公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2023 | Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases | Chen, Chi-Bo; Jacob Shujui Hsu ; PEI-LUNG CHEN ; JIA-FENG WU ; Li, Huei-Ying; Liou, Bang-Yu; MEI-HWEI CHANG ; YEN-HSUAN NI ; WUH-LIANG HWU ; YIN-HSIU CHIEN ; Chou, Yen-Yin; Yang, Yao-Jong; NI-CHUNG LEE ; HUEY-LING CHEN | The Journal of Pediatrics | 1 | 0 | |
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 | CHIH-HAO CHEN ; Chu, Yung-Tsai; YA-FANG CHEN ; Ko, Tzu-Yu; Cheng, Yu-Wen; MING-JEN LEE ; PEI-LUNG CHEN ; SUNG-CHUN TANG ; JIANN-SHING JENG | European journal of neurology | 4 | 4 | |
2024 | Complete genomic profiles of 1496 Taiwanese reveal curated medical insights | Jacob Shujui Hsu ; Wu, Dung Chi; Shih, Shang Hung; Liu, Jen Feng; Tsai, Ya Chen; Lee, Tung Lin; Chen, Wei An; Tseng, Yi Hsuan; Lo, Yi Chung; Lin, Hong Ye; Chen, Yi Chieh; Chen, Jing Yi; Chou, Ting Hsuan; Chang, Darby Tien Hao; Su, Ming Wei; Guo, Wei Hong; Mao, Hsin Hsiang; CHIEN-YU CHEN ; PEI-LUNG CHEN | Journal of Advanced Research | 0 | | |
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 | 4 | 5 | |
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 | 55 | 52 | |
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 | 7 | 6 | |
2015 | Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome | MEI-JOU CHEN ; Wei S.-Y; WEI-SHIUNG YANG ; Wu T.-T; Li H.-Y; HONG-NERNG HO ; YU-SHIH YANG ; PEI-LUNG CHEN | Human Reproduction | 19 | 16 | |
2023 | Diagnostic rate of germline pathogenic variants in pancreatic ductal adenocarcinoma patients using whole genome sequencing | Chung, An-Ko; Lin, Ro-Ting; Yeh, Chun-Chieh; Yang, Chi-Ying; Wu, Chang-Jiun; PEI-LUNG CHEN ; JAW-TOWN LIN | Frontiers in Genetics | 1 | 0 | |
2022 | Different clinical and genetic features of Alagille patients with progressive disease versus a jaundice-free course | Chiang, Che-Ming; YUNG-MING JENG ; MING-CHIH HO ; Lai, Ming-Wei; Li, Huei-Ying; PEI-LUNG CHEN ; NI-CHUNG LEE ; JIA-FENG WU ; YU-CHUN CHIU ; Liou, Bang-Yu; YEN-HSUAN NI ; HONG-YUAN HSU ; MEI-HWEI CHANG ; HUEY-LING CHEN | JGH open : an open access journal of gastroenterology and hepatology | 1 | 1 | |
2019 | Distinctive genetic variation of long-segment Hirschsprung's disease in Taiwan | Yang W.; Chen S.-C.; Lai J.-Y.; Ming Y.-C.; Chen J.-C.; PEI-LUNG CHEN | Neurogastroenterology and Motility | 6 | 5 | |
2017 | Early measurement of IL-10 predicts the outcomes of patients with acute respiratory distress syndrome receiving extracorporeal membrane oxygenation /631/250/127 /692/53/2422 /13 /13/21 /13/31 /45/23 article | Liu C.-H.; SHUENN-WEN KUO ; Ko W.-J.; Tsai P.-R.; Wu S.-W.; Lai C.-H.; CHIH-HSIEN WANG ; YIH-SHARNG CHEN ; PEI-LUNG CHEN ; Liu T.-T.; SHU-CHIEN HUANG ; TZUU-SHUH JOU | Scientific Reports | 24 | 20 | |
2020 | The efficacy and safety of topical rapamycin–calcitriol for facial angiofibromas in patients with tuberous sclerosis complex: a prospective, double-blind, randomized clinical trial | PEI-LUNG CHEN ; Hong J.B.; LI-JIUAN SHEN ; Chen Y.T.; Wang S.J.; YI-HUA LIAO | British Journal of Dermatology | 13 | 12 | |
2019 | Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study | PEI-LUNG CHEN | Epilepsia Open | 108 | 93 | |
2021 | Evaluation of using WGS/WES to characterize ACMG actionable genes in genetic testing reports | Yang W.-T.; Wu D.-C.; Liu J.-F.; JIN-BON HONG ; Wu J.-T.; PEI-LUNG CHEN ; CHIEN-YU CHEN | Proceedings - 2021 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2021 | 0 | 0 | |
2009 | Familiality of novel factorial dimensions of schizophrenia | McGrath J.A.; Avramopoulos D.; Lasseter V.K.; Wolyniec P.S.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Thornquist M.H.; Luke J.R.; PEI-LUNG CHEN ; Valle D.; Pulver A.E. | Archives of General Psychiatry | 62 | 55 | |
2008 | Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of Taiwan | PEI-LUNG CHEN ; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; WEI-YIH CHIU ; Lin C.-Y.; WEI-SHIUNG YANG ; TIEN-CHUN CHANG | Genes and Immunity | 14 | 13 | |
2014 | A fault-tolerant method for HLA typing with PacBio data | Chang, Chia-Jung; PEI-LUNG CHEN ; WEI-SHIUNG YANG ; KUN-MAO CHAO | BMC Bioinformatics | 12 | 12 | |
2009 | Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia | PEI-LUNG CHEN ; Avramopoulos D.; Lasseter V.K.; McGrath J.A.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Feng N.; Steel G.; Cutting A.S.; Wolyniec P.; Pulver A.E.; Valle D. | American Journal of Human Genetics | 74 | 70 | |
2016 | First step towards precision medicine for antithyroid drug-induced agranulocytosis | PEI-LUNG CHEN ; Fann C.S.-J.; SHYANG-RONG SHIH ; WEI-SHIUNG YANG ; TIEN-CHUN CHANG | The Lancet Diabetes and Endocrinology | 1 | 1 | |