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Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.ccell.2014.09.010openalex-snapshot
The Architecture and Evolution of Cancer Neochromosomes
inferredcites →https://doi.org/10.1016/j.ccr.2014.07.014openalex-snapshot
The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma
inferredcites →https://doi.org/10.1016/j.cell.2010.10.027openalex-snapshot
A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms
inferredcites →https://doi.org/10.1016/j.cell.2010.11.055openalex-snapshot
Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development
inferredcites →https://doi.org/10.1016/j.cell.2011.07.042openalex-snapshot
Chromosome Catastrophes Involve Replication Mechanisms Generating Complex Genomic Rearrangements
inferredcites →https://doi.org/10.1016/j.cell.2011.12.013openalex-snapshot
Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations
inferredcites →https://doi.org/10.1016/j.cell.2012.04.024openalex-snapshot
Mutational Processes Molding the Genomes of 21 Breast Cancers
inferredcites →https://doi.org/10.1016/j.cell.2013.02.023openalex-snapshot
Criteria for Inference of Chromothripsis in Cancer Genomes
inferredcites →https://doi.org/10.1016/j.cell.2013.04.010openalex-snapshot
Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes
inferredcites →https://doi.org/10.1016/j.cell.2013.10.011openalex-snapshot
Cumulative Haploinsufficiency and Triplosensitivity Drive Aneuploidy Patterns and Shape the Cancer Genome
inferredcites →https://doi.org/10.1016/j.cell.2015.05.044openalex-snapshot
Genomic Classification of Cutaneous Melanoma
inferredcites →https://doi.org/10.1016/j.cell.2015.11.054openalex-snapshot
Chromothripsis and Kataegis Induced by Telomere Crisis
inferredcites →https://doi.org/10.1016/j.cell.2018.02.020openalex-snapshot
Timing the Landmark Events in the Evolution of Clear Cell Renal Cell Cancer: TRACERx Renal
inferredcites →https://doi.org/10.1016/j.celrep.2012.05.009openalex-snapshot
Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms
inferredcites →https://doi.org/10.1016/j.celrep.2014.04.053openalex-snapshot
Break-Induced Replication Is a Source of Mutation Clusters Underlying Kataegis
inferredcites →https://doi.org/10.1016/j.molcel.2016.06.020openalex-snapshot
Essential Roles for Polymerase θ-Mediated End Joining in the Repair of Chromosome Breaks
inferredcites →https://doi.org/10.1038/nature10802openalex-snapshot
DNA breaks and chromosome pulverization from errors in mitosis
inferredcites →https://doi.org/10.1038/nature10910openalex-snapshot
Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes
inferredcites →https://doi.org/10.1038/nature13115openalex-snapshot
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
inferredcites →https://doi.org/10.1038/nature14493openalex-snapshot
Chromothripsis from DNA damage in micronuclei
inferredcites →https://doi.org/10.1038/nature17676openalex-snapshot
Landscape of somatic mutations in 560 breast cancer whole-genome sequences
inferredcites →https://doi.org/10.1038/nature19823openalex-snapshot
A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns
inferredcites →https://doi.org/10.1038/nature20788openalex-snapshot
Genomic hallmarks of localized, non-indolent prostate cancer
inferredcites →https://doi.org/10.1038/nature25480openalex-snapshot
The landscape of genomic alterations across childhood cancers
inferredcites →https://doi.org/10.1038/nature25795openalex-snapshot
Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours
inferredcites →https://doi.org/10.1038/ncb3450openalex-snapshot
Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining
inferredcites →https://doi.org/10.1038/ncomms15180openalex-snapshot
A molecular portrait of microsatellite instability across multiple cancers
inferredcites →https://doi.org/10.1038/ncomms15936openalex-snapshot
Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma
inferredcites →https://doi.org/10.1038/ncomms6224openalex-snapshot
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis
inferredcites →https://doi.org/10.1038/ncomms6690openalex-snapshot
Extrachromosomal driver mutations in glioblastoma and low-grade glioma
inferredcites →https://doi.org/10.1038/ng.2702openalex-snapshot
An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers
inferredcites →https://doi.org/10.1038/ng.2760openalex-snapshot
Pan-cancer patterns of somatic copy number alteration
inferredcites →https://doi.org/10.1038/nmeth.2642openalex-snapshot
IntOGen-mutations identifies cancer drivers across tumor types
inferredcites →https://doi.org/10.1038/nrg2593openalex-snapshot
Mechanisms of change in gene copy number
inferredcites →https://doi.org/10.1038/s41375-018-0035-yopenalex-snapshot
Chromothripsis in acute myeloid leukemia: biological features and impact on survival
inferredcites →https://doi.org/10.1038/s41467-017-02602-0openalex-snapshot
Integrative genomic and transcriptomic analysis of leiomyosarcoma
inferredcites →https://doi.org/10.1038/s41467-020-18688-yopenalex-snapshot
Framework for quality assessment of whole genome cancer sequences
inferredcites →https://doi.org/10.1083/jcb.201210040openalex-snapshot
Linking abnormal mitosis to the acquisition of DNA damage
inferredcites →https://doi.org/10.1093/bioinformatics/btp120openalex-snapshot
TopHat: discovering splice junctions with RNA-Seq
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp698openalex-snapshot
Fast and accurate long-read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot
STAR: ultrafast universal RNA-seq aligner
inferredcites →https://doi.org/10.1093/genetics/26.2.234openalex-snapshot
THE STABILITY OF BROKEN ENDS OF CHROMOSOMES IN ZEA MAYS
inferredcites →https://doi.org/10.1093/hmg/ddr073openalex-snapshot
Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†
inferredcites →https://doi.org/10.1093/jnci/djs177openalex-snapshot
A DNA Repair Pathway–Focused Score for Prediction of Outcomes in Ovarian Cancer Treated With Platinum-Based Chemotherapy
inferredcites →https://doi.org/10.1093/nar/gkq603openalex-snapshot
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
inferredcites →https://doi.org/10.1093/nar/gkw1121openalex-snapshot
COSMIC: somatic cancer genetics at high-resolution
inferredcites →https://doi.org/10.1101/181339openalex-snapshot
Patterns of structural variation in human cancer
inferredcites →https://doi.org/10.1101/gr.115782.110openalex-snapshot
RAFgene fusion breakpoints in pediatric brain tumors are characterized by significant enrichment of sequence microhomology
inferredcites →https://doi.org/10.1101/gr.140301.112openalex-snapshot
Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes
inferredcites →https://doi.org/10.1126/science.1219580openalex-snapshot
Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative Potential
inferredcites →https://doi.org/10.1126/science.aaf8399openalex-snapshot
Tumor aneuploidy correlates with markers of immune evasion and with reduced response to immunotherapy
inferredcites →https://doi.org/10.1146/annurev-genet-120213-092228openalex-snapshot
Chromothripsis: A New Mechanism for Rapid Karyotype Evolution
inferredcites →https://doi.org/10.1158/0008-5472.can-13-0186openalex-snapshot
Double Minute Chromosomes in Glioblastoma Multiforme Are Revealed by Precise Reconstruction of Oncogenic Amplicons
inferredcites →https://doi.org/10.1158/2159-8290.cd-13-0285openalex-snapshot
Tolerance of Whole-Genome Doubling Propagates Chromosomal Instability and Accelerates Cancer Genome Evolution
inferredcites →https://doi.org/10.1158/2159-8290.cd-13-0879openalex-snapshot
EGFR Variant Heterogeneity in Glioblastoma Resolved through Single-Nucleus Sequencing
inferredcites →https://doi.org/10.1177/1947601912455199openalex-snapshot
Dual Roles of MDM2 in the Regulation of p53: Ubiquitination Dependent and Ubiquitination Independent Mechanisms of MDM2 Repression of p53 Activity
inferredcites →https://doi.org/10.1186/1471-2105-15-78openalex-snapshot
ShatterProof: operational detection and quantification of chromothripsis
inferredcites →https://doi.org/10.1186/1471-2164-15-82openalex-snapshot
Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens
inferredcites →https://doi.org/10.1186/1751-0473-9-13openalex-snapshot
biobambam: tools for read pair collation based algorithms on BAM files
inferredcites →https://doi.org/10.1371/journal.pgen.1000327openalex-snapshot
A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation
inferredcites →https://doi.org/10.1371/journal.pone.0006564openalex-snapshot
Multipolar Spindle Pole Coalescence Is a Major Source of Kinetochore Mis-Attachment and Chromosome Mis-Segregation in Cancer Cells
inferredcites →https://doi.org/10.15252/msb.20156505openalex-snapshot
A cell‐based model system links chromothripsis with hyperploidy
inferredcites →https://doi.org/10.7554/elife.06516openalex-snapshot
Catastrophic chromosomal restructuring during genome elimination in plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ajh.27575openalex-snapshot
Chromoanagenesis Is Frequently Associated With Highly Complex Karyotypes, Extensive Clonal Heterogeneity, and Treatment Refractoriness in Acute Myeloid Leukemia
inferred← citeshttps://doi.org/10.1002/ajmg.a.63975openalex-snapshot
De Novo Chromosomes 3q and 5q Chromothripsis Leads to a 5q14.3 Microdeletion Syndrome Presentation: Case Report and Review of the Literature
inferred← citeshttps://doi.org/10.1002/gcc.23027openalex-snapshot
ERG amplification is a secondary recurrent driver event in myeloid malignancy with complex karyotype and TP53 mutations
inferred← citeshttps://doi.org/10.1002/gcc.23253openalex-snapshot
The Variable Genomic Landscape During Osteosarcoma Progression: Insights From a Longitudinal WGS Analysis
inferred← citeshttps://doi.org/10.1002/ijc.33300openalex-snapshot
Small but strong: Mutational and functional landscapes of micronuclei in cancer genomes
inferred← citeshttps://doi.org/10.1002/ijc.33618openalex-snapshot
Cell‐based model systems for genome instability: Dissecting the mechanistic basis of chromothripsis in cancer
inferred← citeshttps://doi.org/10.1002/ijc.34027openalex-snapshot
A synergistic interaction between HDAC‐ and PARP inhibitors in childhood tumors with chromothripsis
inferred← citeshttps://doi.org/10.1002/ijc.34051openalex-snapshot
The landscape of genetic aberrations in myxofibrosarcoma
inferred← citeshttps://doi.org/10.1002/path.5891openalex-snapshot
Genomic catastrophe, the peritoneal cavity and ovarian cancer prevention
inferred← citeshttps://doi.org/10.1002/path.6219openalex-snapshot
Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway
inferred← citeshttps://doi.org/10.1007/s10555-021-09969-zopenalex-snapshot
Decoding human cancer with whole genome sequencing: a review of PCAWG Project studies published in February 2020
inferred← citeshttps://doi.org/10.1007/s11427-024-2710-3openalex-snapshot
Exploring the potential of extrachromosomal DNA as a novel oncogenic driver
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.09.071openalex-snapshot
Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design
inferred← citeshttps://doi.org/10.1016/j.gde.2020.02.009openalex-snapshot
Chromothripsis and telomere crisis: engines of genome instability
inferred← citeshttps://doi.org/10.1016/j.jtho.2026.104204openalex-snapshot
Integrated Multi-Omic Profiling Enables Recurrence Risk Stratification Beyond Pathological Stage in Resected EGFR-Mutant Lung Adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.semcancer.2019.11.009openalex-snapshot
The genomics of undifferentiated sarcoma of soft tissue: Progress, challenges and opportunities
inferred← citeshttps://doi.org/10.1016/j.tcb.2018.10.006openalex-snapshot
Homologous Recombination and the Formation of Complex Genomic Rearrangements
inferred← citeshttps://doi.org/10.1038/s12276-020-00529-zopenalex-snapshot
Small but mighty: the causes and consequences of micronucleus rupture
inferred← citeshttps://doi.org/10.1038/s12276-021-00668-xopenalex-snapshot
Genomic and transcriptomic analyses reveal a tandem amplification unit of 11 genes and mutations in mismatch repair genes in methotrexate-resistant HT-29 cells
inferred← citeshttps://doi.org/10.1038/s41374-021-00709-zopenalex-snapshot
A murine mesenchymal stem cell model for initiating events in osteosarcomagenesis points to CDK4/CDK6 inhibition as a therapeutic target
inferred← citeshttps://doi.org/10.1038/s41375-022-01671-5openalex-snapshot
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults
inferred← citeshttps://doi.org/10.1038/s41388-022-02588-0openalex-snapshot
Spatiotemporal view of malignant histogenesis and macroevolution via formation of polyploid giant cancer cells
inferred← citeshttps://doi.org/10.1038/s41408-021-00570-9openalex-snapshot
Cancer drivers and clonal dynamics in acute lymphoblastic leukaemia subtypes
inferred← citeshttps://doi.org/10.1038/s41417-021-00347-zopenalex-snapshot
Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies
inferred← citeshttps://doi.org/10.1038/s41467-019-13084-7openalex-snapshot
The genomic landscape of metastatic castration-resistant prostate cancers reveals multiple distinct genotypes with potential clinical impact
inferred← citeshttps://doi.org/10.1038/s41467-019-14261-4openalex-snapshot
Mutational signatures in tumours induced by high and low energy radiation in Trp53 deficient mice
inferred← citeshttps://doi.org/10.1038/s41467-020-18688-yopenalex-snapshot
Framework for quality assessment of whole genome cancer sequences
inferred← citeshttps://doi.org/10.1038/s41467-021-22671-6openalex-snapshot
Integrative reconstruction of cancer genome karyotypes using InfoGenomeR
inferred← citeshttps://doi.org/10.1038/s41467-022-31666-wopenalex-snapshot
Machine learning-based tissue of origin classification for cancer of unknown primary diagnostics using genome-wide mutation features
inferred← citeshttps://doi.org/10.1038/s41467-023-44287-8openalex-snapshot
The ALT pathway generates telomere fusions that can be detected in the blood of cancer patients
inferred← citeshttps://doi.org/10.1038/s41467-024-47031-yopenalex-snapshot
Systematic analysis of RNA-binding proteins identifies targetable therapeutic vulnerabilities in osteosarcoma
inferred← citeshttps://doi.org/10.1038/s41467-024-52147-2openalex-snapshot
Yeast EndoG prevents genome instability by degrading extranuclear DNA species
inferred← citeshttps://doi.org/10.1038/s41467-024-52916-zopenalex-snapshot
53BP1 deficiency leads to hyperrecombination using break-induced replication (BIR)
inferred← citeshttps://doi.org/10.1038/s41467-025-58245-zopenalex-snapshot
Cell-cycle dependent DNA repair and replication unifies patterns of chromosome instability
inferred← citeshttps://doi.org/10.1038/s41523-021-00342-5openalex-snapshot
A careful reassessment of anthracycline use in curable breast cancer
inferred← citeshttps://doi.org/10.1038/s41568-020-00321-1openalex-snapshot
Aneuploidy as a promoter and suppressor of malignant growth
inferred← citeshttps://doi.org/10.1038/s41568-021-00418-1openalex-snapshot
Pancreatic cancer evolution and heterogeneity: integrating omics and clinical data
inferred← citeshttps://doi.org/10.1038/s41568-022-00488-9openalex-snapshot
Structural variations in cancer and the 3D genome
inferred← citeshttps://doi.org/10.1038/s41568-026-00970-8openalex-snapshot
A single-cell lens into the co-evolution of genotypes and phenotypes in cancer
inferred← citeshttps://doi.org/10.1038/s41571-021-00519-8openalex-snapshot
Advancing therapy for osteosarcoma
inferred← citeshttps://doi.org/10.1038/s41571-022-00696-0openalex-snapshot
Neuroendocrine neoplasms of the lung and gastrointestinal system: convergent biology and a path to better therapies
inferred← citeshttps://doi.org/10.1038/s41575-021-00463-zopenalex-snapshot
The pancreatic cancer genome revisited
inferred← citeshttps://doi.org/10.1038/s41576-020-00299-4openalex-snapshot
Mutation–selection balance and compensatory mechanisms in tumour evolution
inferred← citeshttps://doi.org/10.1038/s41576-021-00431-yopenalex-snapshot
Computational analysis of cancer genome sequencing data
inferred← citeshttps://doi.org/10.1038/s41576-024-00808-9openalex-snapshot
Diversity and consequences of structural variation in the human genome
inferred← citeshttps://doi.org/10.1038/s41586-020-2135-xopenalex-snapshot
A genomic and epigenomic atlas of prostate cancer in Asian populations
inferred← citeshttps://doi.org/10.1038/s41586-022-04938-0openalex-snapshot
Nuclear chromosome locations dictate segregation error frequencies
inferred← citeshttps://doi.org/10.1038/s41586-022-05154-6openalex-snapshot
African-specific molecular taxonomy of prostate cancer
inferred← citeshttps://doi.org/10.1038/s41586-022-05504-4openalex-snapshot
Structural variants drive context-dependent oncogene activation in cancer
inferred← citeshttps://doi.org/10.1038/s41586-023-05923-xopenalex-snapshot
Chromosomal fragile site breakage by EBV-encoded EBNA1 at clustered repeats
inferred← citeshttps://doi.org/10.1038/s41586-023-06157-7openalex-snapshot
Heritable transcriptional defects from aberrations of nuclear architecture
inferred← citeshttps://doi.org/10.1038/s41586-023-06216-zopenalex-snapshot
Mitotic tethering enables inheritance of shattered micronuclear chromosomes
inferred← citeshttps://doi.org/10.1038/s41586-024-07054-3openalex-snapshot
Deep whole-genome analysis of 494 hepatocellular carcinomas
inferred← citeshttps://doi.org/10.1038/s41586-024-07747-9openalex-snapshot
The genomic landscape of 2,023 colorectal cancers
inferred← citeshttps://doi.org/10.1038/s41586-025-08671-2openalex-snapshot
Evolutionary fingerprints of epithelial-to-mesenchymal transition
inferred← citeshttps://doi.org/10.1038/s41587-022-01551-4openalex-snapshot
Functional analysis of structural variants in single cells using Strand-seq
inferred← citeshttps://doi.org/10.1038/s41588-019-0360-8openalex-snapshot
Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangements
inferred← citeshttps://doi.org/10.1038/s41588-019-0566-9openalex-snapshot
Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution
inferred← citeshttps://doi.org/10.1038/s41588-021-00951-7openalex-snapshot
Chromothripsis followed by circular recombination drives oncogene amplification in human cancer
inferred← citeshttps://doi.org/10.1038/s41588-022-01211-yopenalex-snapshot
Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features
inferred← citeshttps://doi.org/10.1038/s41588-023-01321-1openalex-snapshot
Multiomic analysis of malignant pleural mesothelioma identifies molecular axes and specialized tumor profiles driving intertumor heterogeneity
inferred← citeshttps://doi.org/10.1038/s41588-023-01395-xopenalex-snapshot
Clonal evolution during metastatic spread in high-risk neuroblastoma
inferred← citeshttps://doi.org/10.1038/s41588-024-01981-7openalex-snapshot
Engineering structural variants to interrogate genome function
inferred← citeshttps://doi.org/10.1038/s41588-024-01988-0openalex-snapshot
Luminal breast epithelial cells of BRCA1 or BRCA2 mutation carriers and noncarriers harbor common breast cancer copy number alterations
inferred← citeshttps://doi.org/10.1038/s41591-023-02304-9openalex-snapshot
Multi-organ landscape of therapy-resistant melanoma
inferred← citeshttps://doi.org/10.1038/s41592-023-01932-wopenalex-snapshot
A survey of algorithms for the detection of genomic structural variants from long-read sequencing data
inferred← citeshttps://doi.org/10.1038/s41594-022-00893-6openalex-snapshot
Multiscale reorganization of the genome following DNA damage facilitates chromosome translocations via nuclear actin polymerization
inferred← citeshttps://doi.org/10.1038/s41597-025-04801-7openalex-snapshot
Genome assembly resources of genitourinary cancers for chromosomal aberration at the single nucleotide level
inferred← citeshttps://doi.org/10.1038/s41598-022-07211-6openalex-snapshot
Clustering and graph mining techniques for classification of complex structural variations in cancer genomes
inferred← citeshttps://doi.org/10.1038/s41598-023-37764-zopenalex-snapshot
The genomic and transcriptomic landscape of advanced renal cell cancer for individualized treatment strategies
inferred← citeshttps://doi.org/10.1038/s41598-024-60628-zopenalex-snapshot
Establishment, characterization, and genetic profiling of patient-derived osteosarcoma cells from a patient with retinoblastoma
inferred← citeshttps://doi.org/10.1038/s41598-024-69382-8openalex-snapshot
Whole genome and reverse protein phase array landscapes of patient derived osteosarcoma xenograft models
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/s42003-022-03238-7openalex-snapshot
Rearrangement processes and structural variations show evidence of selection in oesophageal adenocarcinomas
inferred← citeshttps://doi.org/10.1038/s42003-022-04392-8openalex-snapshot
Profilin 1 deficiency drives mitotic defects and reduces genome stability
inferred← citeshttps://doi.org/10.1038/s43018-026-01242-yopenalex-snapshot
Unraveling the lexicon of complex mutational phenomena in human cancers
inferred← citeshttps://doi.org/10.1093/bioinformatics/btad719openalex-snapshot
ReConPlot: an R package for the visualization and interpretation of genomic rearrangements
inferred← citeshttps://doi.org/10.1093/gigascience/giac128openalex-snapshot
A molecular phenotypic map of malignant pleural mesothelioma
inferred← citeshttps://doi.org/10.1097/pas.0000000000002229openalex-snapshot
Genomic Catastrophe (Chromothripsis and Polyploidy) Correlates With Tumor Distribution in Extrauterine High-grade Serous Carcinoma
inferred← citeshttps://doi.org/10.1101/163907openalex-snapshot
A user’s guide to the online resources for data exploration, visualization, and discovery for the Pan-Cancer Analysis of Whole Genomes project (PCAWG)
inferred← citeshttps://doi.org/10.1101/2019.12.18.881086openalex-snapshot
Revealing the impact of recurrent and rare structural variants in multiple myeloma
inferred← citeshttps://doi.org/10.1101/2022.05.03.490481openalex-snapshot
Genomic patterns of malignant peripheral nerve sheath tumour (MPNST) evolution correlate with clinical outcome and are detectable in cell-free DNA
inferred← citeshttps://doi.org/10.1101/2023.12.29.573403openalex-snapshot
Mechanisms Underpinning Osteosarcoma Genome Complexity and Evolution
inferred← citeshttps://doi.org/10.1101/546051openalex-snapshot
The genomic landscape of metastatic castration-resistant prostate cancers using whole genome sequencing reveals multiple distinct genotypes with potential clinical impact
inferred← citeshttps://doi.org/10.1101/566455openalex-snapshot
Genomic profiling of childhood tumor patient-derived xenograft models to enable rational clinical trial design
inferred← citeshttps://doi.org/10.1101/mcs.a003251openalex-snapshot
A case study of a long-term glioblastoma survivor with unmethylated MGMT and hypermutated genotype
inferred← citeshttps://doi.org/10.1111/cas.70159openalex-snapshot
Allelic Imbalance and Chromothripsis Lead to Diversity in Japanese Tumor Genomes With Whole‐Genome Duplication
inferred← citeshttps://doi.org/10.1111/his.14446openalex-snapshot
Unravelling undifferentiated soft tissue sarcomas: insights from genomics
inferred← citeshttps://doi.org/10.1111/his.14845openalex-snapshot
Molecular and immunohistochemical testing of bone tumours: review and update
inferred← citeshttps://doi.org/10.1111/jerd.12844openalex-snapshot
Applications of artificial intelligence in dentistry: A comprehensive review
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-1920openalex-snapshot
Chromothripsis in Human Breast Cancer
inferred← citeshttps://doi.org/10.1158/2159-8290.cd-25-2063openalex-snapshot
Immunologic Consequences of Genomic Instabilities
inferred← citeshttps://doi.org/10.11606/d.17.2019.tde-19022019-110314openalex-snapshot
Caracterização de alterações genômicas caóticas em osteossarcoma
inferred← citeshttps://doi.org/10.11606/t.17.2020.tde-14052020-090705openalex-snapshot
Caracterização de alterações genômicas caóticas em osteossarcoma
inferred← citeshttps://doi.org/10.1186/s12864-021-07739-3openalex-snapshot
Uphyloplot2: visualizing phylogenetic trees from single-cell RNA-seq data
inferred← citeshttps://doi.org/10.1186/s12911-026-03862-xopenalex-snapshot
MyeGPT: an AI agent for multiple myeloma
inferred← citeshttps://doi.org/10.1186/s12920-020-0729-7openalex-snapshot
ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer
inferred← citeshttps://doi.org/10.1186/s13073-018-0596-4openalex-snapshot
The ins and outs of telomere crisis in cancer
inferred← citeshttps://doi.org/10.14735/amko2019101openalex-snapshot
Chromothripsis – Extensive Chromosomal Rearrangements and Their Significance in Cancer
inferred← citeshttps://doi.org/10.15252/embj.2020104844openalex-snapshot
Centriolar distal appendages activate the centrosome‐PIDDosome‐p53 signalling axis via ANKRD26
inferred← citeshttps://doi.org/10.20892/j.issn.2095-3941.2020.0177openalex-snapshot
Evolving insights: how DNA repair pathways impact cancer evolution
inferred← citeshttps://doi.org/10.20944/preprints202401.0111.v1openalex-snapshot
Repair and misrepair of telomeric DNA in dynamic interactions with PML nuclear bodies and lamin B1. A gear-wheel nuclear traffic.
inferred← citeshttps://doi.org/10.20944/preprints202401.0111.v2openalex-snapshot
Repair and Misrepair of Telomeric DNA in Dynamic Interactions with PML Nuclear Bodies and Lamin B1. A Gear-Wheel Nuclear Traffic.
inferred← citeshttps://doi.org/10.21037/tlcr.2019.11.12openalex-snapshot
Chromosomal rearrangements and their neoantigenic potential in mesothelioma
inferred← citeshttps://doi.org/10.21203/rs.3.rs-11096418/v1openalex-snapshot
A transcriptomic readout of chromosomal instability reveals genome-stress states beyond proliferation in colorectal cancer
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1333557/v1openalex-snapshot
Extrachromosomal circular DNA harboring targeted tumor suppressor gene mutations supports intratumor heterogeneity in mouse liver cancer induced by multiplexed CRISPR/Cas9
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1354631/v1openalex-snapshot
Distinct Genomic Features Between Osteosarcomas Firstly Metastasing to Bone and to Lung
inferred← citeshttps://doi.org/10.21203/rs.3.rs-137969/v1openalex-snapshot
Development and Validation an Epigenetic Modification-related Signals for Diagnosis and Prognosis of Hepatocellular Carcinoma
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1396291/v1openalex-snapshot
Mutational topography reflects clinical neuroblastoma heterogeneity
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1813320/v1openalex-snapshot
Transmission Dynamics of Human Herpesvirus 6 and 7 from Whole Genome Sequences of Families
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3675752/v1openalex-snapshot
Whole genome sequencing refines stratification and therapy of patients with clear cell renal cell carcinoma
inferred← citeshttps://doi.org/10.21203/rs.3.rs-535468/v1openalex-snapshot
Mutational signatures of complex genomic rearrangements in human cancer
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8554974/v1openalex-snapshot
Age-dependent chromosomal instability in osteosarcoma: younger patients exhibit paradoxically higher genomic damage
inferred← citeshttps://doi.org/10.25236/ajets.2022.050207openalex-snapshot
Genome Sequencing and Drought Resistance Expression Analysis of Mulberry Hybrids
inferred← citeshttps://doi.org/10.32388/545bgmopenalex-snapshot
Darwin, Gödel, Luria, Delbrück: Biomedical, Mathematical, and Metamathematical Perspectives on Attributes and Consequences of Random Somatic Mutations Subject to Selection
inferred← citeshttps://doi.org/10.3390/cancers11081123openalex-snapshot
Interphase Cytogenetic Analysis of Micronucleated and Multinucleated Cells Supports the Premature Chromosome Condensation Hypothesis as the Mechanistic Origin of Chromothripsis
inferred← citeshttps://doi.org/10.3390/cancers13153778openalex-snapshot
Targeting BRF2 in Cancer Using Repurposed Drugs
inferred← citeshttps://doi.org/10.3390/genes10110865openalex-snapshot
The Many Faces of Gene Regulation in Cancer: A Computational Oncogenomics Outlook
inferred← citeshttps://doi.org/10.3390/ijms21072477openalex-snapshot
Extrachromosomal Circular DNA: Current Knowledge and Implications for CNS Aging and Neurodegeneration
inferred← citeshttps://doi.org/10.3390/jcm9030613openalex-snapshot
Chromothripsis and DNA Repair Disorders
inferred← citeshttps://doi.org/10.3410/f.735233641.793563131openalex-snapshot
Faculty Opinions recommendation of Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangements.
inferred← citeshttps://doi.org/10.3760/cma.j.issn.0253-2727.2021.07.017openalex-snapshot
[Progress in clonal evolution of multiple myeloma].
inferred← citeshttps://doi.org/10.3779/j.issn.1009-3419.2020.101.48openalex-snapshot
[Amplification of Extrachromosomal Oncogene and Tumorigenesis and Development].
inferred← citeshttps://doi.org/10.54254/2753-8818/32/20240802openalex-snapshot
Current research progress of whole genome sequencing in practical
inferred← citeshttps://doi.org/10.64898/2026.09.14.751472openalex-snapshot
Clustered structural variant hotspots enable oncogenic addiction and plasticity in osteosarcoma
inferred← citeshttps://doi.org/10.7150/jca.92844openalex-snapshot
Revisiting 'Hallmarks of Cancer' In Sarcomas
inferred← citeshttps://doi.org/10.7150/thno.81350openalex-snapshot
Chromothripsis is correlated with reduced cytotoxic immune infiltration and diminished responsiveness to checkpoint blockade immunotherapy
inferred← citeshttps://doi.org/10.7717/peerj.9294openalex-snapshot
Whole genome sequencing analysis identifies recurrent structural alterations in esophageal squamous cell carcinoma
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