Tao Chen
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Also affiliated: Ningbo University (2024–2025); Tongji University (2006–2025); Beijing Tongren Hospital (2016); Fujian Medical University (2023); Apple (Israel) (2018); United States Food and Drug Administration (2025); Ministry of Education of the People's Republic of China (2018); Kyushu University (2001–2020); Harvard University (2016); Xidian University (2018); National University of Singapore (2019); City University of Hong Kong (2024–2025); Guangdong Medical College (2021); Second Military Medical University (2017); Zunyi Medical University (2019–2020); Shanghai Jiao Tong University (2025); Capital Medical University (2016); King's College London (2017); Chinese Center For Disease Control and Prevention (2012); Liverpool School of Tropical Medicine (2022); Chinese Academy of Medical Sciences & Peking Union Medical College (2011); Yichun University (2025); Southwestern University of Finance and Economics (2009); Sichuan University (2020–2025); Edinburgh Napier University (2012–2019); National Health and Family Planning Commission (2019); Diabetes Australia (2021); Chinese PLA General Hospital (2020–2024); Guangzhou Sport University (2025); Sichuan Agricultural University (2009); Haikou City People's Hospital (2014); West China Hospital of Sichuan University (2020–2025); Ganzhou People's Hospital (2024); Xinjiang Uygur Autonomous Region Disease Prevention and Control Center (2022); Jiangsu University of Science and Technology (2023–2024); Counseling Center (2020); 302 Military Hospital of China (2021); Gannan Medical University (2025); Changhai Hospital (2017); First Affiliated Hospital of Fujian Medical University (2023); First Affiliated Hospital of Xi'an Jiaotong University (2011–2019); Shanghai Pulmonary Hospital (2016–2025); State Council of the People's Republic of China (2019); Ningxia Medical University (2019); Hainan General Hospital (2014); Shanghai First People's Hospital (2025); Chinese Academy of Agricultural Sciences (2024); Sericultural Research Institute (2023–2025); People's Government of Shaanxi Province (2019); National Institute for Viral Disease Control and Prevention (2013–2019); Ministry of Education (2019); The First People's Hospital of Guiyang (2024); Ministry of Education (2019); Ministry of Agriculture and Rural Affairs (2024); Harvard Stem Cell Institute (2016); Second Affiliated Hospital of Zhejiang University (2021); Tongji Hospital (2020); Chinese People's Liberation Army (2020); Fu Wai Hospital (2009); Hainan 301 Hospital (2014); Affiliated Hospital of Zunyi Medical College (2019–2020); Dong-A University (2020); Chengdu University of Traditional Chinese Medicine (2022); Shandong Agricultural University (2019); University of Birmingham (2009); Xi'an Jiaotong University (2019); American College of Surgeons (2015)
Upstream record may be merged OpenAlex, the source of these figures, lists 68 institutions in 11 countries for this author record — a pattern that usually means it combines several researchers with similar names. The totals above may include work by other people.
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Tao Chen's research has investigated various aspects of human health, including susceptibility to exercise-induced muscle damage, determinants of cognitive performance and decline across diverse ethno-regional groups, and sex differences in dementia risk. Chen's work has also examined the relationship between sedentary behavior and metabolic syndrome in working adults. In addition, Chen has conducted studies on DNA adduct formation and mutation induction by aristolochic acid in animal models, and explored population aging, gender, and transportation systems.
Chen's scholarly contributions are reflected in a high-impact researcher designation, with a current h-index of 29, 151 total publications, and 2,729 citations. Key collaborators include Ying Chen, Robert H. Heflich, and Li Xia, all from the National Center for Toxicological Research, with whom Chen has co-authored multiple publications. Chen remains recently active, with the most recent publication listed as 2026.
Metrics
- h-index: 29
- Publications: 151
- Citations: 2,729
Selected Publications
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Key challenges for in vitro testing of tobacco and next generation products for regulatory applications: Recommendations for the Ames test (2026)
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N-nitroso-ethylisopropylamine mutagenicity in rat liver using the cII transgenic mutation assay and duplex sequencing analysis of genomic DNA (2025)
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Germline mutagenicity of molnupiravir and its active form, β-d-N4-hydroxycytidine, in Caenorhabditis elegans evaluated using whole-genome sequencing (2025)
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Integration of the rat liver micronucleus assay into a 28-day treatment protocol: testing the genotoxicity of 4 small-molecule nitrosamines with different carcinogenic potencies and tumor target specificities (2025)
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Application of duplex sequencing to evaluate mutagenicity of aristolochic acid and methapyrilene in Fisher 344 rats (2024)
Collaboration Network
Top Collaborators
- Integrated microRNA, mRNA, and protein expression profiling reveals microRNA regulatory networks in rat kidney treated with a carcinogenic dose of aristolochic acid
- Decrease of 5‐hydroxymethylcytosine in rat liver with subchronic exposure to genotoxic carcinogens riddelliine and aristolochic acid
- Application of duplex sequencing to evaluate mutagenicity of aristolochic acid and methapyrilene in Fisher 344 rats
- Evaluation of mutagenic susceptibility of different stages in germ cell development of Caenorhabditis elegans using whole genome sequencing
- Germline mutagenicity of molnupiravir and its active form, β-d-N4-hydroxycytidine, in Caenorhabditis elegans evaluated using whole-genome sequencing
Showing 5 of 8 shared publications
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- DNA adduct formation and mutation induction by aristolochic acid in rat kidney and liver
- Gene Expression Profiles Distinguish the Carcinogenic Effects of Aristolochic Acid in Target (Kidney) and Non-target (Liver) Tissues in Rats
- Aristolochic acid-induced genotoxicity and toxicogenomic changes in rodents
- Comparison of gene expression profiles altered by comfrey and riddelliine in rat liver
Showing 5 of 7 shared publications
- DNA adduct formation and mutation induction by aristolochic acid in rat kidney and liver
- Molecular analysis of in vivo mutations induced byN-ethyl-N-nitrosourea in the autosomalTk and the X-linkedHprt genes of mouse lymphocytes
- Differential mutagenicity of aflatoxin B1 in the liver of neonatal and adult mice
- Sequence specificity of Hprt lymphocyte mutation in rats fed the hepatocarcinogen 2-acetylaminofluorene
- N-nitroso-ethylisopropylamine mutagenicity in rat liver using the cII transgenic mutation assay and duplex sequencing analysis of genomic DNA
Showing 5 of 6 shared publications
- Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
- Integrated microRNA, mRNA, and protein expression profiling reveals microRNA regulatory networks in rat kidney treated with a carcinogenic dose of aristolochic acid
- Microarray platform consistency is revealed by biologically functional analysis of gene expression profiles
- Abstract LB-438: Proteomic analysis of aristolochic acid-induced nephrotoxicity in rats
- Expression of miR-34a is a sensitive biomarker for exposure to genotoxic agents in human lymphoblastoid TK6 cells
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
- Integrated microRNA, mRNA, and protein expression profiling reveals microRNA regulatory networks in rat kidney treated with a carcinogenic dose of aristolochic acid
- Microarray platform consistency is revealed by biologically functional analysis of gene expression profiles
- Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
- Gene Expression Profiles Distinguish the Carcinogenic Effects of Aristolochic Acid in Target (Kidney) and Non-target (Liver) Tissues in Rats
- Microarray platform consistency is revealed by biologically functional analysis of gene expression profiles
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- Gene Expression Profiles Distinguish the Carcinogenic Effects of Aristolochic Acid in Target (Kidney) and Non-target (Liver) Tissues in Rats
- Comparison of gene expression profiles altered by comfrey and riddelliine in rat liver
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- Gene Expression Profiles Distinguish the Carcinogenic Effects of Aristolochic Acid in Target (Kidney) and Non-target (Liver) Tissues in Rats
- Comparison of gene expression profiles altered by comfrey and riddelliine in rat liver
- Aristolochic acid-induced genotoxicity and toxicogenomic changes in rodents
- Mutagenicity and DNA adduct formation by aristolochic acid in the spleen of Big Blue® rats
- Integration of the rat liver micronucleus assay into a 28-day treatment protocol: testing the genotoxicity of 4 small-molecule nitrosamines with different carcinogenic potencies and tumor target specificities
- Integrated microRNA, mRNA, and protein expression profiling reveals microRNA regulatory networks in rat kidney treated with a carcinogenic dose of aristolochic acid
- Abstract LB-438: Proteomic analysis of aristolochic acid-induced nephrotoxicity in rats
- Differential mutagenicity of aflatoxin B1 in the liver of neonatal and adult mice
- Key challenges for in vitro testing of tobacco and next generation products for regulatory applications: Recommendations for the Ames test
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium
- Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
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