| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
| 2018 | A 1204-single nucleotide polymorphism and insertion–deletion polymorphism panel for massively parallel sequencing analysis of DNA mixtures | HSIAO-LIN HWA ; Chung W.-C.; PEI-LUNG CHEN ; Lin C.-P.; Li H.-Y.; Yin H.-I.; JAMES CHUN-I LEE | Forensic Science International: Genetics | 26 | 20 | |
| 2018 | ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies | Wu P.C.; Lin Y.-H.; Tsai L.F.; Chen M.H.; PEI-LUNG CHEN ; Pai S.-C. | Transfusion | 27 | 23 | |
| 2013 | Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment | Chen-Chi Wu ; Lin Y.-H.; Lu Y.-C.; PEI-JER CHEN ; WEI-SHIUNG YANG ; Hsu C.-J.; PEI-LUNG CHEN | PLoS ONE | 29 | 47 | |
| 2015 | Association Between Serum Levels of Adipocyte Fatty Acid-binding Protein and Free Thyroxine | FEN-YU TSENG ; PEI-LUNG CHEN ; Chen, Yen-Ting; Chi, Yu-Chao; SHYANG-RONG SHIH ; CHIH-YUAN WANG ; CHI-LING CHEN ; WEI-SHIUNG YANG | Medicine | 6 | 6 | |
| 2020 | Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA Study | PEI-LUNG CHEN | Frontiers in Neurology | 15 | 14 | |
| 2020 | Cerebral microbleeds in autosomal dominant polycystic kidney disease | LI-KAI TSAI ; PEI-LUNG CHEN ; Tsai H.-H.; YA-FANG CHEN ; Wu P.-C.; JIANN-SHING JENG ; JENQ-WEN HUANG ; TZONG-SHINN CHU ; Kao J.T.-W. | Journal of Stroke | 3 | 3 | |
| 2019 | A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing | CHIN-HSIEN LIN ; PEI-LUNG CHEN ; CHUN-HWEI TAI ; Lin H.-I.; Chen C.-S.; Chen M.-L.; RUEY-MEEI WU | Movement Disorders | 55 | 54 | |
| 2022 | A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan | MENG-CHEN WU ; Chang, Yung-Yee; Lan, Min-Yu; Chen, Ying-Fa; Tai, Chun-Hwei; Lin, Yung-Feng; Tsai, Shih-Feng; PEI-LUNG CHEN ; CHIN-HSIEN LIN | Journal of Molecular Diagnostics | 1 | 1 | |
| 2019 | Clinical characteristics of subependymal giant cell astrocytoma in tuberous sclerosis complex | PEI-LUNG CHEN | Frontiers in Neurology | 17 | 14 | |
| 2021 | The clinical contribution of full-field electroretinography and 8-year experiences of application in a tertiary medical center | Yang J.-J.; Huang C.-H.; CHANG-HAO YANG ; CHUNG-MAY YANG ; Lin C.-W.; TZYY-CHANG HO ; Lin C.-P.; Hsieh Y.-T.; PO-TING YEH ; Lai T.-T.; PEI-LUNG CHEN ; Chen T.-C. | Journal of Personalized Medicine | 1 | 1 | |
| 2016 | Clinical heterogeneity of LRRK2 p.I2012T mutation | Fan T.-S.; RUEY-MEEI WU ; PEI-LUNG CHEN ; TA-FU CHEN ; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; CHUN-HWEI TAI ; Lin H.-I.; CHIEN-YU CHEN | Parkinsonism and Related Disorders | 13 | 13 | |
| 2011 | Clinical implication of the C allele of the ITPKC gene SNP rs28493229 in kawasaki disease: Association with disease susceptibility and BCG scar reactivation | MING-TAI LIN ; JOU-KOU WANG ; Yeh J.-I.; Sun L.-C.; PEI-LUNG CHEN ; JIA-FENG WU ; Chang C.-C.; Lee W.-L.; Shen C.-T.; Wang N.-K.; Wu C.-S.; Yeh S.-Z.; CHUN-AN CHEN ; SHUENN-NAN CHIU ; MEI-HWAN WU | Pediatric Infectious Disease Journal | 51 | 47 | |
| 2022 | Clinical manifestations and genetic characteristics in the Taiwan thoracic aortic aneurysm and dissection cohort - a prospective cohort study | Duan, De-Min; Chiu, Hsin-Hui; PEI-LUNG CHEN ; PO-TING YEH ; CHIH-WEI YU ; KAI-CHIEN YANG ; CHIH-CHIEH YU | Journal of the Formosan Medical Association | 3 | 2 | |
| 2022 | Cochlear implantation in LEOPARD syndrome: Our experience with three patients | Tseng Y.-C.; Tsai C.-Y.; TIEN-CHEN LIU ; Hsieh Y.-S.; Huang F.-L.; PEI-LUNG CHEN ; Shiao J.-Y.; Liu T.-C.; Hsu C.-J.; Huang C.-W.; Chen-Chi Wu | Clinical Otolaryngology | 0 | 0 | |
| 2022 | Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study | Lin, Pei-Hsuan; Wu, Hung-Pin; Wu, Che-Ming; Chiang, Yu-ting ; Jacob Shujui Hsu ; Tsai, Cheng-Yu; Wang, Han; Tseng, Li-Hui; Chen, Pey-Yu; Yang, Ting-Hua; Hsu, Chuan-Jen; PEI-LUNG CHEN ; CHEN-CHI WU ; TIEN-CHEN LIU | Biomedicines | 3 | 3 | |
| 2012 | Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas | CHENG-PING WANG ; TSENG-CHENG CHEN ; YIH-LEONG CHANG ; JENG-YUH KO ; TSUNG-LIN YANG ; Lo F.-Y.; Hu Y.-L.; PEI-LUNG CHEN ; Chen-Chi Wu ; PEI-JEN LOU | Oral Oncology | 10 | 9 | |
| 2022 | Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage | Chen, Chih-Hao; Chu, Yung-Tsai; YA-FANG CHEN ; Ko, Tzu-Yu; Cheng, Yu-Wen; Lee, Ming-Jen; PEI-LUNG CHEN ; Tang, Sung-Chun; JIANN-SHING JENG | European journal of neurology | 1 | 1 | |
| 2022 | Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications | Lee, Chee-Yee; PEI-HSUAN LIN ; Tsai, Cheng-Yu; Chiang Yu-ting ; Chiou, Hong-Ping; Chiang, Ko-Yin; PEI-LUNG CHEN ; Jacob Shujui Hsu ; TIEN-CHEN LIU ; Wu, Hung-Pin; CHEN-CHI WU ; Hsu, Chuan-Jen | Biomedicines | 1 | 2 | |
| 2011 | Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles | PEI-LUNG CHEN ; Fann C.-S.-J.; Chu C.-C.; Chang C.-C.; Chang S.-W.; Hsieh H.-Y.; Lin M.; WEI-SHIUNG YANG ; TIEN-CHUN CHANG | PLoS ONE | 54 | 51 | |
| 2018 | Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan | YI-CHING TUNG ; Fann C.S.-J.; Chang C.-C.; Chu C.-C.; WEI-SHIUNG YANG ; WUH-LIANG HWU ; PEI-LUNG CHEN ; Tsai W.-Y. | Pediatric Diabetes | 4 | 3 | |
