公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
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 | |
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 | |