Identification of common genetic variants controlling transcript isoform variation in human whole blood.
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Tracks through the genome to physiological eventsC5orf30 is a negative regulator of tissue damage in rheumatoid arthritisreGenotyper: Detecting mislabeled samples in genetic dataWhole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosusInsight into Genotype-Phenotype Associations through eQTL Mapping in Multiple Cell Types in Health and Immune-Mediated DiseaseDiscovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.Non-coding genetic variants in human disease.Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.ulfasQTL: an ultra-fast method of composite splicing QTL analysis.PExFInS: An Integrative Post-GWAS Explorer for Functional Indels and SNPsGenome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.Integrative approaches for large-scale transcriptome-wide association studiesDiscovery of Cancer Driver Long Noncoding RNAs across 1112 Tumour Genomes: New Candidates and Distinguishing Features.Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci.The roles of RNA processing in translating genotype to phenotypePeripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations.Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues.The Expanding Landscape of Alternative Splicing Variation in Human Populations.Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traitsGenetic architecture of gene expression traits across diverse populations
P2860
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P2860
Identification of common genetic variants controlling transcript isoform variation in human whole blood.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
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2015年學術文章
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2015年學術文章
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name
Identification of common genet ...... ariation in human whole blood.
@en
Identification of common genet ...... ariation in human whole blood.
@nl
type
label
Identification of common genet ...... ariation in human whole blood.
@en
Identification of common genet ...... ariation in human whole blood.
@nl
prefLabel
Identification of common genet ...... ariation in human whole blood.
@en
Identification of common genet ...... ariation in human whole blood.
@nl
P2093
P2860
P356
P1433
P1476
Identification of common genet ...... ariation in human whole blood.
@en
P2093
Andrew D Johnson
Christopher J O'Donnell
Daniel Levy
Peter J Munson
Roby Joehanes
Saixia Ying
Tianxiao Huan
Xiaoling Zhang
P2860
P2888
P304
P356
10.1038/NG.3220
P407
P50
P577
2015-02-16T00:00:00Z