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Radiation‐induced genomic instability in breast carcinomas of the Swedish hemangioma cohort

https://doi.org/10.1002/gcc.22757
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Radiobiology for the Radiologist
inferredcites →https://doi.org/10.1002/path.4299openalex-snapshot
Responses to ionizing radiation mediated by inflammatory mechanisms
inferredcites →https://doi.org/10.1007/s10555-013-9429-5openalex-snapshot
The detection and implication of genome instability in cancer
inferredcites →https://doi.org/10.1016/b978-0-12-035416-0.50009-4openalex-snapshot
Commentary to Thacker: A Consideration of the Mechanisms of Induction of Mutations in Mammalian Cells by Low Doses and Dose Rates of Ionizing Radiation
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.ctrv.2005.03.004openalex-snapshot
The controversial abscopal effect
inferredcites →https://doi.org/10.1016/j.jrras.2015.03.003openalex-snapshot
Targeted and non-targeted effects of ionizing radiation
inferredcites →https://doi.org/10.1016/j.molonc.2014.07.019openalex-snapshot
A tumor DNA complex aberration index is an independent predictor of survival in breast and ovarian cancer
inferredcites →https://doi.org/10.1016/j.mrfmmm.2009.04.009openalex-snapshot
Breast cancer risk among Swedish hemangioma patients and possible consequences of radiation-induced genomic instability
inferredcites →https://doi.org/10.1016/j.mrfmmm.2010.01.014openalex-snapshot
Manifestations and mechanisms of non-targeted effects of ionizing radiation
inferredcites →https://doi.org/10.1016/j.mrfmmm.2015.03.002openalex-snapshot
Breast cancer risk and possible mechanisms of radiation-induced genomic instability in the Swedish hemangioma cohort after reanalyzed dosimetry
inferredcites →https://doi.org/10.1016/j.mrrev.2018.06.004openalex-snapshot
Mutational game changer: Chromothripsis and its emerging relevance to cancer
inferredcites →https://doi.org/10.1016/j.radmeas.2018.05.013openalex-snapshot
Microdosimetry and nanodosimetry for internal emitters
inferredcites →https://doi.org/10.1038/nature11412openalex-snapshot
Comprehensive molecular portraits of human breast tumours
inferredcites →https://doi.org/10.1038/nature11935openalex-snapshot
Replication stress links structural and numerical cancer chromosomal instability
inferredcites →https://doi.org/10.1038/nature12369openalex-snapshot
Erratum: Corrigendum: Replication stress links structural and numerical cancer chromosomal instability
inferredcites →https://doi.org/10.1038/nrc2603openalex-snapshot
Radiation-induced bystander signalling in cancer therapy
inferredcites →https://doi.org/10.1038/sj.onc.1206988openalex-snapshot
Genomic instability and bystander effects: a historical perspective
inferredcites →https://doi.org/10.1054/bjoc.2001.1868openalex-snapshot
Excess breast cancer risk and the role of parity, age at first childbirth and exposure to radiation in infancy
inferredcites →https://doi.org/10.1056/nejm198911093211902openalex-snapshot
Mortality from Breast Cancer after Irradiation during Fluoroscopic Examinations in Patients Being Treated for Tuberculosis
inferredcites →https://doi.org/10.1073/pnas.1009843107openalex-snapshot
Allele-specific copy number analysis of tumors
inferredcites →https://doi.org/10.1080/09553008914550091openalex-snapshot
Increased Chromosome Aberration Levels in Cells from Mouse Fetuses after Zygote X-irradiation
inferredcites →https://doi.org/10.1093/annonc/mdr304openalex-snapshot
Strategies for subtypes—dealing with the diversity of breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2011
inferredcites →https://doi.org/10.1093/jnci/85.20.1679openalex-snapshot
Radiation-Induced Breast Cancer: Long-Term Follow-up of Radiation Therapy for Benign Breast Disease
inferredcites →https://doi.org/10.1093/rpd/ncq473openalex-snapshot
Breast cancer risk after radiation treatment at infancy: potential consequences of radiation-induced genomic instability
inferredcites →https://doi.org/10.1097/hp.0b013e3182082f12openalex-snapshot
RADIATION-INDUCED GENOMIC INSTABILITY
inferredcites →https://doi.org/10.1126/science.66.1699.84openalex-snapshot
Artificial Transmutation of the Gene
inferredcites →https://doi.org/10.1126/scitranslmed.3000611openalex-snapshot
Genomic Architecture Characterizes Tumor Progression Paths and Fate in Breast Cancer Patients
inferredcites →https://doi.org/10.1158/0008-5472.can-10-3604openalex-snapshot
Chromosomal Instability Confers Intrinsic Multidrug Resistance
inferredcites →https://doi.org/10.1186/1471-2164-13-591openalex-snapshot
Copynumber: Efficient algorithms for single- and multi-track copy number segmentation
inferredcites →https://doi.org/10.1186/1471-2164-15-579openalex-snapshot
Chromosome-breakage genomic instability and chromothripsis in breast cancer
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/10.1186/1748-717x-6-168openalex-snapshot
Significance of genomic instability in breast cancer in atomic bomb survivors: analysis of microarray-comparative genomic hybridization
inferredcites →https://doi.org/10.1186/1755-8794-5-54openalex-snapshot
An array CGH based genomic instability index (G2I) is predictive of clinical outcome in breast cancer and reveals a subset of tumors without lymph node involvement but with poor prognosis
inferredcites →https://doi.org/10.1186/bcr970openalex-snapshot
Radiation and breast cancer: a review of current evidence
inferredcites →https://doi.org/10.1186/gb-2007-8-10-r215openalex-snapshot
High-resolution aCGH and expression profiling identifies a novel genomic subtype of ER negative breast cancer
inferredcites →https://doi.org/10.1186/gb-2011-12-10-r108openalex-snapshot
Allele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneity
inferredcites →https://doi.org/10.1186/s13073-017-0442-0openalex-snapshot
The genomic road to invasion—examining the similarities and differences in the genomes of associated oral pre-cancer and cancer samples
inferredcites →https://doi.org/10.1667/0033-7587(2003)159[0567:nadeoe]2.0.co;2openalex-snapshot
Non-targeted and Delayed Effects of Exposure to Ionizing Radiation: I. Radiation-Induced Genomic Instability and Bystander EffectsIn Vitro
inferredcites →https://doi.org/10.1667/0033-7587(2003)159[0581:nadeoe]2.0.co;2openalex-snapshot
Non-targeted and Delayed Effects of Exposure to Ionizing Radiation: II. Radiation-Induced Genomic Instability and Bystander EffectsIn Vivo,Clastogenic Factors and Transgenerational Effects
inferredcites →https://doi.org/10.1667/rr13675.1openalex-snapshot
Linking the History of Radiation Biology to the Hallmarks of Cancer
inferredcites →https://doi.org/10.1667/rr3082openalex-snapshot
Incidence of Female Breast Cancer among Atomic Bomb Survivors, Hiroshima and Nagasaki, 1950–1990
inferredcites →https://doi.org/10.18632/oncotarget.7186openalex-snapshot
Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system
inferredcites →https://doi.org/10.2307/3577890openalex-snapshot
Frequent Chest X-Ray Fluoroscopy and Breast Cancer Incidence among Tuberculosis Patients in Massachusetts
inferredcites →https://doi.org/10.2307/3579454openalex-snapshot
Genomic Instability Induced by Ionizing Radiation
inferredcites →https://doi.org/10.2307/3580039openalex-snapshot
Breast Cancer Risk after Radiotherapy in Infancy: A Pooled Analysis of Two Swedish Cohorts of 17,202 Infants
inferredcites →https://doi.org/10.2307/3580153openalex-snapshot
Unexpected Sensitivity to the Induction of Mutations by Very Low Doses of Alpha-Particle Radiation: Evidence for a Bystander Effect
inferredcites →https://doi.org/10.3390/ijms140715059openalex-snapshot
Epigenetics Meets Radiation Biology as a New Approach in Cancer Treatment
inferredcites →https://doi.org/10.3892/ijo.21.2.337openalex-snapshot
Radiation-induced effects in unirradiated cells: A review and implications in cancer

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4679863openalex-extracted
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e34460openalex-snapshot
Mediation of radiation-induced bystander effect and epigenetic modification: The role of exosomes in cancer radioresistance
inferred← citeshttps://doi.org/10.1097/md.0000000000021719openalex-snapshot
Image quality and clinical usefulness of automatic tube current modulation technology in female chest computed tomography screening
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-1920openalex-snapshot
Chromothripsis in Human Breast Cancer
inferred← citeshttps://doi.org/10.1371/journal.pone.0235998openalex-snapshot
Replication stress and FOXM1 drive radiation induced genomic instability and cell transformation
inferred← citeshttps://doi.org/10.22038/ijbms.2023.71259.15482openalex-snapshot
Insights into the radiotherapy-induced deferentially expressed RNAs in colorectal cancer management.
inferred← citeshttps://doi.org/10.3390/ijms20194723openalex-snapshot
DNA Copy Number Variations as Markers of Mutagenic Impact
inferred← citeshttps://doi.org/10.3390/ijms24010794openalex-snapshot
Chromosomal Rearrangements and Chromothripsis: The Alternative End Generation Model
inferred← citeshttps://doi.org/10.66224/ijrr.24.1.37openalex-snapshot
Cell cycle dependent modulating effects of melatonin on radiation induced cytogenetic damages in lymphocytes of normal individuals and breast cancer patients
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