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Highlights

  1. 1
    Nature biotechnology · 2022
    PMID: 35165384PMCID: PMC9232935DOISenior author95 citations
  2. 2
    Nature biotechnology · 2023
    PMID: 37563300PMCID: PMC11295146DOISenior author30 citations
  3. 3
    Cancer discovery · 2020
    PMID: 32792368PMCID: PMC7642097DOISenior author114 citations

Publications

107 publications

Active

8 grants
  • PI
    Mechanisms of genetic and non-genetic resistance to KRAS inhibition
    National Cancer Institute · 2025–2030
    R01CA297721-02
  • Sub-PI
    The Genetic Epidemiology of Radiation-Associated Contralateral Breast Cancer
    National Cancer Institute · 2026–2030 · via Memorial Sloan Kettering Cancer Center
    R01CA289804-02
  • MPI
    Defining the oncogenic potential and therapeutic dependencies of PDAC-associated KRAS variants
    National Cancer Institute · 2024–2029
    R01CA290616-02
  • KP
    Understanding Kras Mutation Heterogeneity in PDAC
    National Cancer Institute · 2024–2027Fellowship
    F31CA288132-01
  • PI
    Tumor selective inhibition of the WNT pathway
    National Cancer Institute · 2022–2027
    R01CA273106-03
  • PI
    Agmen SRA : Understanding WNT dependence in CRC
    Amgen Inc. · 2025–2027Contract
    SRA 250524-01
  • Sub-PI
    Biology of R-Spondin-Induced Sensitization to Asparaginase in Colorectal Cancer
    National Cancer Institute · 2021–2026 · via St. Jude Children's Research Hospital· 2 renewals
    R01CA249678-04
  • PI
    Defining the impact of Kras mutational heterogeneity on the tumor microenvironment in pancreatic cancer
    U.S. Department of Defense · 2023–2026
    HT9425-23-1-0728
Completed grants (23)
  • KP
    Interrogating the role of mutant KRAS allelic imbalance and co-mutated genes in targeted therapy response of NSCLC
    National Cancer Institute · 2021–2025Fellowship
    F31CA261061-01A1
  • Co-I
    Modeling Hepatoblastoma using pluripotent stem cell derived hepatocyte-like cells
    National Cancer Institute · 2019–2025
    R01CA234614-01A1
  • PI
    In Vivo Base Editing for Precision Oncology Models
    NCI · 2019–2025 · via NIH RePORTER
    R01CA229773-05
  • PI
    In Vivo Base Editing for Precision Oncology Models
    National Cancer Institute · 2019–2025
    5 R01C A229773-05
  • PI
    Identifying acquired vulnerabilities driven by lineage plasticity and drug resistance in CRC
    Starr Cancer Consortium · 2023–2024
    SCC I16-0062
  • KP
    Differential role of different NAD+ kinase Isoforms in melanoma metastasis
    National Cancer Institute · 2022–2024
    R01CA270885-01
  • KP
    Investigating the non-cell autonomous immune effects of mutant p53 in pancreatic cancer
    National Cancer Institute · 2021–2024
    K08CA241341-03
  • PI
    Revolution Medicines, Inc. Biopharma
    Revolution Medicines, Inc. · 2020–2024BioPharma Alliance
    RMI 212909-01
  • Co-I
    Targeting Genomic, Metabolic and Immunological Vulnerabilities of Colorectal Cancer
    American Association for Cancer Research · 2017–2024 · via Sloan-Kettering Institute for Cancer Research
    SU2C-AACR-DT22-17
  • PI
    Progression, response, and resistance of RSPO fusion colorectal cancer
    National Cancer Institute · 2018–2023
    R01CA222517-05
  • PI
    Defining the Genetic Determinants of Response to B-Catenin Blockade in CRC
    Fog Pharmaceuticals, Inc. · 2022–2023BioPharma Alliance
    BP 226002-01
  • PI
    Defining the cancer stem cell niche
    Starr Cancer Consortium · 2021–2022
    SCC I14-0023
  • KP
    Sensitizing Colorectal Cancer to Checkpoint Inhibitors by WNT Pathway Suppression
    National Cancer Institute · 2020–2022Fellowship
    F31CA247351-01
  • PI
    Tumor Dormancy and Therapy Resistance in RSPO Fusion CRC
    American Cancer Society · 2018–2021
    RSG-17-202-01-TBG
  • PI
    OVERCOMING OBSTACLES IN BASE EDITING WITH SYTHETIC GUIDE RNAs
    Synthego · 2019–2021
    SYN 194391-01
  • KP
    Targeting the WNT Pathway in Colorectal Cancer
    National Cancer Institute · 2017–2021Fellowship
    F31CA224800-02
  • Co-I
    Targeting the Epithelial to Mesenchymal Transition-Related Chemoresistance in Breast Cancer
    National Cancer Institute · 2016–2021
    R01CA205418-03
  • KP
    Propionate Metabolism as an Essential Metabolic Adaptation for Tumor Progression
    National Cancer Institute · 2017–2020Career
    K99CA218686-02
  • PI
    Targeting cancer-specific vulnerabilities in the WNT pathway
    Concern Foundation · 2018–2020
    CONCERN 194724-01
  • PI
    Investigating Cancer-Associated Structural Genomic Rearrangements Using in vivo Genome Editing
    Starr Cancer Consortium · 2017–2018
    SCC 17070948-01
  • PI
    Selective TNKS2 inhibition as a Collateral Vulnerability in Colorectal Cancer
    Daedalus Fund for Innovation (Weill Cornell) · 2017–2018
    DFI 180426-01
  • Sub-PI
    A scalable platform for target validation in GEMM models of gastrointestinalmalignancies.
    National Cancer Institute · 2015–2018 · via Sloan-Kettering Institute for Cancer Research
    R01CA195787-03
  • PI
    Defining the genetic requirements for maintenance of colorectal cancer
    NCI · 2014–2017 · via NIH RePORTER
    K22CA181280-03

Available technologies

News mentions

Show 1 more mention
  • Gene Editing Yields New Models for Studying Common Cancer Mutations
    August 12, 2020

    A new set of laboratory models designed to study variations in one of the most commonly mutated genes in cancer has revealed that each variation has a different effect on the colon and pancreas, according to investigators at Weill Cornell Medicine. The models also provide a new platform for screening potential therapies.

Media highlights

1 clip
11 PhD students · 4 Postdocs

External relationships

Other

Revolution Medicines, Inc.