Pages that link to "Q33839438"
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The following pages link to Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals (Q33839438):
Displaying 50 items.
- MicroRNA-driven developmental remodeling in the brain distinguishes humans from other primates (Q21145751) (← links)
- Detection of identity by descent using next-generation whole genome sequencing data (Q21284324) (← links)
- Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population (Q21563374) (← links)
- Heritability in the genome-wide association era (Q27024251) (← links)
- Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular disease (Q27311664) (← links)
- Linear mixed model for heritability estimation that explicitly addresses environmental variation (Q27320867) (← links)
- A statistical framework for joint eQTL analysis in multiple tissues (Q28397927) (← links)
- The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics (Q28482577) (← links)
- The genetic and mechanistic basis for variation in gene regulation (Q28542978) (← links)
- Aberrant gene expression in humans (Q28543078) (← links)
- Context Sensitive Modeling of Cancer Drug Sensitivity (Q28547285) (← links)
- A gene-based association method for mapping traits using reference transcriptome data (Q28608356) (← links)
- An Expanded View of Complex Traits: From Polygenic to Omnigenic (Q30322686) (← links)
- Improving the accuracy and efficiency of identity-by-descent detection in population data (Q30608038) (← links)
- Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data (Q30630709) (← links)
- Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals. (Q33637547) (← links)
- An independent component analysis confounding factor correction framework for identifying broad impact expression quantitative trait loci (Q33739437) (← links)
- Differential expression analysis for RNAseq using Poisson mixed models (Q33878991) (← links)
- PedBLIMP: extending linear predictors to impute genotypes in pedigrees (Q34022023) (← links)
- Integrating autoimmune risk loci with gene-expression data identifies specific pathogenic immune cell subsets (Q34036705) (← links)
- Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression (Q34139984) (← links)
- Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits (Q34221082) (← links)
- Length distributions of identity by descent reveal fine-scale demographic history (Q34308519) (← links)
- Mechanisms of dietary response in mice and primates: a role for EGR1 in regulating the reaction to human-specific nutritional content. (Q34399564) (← links)
- Efficient multivariate linear mixed model algorithms for genome-wide association studies (Q34415454) (← links)
- Transcriptional Enhancers: Bridging the Genome and Phenome (Q34502174) (← links)
- Carboxylesterase 1 gene duplication and mRNA expression in adipose tissue are linked to obesity and metabolic function (Q34611588) (← links)
- Robust prediction of expression differences among human individuals using only genotype information (Q34649950) (← links)
- Global properties and functional complexity of human gene regulatory variation (Q34758225) (← links)
- Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits (Q34758236) (← links)
- Impact of natural genetic variation on gene expression dynamics. (Q34765325) (← links)
- Parente2: a fast and accurate method for detecting identity by descent (Q35042987) (← links)
- The evolution and adaptive potential of transcriptional variation in sticklebacks--signatures of selection and widespread heritability. (Q35081187) (← links)
- A systematic heritability analysis of the human whole blood transcriptome (Q35119592) (← links)
- Geographical, environmental and pathophysiological influences on the human blood transcriptome. (Q35226568) (← links)
- Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance. (Q35236390) (← links)
- The genetic architecture of gene expression levels in wild baboons (Q35249398) (← links)
- Expression quantitative trait locus analysis for translational medicine (Q35775535) (← links)
- Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent (Q35791545) (← links)
- Which Genetics Variants in DNase-Seq Footprints Are More Likely to Alter Binding? (Q35930706) (← links)
- Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder (Q36017055) (← links)
- Transethnic Genetic-Correlation Estimates from Summary Statistics (Q36056569) (← links)
- Functional genomics bridges the gap between quantitative genetics and molecular biology (Q36084283) (← links)
- Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues (Q36189755) (← links)
- A mixed-model approach for genome-wide association studies of correlated traits in structured populations (Q36204938) (← links)
- Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins (Q36276125) (← links)
- Large-scale identification of sequence variants influencing human transcription factor occupancy in vivo (Q36338647) (← links)
- Coordinating GWAS results with gene expression in a systems immunologic paradigm in autoimmunity (Q36371313) (← links)
- Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort (Q36528366) (← links)
- Intersection of population variation and autoimmunity genetics in human T cell activation (Q36572940) (← links)