Ming-Ching Shen

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 23

Top Topics

Recombinant Human

Top Venues

Haemophilia : the official journal of the World Federation of Hemophilia

International journal of molecular sciences

International journal of hematology

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

Publications

Ming Chen, Ming-Ching Shen, Shun-Ping Chang, Gwo-Chin Ma, Dong-Jay Lee, Adeline Yan
De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study. International journal of molecular sciences 25 (3) (2024)
Ming Chen, Ming-Ching Shen, Shun-Ping Chang, Gwo-Chin Ma, Dong-Jay Lee, Adeline Yan
De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study. International journal of molecular sciences 25 (3) (2024)
Hsuan-Yu Lin, Ching-Yeh Lin, Su-Feng Kuo, Jen-Shiou Lin, Po-Te Lin, Ying-Chih Huang, Han-Ni Hsieh, Ming-Ching Shen
Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients. Haemophilia : the official journal of the World Federation of Hemophilia (2024)
Ming Chen, Ming-Ching Shen, Shun-Ping Chang, Gwo-Chin Ma, Dong-Jay Lee, Adeline Yan
De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study. International journal of molecular sciences 25 (3) (2024)
Ming Chen, Ming-Ching Shen, Shun-Ping Chang, Gwo-Chin Ma, Dong-Jay Lee, Adeline Yan
De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study. International journal of molecular sciences 25 (3) (2024)
Ming Chen, Ming-Ching Shen, Shun-Ping Chang, Gwo-Chin Ma, Dong-Jay Lee, Adeline Yan
De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study. International journal of molecular sciences 25 (3) (2024)
Hsuan-Yu Lin, Ching-Yeh Lin, Su-Feng Kuo, Jen-Shiou Lin, Po-Te Lin, Ying-Chih Huang, Han-Ni Hsieh, Ming-Ching Shen
Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients. Haemophilia : the official journal of the World Federation of Hemophilia 30 (4) (2024)
Hsuan-Yu Lin, Ching-Yeh Lin, Su-Feng Kuo, Jen-Shiou Lin, Po-Te Lin, Ying-Chih Huang, Han-Ni Hsieh, Ming-Ching Shen
Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients. Haemophilia : the official journal of the World Federation of Hemophilia 30 (4) (2024)
Yu-Hung Shih, Ying-Chih Huang, Ching-Yeh Lin, Hsuan-Yu Lin, Su-Feng Kuo, Jen-Shiou Lin, Ming-Ching Shen
A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review. Medicine 102 (4) (2023)
Ming-Ching Shen, Sheng-Chieh Chou, Shyh-Shin Chiou, Pei-Chin Lin, Yeu-Chin Chen, Hsuan-Yu Lin, Yang-Cheng Lee, Cih-En Huang, Te-Fu Weng, Ting-Huan Huang, Chih-Yuan Chung, Jiann-Shiuh Chen, Shu-Huey Chen, Shin-Nan Cheng, Chih-Cheng Hsiao, Yen-Min Huang, Shih-Hsiang Chen, Yuan-Bin Yu, Shih-Chiang Lin, Ching-Yeh Lin, Ching-Tien Peng, Jiaan-Der Wang, null null
Efficacy, safety and cost of emicizumab prophylaxis in haemophilia A patients with inhibitors: A nationwide observational study in Taiwan. Haemophilia : the official journal of the World Federation of Hemophilia (2023)
Ravichandran Chandrasekaran, Mauro Dávoli, Zulaiha Muda, Uendy Pérez-Lozano, Naouel Salhi, Nakul Saxena, Ming-Ching Shen, HyeRyoung Haylee Song, Darintr Sosothikul, Veronica Soledad Soto-Arellano, Igor Solev
Estimating the impact of improved management of haemophilia a on clinical outcomes and healthcare utilisation and costs. BMC research notes 16 (1) (2023)
Yu-Hung Shih, Ying-Chih Huang, Ching-Yeh Lin, Hsuan-Yu Lin, Su-Feng Kuo, Jen-Shiou Lin, Ming-Ching Shen
A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review. Medicine 102 (4) (2023)
Ming-Ching Shen, Shun-Ping Chang, Dong-Jay Lee, Wen-Hsiang Lin, Ming Chen, Gwo-Chin Ma
Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients. Diagnostics (Basel, Switzerland) 12 (10) (2022)
Ming Chen, Ming-Ching Shen, Shun-Ping Chang, Gwo-Chin Ma, Ying-Chih Huang, Ching-Yeh Lin
Origin and timing of de novo variants implicated in type 2 von Willebrand disease. Journal of cellular and molecular medicine 26 (21) (2022)
Ming-Ching Shen, Shyh-Shin Chiou, Sheng-Chieh Chou, Te-Fu Weng, Ching-Yeh Lin, Jiaan-Der Wang, Shou-Wu Lee, Ching-Tien Peng
Prevalence of non-Alcoholic Fatty Liver Disease and Associated Factors in Patients with Moderate or Severe Hemophilia: A Multicenter-Based Study. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 28 (2022)
Sheng-Chieh Chou, Ching-Yeh Lin, Hsuan-Yu Lin, Chen-Hsueh Pai, Cheng-Ye Yu, Su-Feng Kuo, Jen-Shiou Lin, Po-Te Lin, Mei-Hua Hung, Han-Ni Hsieh, Hsiang-Chun Liu, Ming-Ching Shen
Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation. International journal of hematology 116 (4) (2022)
Ming-Ching Shen, Jiaan-Der Wang, Woei Tsai, Ching-Yeh Lin, Jen-Shiou Lin, Su-Feng Kuo, Po-Te Lin, Ying-Chih Huang, Mei-Hua Hung
Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population. Haemophilia : the official journal of the World Federation of Hemophilia 27 (6) (2021)
Sheng-Chieh Chou, Dong-Tasmn Lin, Ching-Yeh Lin, Ying-Chih Huang, Han-Ni Hsieh, Ming-Ching Shen
First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene. International journal of hematology 113 (5) (2021)
Hsuan-Yu Lin, Jen-Shiou Lin, Woei Tsay, Po-Te Lin, Ying-Chih Huang, Ming-Ching Shen
A distinct common p.Gln317* mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families. Haemophilia : the official journal of the World Federation of Hemophilia (2021)
Ying-Chih Huang, Yu-Hung Shih, Ching-Yeh Lin, Ping-Fang Chiu, Su-Feng Kuo, Jen-Shiou Lin, Ming-Ching Shen
A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan. International journal of hematology 112 (6) (2020)
Jiaan-Der Wang, Ching-Yeh Lin, Te-Fu Weng, Shyh-Shin Chiou, Ching-Tien Peng, Ming-Ching Shen
Transfusion-transmitted infection and comorbidities in patients with severe haemophilia: A longitudinal birth cohort analysis. Haemophilia : the official journal of the World Federation of Hemophilia 27 (4) (2020)
Hsuan-Yu Lin, Ching-Yeh Lin, Mei-Hua Hung, Su-Feng Kuo, Jen-Shiou Lin, Ming-Ching Shen
Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations. International journal of hematology 112 (2) (2020)
Ming-Ching Shen, Ming Chen, Shung-Ping Chang, Po-Te Lin, Han-Ni Hsieh, Kai-Hsin Lin
Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent. Pediatric hematology and oncology 35 (7-8) (2019)