prognosis phenotype
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| auditory | associated_with | prognosis | — | 1 |
| genetic variants | biomarker_for | prognosis | — | 1 |
Mentioned in (26)
Papers in which this entity is mentioned.
- A guide to transcriptomic deconvolution in cancer. (2026)
- Tracing the evolution of single-cell 3D genomes in Kras-driven cancers. (2025)
- A New Era of Data-Driven Cancer Research and Care: Opportunities and Challenges. (2024)
- Combination of genomic instability score and TP53 status for prognosis prediction in lung adenocarcinoma. (2023)
- Towards understandings of serine/arginine-rich splicing factors. (2023)
- Construction and validation of a novel gene signature for predicting the prognosis of osteosarcoma. (2022)
- Circulating Tumor DNA Is Associated with Response and Survival in Patients with Advanced Leiomyosarcoma. (2022)
- Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology. (2021)
- Choline Kinase: An Unexpected Journey for a Precision Medicine Strategy in Human Diseases. (2021)
- Accurate detection of circulating tumor DNA using nanopore consensus sequencing. (2021)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. (2021)
- Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
- Detection of Somatic Structural Variants Enables Quantification and Characterization of Circulating Tumor DNA in Children With Solid Tumors. (2018)
- The Immune Landscape of Cancer. (2018)
- Detection of circulating tumour DNA is associated with inferior outcomes in Ewing sarcoma and osteosarcoma: a report from the Children's Oncology Group. (2018)
- Estimating the population abundance of tissue-infiltrating immune and stromal cell populations using gene expression. (2016)
- Systematic pan-cancer analysis of tumour purity. (2015)
- Comparison of RNA-seq and microarray-based models for clinical endpoint prediction. (2015)
- Unraveling the clonal hierarchy of somatic genomic aberrations. (2014)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
- Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
- A rare population of CD24(+)ITGB4(+)Notch(hi) cells drives tumor propagation in NSCLC and requires Notch3 for self-renewal. (2013)
- Microsatellites with macro-influence in ewing sarcoma. (2012)
- A novel and universal method for microRNA RT-qPCR data normalization. (2009)
- Finding the missing heritability of complex diseases. (2009)
- Three-dimensional brain growth abnormalities in childhood-onset schizophrenia visualized by using tensor-based morphometry. (2008)
Merged raw entities (1)
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 |
|---|---|---|---|
| prognosis | phenotype | 26 | 36 |