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Author Details

Nicholas J Haradhvala
2015
25
16
PMIDPaper TitleJournal TitlePublished Year
36697836Author Correction: The repertoire of mutational signatures in human cancer.Nature2023
37938768Latent human herpesvirus 6 is reactivated in CAR T cells.Nature2023
37577538Systematic characterization of therapeutic vulnerabilities in Multiple Myeloma with Amp1q reveals increased sensitivity to the combination of MCL1 and PI3K inhibitors.bioRxiv2023
36697832Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.Nature2023
35241837Designing sensitive viral diagnostics with machine learning.Nat Biotechnol2022
36097221Distinct cellular dynamics associated with response to CAR-T therapy for refractory B cell lymphoma.Nat Med2022
35418687CAR T cell killing requires the IFNγR pathway in solid but not liquid tumours.Nature2022
36396631Single cell characterization of myeloma and its precursor conditions reveals transcriptional signatures of early tumorigenesis.Nat Commun2022
36379208Immune biomarkers of response to immunotherapy in patients with high-risk smoldering myeloma.Cancer Cell2022
33355208DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells.Cancer Discov2021
34017125Inflammatory stromal cells in the myeloma microenvironment.Nat Immunol2021
33409501Single-cell RNA sequencing reveals compromised immune microenvironment in precursor stages of multiple myeloma.Nat Cancer2020
32025018The repertoire of mutational signatures in human cancer.Nature2020
32039742A post-transcriptional program of chemoresistance by AU-rich elements and TTP in quiescent leukemic cells.2020
30844029Analyzing Frequently Mutated Genes and the Association With Tumor Mutation Load.JAMA Oncol2019
31675989Scaling computational genomics to millions of individuals with GPUs.Genome Biol2019
31526759Passenger Hotspot Mutations in Cancer.Cancer Cell2019
31171663RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues.Science2019
29717118Distinct mutational signatures characterize concurrent loss of polymerase proofreading and mismatch repair.Nat Commun2018
30459213Quantification of somatic mutation flow across individual cell division events by lineage sequencing.Genome Res2018
29909985Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing.Cell2018
28892075Analysis of somatic microsatellite indels identifies driver events in human tumors.Nat Biotechnol2017
28825726A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer.Nat Genet2017
26806129Mutational Strand Asymmetries in Cancer Genomes Reveal Mechanisms of DNA Damage and Repair.Cell2016
26638776Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution.Nat Commun2015
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Broad Institute of Massachusetts Institute of Technology and Harvard
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Vanderbilt-Ingram Cancer Center, Vanderbilt University
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National Institute of Environmental Health Sciences (NIEHS)
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The Broad Institute of MIT and Harvard
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