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Author Details
Full Name
William C Hahn
Affiliation
Broad Institute of MIT and Harvard, USA Dana-Farber Cancer Institute
ORCID
Career Start Year
1987
Papers
349
H Index
124
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36459568
Spatially Resolved Single-Cell Assessment of Pancreatic Cancer Expression Subtypes Reveals Co-expressor Phenotypes and Extensive Intratumoral Heterogeneity.
Cancer Res
2023
37922313
Functional screening of amplification outlier oncogenes in organoid models of early tumorigenesis.
Cell Rep
2023
37612728
Partial gene suppression improves identification of cancer vulnerabilities when CRISPR-Cas9 knockout is pan-lethal.
Genome Biol
2023
37030295
USP9X mediates an acute adaptive response to MAPK suppression in pancreatic cancer but creates multiple actionable therapeutic vulnerabilities.
Cell Rep Med
2023
37024492
Mapping the landscape of genetic dependencies in chordoma.
Nat Commun
2023
36576405
A Ubiquitination Cascade Regulating the Integrated Stress Response and Survival in Carcinomas.
Cancer Discov
2023
36574667
Discovery of antibodies and cognate surface targets for ovarian cancer by surface profiling.
Proc Natl Acad Sci U S A
2023
37394429
An Atlas of Variant Effects to understand the genome at nucleotide resolution.
Genome Biol
2023
36747859
Compressed phenotypic screens for complex multicellular models and high-content assays.
bioRxiv
2023
36548402
Systematic Interrogation of Tumor Cell Resistance to Chimeric Antigen Receptor T-cell Therapy in Pancreatic Cancer.
Cancer Res
2023
37237081
Genome-scale functional genomics identify genes preferentially essential for multiple myeloma cells compared to other neoplasias.
Nat Cancer
2023
36989360
Aberrant cell state plasticity mediated by developmental reprogramming precedes colorectal cancer initiation.
Sci Adv
2023
36459568
Spatially Resolved Single-Cell Assessment of Pancreatic Cancer Expression Subtypes Reveals Co-expressor Phenotypes and Extensive Intratumoral Heterogeneity.
Cancer Res
2023
37612728
Partial gene suppression improves identification of cancer vulnerabilities when CRISPR-Cas9 knockout is pan-lethal.
Genome Biol
2023
37922313
Functional screening of amplification outlier oncogenes in organoid models of early tumorigenesis.
Cell Rep
2023
37394429
An Atlas of Variant Effects to understand the genome at nucleotide resolution.
Genome Biol
2023
37024492
Mapping the landscape of genetic dependencies in chordoma.
Nat Commun
2023
36989360
Aberrant cell state plasticity mediated by developmental reprogramming precedes colorectal cancer initiation.
Sci Adv
2023
37237081
Genome-scale functional genomics identify genes preferentially essential for multiple myeloma cells compared to other neoplasias.
Nat Cancer
2023
37030295
USP9X mediates an acute adaptive response to MAPK suppression in pancreatic cancer but creates multiple actionable therapeutic vulnerabilities.
Cell Rep Med
2023
36548402
Systematic Interrogation of Tumor Cell Resistance to Chimeric Antigen Receptor T-cell Therapy in Pancreatic Cancer.
Cancer Res
2023
36747859
Compressed phenotypic screens for complex multicellular models and high-content assays.
bioRxiv
2023
36576405
A Ubiquitination Cascade Regulating the Integrated Stress Response and Survival in Carcinomas.
Cancer Discov
2023
36574667
Discovery of antibodies and cognate surface targets for ovarian cancer by surface profiling.
Proc Natl Acad Sci U S A
2023
35058622
Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
36040810
VRK1 as a synthetic lethal target in VRK2 promoter-methylated cancers of the nervous system.
JCI Insight
2022
35831509
Structure-function analysis of the SHOC2-MRAS-PP1C holophosphatase complex.
Nature
2022
35437317
Phosphate dysregulation via the XPR1-KIDINS220 protein complex is a therapeutic vulnerability in ovarian cancer.
Nat Cancer
2022
35365656
Author Correction: Identification of ADAR1 adenosine deaminase dependency in a subset of cancer cells.
Nat Commun
2022
35550030
CREB5 reprograms FOXA1 nuclear interactions to promote resistance to androgen receptor-targeting therapies.
Elife
2022
36258042
Author Correction: Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
35058622
Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
35085500
Sparse dictionary learning recovers pleiotropy from human cell fitness screens.
Cell Syst
2022
35550030
CREB5 reprograms FOXA1 nuclear interactions to promote resistance to androgen receptor-targeting therapies.
Elife
2022
35437317
Phosphate dysregulation via the XPR1-KIDINS220 protein complex is a therapeutic vulnerability in ovarian cancer.
Nat Cancer
2022
35831509
Structure-function analysis of the SHOC2-MRAS-PP1C holophosphatase complex.
Nature
2022
35365656
Author Correction: Identification of ADAR1 adenosine deaminase dependency in a subset of cancer cells.
Nat Commun
2022
36040810
VRK1 as a synthetic lethal target in VRK2 promoter-methylated cancers of the nervous system.
JCI Insight
2022
36258042
Author Correction: Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
35085500
Sparse dictionary learning recovers pleiotropy from human cell fitness screens.
Cell Syst
2022
33406420
Functional Genomics Identify Distinct and Overlapping Genes Mediating Resistance to Different Classes of Heterobifunctional Degraders of Oncoproteins.
Cell Rep
2021
33753930
A first-generation pediatric cancer dependency map.
Nat Genet
2021
33534641
Predicting cell health phenotypes using image-based morphology profiling.
Mol Biol Cell
2021
33526449
A Leucine-Rich Repeat Protein Provides a SHOC2 the RAS Circuit: a Structure-Function Perspective.
Mol Cell Biol
2021
33785741
Reprogramming of the FOXA1 cistrome in treatment-emergent neuroendocrine prostate cancer.
Nat Commun
2021
34261517
Haplotype-resolved germline and somatic alterations in renal medullary carcinomas.
Genome Med
2021
34260938
Synthetic Lethal Interaction between the ESCRT Paralog Enzymes VPS4A and VPS4B in Cancers Harboring Loss of Chromosome 18q or 16q.
Cell Rep
2021
33926920
<i>FGFR2</i> Extracellular Domain In-Frame Deletions Are Therapeutically Targetable Genomic Alterations That Function as Oncogenic Drivers in Cholangiocarcinoma.
Cancer Discov
2021
33500573
Cancer research needs a better map.
Nature
2021
34320363
SMAD4 represses FOSL1 expression and pancreatic cancer metastatic colonization.
Cell Rep
2021
1 - 50 of 698
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Jill P Mesirov
University of California San Diego
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