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Author Details
Full Name
Ignaty Leshchiner
Affiliation
Broad Institute of Massachusetts Institute of Technology and Harvard
ORCID
Career Start Year
2008
Papers
53
H Index
28
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37916958
Allosteric PI3Kα Inhibition Overcomes On-target Resistance to Orthosteric Inhibitors Mediated by Secondary PIK3CA Mutations.
Cancer Discov
2024
36287227
Pirtobrutinib targets BTK C481S in ibrutinib-resistant CLL but second-site BTK mutations lead to resistance.
Blood Adv
2023
37808694
Germline mutations and developmental mosaicism underlying <i>EGFR</i>-mutant lung cancer.
medRxiv
2023
37024582
Genomic and transcriptomic analysis of checkpoint blockade response in advanced non-small cell lung cancer.
Nat Genet
2023
37081260
Inferring early genetic progression in cancers with unobtainable premalignant disease.
Nat Cancer
2023
37146250
Genetic events associated with venetoclax resistance in CLL identified by whole-exome sequencing of patient samples.
Blood
2023
36624313
Evolutionary history of transformation from chronic lymphocytic leukemia to Richter syndrome.
Nat Med
2023
35243413
Combined tumor and immune signals from genomes or transcriptomes predict outcomes of checkpoint inhibition in melanoma.
Cell Rep Med
2022
36215125
Clinical Efficacy and Whole-Exome Sequencing of Liquid Biopsies in a Phase IB/II Study of Bazedoxifene and Palbociclib in Advanced Hormone Receptor-Positive Breast Cancer.
Clin Cancer Res
2022
36359386
<i>osr1</i> Maintains Renal Progenitors and Regulates Podocyte Development by Promoting <i>wnt2ba</i> via the Antagonism of <i>hand2</i>.
Biomedicines
2022
34112698
Longitudinal Single-Cell Dynamics of Chromatin Accessibility and Mitochondrial Mutations in Chronic Lymphocytic Leukemia Mirror Disease History.
Cancer Discov
2021
33684943
Activation of the MAPK pathway mediates resistance to PI3K inhibitors in chronic lymphocytic leukemia.
Blood
2021
34496240
Molecular features of exceptional response to neoadjuvant anti-androgen therapy in high-risk localized prostate cancer.
Cell Rep
2021
34404686
Parallel Genomic Alterations of Antigen and Payload Targets Mediate Polyclonal Acquired Clinical Resistance to Sacituzumab Govitecan in Triple-Negative Breast Cancer.
Cancer Discov
2021
34750583
The RNA helicase Ddx21 controls Vegfc-driven developmental lymphangiogenesis by balancing endothelial cell ribosome biogenesis and p53 function.
Nat Cell Biol
2021
32442065
Genomic Profiling of Smoldering Multiple Myeloma Identifies Patients at a High Risk of Disease Progression.
J Clin Oncol
2020
32973110
The cationic amino acid exporter Slc7a7 is induced and vital in zebrafish tissue macrophages with sustained efferocytic activity.
J Cell Sci
2020
32938797
Distinct evolutionary paths in chronic lymphocytic leukemia during resistance to the graft-versus-leukemia effect.
Sci Transl Med
2020
31160420
Tfap2a is a novel gatekeeper of nephron differentiation during kidney development.
Development
2019
31745334
Author Correction: Liquid versus tissue biopsy for detecting acquired resistance and tumor heterogeneity in gastrointestinal cancers.
Nat Med
2019
31501609
Liquid versus tissue biopsy for detecting acquired resistance and tumor heterogeneity in gastrointestinal cancers.
Nat Med
2019
31543463
Mitochondrial Reprogramming Underlies Resistance to BCL-2 Inhibition in Lymphoid Malignancies.
Cancer Cell
2019
30712845
A Murine Model of Chronic Lymphocytic Leukemia Based on B Cell-Restricted Expression of Sf3b1 Mutation and Atm Deletion.
Cancer Cell
2019
31142838
Growth dynamics in naturally progressing chronic lymphocytic leukaemia.
Nature
2019
29713087
Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.
Nat Med
2018
30107175
Widespread Chromosomal Losses and Mitochondrial DNA Alterations as Genetic Drivers in Hürthle Cell Carcinoma.
Cancer Cell
2018
30131872
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery.
NPJ Genom Med
2018
30123863
Heterogeneity and Coexistence of T790M and T790 Wild-Type Resistant Subclones Drive Mixed Response to Third-Generation Epidermal Growth Factor Receptor Inhibitors in Lung Cancer.
JCO Precis Oncol
2018
29955181
Publisher Correction: Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.
Nat Med
2018
29955182
Author Correction: Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes.
Nat Med
2018
30262473
Comment on "DNA damage is a pervasive cause of sequencing errors, directly confounding variant identification".
Science
2018
29717118
Distinct mutational signatures characterize concurrent loss of polymerase proofreading and mismatch repair.
Nat Commun
2018
28034880
Polyclonal Secondary <i>FGFR2</i> Mutations Drive Acquired Resistance to FGFR Inhibition in Patients with FGFR2 Fusion-Positive Cholangiocarcinoma.
Cancer Discov
2017
29872714
Resolving the phylogenetic origin of glioblastoma via multifocal genomic analysis of pre-treatment and treatment-resistant autopsy specimens.
NPJ Precis Oncol
2017
28162975
Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma.
Cancer Cell
2017
29109393
Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors.
Nat Commun
2017
29259203
The evolutionary landscape of chronic lymphocytic leukemia treated with ibrutinib targeted therapy.
Nat Commun
2017
28825726
A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer.
Nat Genet
2017
28579318
The zebrafish kidney mutant zeppelin reveals that brca2/fancd1 is essential for pronephros development.
Dev Biol
2017
26698910
Resensitization to Crizotinib by the Lorlatinib ALK Resistance Mutation L1198F.
N Engl J Med
2016
26493744
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood.
Rheumatology (Oxford)
2016
27432961
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans.
Proc Natl Acad Sci U S A
2016
27432227
Molecular Mechanisms of Resistance to First- and Second-Generation ALK Inhibitors in ALK-Rearranged Lung Cancer.
Cancer Discov
2016
25341114
Summarizing polygenic risks for complex diseases in a clinical whole-genome report.
Genet Med
2015
26436107
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease.
Mol Genet Genomic Med
2015
26392535
Comprehensive assessment of cancer missense mutation clustering in protein structures.
Proc Natl Acad Sci U S A
2015
26192918
Paired exome analysis of Barrett's esophagus and adenocarcinoma.
Nat Genet
2015
24667040
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Genome Biol
2014
24130329
Rapid identification of kidney cyst mutations by whole exome sequencing in zebrafish.
Development
2013
22555591
Mutation mapping and identification by whole-genome sequencing.
Genome Res
2012
1 - 50 of 53
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Co-authored papers
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Massachusetts General Hospital
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Atanas Kamburov
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Co-authored papers
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Paz Polak
McGill University
Co-authored papers
6
Thomas J Kipps
University of California San Diego
Co-authored papers
5
Laura Z Rassenti
University of California San Diego
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5
Dora Dias-Santagata
Co-authored papers
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Shamil R Sunyaev
Harvard Medical School
Co-authored papers
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Matthew Meyerson
Broad Institute
Co-authored papers
5
François Aguet
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Mara Rosenberg
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Samuel S Freeman
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