Yanjun Lu (Y Lu)

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 14

Top Topics

Respiratory Syndrome Coronavirus

Muscular Dystrophy

Top Venues

BMC medical genetics

Haemophilia : the official journal of the World Federation of Hemophilia

Molecular genetics & genomic medicine

Hematology (Amsterdam, Netherlands)

This page only lists publications with an associated author ORCID identifier.

Publications

Xiong Wang, Weihong Hu, Yong Gao, Dengju Li, Yanjun Lu
Rapid genotyping of F8 intron 22 inversion by nested PCR based on long-distance PCR. Journal of thrombosis and thrombolysis 49 (4) (2021)
Xin Guan, Bo Zhang, Ming Fu, Mengying Li, Xu Yuan, Yaowu Zhu, Jing Peng, Huan Guo, Yanjun Lu
Clinical and inflammatory features based machine learning model for fatal risk prediction of hospitalized COVID-19 patients: results from a retrospective cohort study. Annals of medicine 53 (1) (2021)
Xiong Wang, Ning Tang, Na Shen, Yaowu Zhu, Yanjun Lu, Linna Gao
Normal activated partial thromboplastin time in Chinese patients with mild hemophilia B. Hematology (Amsterdam, Netherlands) 25 (1) (2021)
Xiong Wang, Ning Tang, Na Shen, Yanjun Lu, Dengju Li
Congenital fibrinogen disorder caused by digenic mutations of the FGA and FGB genes. Hematology (Amsterdam, Netherlands) 25 (1) (2020)
Yaowu Zhu, Na Shen, Xiong Wang, Juan Xiao, Yanjun Lu
Alpha and beta-Thalassemia mutations in Hubei area of China. BMC medical genetics 21 (1) (2020)
Xiong Wang, Guijiao Zhang, Yanjun Lu, Xiaoping Luo, Wei Wu
Trio-WES reveals a novel de novo missense mutation of KMT2A in a Chinese patient with Wiedemann-Steiner syndrome: A case report. Molecular genetics & genomic medicine 9 (1) (2020)
Delei Li, Wei Chang, Ning Tang, Na Shen, Yanjun Lu, Xiong Wang, Qun Hu
F8 IVS9+5G>A mutation causes moderate haemophilia A. Haemophilia : the official journal of the World Federation of Hemophilia 25 (2) (2019)
Xiong Wang, Aiguo Liu, Ming Huang, Na Shen, Yanjun Lu, Qun Hu
Hereditary elliptocytosis with variable expression and incomplete penetrance in a Chinese family. British journal of haematology 186 (5) (2019)
Na Shen, Ting Wang, Delei Li, Aiguo Liu, Yanjun Lu
Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese family. BMC medical genetics 20 (1) (2019)
Xiong Wang, Ning Tang, Yanjun Lu, Qun Hu, Dengju Li
Two cases of von Willebrand disease type 3 in consanguineous Chinese families. Molecular genetics & genomic medicine 8 (2) (2019)
Xiong Wang, Ning Tang, Wei Chang, Yanjun Lu, Dengju Li
Hemophagocytic lymphohistiocytosis and congenital factor VII deficiency: a case report. BMC medical genetics 19 (1) (2018)
X Wang, Y Lyu, N Shen, Q Hu, Yanjun Lu
FVIII p.Arg1800His mutation is associated with mild/moderate hemophilia A in Chinese population. International journal of laboratory hematology 40 (5) (2018)
X He, Z Xiong, N Shen, Yanjun Lu, X Wang
Performance of next-generation sequencing in the detection of large exon deletion in patients of haemophilia A. Haemophilia : the official journal of the World Federation of Hemophilia 24 (4) (2018)
X Wang, N Tang, Yanjun Lu, D Li
Congenital factor V deficiency and decreased VWF in a Chinese male patient with hematuria. Haemophilia : the official journal of the World Federation of Hemophilia 24 (1) (2017)