PubRank

Yanhui Jin

Author PubWeight™ 0.77‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Severe female hemophilia A patient caused by a nonsense mutation (p.Gln1686X) of F8 gene combined with skewed X-chromosome inactivation. Blood Coagul Fibrinolysis 2015 0.77
2 [Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2017 0.75
3 [Congenital hypofibrinogenemia associated with a novel mutation in FGG gene]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2015 0.75
4 A novel gene insertion combined with a missense mutation causing factor VII deficiency in two unrelated Chinese families. Blood Coagul Fibrinolysis 2015 0.75
5 Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide. Clin Lab 2016 0.75
6 [Phenotypic and genetic analysis of two pedigrees affected with hereditary antithrombin deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2016 0.75
7 [Identification of a novel mutation of factor XII gene in a family with coagulation FXII deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2013 0.75
8 A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family. Blood Coagul Fibrinolysis 2013 0.75
9 Unique de-novo mutation of fibrinogen gene in a Chinese girl with hypofibrinogenemia. Blood Coagul Fibrinolysis 2014 0.75
10 Double heterozygous mutations Gln100Leu and His348Gln of the F7 gene in a patient with factor VII deficiency. Blood Coagul Fibrinolysis 2013 0.75
11 Genetic analysis of a pedigree with hereditary coagulation factor XI deficiency. Blood Coagul Fibrinolysis 2019 0.75
12 Congenital combined deficiency of factor VII and X in a patient due to accidental diphacinone intoxication. Thromb Haemost 2011 0.75
13 Identification of Genetic Defects Underlying FXII Deficiency in Four Unrelated Chinese Patients. Acta Haematol 2016 0.75
14 [Identification of a novel heterozygous mutation in a pedigree with hereditary coagulation factor XII deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2015 0.75
15 Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140s. Blood Coagul Fibrinolysis 2016 0.75