org/10.1002/humu.21145openalex-snapshot
Allelic imbalance (AI) identifies novel tissue-specificcis-regulatory variation for humanUGT2B15
inferred← citeshttps://doi.org/10.1002/humu.21199openalex-snapshot
An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational history
inferred← citeshttps://doi.org/10.1002/humu.21484openalex-snapshot
Evolutionary genetics evidence of an essential, nonredundant role of the IFN-γ pathway in protective immunity
inferred← citeshttps://doi.org/10.1002/humu.21511openalex-snapshot
Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens
inferred← citeshttps://doi.org/10.1002/humu.21579openalex-snapshot
A functional XPNPEP2 promoter haplotype leads to reduced plasma aminopeptidase P and increased risk of ACE inhibitor-induced angioedema
inferred← citeshttps://doi.org/10.1002/ibd.20223openalex-snapshot
TNFSF15 is an ethnic-specific IBD gene
inferred← citeshttps://doi.org/10.1002/ibd.20754openalex-snapshot
High-frequency Haplotypes in the X Chromosome Locus TLR8 Are Associated With Both CD and UC in Females
inferred← citeshttps://doi.org/10.1002/ibd.20936openalex-snapshot
Genetic variants in surfactant, pulmonary-associated protein D (SFTPD) and Japanese susceptibility to ulcerative colitis
inferred← citeshttps://doi.org/10.1002/ibd.21913openalex-snapshot
Crohnʼs disease-associated polymorphism within the PTPN2 gene affects muramyl-dipeptide-induced cytokine secretion and autophagy
inferred← citeshttps://doi.org/10.1002/ijc.20888openalex-snapshot
Methylenetetrahydrofolate reductase polymorphisms and risk of squamous cell carcinoma of the head and neck: A case‐control analysis
inferred← citeshttps://doi.org/10.1002/ijc.21281openalex-snapshot
TP53BP2 locus is associated with gastric cancer susceptibility
inferred← citeshttps://doi.org/10.1002/ijc.21463openalex-snapshot
Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
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