Complex nature of SNP genotype effects on gene expression in primary human leucocytes - Wikidata - thesis-toulmin - TriplyDB

Complex nature of SNP genotype effects on gene expression in primary human leucocytes

Complex nature of SNP genotype effects on gene expression in primary human leucocytes

http://www.wikidata.org/entity/Q33398161

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Exploiting gene expression variation to capture gene-environment interactions for disease Multiple common variants for celiac disease influencing immune gene expression Human endogenous retroviruses and the nervous system Trans-ethnic meta-analysis of white blood cell phenotypes Population differences in transcript-regulator expression quantitative trait loci Comparing methods for mapping cis acting polymorphisms using allelic expression ratios Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.Modeling expression quantitative trait loci in data combining ethnic populations.XGAP: a uniform and extensible data model and software platform for genotype and phenotype experiments Geographical genomics of human leukocyte gene expression variation in southern Morocco Gene expression and genetic variation data implicate PCLO in bipolar disorder.Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs.Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression.Genome-wide association and functional follow-up reveals new loci for kidney function Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.Genome-wide association of pericardial fat identifies a unique locus for ectopic fat Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.Blood-informative transcripts define nine common axes of peripheral blood gene expression.DeepSAGE reveals genetic variants associated with alternative polyadenylation and expression of coding and non-coding transcripts.Integrative modeling of eQTLs and cis-regulatory elements suggests mechanisms underlying cell type specificity of eQTLs.Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.Peripheral blood gene expression profiles in metabolic syndrome, coronary artery disease and type 2 diabetes.MeDiA: Mean Distance Association and Its Applications in Nonlinear Gene Set Analysis Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.Loci influencing blood pressure identified using a cardiovascular gene-centric array.Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.An expression quantitative trait loci-guided co-expression analysis for constructing regulatory network using a rice recombinant inbred line population.Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.Insights from GWAS into the quantitative genetics of transcription in humans.Systems genetics in "-omics" era: current and future development.Integrative genomics and transcriptomics analysis of human embryonic and induced pluripotent stem cells.eQTL analysis links inflammatory bowel disease associated 1q21 locus to ECM1 gene.HIV-1 Infection Dysregulates Cell Cycle Regulatory Protein p21 in CD4+ T Cells Through miR-20a and miR-106b Regulation.Specific T cell frequency and cytokine expression profile do not correlate with protection against tuberculosis after bacillus Calmette-Guérin vaccination of newborns.

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Complex nature of SNP genotype effects on gene expression in primary human leucocytes

http://www.wikidata.org/entity/Q33398161

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2009 nî lūn-bûn

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2009 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2009 թվականի հունվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Complex nature of SNP genotype effects on gene expression in primary human leucocytes

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Complex nature of SNP genotype effects on gene expression in primary human leucocytes

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Complex nature of SNP genotype effects on gene expression in primary human leucocytes

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Complex nature of SNP genotype effects on gene expression in primary human leucocytes

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Complex nature of SNP genotype effects on gene expression in primary human leucocytes

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Complex nature of SNP genotype effects on gene expression in primary human leucocytes

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BMC Medical Genomics

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Complex nature of SNP genotype effects on gene expression in primary human leucocytes

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David A Vanheel

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Karen A Hunt

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Lotte C Dinesen

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Ritsert C Jansen

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Genome-wide associations of gene expression variation in humans

Recent advances in coeliac disease

A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

Newly identified genetic risk variants for celiac disease related to the immune response

PANTHER version 6: protein sequence and function evolution data with expanded representation of biological pathways

The Biomolecular Interaction Network Database and related tools 2005 update

Human protein reference database--2006 update

The KEGG resource for deciphering the genome

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10.1186/1755-8794-2-1

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Marcel Bruinenberg

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23763312

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