Crohn's disease phenotype

Aliases

CD, Crohn disease, Crohns disease, Crohn×s disease, Crohn’s disease

Related entities (16)

Mentioned in (34)

Papers in which this entity is mentioned.

• Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. (2022)
• Shared genetic architecture across psychiatric disorders. (2021)
• The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
• Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
• The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (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)
• Establishment of human iPSC-based models for the study and targeting of glioma initiating cells. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• Visualizing genomic information across chromosomes with PhenoGram. (2013)
• The role of nutrition in children's neurocognitive development, from pregnancy through childhood. (2013)
• A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. (2013)
• Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
• Inflammaging: disturbed interplay between autophagy and inflammasomes. (2012)
• Myeloid cells in tumor inflammation. (2012)
• Pathway analysis of genomic data: concepts, methods, and prospects for future development. (2012)
• Genome-wide efficient mixed-model analysis for association studies. (2012)
• Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants. (2011)
• The PhenX Toolkit: get the most from your measures. (2011)
• From genotype to EEG endophenotype: a route for post-genomic understanding of complex psychiatric disease? (2010)
• MicroRNAs: master regulators of ethanol abuse and toxicity? (2010)
• Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes. (2010)
• The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
• i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study. (2010)
• The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
• The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
• ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. (2009)
• ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. (2009)
• Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample. (2009)
• Common and rare variants in multifactorial susceptibility to common diseases. (2008)
• Identification of novel bone-specific molecular targets of binge alcohol and ibandronate by transcriptome analysis. (2008)
• Analysis and application of European genetic substructure using 300 K SNP information. (2008)
• Eotaxin and the attraction of eosinophils to the asthmatic lung. (2001)

Merged raw entities (4)

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