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Author Details

Gad Getz
Broad Institute of the Massachusetts Institute of Technology and Harvard
2000
332
157
PMIDPaper TitleJournal TitlePublished Year
37823831Combined Immunotherapy Improves Outcome for Replication-Repair-Deficient (RRD) High-Grade Glioma Failing Anti-PD-1 Monotherapy: A Report from the International RRD Consortium.Cancer Discov2024
37823831Combined Immunotherapy Improves Outcome for Replication-Repair-Deficient (RRD) High-Grade Glioma Failing Anti-PD-1 Monotherapy: A Report from the International RRD Consortium.Cancer Discov2024
37916958Allosteric PI3Kα Inhibition Overcomes On-target Resistance to Orthosteric Inhibitors Mediated by Secondary PIK3CA Mutations.Cancer Discov2024
37916958Allosteric PI3Kα Inhibition Overcomes On-target Resistance to Orthosteric Inhibitors Mediated by Secondary PIK3CA Mutations.Cancer Discov2024
36287227Pirtobrutinib targets BTK C481S in ibrutinib-resistant CLL but second-site BTK mutations lead to resistance.Blood Adv2023
36240479Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset.J Clin Oncol2023
36287227Pirtobrutinib targets BTK C481S in ibrutinib-resistant CLL but second-site BTK mutations lead to resistance.Blood Adv2023
35358998The immune microenvironment shapes transcriptional and genetic heterogeneity in chronic lymphocytic leukemia.Blood Adv2023
37938768Latent human herpesvirus 6 is reactivated in CAR T cells.Nature2023
38019104Clinical Outcomes and Evolution of Clonal Hematopoiesis in Patients with Newly Diagnosed Multiple Myeloma.Cancer Res Commun2023
37738974ZNF683 marks a CD8<sup>+</sup> T cell population associated with anti-tumor immunity following anti-PD-1 therapy for Richter syndrome.Cancer Cell2023
37653227Author Correction: Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling.Nat Biotechnol2023
37808694Germline mutations and developmental mosaicism underlying <i>EGFR</i>-mutant lung cancer.medRxiv2023
37577538Systematic characterization of therapeutic vulnerabilities in Multiple Myeloma with Amp1q reveals increased sensitivity to the combination of MCL1 and PI3K inhibitors.bioRxiv2023
37794034Genomic signatures of past and present chromosomal instability in Barrett's esophagus and early esophageal adenocarcinoma.Nat Commun2023
37474833Clonal origin of KMT2A wild-type lineage-switch leukemia following CAR-T cell and blinatumomab therapy.Nat Cancer2023
37407818Therapy-induced APOBEC3A drives evolution of persistent cancer cells.Nature2023
37024582Genomic and transcriptomic analysis of checkpoint blockade response in advanced non-small cell lung cancer.Nat Genet2023
37146250Genetic events associated with venetoclax resistance in CLL identified by whole-exome sequencing of patient samples.Blood2023
37081260Inferring early genetic progression in cancers with unobtainable premalignant disease.Nat Cancer2023
36821441TGF-β in the microenvironment induces a physiologically occurring immune-suppressive senescent state.Cell Rep2023
36702949Combined PD-1, BRAF and MEK inhibition in BRAF<sup>V600E</sup> colorectal cancer: a phase 2 trial.Nat Med2023
36697832Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.Nature2023
36697836Author Correction: The repertoire of mutational signatures in human cancer.Nature2023
37126021Efficacy of Nivolumab in Pediatric Cancers with High Mutation Burden and Mismatch Repair Deficiency.Clin Cancer Res2023
36624313Evolutionary history of transformation from chronic lymphocytic leukemia to Richter syndrome.Nat Med2023
36477267MinimuMM-seq: Genome Sequencing of Circulating Tumor Cells for Minimally Invasive Molecular Characterization of Multiple Myeloma Pathology.Cancer Discov2023
37053197Clinical Importance of the lncRNA NEAT1 in Cancer Patients Treated with Immune Checkpoint Inhibitors.Clin Cancer Res2023
36468984In Vivo Modeling of CLL Transformation to Richter Syndrome Reveals Convergent Evolutionary Paths and Therapeutic Vulnerabilities.Blood Cancer Discov2023
37535729<i>CXCL9:SPP1</i> macrophage polarity identifies a network of cellular programs that control human cancers.Science2023
37505099IGLV3-21R110 mutation has prognostic value in patients with treatment-naive chronic lymphocytic leukemia.Blood Adv2023
37808694Germline mutations and developmental mosaicism underlying <i>EGFR</i>-mutant lung cancer.medRxiv2023
38019104Clinical Outcomes and Evolution of Clonal Hematopoiesis in Patients with Newly Diagnosed Multiple Myeloma.Cancer Res Commun2023
37794034Genomic signatures of past and present chromosomal instability in Barrett's esophagus and early esophageal adenocarcinoma.Nat Commun2023
37653227Author Correction: Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling.Nat Biotechnol2023
37505099IGLV3-21R110 mutation has prognostic value in patients with treatment-naive chronic lymphocytic leukemia.Blood Adv2023
37738974ZNF683 marks a CD8<sup>+</sup> T cell population associated with anti-tumor immunity following anti-PD-1 therapy for Richter syndrome.Cancer Cell2023
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
37535729<i>CXCL9:SPP1</i> macrophage polarity identifies a network of cellular programs that control human cancers.Science2023
35358998The immune microenvironment shapes transcriptional and genetic heterogeneity in chronic lymphocytic leukemia.Blood Adv2023
37126021Efficacy of Nivolumab in Pediatric Cancers with High Mutation Burden and Mismatch Repair Deficiency.Clin Cancer Res2023
37024582Genomic and transcriptomic analysis of checkpoint blockade response in advanced non-small cell lung cancer.Nat Genet2023
37053197Clinical Importance of the lncRNA NEAT1 in Cancer Patients Treated with Immune Checkpoint Inhibitors.Clin Cancer Res2023
37081260Inferring early genetic progression in cancers with unobtainable premalignant disease.Nat Cancer2023
37146250Genetic events associated with venetoclax resistance in CLL identified by whole-exome sequencing of patient samples.Blood2023
37407818Therapy-induced APOBEC3A drives evolution of persistent cancer cells.Nature2023
37474833Clonal origin of KMT2A wild-type lineage-switch leukemia following CAR-T cell and blinatumomab therapy.Nat Cancer2023
36697832Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.Nature2023
36697836Author Correction: The repertoire of mutational signatures in human cancer.Nature2023
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Collaborators

Broad Institute
Co-authored papers 85
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Broad Institute of MIT and Harvard
Co-authored papers 64
Broad Institute of MIT and Harvard
Co-authored papers 57
Vanderbilt-Ingram Cancer Center, Vanderbilt University
Co-authored papers 55
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Co-authored papers 54
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Co-authored papers 50
Co-authored papers 49
Co-authored papers 49
The Broad Institute of Harvard and MIT
Co-authored papers 43
Co-authored papers 40
Co-authored papers 40
Dana-Farber Cancer Institute
Co-authored papers 37
Co-authored papers 36
Broad Institute of Massachusetts Institute of Technology and Harvard
Co-authored papers 35
Co-authored papers 33
Broad Institute of MIT and Harvard
Co-authored papers 28
Cystic Fibrosis Foundation
Co-authored papers 27
Co-authored papers 27
Broad Institute of Massachusetts Institute of Technology and Harvard
Co-authored papers 26
Co-authored papers 25
Broad Institute of MIT and Harvard
Co-authored papers 23
Co-authored papers 23
Broad Institute of MIT and Harvard, USA Dana-Farber Cancer Institute
Co-authored papers 22
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Co-authored papers 20
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Co-authored papers 19