Resume-aware faculty matching

Find professors who actually fit you

Upload your resume. Four AI agents analyze your background, rank the faculty who fit, inspect their recent research, and help you draft outreach — grounded in their actual work, not templates.

Free to startNo credit cardCancel anytime
Top matches Balanced preset
Dr. Sarah Chen
Stanford · Interpretability · NLP
91
Dr. Marcus Holloway
MIT · Robotics · RL
84
Dr. Aisha Okonkwo
CMU · Fairness · HCI
82
Nova · Professor Researcher · re-ranking top 20…
Amy E Baxter

Amy E Baxter

University of Pennsylvania · Rehabilitation Medicine

Active 1996–2024

h-index55
Citations14.9k
Papers132106 last 5y
Funding
See your match with Amy E Baxter — sign in to PhdFit.Sign in

About

Amy E Baxter, D.Phil, is a Research Assistant Professor of Systems Pharmacology and Translational Therapeutics at the University of Pennsylvania's Perelman School of Medicine. She serves as the Director of Research and Development in Immune Health within the Department of Systems Pharmacology and Translational Therapeutics. Her research expertise encompasses immune oncology, immunology, and virology, with a focus on understanding how the immune system responds to persistent threats such as chronic viral infections and tumor cells. Baxter's work aims to define immune diversity in large populations, investigating how immune health changes over time and how it impacts responses to cancer, infection, autoimmune conditions, and therapeutics. Her laboratory employs cutting-edge technologies to characterize immune responses, contributing to the advancement of immune health research.

Research topics

  • Immunology
  • Medicine
  • Biology
  • Virology
  • Pathology
  • Genetics
  • Computer Science
  • Internal medicine
  • Computational biology

Selected publications

  • Serotonin reduction in post-acute sequelae of viral infection

    Cell · 2023 · 352 citations

    • Biology
    • Virology
    • Immunology
  • Signaling Through FcγRIIA and the C5a-C5aR Pathway Mediate Platelet Hyperactivation in COVID-19

    Frontiers in Immunology · 2022 · 54 citations

    • Medicine
    • Immunology
    • Internal medicine

    platelet activation. Mechanistically, blocking the signaling of the FcγRIIa-Syk and C5a-C5aR pathways on platelets, using antibody-mediated neutralization, IgG depletion or the Syk inhibitor fostamatinib, reversed this hyperactivity driven by COVID-19 plasma and prevented platelet aggregation in endothelial microfluidic chamber conditions. These data identified these potentially actionable pathways as central for platelet activation and/or vascular complications and clinical outcomes in COVID-19 patients. In conclusion, we reveal a key role of platelet-mediated immunothrombosis in COVID-19 and identify distinct, clinically relevant, targetable signaling pathways that mediate this effect.

  • mRNA vaccines induce durable immune memory to SARS-CoV-2 and variants of concern

    Science · 2021 · 929 citations

    • Immunology
    • Biology
    • Virology

    T cell responses correlated with long-term humoral immunity. Recall responses to vaccination in individuals with preexisting immunity primarily increased antibody levels without substantially altering antibody decay rates. Together, these findings demonstrate robust cellular immune memory to SARS-CoV-2 and its variants for at least 6 months after mRNA vaccination.

  • CD8+ T cells contribute to survival in patients with COVID-19 and hematologic cancer

    Nature Medicine · 2021 · 512 citations

    • Medicine
    • Immunology
    • Internal medicine
  • Comprehensive mapping of immune perturbations associated with severe COVID-19

    Science Immunology · 2020 · 799 citations

    • Biology
    • Virology
    • Immunology

    Although critical illness has been associated with SARS-CoV-2-induced hyperinflammation, the immune correlates of severe COVID-19 remain unclear. Here, we comprehensively analyzed peripheral blood immune perturbations in 42 SARS-CoV-2 infected and recovered individuals. We identified extensive induction and activation of multiple immune lineages, including T cell activation, oligoclonal plasmablast expansion, and Fc and trafficking receptor modulation on innate lymphocytes and granulocytes, that distinguished severe COVID-19 cases from healthy donors or SARS-CoV-2-recovered or moderate severity patients. We found the neutrophil to lymphocyte ratio to be a prognostic biomarker of disease severity and organ failure. Our findings demonstrate broad innate and adaptive leukocyte perturbations that distinguish dysregulated host responses in severe SARS-CoV-2 infection and warrant therapeutic investigation.

  • Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications

    Science · 2020 · 1652 citations

    • Computer Science
    • Virology
    • Biology

    Immune profiling of COVID-19 patients Coronavirus disease 2019 (COVID-19) has affected millions of people globally, yet how the human immune system responds to and influences COVID-19 severity remains unclear. Mathew et al. present a comprehensive atlas of immune modulation associated with COVID-19. They performed high-dimensional flow cytometry of hospitalized COVID-19 patients and found three prominent and distinct immunotypes that are related to disease severity and clinical parameters. Arunachalam et al. report a systems biology approach to assess the immune system of COVID-19 patients with mild-to-severe disease. These studies provide a compendium of immune cell information and roadmaps for potential therapeutic interventions. Science , this issue p. eabc8511 , p. 1210

Frequent coauthors

Labs

  • Systems Pharmacology and Translational TherapeuticsPI

Education

  • D.Phil, Sir William Dunn School of Pathology

    University of Oxford

    2013
  • B.A. M.Sci, Natural Sciences (Biochemistry)

    University of Cambridge

    2009

Similar researchers at University of Pennsylvania

  • Resume-aware match score
  • Save to shortlist
  • AI-drafted outreach

See your match with Amy E Baxter

PhdFit ranks faculty by your research interests, methods, and publications — grounded in their actual work, not templates.

  • Free to start
  • No credit card
  • 30-second signup