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Author Details
Full Name
Robert K Bradley
Affiliation
Fred Hutchinson Cancer Research Center, University of Washington
ORCID
Career Start Year
1998
Papers
70
H Index
38
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36627445
RNA splicing dysregulation and the hallmarks of cancer.
Nat Rev Cancer
2023
37502871
DUX4 is a common driver of immune evasion and immunotherapy failure in metastatic cancers.
bioRxiv
2023
37137707
Recursive splicing discovery using lariats in total RNA sequencing.
Life Sci Alliance
2023
37166992
The proto-oncogene SRC phosphorylates cGAS to inhibit an antitumor immune response.
JCI Insight
2023
37396617
pgMAP: a pipeline to enable guide RNA read mapping from dual-targeting CRISPR screens.
ArXiv
2023
36563682
Modulation of RNA splicing enhances response to BCL2 inhibition in leukemia.
Cancer Cell
2023
35241838
Synthetic introns enable splicing factor mutation-dependent targeting of cancer cells.
Nat Biotechnol
2022
34861039
Coordinated missplicing of TMEM14C and ABCB7 causes ring sideroblast formation in SF3B1-mutant myelodysplastic syndrome.
Blood
2022
33473122
Short H2A histone variants are expressed in cancer.
Nat Commun
2021
33846634
Minor intron retention drives clonal hematopoietic disorders and diverse cancer predisposition.
Nat Genet
2021
33527899
Convergent organization of aberrant MYB complex controls oncogenic gene expression in acute myeloid leukemia.
Elife
2021
34880103
Nonsense-mediated mRNA decay uses complementary mechanisms to suppress mRNA and protein accumulation.
Life Sci Alliance
2021
34469736
Discovery of synthetic lethal and tumor suppressor paralog pairs in the human genome.
Cell Rep
2021
34568833
<i>ZBTB33</i> is mutated in clonal hematopoiesis and myelodysplastic syndromes and impacts RNA splicing.
Blood Cancer Discov
2021
34171309
Pharmacologic modulation of RNA splicing enhances anti-tumor immunity.
Cell
2021
34285073
Characterization of neoantigen-specific T cells in cancer resistant to immune checkpoint therapies.
Proc Natl Acad Sci U S A
2021
34373451
Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancer.
Nat Commun
2021
33404013
The origins and consequences of <i>UPF1</i> variants in pancreatic adenosquamous carcinoma.
Elife
2021
32559497
Altered RNA Splicing by Mutant p53 Activates Oncogenic RAS Signaling in Pancreatic Cancer.
Cancer Cell
2020
32001512
Recurrent SRSF2 mutations in MDS affect both splicing and NMD.
Genes Dev
2020
31961934
Rare and private spliceosomal gene mutations drive partial, complete, and dual phenocopies of hotspot alterations.
Blood
2020
31911676
RNA isoform screens uncover the essentiality and tumor-suppressor activity of ultraconserved poison exons.
Nat Genet
2020
32640014
Single-cell genomics reveals the genetic and molecular bases for escape from mutational epistasis in myeloid neoplasms.
Blood
2020
32278354
Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity.
Skelet Muscle
2020
30644821
Quantitative proteomics reveals key roles for post-transcriptional gene regulation in the molecular pathology of facioscapulohumeral muscular dystrophy.
Elife
2019
31327741
DUX4 Suppresses MHC Class I to Promote Cancer Immune Evasion and Resistance to Checkpoint Blockade.
Dev Cell
2019
31434678
RNA components of the spliceosome regulate tissue- and cancer-specific alternative splicing.
Genome Res
2019
31578525
Coordinated alterations in RNA splicing and epigenetic regulation drive leukaemogenesis.
Nature
2019
31597964
Spliceosomal disruption of the non-canonical BAF complex in cancer.
Nature
2019
30842218
The splicing factor U2AF1 contributes to cancer progression through a noncanonical role in translation regulation.
Genes Dev
2019
29681544
Dissecting the Contributions of Cooperating Gene Mutations to Cancer Phenotypes and Drug Responses with Patient-Derived iPSCs.
Stem Cell Reports
2018
30107174
Synthetic Lethal and Convergent Biological Effects of Cancer-Associated Spliceosomal Gene Mutations.
Cancer Cell
2018
30322915
Impaired hematopoiesis and leukemia development in mice with a conditional knock-in allele of a mutant splicing factor gene <i>U2af1</i>.
Proc Natl Acad Sci U S A
2018
30388411
Exon Junction Complex Shapes the Transcriptome by Repressing Recursive Splicing.
Mol Cell
2018
29666160
Most human introns are recognized via multiple and tissue-specific branchpoints.
Genes Dev
2018
27694897
Systematic and functional characterization of novel androgen receptor variants arising from alternative splicing in the ligand-binding domain.
Oncogene
2017
28669802
The RNA Surveillance Factor UPF1 Represses Myogenesis via Its E3Â Ubiquitin Ligase Activity.
Mol Cell
2017
28717044
Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.
Genes Dev
2017
27282250
RNA splicing factors as oncoproteins and tumour suppressors.
Nat Rev Cancer
2016
28171552
Model systems of DUX4 expression recapitulate the transcriptional profile of FSHD cells.
Hum Mol Genet
2016
27646533
Translational plasticity facilitates the accumulation of nonsense genetic variants in the human population.
Genome Res
2016
27776121
Wild-Type U2AF1 Antagonizes the Splicing Program Characteristic of U2AF1-Mutant Tumors and Is Required for Cell Survival.
PLoS Genet
2016
27151974
Spliceosomal gene mutations in myelodysplasia: molecular links to clonal abnormalities of hematopoiesis.
Genes Dev
2016
27270779
Erratum: Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins.
Nat Med
2016
27135740
Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins.
Nat Med
2016
25267526
U2AF1 mutations alter splice site recognition in hematological malignancies.
Genome Res
2015
28843286
Integrative Clinical Genomics of Advanced Prostate Cancer.
Cell
2015
26554309
Expression of androgen receptor splice variants in clinical breast cancers.
Oncotarget
2015
26113877
Widespread intron retention diversifies most cancer transcriptomes.
Genome Med
2015
25965569
SRSF2 Mutations Contribute to Myelodysplasia by Mutant-Specific Effects on Exon Recognition.
Cancer Cell
2015
1 - 50 of 70
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University of California berkeley
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Co-authored papers
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Joaquin Mateo
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