ResearcherHuazhong University of Science and TechnologyActive in the last 2 years
Rong Zhong
Matched on ORCID iD 0000-0002-5060-895X; OpenAlex author ID A5063159905. Sources: OpenAlex.
Their work
- Papers
- 18 (first author 2, last author 1)
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 26
2013: 1 paper · 2014: 3 papers · 2015: 2 papers · 2016: 1 paper · 2017: 1 paper · 2018: 1 paper · 2019: 3 papers · 2020: 2 papers · 2021: 2 papers · 2022: 1 paper · 2023: none · 2024: none · 2025: 1 paper
Papers 18
- Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations. Co-author DOI 10.1038/s41467-025-58613-9↗
- Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis… Co-author DOI 10.1097/cm9.0000000000002180↗
- Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese population. Co-author DOI 10.1007/s00204-021-02978-5↗
- A genetic variant conferred high expression of CAV2 promotes pancreatic cancer progression and associates with poor prognosis. Co-author DOI 10.1016/j.ejca.2021.04.008↗
- Evaluation of polymorphisms in microRNA-binding sites and pancreatic cancer risk in Chinese population. Co-author DOI 10.1111/jcmm.14906↗
- N6-methyladenosine mRNA methylation of PIK3CB regulates AKT signalling to promote PTEN-deficient pancreatic cancer progression. Co-author DOI 10.1136/gutjnl-2019-320179↗
- A genetic variant in PIK3R1 is associated with pancreatic cancer survival in the Chinese population. Co-author DOI 10.1002/cam4.2228↗
- A functional variant rs1537373 in 9p21.3 region is associated with pancreatic cancer risk. Last author DOI 10.1002/mc.22968↗
- A functional variant in the boundary of a topological association domain is associated with pancreatic cancer risk. Co-author DOI 10.1002/mc.23077↗
- Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations. Co-author DOI 10.1038/s41467-018-06136-x↗
- BRCA1 missense polymorphisms are associated with poor prognosis of pancreatic cancer patients in a Chinese population. Co-author DOI 10.18632/oncotarget.16422↗
- A single nucleotide polymorphism in the 3'-UTR of STAT3 regulates its expression and reduces risk of pancreatic cancer in a Chinese population. Co-author DOI 10.18632/oncotarget.11607↗
- Genetic variants in the SWI/SNF complex and smoking collaborate to modify the risk of pancreatic cancer in a Chinese population. Co-author DOI 10.1002/mc.22140↗
- SF3A1 and pancreatic cancer: new evidence for the association of the spliceosome and cancer. Co-author DOI 10.18632/oncotarget.5647↗
- Non-linear dose-response relationship between cigarette smoking and pancreatic cancer risk: evidence from a meta-analysis of 42 observational studies. First author DOI 10.1016/j.ejca.2013.08.014↗
- Parity and pancreatic cancer risk: evidence from a meta-analysis of twenty epidemiologic studies. Co-author DOI 10.1038/srep05313↗
- [Association between pancreatic cancer risk and the interaction of U2AF65 gene polymorphisms and smoking]. Co-author PMID 25174478↗
- [Discussion on the strategy of prevention and control of pancreatic cancer]. First author PMID 24304947↗
Closest collaborators
The 25 strongest of 26 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Xiaoping Miao · 17 shared papers, 2013–2025 · strength 1.30
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD r… DOI 10.1097/cm9.0000000000002180↗
- Paper Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese popu… DOI 10.1007/s00204-021-02978-5↗
- Jianbo Tian · 12 shared papers, 2016–2025 · strength 1.12
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD r… DOI 10.1097/cm9.0000000000002180↗
- Paper Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese popu… DOI 10.1007/s00204-021-02978-5↗
- Jiang Chang · 12 shared papers, 2016–2025 · strength 1.12
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD r… DOI 10.1097/cm9.0000000000002180↗
- Paper Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese popu… DOI 10.1007/s00204-021-02978-5↗
- Ying Zhu · 11 shared papers, 2016–2025 · strength 0.99
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese popu… DOI 10.1007/s00204-021-02978-5↗
- Paper A genetic variant conferred high expression of CAV2 promotes pancreatic cancer progression and associates with poor pro… DOI 10.1016/j.ejca.2021.04.008↗
- Juntao Ke · 10 shared papers, 2014–2025 · strength 0.75
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Evaluation of polymorphisms in microRNA-binding sites and pancreatic cancer risk in Chinese population. DOI 10.1111/jcmm.14906↗
- Paper A functional variant rs1537373 in 9p21.3 region is associated with pancreatic cancer risk. DOI 10.1002/mc.22968↗
- Pingting Ying · 7 shared papers, 2019–2022 · strength 0.69
- Paper Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD r… DOI 10.1097/cm9.0000000000002180↗
- Paper Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese popu… DOI 10.1007/s00204-021-02978-5↗
- Paper A genetic variant conferred high expression of CAV2 promotes pancreatic cancer progression and associates with poor pro… DOI 10.1016/j.ejca.2021.04.008↗
- Beibei Zhu · 8 shared papers, 2014–2025 · strength 0.50
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese … DOI 10.1038/s41467-018-06136-x↗
- Paper [Association between pancreatic cancer risk and the interaction of U2AF65 gene polymorphisms and smoking]. PMID 25174478↗
- Kun Huang · 3 shared papers, 2017–2025 · strength 0.30
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese … DOI 10.1038/s41467-018-06136-x↗
- Paper BRCA1 missense polymorphisms are associated with poor prognosis of pancreatic cancer patients in a Chinese population. DOI 10.18632/oncotarget.16422↗
- Ming Zhang · 3 shared papers, 2019–2022 · strength 0.29
- Paper Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD r… DOI 10.1097/cm9.0000000000002180↗
- Paper N6-methyladenosine mRNA methylation of PIK3CB regulates AKT signalling to promote PTEN-deficient pancreatic cancer prog… DOI 10.1136/gutjnl-2019-320179↗
- Paper A genetic variant in PIK3R1 is associated with pancreatic cancer survival in the Chinese population. DOI 10.1002/cam4.2228↗
- Shufang Mei · 3 shared papers, 2019–2020 · strength 0.24
- Paper Evaluation of polymorphisms in microRNA-binding sites and pancreatic cancer risk in Chinese population. DOI 10.1111/jcmm.14906↗
- Paper A functional variant in the boundary of a topological association domain is associated with pancreatic cancer risk. DOI 10.1002/mc.23077↗
- Paper A genetic variant in PIK3R1 is associated with pancreatic cancer survival in the Chinese population. DOI 10.1002/cam4.2228↗
- Ming Yang · 2 shared papers, 2018–2025 · strength 0.24
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese … DOI 10.1038/s41467-018-06136-x↗
- Li Wang · 2 shared papers, 2018–2025 · strength 0.24
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese … DOI 10.1038/s41467-018-06136-x↗
- Chen Hsuan Wu · 2 shared papers, 2018–2025 · strength 0.24
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese … DOI 10.1038/s41467-018-06136-x↗
- Dongxin Lin · 2 shared papers, 2018–2025 · strength 0.24
- Paper Author Correction: Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic canc… DOI 10.1038/s41467-025-58613-9↗
- Paper Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese … DOI 10.1038/s41467-018-06136-x↗
- Bin Li · 2 shared papers, 2019–2021 · strength 0.17
- Li Zou · 4 shared papers, 2014–2015 · strength 0.16
- Paper SF3A1 and pancreatic cancer: new evidence for the association of the spliceosome and cancer. DOI 10.18632/oncotarget.5647↗
- Paper Parity and pancreatic cancer risk: evidence from a meta-analysis of twenty epidemiologic studies. DOI 10.1038/srep05313↗
- Paper Genetic variants in the SWI/SNF complex and smoking collaborate to modify the risk of pancreatic cancer in a Chinese po… DOI 10.1002/mc.22140↗
- Jing Tian · 3 shared papers, 2014–2015 · strength 0.13
- Paper [Association between pancreatic cancer risk and the interaction of U2AF65 gene polymorphisms and smoking]. PMID 25174478↗
- Paper SF3A1 and pancreatic cancer: new evidence for the association of the spliceosome and cancer. DOI 10.18632/oncotarget.5647↗
- Paper Genetic variants in the SWI/SNF complex and smoking collaborate to modify the risk of pancreatic cancer in a Chinese po… DOI 10.1002/mc.22140↗
- Yao Tian · 3 shared papers, 2014–2015 · strength 0.13
- Paper [Association between pancreatic cancer risk and the interaction of U2AF65 gene polymorphisms and smoking]. PMID 25174478↗
- Paper SF3A1 and pancreatic cancer: new evidence for the association of the spliceosome and cancer. DOI 10.18632/oncotarget.5647↗
- Paper Genetic variants in the SWI/SNF complex and smoking collaborate to modify the risk of pancreatic cancer in a Chinese po… DOI 10.1002/mc.22140↗
- Ying Zhu · 1 shared paper, 2022 · strength 0.13
- Li Wang · 2 shared papers, 2014–2015 · strength 0.09
- Beibei Zhu · 1 shared paper, 2019 · strength 0.08
- Xiaoping Miao · 1 shared paper, 2019 · strength 0.08
- Wei Chen · 2 shared papers, 2014 · strength 0.08
- Bei-bei Zhu · 1 shared paper, 2013 · strength 0.06
- Li Liu · 1 shared paper, 2015 · strength 0.04
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.