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Sarah R. DiNapoli

Howard Hughes Medical Institute · US
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Area of research
Immunology · Oncology
Research interest
Research interests include CAR-T cell therapy research, Immunotherapy and Immune Responses, Immune Cell Function and Interaction, and HIV Research and Treatment.
h-index
18
citations
1,470
works
34
NIH funding
primary concept
email

Recent publications

TRBC2-targeting antibody–drug conjugates for the treatment of T cell cancers
Nature Cancer 2025cited by 1position: middledoi
TRBC1-targeting antibody–drug conjugates for the treatment of T cell cancers
Nature 2024cited by 41position: middledoi
Preclinical studies show that Co-STARs combine the advantages of chimeric antigen and T cell receptors for the treatment of tumors with low antigen densities
Science Translational Medicine 2024cited by 21position: middledoi
Hydrophobic interactions dominate the recognition of a KRAS G12V neoantigen
Nature Communications 2023cited by 25position: middledoi
Targeting a neoantigen derived from a common <i>TP53</i> mutation
Science 2021cited by 341position: middledoi
Targeting public neoantigens for cancer immunotherapy
Nature Cancer 2021cited by 176position: middledoi
Bispecific antibodies targeting mutant<i>RAS</i>neoantigens
Science Immunology 2021cited by 166position: middledoi
TCR β chain–directed bispecific antibodies for the treatment of T cell cancers
Science Translational Medicine 2021cited by 55position: middledoi
Structural engineering of chimeric antigen receptors targeting HLA-restricted neoantigens
Nature Communications 2021cited by 38position: middledoi
Author Correction: Targeting public neoantigens for cancer immunotherapy
Nature Cancer 2021cited by 3position: middledoi
Hallmarks of primate lentiviral immunodeficiency infection recapitulate loss of innate lymphoid cells
Nature Communications 2018cited by 34position: middledoi
Tissue-resident macrophages can contain replication-competent virus in antiretroviral-naive, SIV-infected Asian macaques
JCI Insight 2017cited by 68position: firstdoi
IL-21 and probiotic therapy improve Th17 frequencies, microbial translocation, and microbiome in ARV-treated, SIV-infected macaques
Mucosal Immunology 2015cited by 88position: middledoi
Synergy of Topical Toll-like Receptor 7 Agonist with Radiation and Low-Dose Cyclophosphamide in a Mouse Model of Cutaneous Breast Cancer
Clinical Cancer Research 2012cited by 152position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Alexander H. Pearlman · Howard Hughes Medical Institute7 papers (2021–2024)Maximilian F. Konig · Howard Hughes Medical Institute7 papers (2021–2024)Kenneth W. Kinzler · University of Baltimore7 papers (2021–2024)Brian J. Mog · Howard Hughes Medical Institute7 papers (2021–2024)Drew M. Pardoll · Bloomberg (United States)7 papers (2021–2024)Sandra B. Gabelli · Johns Hopkins Medicine7 papers (2021–2024)Chetan Bettegowda · Seattle University7 papers (2021–2024)Bert Vogelstein · Clinical Pharmacology of Miami7 papers (2021–2024)Emily Han-Chung Hsiue · Howard Hughes Medical Institute7 papers (2021–2024)Shibin Zhou · Bloomberg (United States)7 papers (2021–2024)Jacqueline Douglass · Howard Hughes Medical Institute7 papers (2021–2024)Nickolas Papadopoulos · Ludwig Cancer Research5 papers (2021–2024)Katharine M. Wright · Howard Hughes Medical Institute5 papers (2021–2024)Suman Paul · Johns Hopkins University5 papers (2021–2024)Michael S. Hwang · University of California, San Francisco5 papers (2021–2024)Michelle S. Miller · The University of Melbourne4 papers (2021–2024)P. Aitana Azurmendi · Howard Hughes Medical Institute4 papers (2021–2024)Jason M. Brenchley · University of Cape Town3 papers (2015–2018)Andrew D. Skora · Howard Hughes Medical Institute2 papers (2021–2021)Mirko Paiardini · Emory Healthcare2 papers (2015–2018)
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