公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2016 | Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good (131)I treatment response | JIN-YING LU ; Hung, Po-Ju; PEI-LUNG CHEN ; RUOH-FANG YEN ; KUAN-TING KUO ; TSUNG-LIN YANG ; CHIH-YUAN WANG ; TIEN-CHUN CHANG ; TIEN-SHANG HUANG ; CHING-CHUNG CHANG | Endocrinology, diabetes & metabolism case reports | 5 | 0 | |
2015 | Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling | Liu Y.; Pham X.; Zhang L.; PEI-LUNG CHEN ; Burzynski G.; McGaughey D.M.; He S.; McGrath J.A.; Wolyniec P.; Fallin M.D.; Pierce M.S.; McCallion A.S.; Pulver A.E.; Avramopoulos D.; Valle D. | G3: Genes, Genomes, Genetics | 35 | 32 | |
2013 | Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response | Hung C.-C.; PEI-LUNG CHEN ; Huang W.-M.; Tai J.J.; Hsieh T.-J.; Ding S.-T.; Hsieh Y.-W.; HORNG-HUEI LIOU | Pharmacogenomics | 16 | 17 | |
2022 | Genetic analysis of a family presenting with coexisting cerebral cavernous malformations and polycystic kidney disease | Hsieh, Pei-Feng; SHIH-YAO LIU ; CHIH-HAO CHEN ; PEI-LUNG CHEN ; SUNG-CHUN TANG ; JIANN-SHING JENG | Journal of the Formosan Medical Association | 0 | 0 | |
2014 | Genetic analysis of CARD14 in non-familial pityriasis rubra pilaris: A case series | JIN-BON HONG ; PEI-LUNG CHEN ; YOU-TZUNG CHEN ; TSEN-FANG TSAI | Acta Dermato-Venereologica | 12 | 9 | |
2021 | Genetic characteristics and epidemiology of inherited retinal degeneration in Taiwan | TA-CHING CHEN ; Huang D.-S.; CHAO-WEN LIN ; CHANG-HAO YANG ; CHUNG-MAY YANG ; Wang V.Y.; JOU-WEI LIN ; Luo A.C.; FUNG-RONG HU ; PEI-LUNG CHEN | npj Genomic Medicine | 30 | 29 | |
2015 | Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study | PEI-LUNG CHEN ; SHYANG-RONG SHIH ; Wang, Pei-Wen; Lin, Ying-Chao; Chu, Chen-Chung; Lin, Jung-Hsin; Chen, Szu-Chi; CHING-CHUNG CHANG ; TIEN-SHANG HUANG ; KEH-SUNG TSAI ; FEN-YU TSENG ; CHIH-YUAN WANG ; JIN-YING LU ; WEI-YIH CHIU ; Chang, Chien-Ching; Chen, Yu-Hsuan; Chen, Yuan-Tsong; Fann, Cathy Shen-Jang; WEI-SHIUNG YANG ; TIEN-CHUN CHANG | Nature communications | 77 | 67 | |
2019 | Genetic epidemiology and clinical features of hereditary hearing impairment in the Taiwanese population | CHEN-CHI WU ; Tsai, Cheng-Yu; Lin, Yi-Hsin; Chen, Pey-Yu; PEI-HSUAN LIN ; Cheng, Yen-Fu; Wu, Che-Ming; Lin, Yin-Hung; Lee, Chee-Yee; Erdenechuluun, Jargalkhuu; TIEN-CHEN LIU ; PEI-LUNG CHEN ; Hsu, Chuan-Jen | Genes | 31 | 27 | |
2023 | Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment | Chiang Yu-ting; PEI-HSUAN LIN ; Lo, Ming-Yu; HSIN-LIN CHEN ; Lee, Chen-Yu; Tsai, Cheng-Yu; Lin, Yin-Hung; Tsai, Shih-Feng; TIEN-CHEN LIU ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; Jacob Shujui Hsu ; CHEN-CHI WU | The Journal of molecular diagnostics : JMD | 0 | 0 | |
2021 | Genetic spectrum and characteristics of hereditary optic neuropathy in Taiwan | CHAO-WEN LIN ; Huang C.-W.; Luo A.C.; Chou Y.-T.; Huang Y.-S.; PEI-LUNG CHEN ; TA-CHING CHEN | Genes | 3 | 3 | |
2021 | Genetic study of young-onset dementia using targeted gene panel sequencing in Taiwan | Hsu J.-L.; CHIN-HSIEN LIN ; PEI-LUNG CHEN ; Lin K.-J.; TA-FU CHEN | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 3 | 3 | |
2023 | Genetic Underpinnings and Audiological Characteristics in Children With Unilateral Sensorineural Hearing Loss | Lee, Chen-Yu; PEI-HSUAN LIN ; Chiang Yu-ting; Tsai, Cheng-Yu; Yang, Shu-Yu; Chen, You-Mei; Li, Chao-Hsuan; CHUN-YI LU ; TIEN-CHEN LIU ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; Jacob Shujui Hsu ; CHEN-CHI WU | Otolaryngology - Head and Neck Surgery | 2 | 0 | |
2013 | A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease | MING-TAI LIN ; CHIA-LIN HSU ; PEI-LUNG CHEN ; WEI-SHIUNG YANG ; JOU-KOU WANG ; Fann C.S.J.; MEI-HWAN WU | Translational Research | 13 | 12 | |
2020 | Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: Case series and literature review | Chu Y.-T.; Lin H.-Y.; PEI-LUNG CHEN ; CHIN-HSIEN LIN | BMC Neurology | 30 | 25 | |
2022 | Genotypes Influence Clinical Progression in EYS-Associated Retinitis Pigmentosa | Lo, Jui-En; Cheng, Chia-Yi; CHANG-HAO YANG ; CHUNG-MAY YANG ; Chen, Yi-Chieh; Huang, Yu-Shu; PEI-LUNG CHEN ; TA-CHING CHEN | Translational Vision Science and Technology | 2 | 2 | |
2020 | Genotypes predispose phenotypes—clinical features and genetic spectrum of abca4-associated retinal dystrophies | Sung Y.-C.; CHANG-HAO YANG ; CHUNG-MAY YANG ; CHAO-WEN LIN ; Huang D.-S.; Huang Y.-S.; FUNG-RONG HU ; PEI-LUNG CHEN ; TA-CHING CHEN | Genes | 8 | 6 | |
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 | |