Yanhui Jin

Shanghai Jiao Tong University — China

Medicine · Health Sciences

11h-index342citations85works0.82yr avg
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Research Topics

Blood Coagulation and Thrombosis Mechanisms(34), Hemophilia Treatment and Research(33), Coagulation, Bradykinin, Polyphosphates, and Angioedema(20), Blood properties and coagulation(14), Vitamin K Research Studies(12)

Publications85 total

Insufficient expression of VTN promotes the development of early-onset severe preeclampsia through the HEY1/autophagy signaling pathway
Placenta·2025
Insufficient expression of COL6A1 promotes the development of early-onset severe preeclampsia by inhibiting the APJ/AKT signaling pathway
Cell Death Discovery·2025· 4 citedOpen Access
Interference between main and auxiliary rotors in floating dual-rotor wind turbines under stationary and surge conditions
Ocean Engineering·2025· 2 cited
Two patients with protein S deficiency and cerebral venous sinus thrombosis: nonsense mutations of the PROS1 gene may account for these deficiencies
Blood Coagulation & Fibrinolysis·2025
[Analysis of two consanguineous Chinese pedigrees affected with Hereditary prokallikrein deficiency and High molecular weight kininogen deficiency].
PubMed·2024
Recurrent Founder Variant in Inherited FVII Deficiency: Molecular Spectrum Analysis in Southeast China Recurrent Founder Variant in Inherited FVII Deficiency: Molecular Spectrum Analysis in Southeast China
2024Open Access
[Analysis of three Chinese pedigrees affected with Hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene].
PubMed·2024
Analysis of refractive errors and related risk factors among students in Baotou, Inner Mongolia
2024Open Access
Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events
International Journal of Laboratory Hematology·2024Open Access
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency
Annals of Hematology·2024· 2 cited
Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency
Annals of Hematology·2023· 1 cited
[Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅺ deficiency due to variant of F11 gene].
PubMed·2023
Institutional Investors, CSR Report Readability and the Moderating Role of ESG Performance
SAGE Open·2023· 14 citedOpen Access
Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency
Hämostaseologie·2023Open Access
Preeclampsia complicated with hypofibrinogenemia: 2 case reports and review of the literature
BMC Pregnancy and Childbirth·2023· 3 citedOpen Access
Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*)
Blood Cells Molecules and Diseases·2023· 1 cited
Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations
Hämostaseologie·2023· 2 citedOpen Access
Analysis of an Inherited FXII Deficiency Pedigree Associated with Double Heterozygous Mutations in the F12 Gene
Indian Journal of Hematology and Blood Transfusion·2023Open Access
[Genetic analysis of two Chinese pedigrees affected with Hereditary hypofibrinemia due to missense variants].
PubMed·2023
Joint DDPG and Unsupervised Learning for Channel Allocation and Power Control in Centralized Wireless Cellular Networks
IEEE Access·2023· 22 citedOpen Access
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Frequent Co-authors

Mingshan Wang(30), Lihong Yang(24), Shasha Luo(9), Xiaoli Cheng(9), Lihong Yang(9), Siqi Liu(8), Haixiao Xie(7), Kankan Su(7), Haiyue Zhang(6), Zhiqiang Du(5), Xiuping Hao(5), Xiaolong Li(4), Qiyu Xu(4), Haiyue Zhang(3), Yingyu Wang(3), Meina Liu(3), Yaosheng Xie(3), Fang-xiu Zheng(3), Yi Chen(3), Mingshan Wang(3)