公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2022 | Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study | Chen, Pey-Yu; Tsai, Cheng-Yu; Wu, Jiunn-Liang; Li, Yi-Lu; Wu, Che-Ming; Chen, Kuang-Chao; Hwang, Chung-Feng; Wu, Hung-Pin; Lin, Hung-Ching; Cheng, Yen-Fu; Lo, Ming-Yu; TIEN-CHEN LIU ; TING-HUA YANG ; PEI-LUNG CHEN ; Hsu, Chuan-Jen; CHEN-CHI WU | Ear and hearing | 1 | 1 | |
2021 | Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause? | Lin, Yi-Hsin; Wu, Ping-Che; Tsai, Cheng-Yu; Lin, Yin-Hung; Lo, Ming-Yu; Hsu, Shu-Jui; PEI-HSUAN LIN ; Erdenechuluun, Jargalkhuu; Wu, Hung-Pin; Hsu, Chuan-Jen; CHEN-CHI WU ; PEI-LUNG CHEN | Journal of Molecular Diagnostics | 8 | 4 | |
2021 | Hereditary hearing impairment with cutaneous abnormalities | Lee, Tung-Lin; PEI-HSUAN LIN ; PEI-LUNG CHEN ; JIN-BON HONG ; CHEN-CHI WU | Genes | 4 | 2 | |
2019 | HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome | YI-AN TU ; SUNG-JAN LIN ; PEI-LUNG CHEN ; Chou C.-H.; CHU-CHUN HUANG ; HONG-NERNG HO ; MEI-JOU CHEN | Journal of the Formosan Medical Association | 11 | 10 | |
2009 | Human genetics of diabetes mellitus in Taiwan | PEI-LUNG CHEN ; WEI-SHIUNG YANG | Frontiers in Bioscience | 4 | 3 | |
2015 | Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing | Lin Y.-H.; Chen-Chi Wu ; Hsu T.-Y.; WEI-YIH CHIU ; Hsu C.-J.; PEI-LUNG CHEN | Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis | 12 | 12 | |
2013 | Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual | PEI-LUNG CHEN ; Lai S.-K.; WEI-SHIUNG YANG ; TIEN-CHUN CHANG ; Chu C.-C. | Tissue Antigens | 2 | 2 | |
2017 | Identification of a novel HLA-B allele, HLA-B*40:238, in a Taiwanese individual | Lee H.-L.; Lai S.-K.; PEI-LUNG CHEN ; Chu C.-C. | HLA | 3 | 1 | |
2018 | Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan | Hsiung Y.-C.; Lin P.-C.; Chen C.-S.; YI-CHING TUNG ; WEI-SHIUNG YANG ; PEI-LUNG CHEN ; TA-CHEN SU | Atherosclerosis | 11 | 10 | |
2022 | Identification of nine novel variants across PAX3, SOX10, EDNRB, and MITF genes in Waardenburg syndrome with next-generation sequencing | Lee, Chen-Yu; Lo, Ming-Yu; Chen, You-Mei; PEI-HSUAN LIN ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; CHEN-CHI WU ; Jacob Shujui Hsu | Molecular Genetics & Genomic Medicine | 3 | 2 | |
2017 | Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: A case report and literature review | Chen Y.-F.; Chang Y.-Y.; Lan M.-Y.; PEI-LUNG CHEN ; CHIN-HSIEN LIN | BMC Neurology | 22 | 14 | |
2015 | Identifying children with poor cochlear implantation outcomes using massively parallel sequencing | Chen-Chi Wu ; Lin Y.-H.; TIEN-CHEN LIU ; Lin K.-N.; WEI-SHIUNG YANG ; Hsu C.-J.; PEI-LUNG CHEN ; Wu C.-M. | Medicine (United States) | 49 | 40 | |
2020 | An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response | PEI-HSUAN LIN ; Hsu, Chuan-Jen; Lin, Yin-Hung; Lin, Yi-Hsin; Yang, Shu-Yu; TING-HUA YANG ; PEI-LUNG CHEN ; Chen-Chi Wu ; TIEN-CHEN LIU | Scientific Reports | 6 | 3 | |
2017 | Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: A case report and literature review | Lin H.-C.; CHIN-HSIEN LIN ; PEI-LUNG CHEN ; Cheng S.-J.; Chen P.-H. | BMC Neurology | 12 | 10 | |
2022 | Investigating DYT1 in a Taiwanese dystonia cohort | MENG-CHEN WU ; Chang, Yung-Yee; Chen, Ying-Fa; Lan, Min-Yu; PEI-LUNG CHEN ; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Journal of the Formosan Medical Association | 2 | 2 | |
2015 | An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report | Yu T.-Y.; Lin H.-S.; PEI-LUNG CHEN ; TIEN-SHANG HUANG | Journal of the Formosan Medical Association | 3 | 2 | |
2016 | KCNN2 polymorphisms and cardiac tachyarrhythmias | CHIH-CHIEH YU ; CHIA-TI TSAI ; PEI-LUNG CHEN ; CHO-KAI WU ; Chiu, Fu-Chun; FU-TIEN CHIANG ; Chen, Peng-Sheng; CHI-LING CHEN ; LIAN-YU LIN ; JYH-MING JIMMY JUANG ; LI-TING HO ; Lai, Ling-Ping; WEI-SHIUNG YANG ; JIUNN-LEE LIN | Medicine | 9 | 11 | |
2023 | L1cam alternative shorter transcripts encoding the extracellular domains were overexpressed in the intestine of L1cam knockdown mice | Yang, Wendy; Chen, Szu-Chieh; Wang, Tse-En; PEI-SHIUE TSAI ; Chen, Jeng-Chang; PEI-LUNG CHEN | Gene | 0 | 0 | |
2011 | Linkage and association on 8p21.2-p21.1 in schizophrenia | Fallin M.D.; Lasseter V.K.; Liu Y.; Avramopoulos D.; McGrath J.; Wolyniec P.S.; Nestadt G.; Liang K.-Y.; PEI-LUNG CHEN ; Valle D.; Pulver A.E. | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 25 | 22 | |
2007 | Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in 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 | Clinical Endocrinology | 8 | 9 | |