Pancreatic Cancer Research

ResearcherJohns Hopkins UniversityActive in the last 2 years

Jacquelyn W. Zimmerman

Matched on ORCID iD 0000-0002-7775-2943; OpenAlex author ID A5016005335. Sources: OpenAlex.

Their work

Papers
17 (first author 3, last author 4)
Trials
0
Grants
0
Labs led
1
Collaborators
84
Papers, trials and grants by year

2020: 3 papers · 2021: 1 paper · 2022: 3 papers · 2023: 2 papers · 2024: 3 papers · 2025: 2 papers · 2026: 3 papers

Papers 17

  1. Patient-derived Organoid Pharmacotyping as a Predictive Tool for Therapeutic Selection in Pancreatic Ductal Adenocarcinoma. Co-author DOI 10.1097/sla.0000000000006517↗
  2. Complement-secreting CAFs are associated with better prognosis in pancreatic cancer: single-cell multiomics. Co-author DOI 10.1136/gutjnl-2025-335683↗
  3. Cancer-Associated Fibroblasts Promote Epithelial-Mesenchymal Transition and Classical to Basal Subtype Shift in Pancreatic Cancer. Last author DOI 10.1158/0008-5472.can-25-0331↗
  4. CD137 agonism enhances anti-PD1 induced activation of expanded CD8+ T cell clones in a neoadjuvant pancreatic cancer clinical trial. Co-author DOI 10.1016/j.isci.2024.111569↗
  5. The tumour microenvironment in pancreatic cancer - new clinical challenges, but more opportunities. Co-author DOI 10.1038/s41571-025-01077-z↗
  6. Transfer Learning Reveals Cancer-Associated Fibroblasts Are Associated with Epithelial-Mesenchymal Transition and Inflammation in Cancer Cells in Pancreatic Du… Last author DOI 10.1158/0008-5472.can-23-1660↗
  7. Fibroblasts in the Aged Pancreas Drive Pancreatic Cancer Progression. Co-author DOI 10.1158/0008-5472.can-24-0086↗
  8. Mesothelin CAR T Cells Secreting Anti-FAP/Anti-CD3 Molecules Efficiently Target Pancreatic Adenocarcinoma and its Stroma. Co-author DOI 10.1158/1078-0432.ccr-23-3841↗
  9. Cancer-cell-derived sialylated IgG as a novel biomarker for predicting poor pathological response to neoadjuvant therapy and prognosis in pancreatic cancer. Co-author DOI 10.1097/js9.0000000000000200↗
  10. Morphology-guided transcriptomic analysis of human pancreatic cancer organoids reveals microenvironmental signals that enhance invasion. Co-author DOI 10.1172/jci162054↗
  11. Multi-omic analyses of changes in the tumor microenvironment of pancreatic adenocarcinoma following neoadjuvant treatment with anti-PD-1 therapy. Co-author DOI 10.1016/j.ccell.2022.10.001↗
  12. Inflammatory Signaling in Pancreatic Cancer Transfers Between a Single-cell RNA Sequencing Atlas and Co-Culture Last author DOI 10.1101/2022.07.14.500096↗
  13. Precision Medicine in Pancreatic Cancer: Patient-Derived Organoid Pharmacotyping Is a Predictive Biomarker of Clinical Treatment Response. First author DOI 10.1158/1078-0432.ccr-21-4165↗
  14. Implantation of a neoantigen-targeted hydrogel vaccine prevents recurrence of pancreatic adenocarcinoma after incomplete resection. Co-author DOI 10.1080/2162402x.2021.2001159↗
  15. Patient-derived Organoid Pharmacotyping is a Clinically Tractable Strategy for Precision Medicine in Pancreatic Cancer. First author DOI 10.1097/sla.0000000000004200↗
  16. Inhibition of miR-21 Regulates Mutant KRAS Effector Pathways and Intercepts Pancreatic Ductal Adenocarcinoma Development. Last author DOI 10.1158/1940-6207.capr-20-0053↗
  17. Modeling human pancreatic ductal adenocarcinoma for translational research: current options, challenges, and prospective directions. First author DOI 10.21037/apc-20-29↗

Closest collaborators

The 25 strongest of 84 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.

  1. Elizabeth M. Jaffee · 12 shared papers, 2020–2026 · strength 1.65
  2. Lei Zheng · 10 shared papers, 2021–2026 · strength 1.55
  3. Jin Peng He · 9 shared papers, 2020–2026 · strength 1.21
  4. Elana Judith Fertig · 8 shared papers, 2020–2026 · strength 1.19
  5. Richard Andrew Burkhart · 9 shared papers, 2020–2026 · strength 1.19
  6. Samantha R. Guinn · 7 shared papers, 2021–2026 · strength 1.07
  7. Reecha Suri · 6 shared papers, 2020–2024 · strength 0.73
  8. Jacob T. Mitchell · 5 shared papers, 2022–2026 · strength 0.71
  9. Christopher L. Wolfgang · 6 shared papers, 2021–2024 · strength 0.70
  10. Luciane Tsukamoto Kagohara · 5 shared papers, 2021–2026 · strength 0.70
  11. Toni T. Seppälä · 5 shared papers, 2020–2026 · strength 0.69
  12. Christopher R. Shubert · 4 shared papers, 2022–2026 · strength 0.68
  13. Kelly J. Lafaro · 4 shared papers, 2022–2026 · strength 0.68
  14. Robert A. Anders · 4 shared papers, 2020–2026 · strength 0.64
  15. Heng‐Chung Kung · 2 shared papers, 2025–2026 · strength 0.63
  16. Benedict Kinny‐Köster · 5 shared papers, 2022–2024 · strength 0.63
  17. Daniel J. Zabransky · 4 shared papers, 2021–2026 · strength 0.59
  18. David Tsai Ting · 5 shared papers, 2020–2024 · strength 0.58
  19. William Reece Burns · 3 shared papers, 2021–2026 · strength 0.52
  20. Won Jin Ho · 3 shared papers, 2021–2026 · strength 0.45
  21. David P. Ryan · 4 shared papers, 2020–2024 · strength 0.45
  22. Norman G. Nicolson · 2 shared papers, 2026 · strength 0.43
  23. Dimitrios N. Sidiropoulos · 3 shared papers, 2022–2025 · strength 0.41
  24. Laura DeLong Wood · 3 shared papers, 2022–2024 · strength 0.39
  25. Jun Yu · 3 shared papers, 2022–2024 · strength 0.38

How to reach this person

A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.