inflammatory bowel disease phenotype

Aliases

IBD

Related entities (8)

Mentioned in (35)

Papers in which this entity is mentioned.

• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
• Identifying Spatial Co-occurrence in Healthy and InflAmed tissues (ISCHIA). (2024)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (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)
• A saturated map of common genetic variants associated with human height. (2022)
• Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. (2022)
• Evidence for long-lasting alterations in the fecal microbiota following prenatal alcohol exposure. (2022)
• Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (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)
• Psychiatric Genomics: An Update and an Agenda. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. (2018)
• Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
• Demystifying the cytokine network: Mathematical models point the way. (2017)
• A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles. (2017)
• The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• An introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disorders. (2015)
• Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
• Heritability and genomics of gene expression in peripheral blood. (2014)
• A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
• Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder. (2013)
• The role of nutrition in children's neurocognitive development, from pregnancy through childhood. (2013)
• Inflammaging: disturbed interplay between autophagy and inflammasomes. (2012)
• Alcoholic liver disease and malnutrition. (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)
• The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. (2009)

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