esophageal cancer phenotype
Evidence from:
primary |
all sources
Related entities (6)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| alcohol | risk_factor_for | esophageal cancer | — | 1 |
| ALDH2 | risk_factor_for | esophageal cancer | — | 1 |
| ALDH2 | biomarker_for | esophageal cancer | — | 1 |
| cancer | associated_with | esophageal cancer | — | 1 |
| East Asian | associated_with | esophageal cancer | — | 1 |
| rs1229984 | associated_with | esophageal cancer | — | 1 |
Mentioned in (30)
Papers in which this entity is mentioned.
- Extrachromosomal DNA-Driven Oncogene Spatial Heterogeneity and Evolution in Glioblastoma. (2025)
- Functional analysis of cancer-associated germline risk variants. (2025)
- Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology. (2024)
- Alternative splicing: Human disease and quantitative analysis from high-throughput sequencing. (2021)
- Evaluating the transcriptional fidelity of cancer models. (2021)
- Therapeutic Implications of Germline Testing in Patients With Advanced Cancers. (2021)
- Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
- CHASMplus Reveals the Scope of Somatic Missense Mutations Driving Human Cancers. (2019)
- The mutational footprints of cancer therapies. (2019)
- The Clonal Evolution of Metastatic Osteosarcoma as Shaped by Cisplatin Treatment. (2019)
- Assessment of tumor mutation burden calculation from gene panel sequencing data. (2019)
- RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
- SvABA: genome-wide detection of structural variants and indels by local assembly. (2018)
- Patterns and mechanisms of structural variations in human cancer. (2018)
- Copy number signatures and mutational processes in ovarian carcinoma. (2018)
- Integrated analysis of gene expression and copy number identified potential cancer driver genes with amplification-dependent overexpression in 1,454 solid tumors. (2017)
- The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
- The impact of structural variation on human gene expression. (2017)
- G = E: What GWAS Can Tell Us about the Environment. (2016)
- DeconstructSigs: delineating mutational processes in single tumors distinguishes DNA repair deficiencies and patterns of carcinoma evolution. (2016)
- Substantial contribution of extrinsic risk factors to cancer development. (2016)
- Signatures of mutational processes in human cancer. (2013)
- Mutational heterogeneity in cancer and the search for new cancer-associated genes. (2013)
- Gene-environment interactions in cancer epidemiology: a National Cancer Institute Think Tank report. (2013)
- Neuroprotective actions of perinatal choline nutrition. (2013)
- Absolute quantification of somatic DNA alterations in human cancer. (2012)
- Blood cell origin of circulating microRNAs: a cautionary note for cancer biomarker studies. (2012)
- The genetic basis of addictive disorders. (2012)
- Massive genomic rearrangement acquired in a single catastrophic event during cancer development. (2011)
- A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (2011)
Merged raw entities (4)
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.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| esophageal cancer | phenotype | 26 | 40 |
| esophageal carcinoma | phenotype | 5 | 5 |
| cancers of the esophagus | phenotype | — | — |
| esophageal cancers | phenotype | — | — |