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Peng Cheng

Observed names: Cheng Peng, Cheng, Peng, PENG CHENG
ORCID: 0000-0003-0716-8124
Observed ORCID: 0000-0003-0716-8124
OpenAlex ID: A5100700050
Three cases of congenital dysfibrinogenemia in unrelated Chinese families
2016 · Meiling Luo, Donghong Deng, et al. · Medicine · 99
Combined use of Clauss and prothrombin time‐derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia
2017 · Liqun Xiang, Meiling Luo, et al. · Journal of Clinical Laboratory Analysis · 47
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Key immune-related gene ITGB2 as a prognostic signature for acute myeloid leukemia
2021 · Jie Wei, Xun-Jun Huang, et al. · Annals of Translational Medicine · 38
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Dipetidyl peptidase-4 and transferrin receptor serve as prognostic biomarkers for acute myeloid leukemia
2021 · Jie Wei, Guan Ye Nai, et al. · Annals of Translational Medicine · 27
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Alterations of anticoagulant proteins and soluble endothelial protein C receptor in thalassemia patients of Chinese origin
2018 · Yulan Huang, Yuan Long, et al. · Thrombosis Research · 25
Liproxstatin‑1 induces cell cycle arrest, apoptosis, and caspase‑3/GSDME‑dependent secondary pyroptosis in K562 cells
2022 · Hai-Qun Dong, Shi-Jing Liang, et al. · International Journal of Oncology · 23
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Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature
2015 · Jie Yan, Donghong Deng, et al. · Clinica Chimica Acta · 16
Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report
2019 · Yu-Ling Xu, Wei-Hua Zhao, et al. · World Journal of Clinical Cases · 14
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Participation of Proteinase-Activated Receptor-2 in Passive Cutaneous Anaphylaxis-Induced Scratching Behavior and the Inhibitory Effect of Tacrolimus
2009 · Yu Zhu, Cheng Peng, et al. · Biological and Pharmaceutical Bulletin · 14
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Management of dysfibrinogenemia in pregnancy: A case report
2017 · Jie Yan, Donghong Deng, et al. · Journal of Clinical Laboratory Analysis · 13
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Guideline for diagnosis and management of congenital dysfibrinogenemia
2024 · Jie Yan, Lin Liao, et al. · Clinica Chimica Acta · 10
Abnormal fibrinogen with an Aα 16Arg → Cys substitution is associated with multiple cerebral infarctions
2018 · Meiling Luo, Aiqiu Wei, et al. · Journal of Thrombosis and Thrombolysis · 9
A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release
2016 · Jie Yan, Meiling Luo, et al. · International Journal of Hematology · 9
Fibrinogen Clauss and prothrombin time derived method ratio can differentiate dysfibrinogenemia from hypofibrinogenemia and hyperfibrinogenemia
2020 · Meiling Luo, Liqun Xiang, et al. · Thrombosis Research · 8
A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the γ165Cys–Bβ227Cys disulfide bond and ultimately leads to hypofibrinogenemia
2018 · WeiJie Zhou, Meiling Luo, et al. · Thrombosis Research · 8
Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region
2021 · Aiqiu Wei, Yangyang Wu, et al. · Hematology · 7
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Selection of reference genes in liproxstatin-1-treated K562 Leukemia cells via RT-qPCR and RNA sequencing
2024 · Hai-Qun Dong, Xue-Ying Hu, et al. · Molecular Biology Reports · 5
Analysis of the genetic variants associated with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy: A case report
2016 · NA SUN, PENG CHENG, et al. · Biomedical Reports · 4
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[Expression of miR-550a-5p in Myelodysplastic Syndrome and Its Prediction of Target Genes].
2016 · Ying Huang, Jing Wen, et al. · PubMed · 2
[Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].
2016 · Jie Yan, Donghong Deng, et al. · PubMed · 2
[Expression and Function of miR-99a-5p in Bone Marrow of Patients with MDS].
2019 · Ying LE, Xu-Pai Zhang, et al. · PubMed · 1
[Advances in Pathogenesis and Related Clinical Research of Thromboembolism in Patients with Thalassemia after Splenectomy].
2016 · Na Sun, Peng Cheng, et al. · PubMed · 1
Comprehensive Genetic Analysis of Hemophilia A in a Chinese Cohort: Insights from Next-Generation and Long-Read Sequencing
2026 · Yuling Xu, Xianli Qin, et al. · Turkish Journal of Hematology
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Clinical profiling and outcomes of ischaemic stroke patients with immune thrombocytopenia: A multicentre retrospective study
2026 · LiQin Cao, Jin Wu, et al. · British Journal of Haematology
A novel fibrinogen gamma-chain mutation, p. γAla327Val, causes structural abnormality of D region and ultimately leads to congenital dysfibrinogenemia
2020 · Aiqiu Wei, Yangyang Wu, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Works count: 32
Citation count: 382
H-index: 10
I10-index: 11
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