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Timing the Onset of Homologous Recombination Deficiency Before Cancer Diagnosis

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

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Radiological audit of interval breast cancers: Estimation of tumour growth rates

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Genomic Evolution of Breast Cancer Metastasis and Relapse

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Timing the Landmark Events in the Evolution of Clear Cell Renal Cell Cancer: TRACERx Renal

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Unscrambling cancer genomes via integrated analysis of structural variation and copy number

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The topography of mutational processes in breast cancer genomes

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Clock-like mutational processes in human somatic cells

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HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures

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Pan-cancer landscape of homologous recombination deficiency

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Tumour lineage shapes BRCA-mediated phenotypes

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The evolutionary history of 2,658 cancers

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Pan-cancer analysis of whole genomes

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Pan-cancer whole-genome comparison of primary and metastatic solid tumours

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Evolutionary histories of breast cancer and related clones

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Haplotype-aware analysis of somatic copy number variations from single-cell transcriptomes

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Preneoplastic stromal cells promote BRCA1-mediated breast tumorigenesis

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Genetic immune escape landscape in primary and metastatic cancer

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Accurate and sensitive mutational signature analysis with MuSiCal

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Luminal breast epithelial cells of BRCA1 or BRCA2 mutation carriers and noncarriers harbor common breast cancer copy number alterations

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Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study

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A practical framework and online tool for mutational signature analyses show intertissue variation and driver dependencies

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Inferring early genetic progression in cancers with unobtainable premalignant disease

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The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

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A decade of clinical development of PARP inhibitors in perspective

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Cancer Risk Estimates for BRCA1 Mutation Carriers Identified in a Risk Evaluation Program

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CIP2A is a prime synthetic-lethal target for BRCA-mutated cancers

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Characterization of Cancer Evolution Landscape Based on Accurate Detection of Somatic Mutations in Single Tumor Cells

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TNscope: Accurate Detection of Somatic Mutations with Haplotype-based Variant Candidate Detection and Machine Learning Filtering

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Aneuploidy and a deregulated DNA damage response suggest haploinsufficiency in breast tissues of BRCA2 mutation carriers

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Population sequencing data reveal a compendium of mutational processes in the human germ line

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Homologous Recombination Deficiency (HRD) Score Predicts Response to Platinum-Containing Neoadjuvant Chemotherapy in Patients with Triple-Negative Breast Cancer

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Timing somatic events in the evolution of cancer

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CellPhy: accurate and fast probabilistic inference of single-cell phylogenies from scDNA-seq data

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TBCRC 031: Randomized Phase II Study of Neoadjuvant Cisplatin Versus Doxorubicin-Cyclophosphamide in Germline BRCA Carriers With HER2-Negative Breast Cancer (the INFORM trial)

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Whole-genome-sequencing of triple negative breast cancers: a population study

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