ResearcherChinese Academy of Medical Sciences & Peking Union Medical CollegeActive in the last 2 years
Jiang Chang
Matched on ORCID iD 0000-0001-8551-9458; OpenAlex author ID A5006101921. Sources: OpenAlex.
Their work
- Papers
- 15 (first author 0, last author 2)
- Trials
- 0
- Grants
- 0
- Labs led
- 1
- Collaborators
- 39
2011: 1 paper · 2012: none · 2013: none · 2014: none · 2015: none · 2016: 2 papers · 2017: 1 paper · 2018: 1 paper · 2019: 3 papers · 2020: 2 papers · 2021: 2 papers · 2022: 2 papers · 2023: none · 2024: none · 2025: 1 paper
Papers 15
- 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↗
- Aberrant RNA Splicing Is a Primary Link between Genetic Variation and Pancreatic Cancer Risk. Co-author DOI 10.1158/0008-5472.can-21-4367↗
- Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese population. Last 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. Last author DOI 10.1002/cam4.2228↗
- A functional variant rs1537373 in 9p21.3 region is associated with pancreatic cancer risk. Co-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↗
- Pancreatic cancer risk variant in LINC00673 creates a miR-1231 binding site and interferes with PTPN11 degradation. Co-author DOI 10.1038/ng.3568↗
- 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↗
- Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations. Co-author DOI 10.1038/ng.1020↗
Closest collaborators
The 25 strongest of 39 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Jianbo Tian · 13 shared papers, 2016–2025 · strength 1.22
- 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↗
- Xiaoping Miao · 14 shared papers, 2011–2025 · strength 1.20
- 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↗
- Rong Zhong · 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↗
- Pingting Ying · 8 shared papers, 2019–2022 · strength 0.79
- 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 Aberrant RNA Splicing Is a Primary Link between Genetic Variation and Pancreatic Cancer Risk. DOI 10.1158/0008-5472.can-21-4367↗
- Juntao Ke · 8 shared papers, 2016–2025 · strength 0.67
- 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↗
- Ming Zhang · 4 shared papers, 2019–2022 · strength 0.40
- 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 Aberrant RNA Splicing Is a Primary Link between Genetic Variation and Pancreatic Cancer Risk. DOI 10.1158/0008-5472.can-21-4367↗
- Paper N6-methyladenosine mRNA methylation of PIK3CB regulates AKT signalling to promote PTEN-deficient pancreatic cancer prog… DOI 10.1136/gutjnl-2019-320179↗
- Chen Hsuan Wu · 4 shared papers, 2011–2025 · 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 Pancreatic cancer risk variant in LINC00673 creates a miR-1231 binding site and interferes with PTPN11 degradation. DOI 10.1038/ng.3568↗
- Dongxin Lin · 4 shared papers, 2011–2025 · 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 Pancreatic cancer risk variant in LINC00673 creates a miR-1231 binding site and interferes with PTPN11 degradation. DOI 10.1038/ng.3568↗
- 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↗
- Beibei Zhu · 3 shared papers, 2016–2025 · strength 0.29
- 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 A single nucleotide polymorphism in the 3'-UTR of STAT3 regulates its expression and reduces risk of pancreatic cancer … DOI 10.18632/oncotarget.11607↗
- 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↗
- Ying Zhu · 2 shared papers, 2022 · strength 0.24
- Bin Li · 2 shared papers, 2019–2021 · strength 0.17
- Zhiyong Yang · 1 shared paper, 2022 · strength 0.11
- Min Wang · 1 shared paper, 2022 · strength 0.11
- Beibei Zhu · 1 shared paper, 2019 · strength 0.08
- Xiaoping Miao · 1 shared paper, 2019 · strength 0.08
- Chaohui Zuo · 2 shared papers, 2011–2016 · strength 0.06
- Xu Che · 2 shared papers, 2011–2016 · strength 0.06
- Dianke Yu · 2 shared papers, 2011–2016 · strength 0.06
- Guoliang Jiang · 2 shared papers, 2011–2016 · strength 0.06
- Chengfeng Wang · 2 shared papers, 2011–2016 · strength 0.06
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.