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Author Details
Full Name
Glenn S Cowley
Affiliation
Broad Institute of Harvard and MIT
ORCID
Career Start Year
1990
Papers
58
H Index
38
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37773632
Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma.
Clin Cancer Res
2023
35016204
Genetic barcoding systematically compares genes in del(5q) MDS and reveals a central role for CSNK1A1 in clonal expansion.
Blood Adv
2022
36329185
The methyltransferase domain of DNMT1 is an essential domain in acute myeloid leukemia independent of DNMT3A mutation.
Commun Biol
2022
32483149
A genome-wide gain-of-function screen identifies CDKN2C as a HBV host factor.
Nat Commun
2020
30664779
Small-molecule targeting of brachyury transcription factor addiction in chordoma.
Nat Med
2019
31070582
Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesis.
Elife
2019
31160565
Neuronal differentiation and cell-cycle programs mediate response to BET-bromodomain inhibition in MYC-driven medulloblastoma.
Nat Commun
2019
30373918
Cells Lacking the <i>RB1</i> Tumor Suppressor Gene Are Hyperdependent on Aurora B Kinase for Survival.
Cancer Discov
2019
29202477
CRISPR-Cas9 screen reveals a MYCN-amplified neuroblastoma dependency on EZH2.
J Clin Invest
2018
30181297
Reply to Haffner et al.: DNA hypomethylation renders tumors more immunogenic.
Proc Natl Acad Sci U S A
2018
30042095
Genome-wide screen identifies cullin-RING ligase machinery required for lenalidomide-dependent CRL4[CRBN] activity.
Blood
2018
28655788
PRMT1-Mediated Translation Regulation Is a Crucial Vulnerability of Cancer.
Cancer Res
2017
28436985
Functional screen of MSI2 interactors identifies an essential role for SYNCRIP in myeloid leukemia stem cells.
Nat Genet
2017
28396387
<i>PIK3CA</i> mutant tumors depend on oxoglutarate dehydrogenase.
Proc Natl Acad Sci U S A
2017
28178529
ATXN1L, CIC, and ETS Transcription Factors Modulate Sensitivity to MAPK Pathway Inhibition.
Cell Rep
2017
28177281
Copy-number and gene dependency analysis reveals partial copy loss of wild-type SF3B1 as a novel cancer vulnerability.
Elife
2017
29083409
Computational correction of copy number effect improves specificity of CRISPR-Cas9 essentiality screens in cancer cells.
Nat Genet
2017
28988802
A Community Challenge for Inferring Genetic Predictors of Gene Essentialities through Analysis of a Functional Screen of Cancer Cell Lines.
Cell Syst
2017
29203668
Epigenetic therapy activates type I interferon signaling in murine ovarian cancer to reduce immunosuppression and tumor burden.
Proc Natl Acad Sci U S A
2017
28753430
Defining a Cancer Dependency Map.
Cell
2017
28701475
HIF activation causes synthetic lethality between the <i>VHL</i> tumor suppressor and the <i>EZH1</i> histone methyltransferase.
Sci Transl Med
2017
27058663
Core Circadian Clock Genes Regulate Leukemia Stem Cells in AML.
Cell
2016
27329820
Integrated genetic and pharmacologic interrogation of rare cancers.
Nat Commun
2016
27260156
Genomic Copy Number Dictates a Gene-Independent Cell Response to CRISPR/Cas9 Targeting.
Cancer Discov
2016
26912360
MTAP deletion confers enhanced dependency on the PRMT5 arginine methyltransferase in cancer cells.
Science
2016
25535386
Synthetic lethal screening in the mammalian central nervous system identifies Gpx6 as a modulator of Huntington's disease.
Proc Natl Acad Sci U S A
2015
26351322
Combined Pan-RAF and MEK Inhibition Overcomes Multiple Resistance Mechanisms to Selective RAF Inhibitors.
Mol Cancer Ther
2015
26337082
Functional, chemical genomic, and super-enhancer screening identify sensitivity to cyclin D1/CDK4 pathway inhibition in Ewing sarcoma.
Oncotarget
2015
25848864
The receptor TREML4 amplifies TLR7-mediated signaling during antiviral responses and autoimmunity.
Nat Immunol
2015
25646658
Probing the virus host interaction in high containment: an approach using pooled short hairpin RNA.
Assay Drug Dev Technol
2015
25548173
Inducible RNAi in vivo reveals that the transcription factor BATF is required to initiate but not maintain CD8+ T-cell effector differentiation.
Proc Natl Acad Sci U S A
2015
23584476
Genome-wide functional screening identifies CDC37 as a crucial HSP90-cofactor for KIT oncogenic expression in gastrointestinal stromal tumors.
Oncogene
2014
25512523
Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma.
Proc Natl Acad Sci U S A
2014
24616378
Csnk1a1 inhibition has p53-dependent therapeutic efficacy in acute myeloid leukemia.
J Exp Med
2014
24516381
The master regulator of the cellular stress response (HSF1) is critical for orthopoxvirus infection.
PLoS Pathog
2014
24476824
In vivo discovery of immunotherapy targets in the tumour microenvironment.
Nature
2014
23288408
A genome-scale RNA interference screen implicates NF1 loss in resistance to RAF inhibition.
Cancer Discov
2013
24332042
SQSTM1 is a pathogenic target of 5q copy number gains in kidney cancer.
Cancer Cell
2013
23715154
Metabolic and functional genomic studies identify deoxythymidylate kinase as a target in LKB1-mutant lung cancer.
Cancer Discov
2013
23770013
In Vivo RNAi screening identifies a leukemia-specific dependence on integrin beta 3 signaling.
Cancer Cell
2013
23393090
(R)-2-hydroxyglutarate is sufficient to promote leukemogenesis and its effects are reversible.
Science
2013
22896676
Targeted tumor-penetrating siRNA nanocomplexes for credentialing the ovarian cancer oncogene ID4.
Sci Transl Med
2012
23245941
β-Catenin-driven cancers require a YAP1 transcriptional complex for survival and tumorigenesis.
Cell
2012
22863534
Gene sets identified with oncogene cooperativity analysis regulate in vivo growth and survival of leukemia stem cells.
Cell Stem Cell
2012
22901813
Cancer vulnerabilities unveiled by genomic loss.
Cell
2012
21760589
Functional genomics reveal that the serine synthesis pathway is essential in breast cancer.
Nature
2011
21548937
A comprehensive platform for highly multiplexed mammalian functional genetic screens.
BMC Genomics
2011
21746896
Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer.
Proc Natl Acad Sci U S A
2011
17114577
Reduced growth of Drosophila neurofibromatosis 1 mutants reflects a non-cell-autonomous requirement for GTPase-Activating Protein activity in larval neurons.
Genes Dev
2006
9919310
Genetic variation in the 3' untranslated region of the neurofibromatosis 1 gene: application to unequal allelic expression.
Somat Cell Mol Genet
1998
1 - 50 of 58
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Stephen J Elledge
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row(s) 1 - 30 of 30
Collaborators
David E Root
Broad Institute of Harvard and MIT
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Co-authored papers
17
Barbara A Weir
Janssen Research and Development LLC
Co-authored papers
16
Aviad Tsherniak
Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard
Co-authored papers
16
Francisca Vazquez
Broad Institute of MIT and Harvard
Co-authored papers
14
Benjamin L Ebert
Co-authored papers
10
Levi A Garraway
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Co-authored papers
9
Jesse S Boehm
Broad Institute of Harvard and MIT
Co-authored papers
7
Kimberly Stegmaier
Dana-Farber Cancer Institute
Co-authored papers
7
Todd R Golub
Broad Institute of MIT and Harvard
Co-authored papers
6
Rameen Beroukhim
Co-authored papers
5
Jill P Mesirov
University of California San Diego
Co-authored papers
4
Gregory V Kryukov
Co-authored papers
4
James E Bradner
Co-authored papers
4
Nir Hacohen
Broad Institute of MIT and Harvard
Co-authored papers
4
Charles W M Roberts
Co-authored papers
4
F??tima Al-Shahrour
Spanish National Cancer Research Centre (CNIO)
Co-authored papers
4
Pablo Tamayo
University of California San Diego
Co-authored papers
3
Travis I Zack
Co-authored papers
3
Gabriela Alexe
Dana-Farber Cancer Institute
Co-authored papers
3
Sangeeta N Bhatia
Brigham and Women's Hospital and Harvard Medical School
Co-authored papers
3
Sara Howell
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3
Federica Piccioni
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Jun Qi
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