ResearcherBrighton and Sussex Medical SchoolActive in the last 2 years
Gordon A. Ferns
Matched on ORCID iD 0000-0002-0957-8349; OpenAlex author ID A5038854437. Sources: OpenAlex.
Their work
- Papers
- 11 (first author 1, last author 2)
- Trials
- 0
- Grants
- 0
- Labs led
- 1
- Collaborators
- 21
2017: 1 paper · 2018: 1 paper · 2019: 1 paper · 2020: none · 2021: 2 papers · 2022: 2 papers · 2023: 2 papers · 2024: 2 papers
Papers 11
- Microbiome as a biomarker and therapeutic target in pancreatic cancer. Co-author DOI 10.1186/s12866-023-03166-4↗
- Elucidating the Role of Pro-renin Receptors in Pancreatic Ductal Adenocarcinoma Progression: A Novel Therapeutic Target in Cancer Therapy. First author DOI 10.2174/0115680096279288231205105904↗
- Down regulation of Cathepsin W is associated with poor prognosis in pancreatic cancer. Co-author DOI 10.1038/s41598-023-42928-y↗
- Therapeutic Potential of Targeting Transforming Growth Factor-beta (TGF-β) and Programmed Death-ligand 1 (PD-L1) in Pancreatic Cancer. Co-author DOI 10.2174/0113894501264450231129042256↗
- Angiotensin-converting Enzyme Inhibitors and Angiotensin Receptor Blockers as Potential Therapeutic Options for Pancreatic Cancer. Last author DOI 10.2174/1568009622666220517104411↗
- Association of a Genetic Variant in the Cyclin-Dependent Kinase Inhibitor 2B with Risk of Pancreatic Cancer. Co-author DOI 10.52547/rbmb.11.2.336↗
- The therapeutic potential of renin-angiotensin system inhibitors in the treatment of pancreatic cancer. Co-author DOI 10.1016/j.lfs.2021.119118↗
- PNU-74654 enhanced the antiproliferative activity of gemcitabine via targeting Wnt/β-catenin Pathway in Pancreatic cancer Co-author DOI 10.21203/rs.3.rs-881431/v1↗
- Therapeutic potential of targeting the Wnt/β-catenin pathway in the treatment of pancreatic cancer. Co-author DOI 10.1002/jcb.27835↗
- Targeting the C-MET/HGF Signaling Pathway in Pancreatic Ductal Adenocarcinoma. Last author DOI 10.2174/1381612825666190110145855↗
- Targeting the Akt/PI3K Signaling Pathway as a Potential Therapeutic Strategy for the Treatment of Pancreatic Cancer. Co-author DOI 10.2174/0929867324666170206142658↗
Closest collaborators
The 21 strongest of 21 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Majid Khazaei · 8 shared papers, 2019–2024 · strength 1.15
- Paper Microbiome as a biomarker and therapeutic target in pancreatic cancer. DOI 10.1186/s12866-023-03166-4↗
- Paper Therapeutic Potential of Targeting Transforming Growth Factor-beta (TGF-β) and Programmed Death-ligand 1 (PD-L1) in Pan… DOI 10.2174/0113894501264450231129042256↗
- Paper Angiotensin-converting Enzyme Inhibitors and Angiotensin Receptor Blockers as Potential Therapeutic Options for Pancrea… DOI 10.2174/1568009622666220517104411↗
- Amir Avan · 7 shared papers, 2017–2024 · strength 0.84
- Paper Microbiome as a biomarker and therapeutic target in pancreatic cancer. DOI 10.1186/s12866-023-03166-4↗
- Paper Down regulation of Cathepsin W is associated with poor prognosis in pancreatic cancer. DOI 10.1038/s41598-023-42928-y↗
- Paper The therapeutic potential of renin-angiotensin system inhibitors in the treatment of pancreatic cancer. DOI 10.1016/j.lfs.2021.119118↗
- Ghazaleh Pourali · 3 shared papers, 2023–2024 · strength 0.50
- Paper Microbiome as a biomarker and therapeutic target in pancreatic cancer. DOI 10.1186/s12866-023-03166-4↗
- Paper Therapeutic Potential of Targeting Transforming Growth Factor-beta (TGF-β) and Programmed Death-ligand 1 (PD-L1) in Pan… DOI 10.2174/0113894501264450231129042256↗
- Paper Down regulation of Cathepsin W is associated with poor prognosis in pancreatic cancer. DOI 10.1038/s41598-023-42928-y↗
- Amir Avan · 3 shared papers, 2022–2023 · strength 0.49
- Paper Therapeutic Potential of Targeting Transforming Growth Factor-beta (TGF-β) and Programmed Death-ligand 1 (PD-L1) in Pan… DOI 10.2174/0113894501264450231129042256↗
- Paper Angiotensin-converting Enzyme Inhibitors and Angiotensin Receptor Blockers as Potential Therapeutic Options for Pancrea… DOI 10.2174/1568009622666220517104411↗
- Paper Association of a Genetic Variant in the Cyclin-Dependent Kinase Inhibitor 2B with Risk of Pancreatic Cancer. DOI 10.52547/rbmb.11.2.336↗
- Majid Ghayour‐Mobarhan · 3 shared papers, 2017–2024 · strength 0.40
- Paper Microbiome as a biomarker and therapeutic target in pancreatic cancer. DOI 10.1186/s12866-023-03166-4↗
- Paper Down regulation of Cathepsin W is associated with poor prognosis in pancreatic cancer. DOI 10.1038/s41598-023-42928-y↗
- Paper Targeting the Akt/PI3K Signaling Pathway as a Potential Therapeutic Strategy for the Treatment of Pancreatic Cancer. DOI 10.2174/0929867324666170206142658↗
- Mohsen Aliakbarian · 2 shared papers, 2022–2024 · strength 0.36
- Paper Elucidating the Role of Pro-renin Receptors in Pancreatic Ductal Adenocarcinoma Progression: A Novel Therapeutic Target… DOI 10.2174/0115680096279288231205105904↗
- Paper Association of a Genetic Variant in the Cyclin-Dependent Kinase Inhibitor 2B with Risk of Pancreatic Cancer. DOI 10.52547/rbmb.11.2.336↗
- Fatemeh Khojasteh‐Leylakoohi · 2 shared papers, 2022–2023 · strength 0.27
- Mohammad‐Hassan Arjmand · 1 shared paper, 2024 · strength 0.23
- Rozita Khodashahi · 1 shared paper, 2024 · strength 0.23
- Fereshteh Asgharzadeh · 1 shared paper, 2022 · strength 0.17
- Zahra Yousefli · 1 shared paper, 2023 · strength 0.14
- Alfred King-yin Lam · 1 shared paper, 2023 · strength 0.14
- Elisa Giovannetti · 1 shared paper, 2023 · strength 0.14
- Negar Khoshghamat · 1 shared paper, 2021 · strength 0.13
- Newsha Sardarzade · 1 shared paper, 2022 · strength 0.13
- Sajjad Sharifi · 1 shared paper, 2021 · strength 0.12
- Sadaf Ghanaatgar‐Kasbi · 1 shared paper, 2018 · strength 0.11
- Seyed Alireza Javadinia · 1 shared paper, 2019 · strength 0.09
- Mina Hosseini · 1 shared paper, 2017 · strength 0.07
- Mina Maftouh · 1 shared paper, 2017 · strength 0.07
- Safieh Ebrahimi · 1 shared paper, 2017 · strength 0.07
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.