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  1. NTU Scholars
  2. Research Outputs

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Showing results 1 to 20 of 108  next >
Issue DateTitleAuthor(s)SourcescopusWOSFulltext/Archive link
2018A 1204-single nucleotide polymorphism and insertion–deletion polymorphism panel for massively parallel sequencing analysis of DNA mixturesHSIAO-LIN HWA ; Chung W.-C.; PEI-LUNG CHEN ; Lin C.-P.; Li H.-Y.; Yin H.-I.; JAMES CHUN-I LEE Forensic Science International: Genetics2722
2018ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepanciesWu P.C.; Lin Y.-H.; Tsai L.F.; Chen M.H.; PEI-LUNG CHEN ; Pai S.-C.Transfusion2724
2013Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing ImpairmentChen-Chi Wu ; Lin Y.-H.; Lu Y.-C.; PEI-JER CHEN ; WEI-SHIUNG YANG ; Hsu C.-J.; PEI-LUNG CHEN PLoS ONE3247
2015Association Between Serum Levels of Adipocyte Fatty Acid-binding Protein and Free ThyroxineFEN-YU TSENG ; PEI-LUNG CHEN ; Chen, Yen-Ting; Chi, Yu-Chao; SHYANG-RONG SHIH ; CHIH-YUAN WANG ; CHI-LING CHEN ; WEI-SHIUNG YANG Medicine66
2020Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA StudyPEI-LUNG CHEN Frontiers in Neurology1515
2020Cerebral microbleeds in autosomal dominant polycystic kidney diseaseLI-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 Stroke33
2019A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencingCHIN-HSIEN LIN ; PEI-LUNG CHEN ; CHUN-HWEI TAI ; Lin H.-I.; Chen C.-S.; Chen M.-L.; RUEY-MEEI WU Movement Disorders5756
2022A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in TaiwanMENG-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 Diagnostics55
2019Clinical characteristics of subependymal giant cell astrocytoma in tuberous sclerosis complexPEI-LUNG CHEN Frontiers in Neurology1814
2021The clinical contribution of full-field electroretinography and 8-year experiences of application in a tertiary medical centerYang J.-J.; Huang C.-H.; CHANG-HAO YANG ; CHUNG-MAY YANG ; CHAO-WEN LIN ; TZYY-CHANG HO ; CHANG-PING LIN ; YI-TING HSIEH ; PO-TING YEH ; TSO-TING LAI ; PEI-LUNG CHEN ; TA-CHING CHEN Journal of Personalized Medicine21
2016Clinical heterogeneity of LRRK2 p.I2012T mutationFan 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 Disorders1414
2011Clinical implication of the C allele of the ITPKC gene SNP rs28493229 in kawasaki disease: Association with disease susceptibility and BCG scar reactivationMING-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 Journal5347
2022Clinical manifestations and genetic characteristics in the Taiwan thoracic aortic aneurysm and dissection cohort - a prospective cohort studyDuan, 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 Association32
2022Cochlear implantation in LEOPARD syndrome: Our experience with three patientsTseng 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 Otolaryngology00
2022Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter StudyLin, 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 Biomedicines53
2023Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver DiseasesChen, 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 Pediatrics00
2012Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomasCHENG-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 Oncology109
2022Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhageCHIH-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 neurology22
2022Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical ImplicationsLee, 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-JenBiomedicines43
2011Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association allelesPEI-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 ONE5451
Showing results 1 to 20 of 108  next >

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

總館學科館員 (Main Library)
醫學圖書館學科館員 (Medical Library)
社會科學院辜振甫紀念圖書館學科館員 (Social Sciences Library)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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    Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
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    Please use Sherpa Romeo to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.
  • 網站簡介 (Quickstart Guide)
  • 使用手冊 (Instruction Manual)
  • 線上預約服務 (Booking Service)
  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入 (With ORCID)
  • 方案一:定期更新ORCID者,以ID匯入 (Search for identifier (ORCID))
  • 方案二:自行建檔 (Default mode Submission)
  • 方案三:學科館員協助匯入 (Email worklist to subject librarians)
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