Pei-Lung Chen

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 19

Top Topics

Spectrum Disorder

Ejection Fraction

Top Venues

International journal of molecular sciences

JGH open : an open access journal of gastroenterology and hepatology

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

Publications

Mei-Chi Huang, Pei-Lung Chen, Chia-Lang Hsu
Transcriptome Analysis of Mesenchymal Progenitor Cells Revealed Molecular Insights into Metabolic Dysfunction and Inflammation in Polycystic Ovary Syndrome. International journal of molecular sciences 25 (14) (2024)
Mei-Chi Huang, Pei-Lung Chen, Chia-Lang Hsu
Transcriptome Analysis of Mesenchymal Progenitor Cells Revealed Molecular Insights into Metabolic Dysfunction and Inflammation in Polycystic Ovary Syndrome. International journal of molecular sciences 25 (14) (2024)
Tsung-Kai Hung, Wan-Chi Liu, Sheng-Kai Lai, Hui-Wen Chuang, Yi-Che Lee, Hong-Ye Lin, Chia-Lang Hsu, Chien-Yu Chen, Ya-Chien Yang, Jacob Shu-Jui Hsu, Pei-Lung Chen
Genetic complexity of killer-cell immunoglobulin-like receptor genes in human pangenome assemblies. Genome research (2024)
Wei-Chieh Wang, Chu-Hsuan Huang, Hsin-Hsiang Chung, Pei-Lung Chen, Fung-Rong Hu, Chang-Hao Yang, Chung-May Yang, Chao-Wen Lin, Cheng-Chih Hsu, Ta-Ching Chen
Metabolomics facilitates differential diagnosis in common inherited retinal degenerations by exploring their profiles of serum metabolites. Nature communications 15 (1) (2024)
Mei-Chi Huang, Pei-Lung Chen, Chia-Lang Hsu
Transcriptome Analysis of Mesenchymal Progenitor Cells Revealed Molecular Insights into Metabolic Dysfunction and Inflammation in Polycystic Ovary Syndrome. International journal of molecular sciences 25 (14) (2024)
Wei-Chieh Wang, Chu-Hsuan Huang, Hsin-Hsiang Chung, Pei-Lung Chen, Fung-Rong Hu, Chang-Hao Yang, Chung-May Yang, Chao-Wen Lin, Cheng-Chih Hsu, Ta-Ching Chen
Metabolomics facilitates differential diagnosis in common inherited retinal degenerations by exploring their profiles of serum metabolites. Nature communications 15 (1) (2024)
Yen-Hui Lee, Cheng-Yu Tsai, Yue-Sheng Lu, Pei-Hsuan Lin, Yu-Ting Chiang, Ting-Hua Yang, Jacob Shu-Jui Hsu, Chuan-Jen Hsu, Pei-Lung Chen, Tien-Chen Liu, Chen-Chi Wu
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population. Genes 14 (4) (2023)
Yen-Hui Lee, Cheng-Yu Tsai, Yue-Sheng Lu, Pei-Hsuan Lin, Yu-Ting Chiang, Ting-Hua Yang, Jacob Shu-Jui Hsu, Chuan-Jen Hsu, Pei-Lung Chen, Tien-Chen Liu, Chen-Chi Wu
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population. Genes 14 (4) (2023)
Yen-Hui Lee, Cheng-Yu Tsai, Yue-Sheng Lu, Pei-Hsuan Lin, Yu-Ting Chiang, Ting-Hua Yang, Jacob Shu-Jui Hsu, Chuan-Jen Hsu, Pei-Lung Chen, Tien-Chen Liu, Chen-Chi Wu
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population. Genes 14 (4) (2023)
Yen-Hui Lee, Cheng-Yu Tsai, Yue-Sheng Lu, Pei-Hsuan Lin, Yu-Ting Chiang, Ting-Hua Yang, Jacob Shu-Jui Hsu, Chuan-Jen Hsu, Pei-Lung Chen, Tien-Chen Liu, Chen-Chi Wu
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population. Genes 14 (4) (2023)
Che-Ming Chiang, Yung-Ming Jeng, Ming-Chih Ho, Ming-Wei Lai, Huei-Ying Li, Pei-Lung Chen, Hung-Chang Lee, Jia-Feng Wu, Yu-Chun Chiu, Bang-Yu Liou, Yen-Hsuan Ni, Hong-Yuan Hsu, Mei-Hwei Chang, Huey-Ling Chen
Different clinical and genetic features of Alagille patients with progressive disease versus a jaundice-free course. JGH open : an open access journal of gastroenterology and hepatology 6 (12) (2022)
Che-Ming Chiang, Yung-Ming Jeng, Ming-Chih Ho, Ming-Wei Lai, Huei-Ying Li, Pei-Lung Chen, Hung-Chang Lee, Jia-Feng Wu, Yu-Chun Chiu, Bang-Yu Liou, Yen-Hsuan Ni, Hong-Yuan Hsu, Mei-Hwei Chang, Huey-Ling Chen
Different clinical and genetic features of Alagille patients with progressive disease versus a jaundice-free course. JGH open : an open access journal of gastroenterology and hepatology 6 (12) (2022)
Pei-Hsuan Lin, Hung-Pin Wu, Che-Ming Wu, Yu-Ting Chiang, Jacob Shu-Jui Hsu, Cheng-Yu Tsai, Han Wang, Li-Hui Tseng, Pey-Yu Chen, Ting-Hua Yang, Chuan-Jen Hsu, Pei-Lung Chen, Chen-Chi Wu, Tien-Chen Liu
Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study. Biomedicines 10 (7) (2022)
Chee-Yee Lee, Pei-Hsuan Lin, Cheng-Yu Tsai, Yu-Ting Chiang, Hong-Ping Chiou, Ko-Yin Chiang, Pei-Lung Chen, Jacob Shu-Jui Hsu, Tien-Chen Liu, Hung-Pin Wu, Chen-Chi Wu, Chuan-Jen Hsu
Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications. Biomedicines 10 (8) (2022)
Ta-Ching Chen, Ding-Siang Huang, Chao-Wen Lin, Chang-Hao Yang, Chung-May Yang, Victoria Y Wang, Jou-Wei Lin, Allen Chilun Luo, Fung-Rong Hu, Pei-Lung Chen
Genetic characteristics and epidemiology of inherited retinal degeneration in Taiwan. NPJ genomic medicine 6 (1) (2021)
Chao-Wen Lin, Ching-Wen Huang, Allen Chilun Luo, Yuh-Tsyr Chou, Yu-Shu Huang, Pei-Lung Chen, Ta-Ching Chen
Genetic Spectrum and Characteristics of Hereditary Optic Neuropathy in Taiwan. Genes 12 (9) (2021)
Guann-Jye Chiou, Ding-Siang Huang, Fung-Rong Hu, Chung-May Yang, Chang-Hao Yang, Ching-Wen Huang, Jou-Wei Lin, Chao-Wen Lin, Tzyy-Chang Ho, Yi-Ting Hsieh, Tzo-Ting Lai, Ho-Min Chen, Pei-Lung Chen, Chuhsing Kate Hsiao, Ta-Ching Chen
Metabolic Syndromes as Important Comorbidities in Patients of Inherited Retinal Degenerations: Experiences from the Nationwide Health Database and a Large Hospital-Based Cohort. International journal of environmental research and public health 18 (4) (2021)
Tung-Lin Lee, Pei-Hsuan Lin, Pei-Lung Chen, Jin-Bon Hong, Chen-Chi Wu
Hereditary Hearing Impairment with Cutaneous Abnormalities. Genes 12 (1) (2020)
Yu-Chi Sung, Chang-Hao Yang, Chung-May Yang, Chao-Wen Lin, Ding-Siang Huang, Yu-Shu Huang, Fung-Rong Hu, Pei-Lung Chen, Ta-Ching Chen
Genotypes Predispose Phenotypes-Clinical Features and Genetic Spectrum of ABCA4-Associated Retinal Dystrophies. Genes 11 (12) (2020)