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Author Details
Full Name
Alice H Berger
Affiliation
Fred Hutchinson Cancer Research Center
ORCID
Career Start Year
2005
Papers
38
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36712079
Somatic mutation but not aneuploidy differentiates lung cancer in never-smokers and smokers.
bioRxiv
2023
36712079
Somatic mutation but not aneuploidy differentiates lung cancer in never-smokers and smokers.
bioRxiv
2023
37396617
pgMAP: a pipeline to enable guide RNA read mapping from dual-targeting CRISPR screens.
ArXiv
2023
37396617
pgMAP: a pipeline to enable guide RNA read mapping from dual-targeting CRISPR screens.
ArXiv
2023
35058622
Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
35512219
All About That Ras: Novel Fusion Drives Ras Pathway Activation in Lung Cancer.
Clin Cancer Res
2022
35418694
Correction to: Oncogenic RIT1 mutations in lung adenocarcinoma.
Oncogene
2022
36258042
Author Correction: Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
35353015
Cell Painting predicts impact of lung cancer variants.
Mol Biol Cell
2022
36522653
Oncogenic KRAS alters splicing factor phosphorylation and alternative splicing in lung cancer.
BMC Cancer
2022
35058622
Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
35512219
All About That Ras: Novel Fusion Drives Ras Pathway Activation in Lung Cancer.
Clin Cancer Res
2022
35353015
Cell Painting predicts impact of lung cancer variants.
Mol Biol Cell
2022
35418694
Correction to: Oncogenic RIT1 mutations in lung adenocarcinoma.
Oncogene
2022
36522653
Oncogenic KRAS alters splicing factor phosphorylation and alternative splicing in lung cancer.
BMC Cancer
2022
36258042
Author Correction: Massively parallel phenotyping of coding variants in cancer with Perturb-seq.
Nat Biotechnol
2022
34373451
Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancer.
Nat Commun
2021
35419481
Genome-wide CRISPR screening reveals novel therapeutic targets in RIT1-driven lung cancer.
Mol Cell Oncol
2021
34236315
Loss of MGA repression mediated by an atypical polycomb complex promotes tumor progression and invasiveness.
Elife
2021
33626341
Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway.
Cell Rep
2021
33606973
CRISPR base editor screens identify variant function at scale.
Mol Cell
2021
34469736
Discovery of synthetic lethal and tumor suppressor paralog pairs in the human genome.
Cell Rep
2021
34846918
Multiomic characterization of oncogenic signaling mediated by wild-type and mutant RIT1.
Sci Signal
2021
34373451
Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancer.
Nat Commun
2021
35419481
Genome-wide CRISPR screening reveals novel therapeutic targets in RIT1-driven lung cancer.
Mol Cell Oncol
2021
33626341
Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway.
Cell Rep
2021
33606973
CRISPR base editor screens identify variant function at scale.
Mol Cell
2021
34469736
Discovery of synthetic lethal and tumor suppressor paralog pairs in the human genome.
Cell Rep
2021
34846918
Multiomic characterization of oncogenic signaling mediated by wild-type and mutant RIT1.
Sci Signal
2021
34236315
Loss of MGA repression mediated by an atypical polycomb complex promotes tumor progression and invasiveness.
Elife
2021
31911676
RNA isoform screens uncover the essentiality and tumor-suppressor activity of ultraconserved poison exons.
Nat Genet
2020
31911676
RNA isoform screens uncover the essentiality and tumor-suppressor activity of ultraconserved poison exons.
Nat Genet
2020
30475228
Compound haploinsufficiency of Dok2 and Dusp4 promotes lung tumorigenesis.
J Clin Invest
2019
31862013
Recommendations for the collection and use of multiplexed functional data for clinical variant interpretation.
Genome Med
2019
30475228
Compound haploinsufficiency of Dok2 and Dusp4 promotes lung tumorigenesis.
J Clin Invest
2019
31862013
Recommendations for the collection and use of multiplexed functional data for clinical variant interpretation.
Genome Med
2019
29625050
Oncogenic Signaling Pathways in The Cancer Genome Atlas.
Cell
2018
29625050
Oncogenic Signaling Pathways in The Cancer Genome Atlas.
Cell
2018
28522754
<i>MET</i> Exon 14 Mutation Encodes an Actionable Therapeutic Target in Lung Adenocarcinoma.
Cancer Res
2017
28522754
<i>MET</i> Exon 14 Mutation Encodes an Actionable Therapeutic Target in Lung Adenocarcinoma.
Cancer Res
2017
29195078
A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles.
Cell
2017
29232558
High-throughput Phenotyping of Lung Cancer Somatic Mutations.
Cancer Cell
2017
29232558
High-throughput Phenotyping of Lung Cancer Somatic Mutations.
Cancer Cell
2017
29195078
A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles.
Cell
2017
27158780
Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas.
Nat Genet
2016
27478040
High-throughput Phenotyping of Lung Cancer Somatic Mutations.
Cancer Cell
2016
27158780
Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas.
Nat Genet
2016
27882345
Institutional implementation of clinical tumor profiling on an unselected cancer population.
JCI Insight
2016
27882345
Institutional implementation of clinical tumor profiling on an unselected cancer population.
JCI Insight
2016
27478040
High-throughput Phenotyping of Lung Cancer Somatic Mutations.
Cancer Cell
2016
1 - 50 of 76
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