tumorigenesis phenotype

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Mentioned in (51)

Papers in which this entity is mentioned.

• Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models. (2026)
• Integrated in vivo combinatorial functional genomics and spatial transcriptomics of tumours to decode genotype-to-phenotype relationships. (2026)
• Whole-genome landscapes of 1,364 breast cancers. (2026)
• Extrachromosomal DNA-Driven Oncogene Spatial Heterogeneity and Evolution in Glioblastoma. (2025)
• Chromosomal instability as a driver of cancer progression. (2025)
• Functional analysis of cancer-associated germline risk variants. (2025)
• Transient loss of Polycomb components induces an epigenetic cancer fate. (2024)
• Human 3D brain organoids: steering the demolecularization of brain and neurological diseases. (2023)
• Deterministic evolution and stringent selection during preneoplasia. (2023)
• RNA splicing dysregulation and the hallmarks of cancer. (2023)
• Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA. (2022)
• Application of third-generation sequencing in cancer research. (2021)
• Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
• Emerging Roles of SRSF3 as a Therapeutic Target for Cancer. (2020)
• Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy. (2019)
• Germline variants associated with leukocyte genes predict tumor recurrence in breast cancer patients. (2019)
• Circular DNA elements of chromosomal origin are common in healthy human somatic tissue. (2018)
• Driver Fusions and Their Implications in the Development and Treatment of Human Cancers. (2018)
• Personal Cancer Genome Reporter: variant interpretation report for precision oncology. (2018)
• Patterns and mechanisms of structural variations in human cancer. (2018)
• Picky comprehensively detects high-resolution structural variants in nanopore long reads. (2018)
• Nanopore Sequencing Reveals High-Resolution Structural Variation in the Cancer Genome (2017)
• Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden. (2017)
• ChimeRScope: a novel alignment-free algorithm for fusion transcript prediction using paired-end RNA-Seq data. (2017)
• PGBD5 promotes site-specific oncogenic mutations in human tumors. (2017)
• Comprehensive Analysis of Hypermutation in Human Cancer. (2017)
• B lymphocytes and cancer: a love-hate relationship. (2016)
• A role for human homologous recombination factors in suppressing microhomology-mediated end joining. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• Global analysis of somatic structural genomic alterations and their impact on gene expression in diverse human cancers. (2016)
• Evolutionary Insights into RNA trans-Splicing in Vertebrates. (2016)
• Systematic pan-cancer analysis of tumour purity. (2015)
• Oncogenic fusion protein EWS-FLI1 is a network hub that regulates alternative splicing. (2015)
• PVT1 dependence in cancer with MYC copy-number increase. (2014)
• Dynamic analyses of alternative polyadenylation from RNA-seq reveal a 3'-UTR landscape across seven tumour types. (2014)
• Inferring tumour purity and stromal and immune cell admixture from expression data. (2013)
• Cancer genome landscapes. (2013)
• Ewing sarcoma protein: a key player in human cancer. (2013)
• Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
• RNA splicing: a new player in the DNA damage response. (2013)
• Differential expression profiles of glycosphingolipids in human breast cancer stem cells vs. cancer non-stem cells. (2013)
• Computational approaches to identify functional genetic variants in cancer genomes. (2013)
• Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. (2013)
• LIN28B promotes growth and tumorigenesis of the intestinal epithelium via Let-7. (2013)
• Absolute quantification of somatic DNA alterations in human cancer. (2012)
• Microsatellites with macro-influence in ewing sarcoma. (2012)
• BRCA1 and BRCA2: different roles in a common pathway of genome protection. (2011)
• Mechanisms and consequences of alternative polyadenylation. (2011)
• Allele-specific copy number analysis of tumors. (2010)
• Insulin-like growth factor-I mitigates motor coordination deficits associated with neonatal alcohol exposure in rats. (2009)
• Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. (2009)

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