ResearcherUniversity of California, Los AngelesActive in the last 2 years
Takayuki Shimizu
Matched on ORCID iD 0000-0002-2727-842X; OpenAlex author ID A5005900553. Sources: OpenAlex.
Their work
- Papers
- 8
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 29
2015: 1 paper · 2016: none · 2017: none · 2018: none · 2019: 1 paper · 2020: none · 2021: 4 papers · 2022: none · 2023: none · 2024: 1 paper · 2025: none · 2026: 1 paper
Papers 8
- Neoadjuvant stereotactic body vs conventionally fractionated radiation therapy for borderline resectable and locally advanced pancreatic cancer: a propensity s… Co-author DOI 10.1016/j.gassur.2026.102358↗
- Clinical and pathological factors associated with survival in patients with pancreatic cancer who receive adjuvant therapy after neoadjuvant therapy: A retrosp… Co-author DOI 10.1016/j.surg.2024.01.008↗
- Impact of adverse events of adjuvant and neoadjuvant chemotherapies on outcomes of patients with pancreatic ductal adenocarcinoma. Co-author DOI 10.1007/s00280-021-04267-5↗
- Predictors of Poor Pathological Response to Neoadjuvant Gemcitabine Plus S-1 Chemotherapy in Patients With Pancreatic Ductal Adenocarcinoma. Co-author DOI 10.1097/mpa.0000000000001826↗
- Efficacy of Adjuvant Chemotherapy According to the Pathological Response to Neoadjuvant Chemotherapy Among Patients With Pancreatic Ductal Adenocarcinoma. Co-author DOI 10.21873/anticanres.14925↗
- Clinical Predictors of Unresectable Disease at Laparotomy in Patients With Pancreatic Ductal Adenocarcinoma Planning to Undergo Surgical Resection. Co-author DOI 10.21873/anticanres.15335↗
- Clinical Significance of Neoadjuvant Chemotherapy With Gemcitabine Plus S-1 for Resectable Pancreatic Ductal Adenocarcinoma. Co-author DOI 10.21873/invivo.11700↗
- Randomized clinical trial of adjuvant chemotherapy with S-1 versus gemcitabine after pancreatic cancer resection. Co-author DOI 10.1002/bjs.9775↗
Closest collaborators
The 25 strongest of 29 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Keiichi Kubota · 6 shared papers, 2015–2021 · strength 0.67
- Paper Impact of adverse events of adjuvant and neoadjuvant chemotherapies on outcomes of patients with pancreatic ductal aden… DOI 10.1007/s00280-021-04267-5↗
- Paper Predictors of Poor Pathological Response to Neoadjuvant Gemcitabine Plus S-1 Chemotherapy in Patients With Pancreatic D… DOI 10.1097/mpa.0000000000001826↗
- Paper Efficacy of Adjuvant Chemotherapy According to the Pathological Response to Neoadjuvant Chemotherapy Among Patients Wit… DOI 10.21873/anticanres.14925↗
- Taku Aoki · 5 shared papers, 2019–2021 · strength 0.60
- Paper Impact of adverse events of adjuvant and neoadjuvant chemotherapies on outcomes of patients with pancreatic ductal aden… DOI 10.1007/s00280-021-04267-5↗
- Paper Predictors of Poor Pathological Response to Neoadjuvant Gemcitabine Plus S-1 Chemotherapy in Patients With Pancreatic D… DOI 10.1097/mpa.0000000000001826↗
- Paper Efficacy of Adjuvant Chemotherapy According to the Pathological Response to Neoadjuvant Chemotherapy Among Patients Wit… DOI 10.21873/anticanres.14925↗
- Shozo Mori · 5 shared papers, 2019–2021 · strength 0.60
- Paper Impact of adverse events of adjuvant and neoadjuvant chemotherapies on outcomes of patients with pancreatic ductal aden… DOI 10.1007/s00280-021-04267-5↗
- Paper Predictors of Poor Pathological Response to Neoadjuvant Gemcitabine Plus S-1 Chemotherapy in Patients With Pancreatic D… DOI 10.1097/mpa.0000000000001826↗
- Paper Efficacy of Adjuvant Chemotherapy According to the Pathological Response to Neoadjuvant Chemotherapy Among Patients Wit… DOI 10.21873/anticanres.14925↗
- Takatsugu Matsumoto · 4 shared papers, 2021 · strength 0.51
- Paper Impact of adverse events of adjuvant and neoadjuvant chemotherapies on outcomes of patients with pancreatic ductal aden… DOI 10.1007/s00280-021-04267-5↗
- Paper Predictors of Poor Pathological Response to Neoadjuvant Gemcitabine Plus S-1 Chemotherapy in Patients With Pancreatic D… DOI 10.1097/mpa.0000000000001826↗
- Paper Efficacy of Adjuvant Chemotherapy According to the Pathological Response to Neoadjuvant Chemotherapy Among Patients Wit… DOI 10.21873/anticanres.14925↗
- Timothy R. Donahue · 2 shared papers, 2024–2026 · strength 0.39
- Paper Neoadjuvant stereotactic body vs conventionally fractionated radiation therapy for borderline resectable and locally ad… DOI 10.1016/j.gassur.2026.102358↗
- Paper Clinical and pathological factors associated with survival in patients with pancreatic cancer who receive adjuvant ther… DOI 10.1016/j.surg.2024.01.008↗
- Zev A. Wainberg · 2 shared papers, 2024–2026 · strength 0.39
- Paper Neoadjuvant stereotactic body vs conventionally fractionated radiation therapy for borderline resectable and locally ad… DOI 10.1016/j.gassur.2026.102358↗
- Paper Clinical and pathological factors associated with survival in patients with pancreatic cancer who receive adjuvant ther… DOI 10.1016/j.surg.2024.01.008↗
- Shimpei Maeda · 2 shared papers, 2024–2026 · strength 0.39
- Paper Neoadjuvant stereotactic body vs conventionally fractionated radiation therapy for borderline resectable and locally ad… DOI 10.1016/j.gassur.2026.102358↗
- Paper Clinical and pathological factors associated with survival in patients with pancreatic cancer who receive adjuvant ther… DOI 10.1016/j.surg.2024.01.008↗
- Jason M. Link · 2 shared papers, 2024–2026 · strength 0.39
- Paper Neoadjuvant stereotactic body vs conventionally fractionated radiation therapy for borderline resectable and locally ad… DOI 10.1016/j.gassur.2026.102358↗
- Paper Clinical and pathological factors associated with survival in patients with pancreatic cancer who receive adjuvant ther… DOI 10.1016/j.surg.2024.01.008↗
- Keith D. Lillemoe · 2 shared papers, 2024–2026 · strength 0.39
- Paper Neoadjuvant stereotactic body vs conventionally fractionated radiation therapy for borderline resectable and locally ad… DOI 10.1016/j.gassur.2026.102358↗
- Paper Clinical and pathological factors associated with survival in patients with pancreatic cancer who receive adjuvant ther… DOI 10.1016/j.surg.2024.01.008↗
- William Reece Burns · 1 shared paper, 2026 · strength 0.23
- Theodore Sunki Hong · 1 shared paper, 2026 · strength 0.23
- Carlos Fernández-del Castillo · 1 shared paper, 2026 · strength 0.23
- Jin He · 1 shared paper, 2026 · strength 0.23
- Motaz Qadan · 1 shared paper, 2026 · strength 0.23
- Jonathan C. King · 1 shared paper, 2026 · strength 0.23
- Jennifer Yon-Li Wo · 1 shared paper, 2026 · strength 0.23
- Oscar Joe Hines · 1 shared paper, 2026 · strength 0.23
- Amol Kumar Narang · 1 shared paper, 2026 · strength 0.23
- Carlos F. Fernandez-del Castillo · 1 shared paper, 2024 · strength 0.17
- William R. Burns · 1 shared paper, 2024 · strength 0.17
- Joon Y. Park · 1 shared paper, 2024 · strength 0.17
- Mark D. Girgis MD · 1 shared paper, 2024 · strength 0.17
- Nikhil L. Chervu · 1 shared paper, 2024 · strength 0.17
- Jun Yu · 1 shared paper, 2024 · strength 0.17
- Christopher Lee Wolfgang · 1 shared paper, 2024 · strength 0.17
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.