The role of regulatory variation in complex traits and disease.
about
Next generation sequencing technology and genomewide data analysis: Perspectives for retinal researchMaking sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genomeCracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and PerspectivesMolecular neurobiological clues to the pathogenesis of bipolar disorderShared genetic control of expression and methylation in peripheral bloodPrediction of Causal Candidate Genes in Coronary Artery Disease LociFrom integrative genomics to systems genetics in the rat to link genotypes to phenotypesGETPrime 2.0: gene- and transcript-specific qPCR primers for 13 species including polymorphismsMassively parallel cis-regulatory analysis in the mammalian central nervous systemAssociating cellular epigenetic models with human phenotypesGenetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.Using GWAS to identify novel therapeutic targets for osteoporosis.Deep phenotyping unveils hidden traits and genetic relations in subtle mutants.Genetic assimilation: a review of its potential proximate causes and evolutionary consequences.Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood.Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data setEnhancers and chromatin structures: regulatory hubs in gene expression and diseases.Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosusGenetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population.Genetic variation in neurodegenerative diseases and its accessibility in the model organism Caenorhabditis elegans.An independent component analysis confounding factor correction framework for identifying broad impact expression quantitative trait lociRegulatory activities of transposable elements: from conflicts to benefits.Epistatic Networks Jointly Influence Phenotypes Related to Metabolic Disease and Gene Expression in Diversity Outbred Mice.Transcriptional Enhancers: Bridging the Genome and Phenome.Expression quantitative trait locus analysis for translational medicine.Fine mapping of QTL and genomic prediction using allele-specific expression SNPs demonstrates that the complex trait of genetic resistance to Marek's disease is predominantly determined by transcriptional regulation.Genome-wide identification of copy number variations between two chicken lines that differ in genetic resistance to Marek's disease.A network based covariance test for detecting multivariate eQTL in saccharomyces cerevisiae.Natural Genetic Variation Influences Protein Abundances in C. elegans Developmental Signalling Pathways.Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar DisorderOligonucleotide-based label-free detection with optical microresonators: strategies and challenges.Genome-wide association study of behavioral, physiological and gene expression traits in outbred CFW mice.Functional genomics bridges the gap between quantitative genetics and molecular biology.Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits.Bipartite Community Structure of eQTLs.Genetics of allergy and allergic sensitization: common variants, rare mutationsSurvey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.Identification of a Putative Quantitative Trait Gene for Resistance to Obesity in Mice Using Transcriptome Analysis and Causal Inference Tests.Dissecting the genetic determinants of hemostasis and thrombosisulfasQTL: an ultra-fast method of composite splicing QTL analysis.
P2860
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P2860
The role of regulatory variation in complex traits and disease.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
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
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
The role of regulatory variation in complex traits and disease.
@en
type
label
The role of regulatory variation in complex traits and disease.
@en
prefLabel
The role of regulatory variation in complex traits and disease.
@en
P356
P1476
The role of regulatory variation in complex traits and disease.
@en
P2093
Leonid Kruglyak
P2888
P304
P356
10.1038/NRG3891
P577
2015-02-24T00:00:00Z
P6179
1040273548