On the public citation graph
Cancer Genome Interpreter annotates the biological and clinical relevance of tumor alterations
0 signed · 98 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/humu.20495openalex-snapshot
Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database
inferredcites →https://doi.org/10.1016/j.ccell.2015.02.007openalex-snapshot
In Silico Prescription of Anticancer Drugs to Cohorts of 28 Tumor Types Reveals Targeting Opportunities
inferredcites →https://doi.org/10.1016/j.ccell.2016.06.022openalex-snapshot
High-throughput Phenotyping of Lung Cancer Somatic Mutations
inferredcites →https://doi.org/10.1016/j.cell.2016.06.017openalex-snapshot
A Landscape of Pharmacogenomic Interactions in Cancer
inferredcites →https://doi.org/10.1038/nature08987openalex-snapshot
International network of cancer genome projects
inferredcites →https://doi.org/10.1038/nature12634openalex-snapshot
Mutational landscape and significance across 12 major cancer types
inferredcites →https://doi.org/10.1038/nature12912openalex-snapshot
Discovery and saturation analysis of cancer genes across 21 tumour types
inferredcites →https://doi.org/10.1038/nature19057openalex-snapshot
Analysis of protein-coding genetic variation in 60,706 humans
inferredcites →https://doi.org/10.1038/ng.3774openalex-snapshot
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer
inferredcites →https://doi.org/10.1038/nmeth.4000openalex-snapshot
DoCM: a database of curated mutations in cancer
inferredcites →https://doi.org/10.1038/srep02650openalex-snapshot
Comprehensive identification of mutational cancer driver genes across 12 tumor types
inferredcites →https://doi.org/10.1073/pnas.1431692100openalex-snapshot
Understanding the function–structure and function–mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis
inferredcites →https://doi.org/10.1093/bioinformatics/btu467openalex-snapshot
OncodriveROLE classifies cancer driver genes in loss of function and activating mode of action
inferredcites →https://doi.org/10.1093/nar/gkv1222openalex-snapshot
ClinVar: public archive of interpretations of clinically relevant variants
inferredcites →https://doi.org/10.1126/science.1073096openalex-snapshot
Addiction to Oncogenes--the Achilles Heal of Cancer
inferredcites →https://doi.org/10.1126/science.1164382openalex-snapshot
An Integrated Genomic Analysis of Human Glioblastoma Multiforme
inferredcites →https://doi.org/10.1126/science.aaf6162openalex-snapshot
A federated ecosystem for sharing genomic, clinical data
inferredcites →https://doi.org/10.1158/0008-5472.can-15-1654openalex-snapshot
Identification of Variant-Specific Functions of PIK3CA by Rapid Phenotyping of Rare Mutations
inferredcites →https://doi.org/10.1158/2159-8290.cd-14-1118openalex-snapshot
Database of Genomic Biomarkers for Cancer Drugs and Clinical Targetability in Solid Tumors
inferredcites →https://doi.org/10.1158/2159-8290.cd-16-0160openalex-snapshot
Systematic Functional Interrogation of Rare Cancer Variants Identifies Oncogenic Alleles
inferredcites →https://doi.org/10.1158/2159-8290.cd-17-0151openalex-snapshot
AACR Project GENIE: Powering Precision Medicine through an International Consortium
inferredcites →https://doi.org/10.1186/s13059-014-0484-1openalex-snapshot
Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations
inferredcites →https://doi.org/10.1186/s13059-016-0994-0openalex-snapshot
OncodriveFML: a general framework to identify coding and non-coding regions with cancer driver mutations
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1878-0261.13710openalex-snapshot
Cell‐free DNA from ascites identifies clinically relevant variants and tumour evolution in patients with advanced ovarian cancer
inferred← citeshttps://doi.org/10.1002/1878-0261.70046openalex-snapshot
Data‐driven discovery of gene expression markers distinguishing pediatric acute lymphoblastic leukemia subtypes
inferred← citeshttps://doi.org/10.1002/hep.31862openalex-snapshot
Molecular Characterization of Biliary Tract Cancer Predicts Chemotherapy and Programmed Death 1/Programmed Death‐Ligand 1 Blockade Responses
inferred← citeshttps://doi.org/10.1007/978-3-030-91836-1_1openalex-snapshot
The Architecture of a Precision Oncology Platform
inferred← citeshttps://doi.org/10.1007/978-3-030-91836-1_10openalex-snapshot
Computational Resources for the Interpretation of Variations in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-030-91836-1_8openalex-snapshot
Pathway Analysis for Cancer Research and Precision Oncology Applications
inferred← citeshttps://doi.org/10.1007/s10120-025-01585-yopenalex-snapshot
Multi-omics sequencing of gastroesophageal junction adenocarcinoma reveals prognosis-relevant key factors and a novel immunogenomic classification
inferred← citeshttps://doi.org/10.1007/s10238-023-01011-6openalex-snapshot
Utility of public knowledge bases for the interpretation of comprehensive tumor molecular profiling results
inferred← citeshttps://doi.org/10.1016/j.bpg.2018.11.013openalex-snapshot
Molecular pathways in the development and treatment of oesophageal cancer
inferred← citeshttps://doi.org/10.1038/s41375-018-0255-1openalex-snapshot
CLL cells cumulate genetic aberrations prior to the first therapy even in outwardly inactive disease phase
inferred← citeshttps://doi.org/10.1038/s41380-021-01256-1openalex-snapshot
Molecular genetics of cocaine use disorders in humans
inferred← citeshttps://doi.org/10.1038/s41388-020-01537-zopenalex-snapshot
Exome sequencing identifies ARID2 as a novel tumor suppressor in early-onset sporadic rectal cancer
inferred← citeshttps://doi.org/10.1038/s41388-021-01928-wopenalex-snapshot
Applicability of liquid biopsies to represent the mutational profile of tumor tissue from different cancer entities
inferred← citeshttps://doi.org/10.1038/s41397-019-0102-4openalex-snapshot
Pharmacogenomics, biomarker network, and allele frequencies in colorectal cancer
inferred← citeshttps://doi.org/10.1038/s41416-021-01558-9openalex-snapshot
Genetic evolution to tyrosine kinase inhibitory therapy in patients with EGFR-mutated non-small-cell lung cancer
inferred← citeshttps://doi.org/10.1038/s41467-019-13915-7openalex-snapshot
Extreme intratumour heterogeneity and driver evolution in mismatch repair deficient gastro-oesophageal cancer
inferred← citeshttps://doi.org/10.1038/s41467-020-16323-4openalex-snapshot
The mutational impact of culturing human pluripotent and adult stem cells
inferred← citeshttps://doi.org/10.1038/s41467-021-24812-3openalex-snapshot
The genomic landscape of 85 advanced neuroendocrine neoplasms reveals subtype-heterogeneity and potential therapeutic targets
inferred← citeshttps://doi.org/10.1038/s41467-022-28348-yopenalex-snapshot
A platform for oncogenomic reporting and interpretation
inferred← citeshttps://doi.org/10.1038/s41540-022-00219-8openalex-snapshot
Functional stratification of cancer drugs through integrated network similarity
inferred← citeshttps://doi.org/10.1038/s41568-020-0290-xopenalex-snapshot
A compendium of mutational cancer driver genes
inferred← citeshttps://doi.org/10.1038/s41576-021-00338-8openalex-snapshot
Clinical cancer genomic profiling
inferred← citeshttps://doi.org/10.1038/s41586-019-1600-xopenalex-snapshot
The Drug Rediscovery protocol facilitates the expanded use of existing anticancer drugs
inferred← citeshttps://doi.org/10.1038/s41586-020-2175-2openalex-snapshot
Landscape and function of multiple mutations within individual oncogenes
inferred← citeshttps://doi.org/10.1038/s41586-021-03771-1openalex-snapshot
In silico saturation mutagenesis of cancer genes
inferred← citeshttps://doi.org/10.1038/s41586-023-06054-zopenalex-snapshot
Pan-cancer whole-genome comparison of primary and metastatic solid tumours
inferred← citeshttps://doi.org/10.1038/s41586-024-07368-2openalex-snapshot
Geographic variation of mutagenic exposures in kidney cancer genomes
inferred← citeshttps://doi.org/10.1038/s41587-022-01342-xopenalex-snapshot
Estimation of tumor cell total mRNA expression in 15 cancer types predicts disease progression
inferred← citeshttps://doi.org/10.1038/s41587-022-01353-8openalex-snapshot
Genome-wide mapping of somatic mutation rates uncovers drivers of cancer
inferred← citeshttps://doi.org/10.1038/s41588-018-0331-5openalex-snapshot
The landscape of selection in 551 esophageal adenocarcinomas defines genomic biomarkers for the clinic
inferred← citeshttps://doi.org/10.1038/s41588-019-0569-6openalex-snapshot
Genomic landscape of lung adenocarcinoma in East Asians
inferred← citeshttps://doi.org/10.1038/s41588-020-0603-8openalex-snapshot
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer
inferred← citeshttps://doi.org/10.1038/s41588-022-01273-yopenalex-snapshot
MHC II immunogenicity shapes the neoepitope landscape in human tumors
inferred← citeshttps://doi.org/10.1038/s41588-023-01333-xopenalex-snapshot
Multiancestry genomic and transcriptomic analysis of gastric cancer
inferred← citeshttps://doi.org/10.1038/s41591-020-0908-2openalex-snapshot
Colibactin DNA-damage signature indicates mutational impact in colorectal cancer
inferred← citeshttps://doi.org/10.1038/s41591-021-01448-wopenalex-snapshot
Limited evolution of the actionable metastatic cancer genome under therapeutic pressure
inferred← citeshttps://doi.org/10.1038/s41598-024-68565-7openalex-snapshot
Unraveling druggable cancer-driving proteins and targeted drugs using artificial intelligence and multi-omics analyses
inferred← citeshttps://doi.org/10.1038/s41598-024-74272-0openalex-snapshot
Evaluation of whole genome sequencing utility in identifying driver alterations in cancer genome
inferred← citeshttps://doi.org/10.1038/s43018-019-0001-2openalex-snapshot
Systematic analysis of alterations in the ubiquitin proteolysis system reveals its contribution to driver mutations in cancer
inferred← citeshttps://doi.org/10.1038/s43018-021-00243-3openalex-snapshot
Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology
inferred← citeshttps://doi.org/10.1038/s43018-022-00332-xopenalex-snapshot
The Molecular Tumor Board Portal supports clinical decisions and automated reporting for precision oncology
inferred← citeshttps://doi.org/10.1055/s-0039-1677931openalex-snapshot
Cancer Informatics in 2018: The Mysteries of the Cancer Genome Continue to Unravel, Deep Learning Approaches the Clinic, and Passive Data Collection Demonstrates Utility
inferred← citeshttps://doi.org/10.1093/nargab/lqaf177openalex-snapshot
A new algorithm Precision OncoPanels (PrOPs) identifies short individualized actionable panels that can guide cancer treatment: a pan-cancer analysis of TCGA cohorts
inferred← citeshttps://doi.org/10.1101/190330openalex-snapshot
The whole-genome panorama of cancer drivers
inferred← citeshttps://doi.org/10.1101/2021.06.25.449889openalex-snapshot
The Personalized Cancer Network Explorer (PeCaX) as a visual analytics tool to support molecular tumor boards
inferred← citeshttps://doi.org/10.1101/2024.09.24.24314298openalex-snapshot
Precise interpretation and prioritization of sequence variants with Onkopus for supporting molecular tumor boards
inferred← citeshttps://doi.org/10.1101/2025.10.12.681753openalex-snapshot
Joint analysis of expression and variation at single cell resolution by scVar
inferred← citeshttps://doi.org/10.1101/507764openalex-snapshot
Disruption of ubiquitin mediated proteolysis is a widespread mechanism of tumorigenesis
inferred← citeshttps://doi.org/10.1101/638866openalex-snapshot
OncoOmics approaches to reveal essential genes in breast cancer: a panoramic view from pathogenesis to precision medicine
inferred← citeshttps://doi.org/10.1111/vco.12944openalex-snapshot
Genomic analysis across 53 canine cancer types reveals novel mutations and high clinical actionability potential
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-17-3509openalex-snapshot
A Pan-cancer Landscape of Interactions between Solid Tumors and Infiltrating Immune Cell Populations
inferred← citeshttps://doi.org/10.1186/s12859-023-05141-2openalex-snapshot
Model performance and interpretability of semi-supervised generative adversarial networks to predict oncogenic variants with unlabeled data
inferred← citeshttps://doi.org/10.1186/s13073-019-0686-yopenalex-snapshot
Text-mining clinically relevant cancer biomarkers for curation into the CIViC database
inferred← citeshttps://doi.org/10.1371/journal.pone.0308176openalex-snapshot
Mutational spectrum of breast cancer by shallow whole-genome sequencing of cfDNA and tumor gene panel analysis
inferred← citeshttps://doi.org/10.15252/msb.20209698openalex-snapshot
CEN‐tools: an integrative platform to identify the contexts of essential genes
inferred← citeshttps://doi.org/10.21037/jtd-22-909openalex-snapshot
Characterization of driver mutations in Chinese non-small cell lung cancer patients using a novel targeted sequencing panel
inferred← citeshttps://doi.org/10.21203/rs.2.20361/v1openalex-snapshot
Comprehensive comparison of immune features between ultra-low and ultra-high mutation burden non-small cell lung cancers
inferred← citeshttps://doi.org/10.21203/rs.2.20361/v2openalex-snapshot
Comprehensive comparison of immune features between ultra-low and ultra-high mutation burden non-small cell lung cancers
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1432636/v1openalex-snapshot
Genetic and epigenetic driven variation in regulatory regions activity contribute to adaptation and evolution under endocrine treatment
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3456496/v1openalex-snapshot
OncoReport: a system for integrative NGS analysis in precision medicine
inferred← citeshttps://doi.org/10.21203/rs.3.rs-783173/v1openalex-snapshot
Clinically Actionable Cancer Somatic Variants (CACSV): A tumor interpreted dataset for analytical workflow
inferred← citeshttps://doi.org/10.33540/946openalex-snapshot
Genomics-based Precision Medicine for Patients with Cancer
inferred← citeshttps://doi.org/10.33612/diss.213504207openalex-snapshot
Clinical decision-making strategies for rare somatic variants in cancer
inferred← citeshttps://doi.org/10.3389/fonc.2017.00214openalex-snapshot
Resources for Interpreting Variants in Precision Genomic Oncology Applications
inferred← citeshttps://doi.org/10.3389/fphar.2019.00557openalex-snapshot
Natural Product Target Network Reveals Potential for Cancer Combination Therapies
inferred← citeshttps://doi.org/10.3390/analytica6020018openalex-snapshot
Evaluation of the Ellman’s Reagent Protocol for Free Sulfhydryls Under Protein Denaturing Conditions
inferred← citeshttps://doi.org/10.3390/cancers16081567openalex-snapshot
Discovery of Novel Potential Prognostic Markers and Targeted Therapy to Overcome Chemotherapy Resistance in an Advanced-Stage Wilms Tumor
inferred← citeshttps://doi.org/10.3390/ijms23031295openalex-snapshot
Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer
inferred← citeshttps://doi.org/10.3410/f.736145192.793584899openalex-snapshot
Faculty Opinions recommendation of Genomic and Transcriptomic Determinants of Therapy Resistance and Immune Landscape Evolution during Anti-EGFR Treatment in Colorectal Cancer.
inferred← citeshttps://doi.org/10.4143/crt.2020.307openalex-snapshot
Genetic Alterations in Preinvasive Lung Synchronous Lesions
inferred← citeshttps://doi.org/10.53846/goediss-7161openalex-snapshot
Guiding Cancer Therapy: Evidence-driven Reporting of Genomic Data
inferred← citeshttps://doi.org/10.6004/jnccn.2022.7097openalex-snapshot
Evaluating Germline Testing Panels in Southern African Males With Advanced Prostate Cancer
inferred← citeshttps://doi.org/10.64898/2025.12.09.25341887openalex-snapshot
Genetic and Health Determinants of Cancer Risk in Bangladeshi and Pakistani South Asians in the UK
inferred← citeshttps://doi.org/10.7717/peerj.10897openalex-snapshot
Bioinformatic strategies for the analysis of genomic aberrations detected by targeted NGS panels with clinical application
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.