rheumatoid arthritis phenotype

Aliases

RA, rheumatoid arthritis

Related entities (8)

Mentioned in (54)

Papers in which this entity is mentioned.

• Integrative epigenetics and transcriptomics identify aging genes in human blood. (2026)
• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Genome-wide association testing beyond SNPs. (2025)
• Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
• Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (2024)
• An overview of DNA methylation-derived trait score methods and applications. (2023)
• Association between the timing of childhood adversity and epigenetic patterns across childhood and adolescence: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) prospective cohort. (2023)
• Osteoclasts in Osteosarcoma: Mechanisms, Interactions, and Therapeutic Prospects. (2023)
• DNA methylation and general psychopathology in childhood: an epigenome-wide meta-analysis from the PACE consortium. (2023)
• Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
• Shared genetic architecture across psychiatric disorders. (2021)
• Choline Kinase: An Unexpected Journey for a Precision Medicine Strategy in Human Diseases. (2021)
• Tutorial: a guide to performing polygenic risk score analyses. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• DNA methylation as a predictor of fetal alcohol spectrum disorder. (2018)
• Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
• Annotation-free quantification of RNA splicing using LeafCutter. (2018)
• Demystifying the cytokine network: Mathematical models point the way. (2017)
• Effects of Antenatal Maternal Depressive Symptoms and Socio-Economic Status on Neonatal Brain Development are Modulated by Genetic Risk. (2017)
• Genetic effects on gene expression across human tissues. (2017)
• One-Carbon Metabolism in Health and Disease. (2017)
• Fetal sex is associated with maternal stimulated cytokine production, but not serum cytokine levels, in human pregnancy. (2017)
• The impact of structural variation on human gene expression. (2017)
• LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. (2017)
• Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses. (2015)
• Fetal Alcohol Spectrum Disorders: An Overview from the Glia Perspective. (2015)
• Recent genetic findings in schizophrenia and their therapeutic relevance. (2015)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• What Happens When Children with Fetal Alcohol Spectrum Disorders Become Adults? (2015)
• A review of the nonpressor and nonantidiuretic actions of the hormone vasopressin. (2015)
• The CXCL12/CXCR4 chemokine ligand/receptor axis in cardiovascular disease. (2014)
• Visualizing genomic information across chromosomes with PhenoGram. (2013)
• Thalidomide-a notorious sedative to a wonder anticancer drug. (2013)
• DNA methylation, genotype and gene expression: who is driving and who is along for the ride? (2013)
• Circulating microRNAs in exosomes indicate hepatocyte injury and inflammation in alcoholic, drug-induced, and inflammatory liver diseases. (2012)
• Myeloid cells in tumor inflammation. (2012)
• Oncostatin M decreases interleukin-1 β secretion by human synovial fibroblasts and attenuates an acute inflammatory reaction in vivo. (2012)
• Pathway analysis of genomic data: concepts, methods, and prospects for future development. (2012)
• Vitamin D and its role during pregnancy in attaining optimal health of mother and fetus. (2012)
• Prenatal alcohol exposure alters the course and severity of adjuvant-induced arthritis in female rats. (2012)
• Teratogenic effects of thalidomide: molecular mechanisms. (2011)
• Epigenetics and psychoneuroimmunology: mechanisms and models. (2011)
• Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
• Using public control genotype data to increase power and decrease cost of case-control genetic association studies. (2010)
• The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
• DT-REFinD: diffusion tensor registration with exact finite-strain differential. (2009)
• Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
• Analysis and application of European genetic substructure using 300 K SNP information. (2008)
• The HLA system: genetics, immunology, clinical testing, and clinical implications. (2007)
• C-reactive protein: a critical update. (2003)

Merged raw entities (2)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.