about
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectFine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effectsGenome-wide associations of gene expression variation in humansFast-evolving noncoding sequences in the human genomeIndependent and population-specific association of risk variants at the IRGM locus with Crohn's diseaseGenome-wide detection and characterization of positive selection in human populationsA second generation human haplotype map of over 3.1 million SNPsExpression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic VariationThe impact of human copy number variation on gene expressionGenome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritisSystems and genome-wide approaches unite to provide a route to personalized medicineGenetics of rheumatoid arthritis contributes to biology and drug discoveryRelative impact of nucleotide and copy number variation on gene expression phenotypesRegulation of gene expression in autoimmune disease loci and the genetic basis of proliferation in CD4+ effector memory T cellsLarge-scale population study of human cell lines indicates that dosage compensation is virtually completeModifier effects between regulatory and protein-coding variation.Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies.Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.Common genetic variants modulate pathogen-sensing responses in human dendritic cells.Integrative eQTL-based analyses reveal the biology of breast cancer risk lociPatterns of cis regulatory variation in diverse human populations.Expression QTL-based analyses reveal candidate causal genes and loci across five tumor types.Progress and promise of genome-wide association studies for human complex trait geneticsMultilocus analysis of variation and speciation in the closely related species Arabidopsis halleri and A. lyrataBalancing selection on a regulatory region exhibiting ancient variation that predates human-neandertal divergenceExtensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysis.Accurate and fast multiple-testing correction in eQTL studies.Human HLA-G+ extravillous trophoblasts: Immune-activating cells that interact with decidual leukocytes.Alzheimer disease susceptibility loci: evidence for a protein network under natural selection.Analysis of case-control association studies with known risk variants.The genetics of regulatory variation in the human genomeThe transcriptional landscape of age in human peripheral blood.Assocplots: a Python package for static and interactive visualization of multiple-group GWAS results.Coordinating GWAS results with gene expression in a systems immunologic paradigm in autoimmunitySex-biased genetic effects on gene regulation in humans.Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.Genetic variation in human gene expression.From DNA to RNA to disease and back: the 'central dogma' of regulatory disease variation.Intersection of population variation and autoimmunity genetics in human T cell activation
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Barbara E Stranger
@nl
Barbara E Stranger
@sl
Barbara E. Stranger
@en
Barbara E. Stranger
@es
Barbara Stranger
@fr
type
label
Barbara E Stranger
@nl
Barbara E Stranger
@sl
Barbara E. Stranger
@en
Barbara E. Stranger
@es
Barbara Stranger
@fr
altLabel
Barbara E Stranger
@en
Barbara Stranger
@en
prefLabel
Barbara E Stranger
@nl
Barbara E Stranger
@sl
Barbara E. Stranger
@en
Barbara E. Stranger
@es
Barbara Stranger
@fr
P106
P1153
6507901873
P21
P31
P496
0000-0001-9021-7331
P569
2000-01-01T00:00:00Z