Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin geneLinkage analysis in the next-generation sequencing eraEvaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancerGenome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaGeneLink: a database to facilitate genetic studies of complex traitsCandidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopiaInferring relationships between pairs of individuals from locus heterozygosities.Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer riskGermline mutations in the ribonuclease L gene in families showing linkage with HPC1A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medicationMajor susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide searchNine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive errorEPHA2 is associated with age-related cortical cataract in mice and humansPleiotropy analysis of quantitative traits at gene level by multivariate functional linear modelsOld lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence dataGenetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scansFamilial Lung Cancer: A Brief History from the Earliest Work to the Most Recent StudiesGenome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorReplicating genotype-phenotype associationsGenome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study.Introduction: association and transmission/disequilibrium test analyses of discrete traits in the GAW12 simulated data.Comparison of novel and existing methods for detection of linkage disequilibrium using parent-child trios in the GAW12 genetic isolate simulated data.Physical and transcript map of the hereditary prostate cancer region at xq27.Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung CancerImportance sampling method of correction for multiple testing in affected sib-pair linkage analysis.Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of two-generation and multigenerational pedigrees in the presence of missing genotype dataRecruitment strategies and comparison of prostate cancer-specific clinical data on African-American and Caucasian males with and without family history.Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 dataNormalization of microarray expression data using within-pedigree pool and its effect on linkage analysisRisk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3.Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits.Application of the propensity score in a covariate-based linkage analysis of the Collaborative Study on the Genetics of Alcoholism.Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium.Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packagesAllele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment.Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies.Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data.Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects.Structure-function correlations using scanning laser polarimetry in primary angle-closure glaucoma and primary open-angle glaucoma
P50
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P50
description
American statistical geneticist
@en
Amerikaans onderzoekster
@nl
cientista estadounidense
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հետազոտող
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name
Joan Bailey-Wilson
@en
Joan Bailey-Wilson
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Joan E Bailey-Wilson
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Joan E Bailey-Wilson
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Joan E Bailey-Wilson
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ജോവാൻ ബെയ്ലി-വിൽസൺ
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type
label
Joan Bailey-Wilson
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Joan Bailey-Wilson
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Joan E Bailey-Wilson
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Joan E Bailey-Wilson
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Joan E Bailey-Wilson
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ജോവാൻ ബെയ്ലി-വിൽസൺ
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Bailey J
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Bailey J. E.
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Bailey J.
@en
Bailey JE
@en
Bailey
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Bailey-Wilson J
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Bailey-Wilson J. E.
@en
Bailey-Wilson J.
@en
Bailey-Wilson JE
@en
Bailey-Wilson
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prefLabel
Joan Bailey-Wilson
@en
Joan Bailey-Wilson
@es
Joan E Bailey-Wilson
@ast
Joan E Bailey-Wilson
@nl
Joan E Bailey-Wilson
@sl
ജോവാൻ ബെയ്ലി-വിൽസൺ
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P214
P244
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35375926200
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0000 0000 2659 9868
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Joan Bailey-Wilson
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0000-0002-9153-2920
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1953-01-01T00:00:00Z
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lccn-n82128668