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Donghong Deng

Observed names: D Deng, D H Deng, D. Deng, DONG-HONG DENG, DONGHONG DENG, Deng Donghong, Dong-Hong Deng, Dong‐Hong Deng
OpenAlex ID: A5045187763
Three cases of congenital dysfibrinogenemia in unrelated Chinese families
2016 · Meiling Luo, Donghong Deng, et al. · Medicine · 99
Identification the prognostic value of glutathione peroxidases expression levels in acute myeloid leukemia
2020 · Jie Wei, Qiongni Xie, et al. · Annals of Translational Medicine · 92
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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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Favorable prognosis of biallelic CEBPA gene mutations in acute myeloid leukemia patients: a meta‐analysis
2014 · Hong‐Ying Li, Dong‐Hong Deng, et al. · European Journal Of Haematology · 40
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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Systematic review/Meta-analysis Anti-epidermal growth factor receptor monoclonal antibody-based therapy for metastatic colorectal cancer: a meta-analysis of the effect of PIK3CA mutations in KRAS wild-type patients
2014 · Lulu Huang, Zhenfang Liu, et al. · Archives of Medical Science · 34
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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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Over-expression of miR-196b-5p is significantly associated with the progression of myelodysplastic syndrome
2017 · Jing Wen, Ying Huang, et al. · International Journal of Hematology · 22
GSTT1 and GSTM1 polymorphisms predict treatment outcome for acute myeloid leukemia: a systematic review and meta-analysis
2014 · Qiang Xiao, Donghong Deng, et al. · Annals of Hematology · 22
Combination of CsA, MTX and low-dose, short-course mycophenolate mofetil for GVHD prophylaxis
2008 · Y Lai, J Ma, et al. · Bone Marrow Transplantation · 21
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
Analyzing the key gene expression and prognostics values for acute myeloid leukemia
2020 · Lingling Shi, Yan Huang, et al. · Translational Cancer Research · 14
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Comprehensively analyze the expression and prognostic role for ten-eleven translocations (TETs) in acute myeloid leukemia
2020 · Yan Huang, Jie Wei, et al. · Translational Cancer Research · 13
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Congenital dysfibrinogenaemia assessed by whole blood thromboelastography
2018 · A. Wei, L. Liao, et al. · International Journal of Laboratory Hematology · 13
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
Polymorphisms in the methylenetetrahydrofolate reductase gene (MTHFR) are associated with susceptibility to adult acute myeloid leukemia in a Chinese population
2015 · Lulu Huang, Donghong Deng, et al. · Cancer Epidemiology · 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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Fas-670A>G polymorphism is not associated with an increased risk of acute myeloid leukemia development
2015 · YING HUANG, DONGHONG DENG, et al. · Biomedical Reports · 5
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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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Works count: 40
Citation count: 609
H-index: 13
I10-index: 18
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