公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
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 | |
2015 | Long-term cochlear implant outcomes in children with GJB2 and SLC26A4 mutations | Wu C.-M.; Ko H.-C.; Tsou Y.-T.; Lin Y.-H.; Lin J.-L.; Chen C.-K.; PEI-LUNG CHEN ; Chen-Chi Wu | PLoS ONE | 39 | 36 | |
2018 | The Lupus-Associated Fcγ Receptor IIb–I232T Polymorphism Results in Impairment in the Negative Selection of Low-Affinity Germinal Center B Cells Via c-Abl in Mice | Jhou J.-P.; Yu I.-S.; Hwai H.; Chen C.-S.; PEI-LUNG CHEN ; SHIANG-JONG TZENG | Arthritis and Rheumatology | 4 | 2 | |
2021 | Metabolic syndromes as important comorbidities in patients of inherited retinal degenerations: Experiences from the nationwide health database and a large hospital-based cohort | Chiou G.-J.; Huang D.-S.; FUNG-RONG HU ; CHUNG-MAY YANG ; CHANG-HAO YANG ; Huang C.-W.; JOU-WEI LIN ; CHAO-WEN LIN ; TZYY-CHANG HO ; YI-TING HSIEH ; TSO-TING LAI ; Chen H.-M.; PEI-LUNG CHEN ; CHUHSING KATE HSIAO ; TA-CHING CHEN | International Journal of Environmental Research and Public Health | 1 | 0 | |
2016 | Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer | PO-HAN LIN ; WEN-HUNG KUO ; Huang A.-C.; YEN-SHEN LU ; CHING-HUNG LIN ; SUNG-HSIN KUO ; Wang M.-Y.; Liu C.-Y.; Cheng F.T.-F.; Yeh M.-H.; Li H.-Y.; Yang Y.-H.; Hsu Y.-H.; Fan S.-C.; Li L.-Y.; SUNG-LIANG YU ; KING-JEN CHANG ; PEI-LUNG CHEN ; YEN-HSUAN NI ; CHIUN-SHENG HUANG | Oncotarget | 74 | 64 | |
2020 | Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): New findings from the TOSCA TAND research project | PEI-LUNG CHEN | Journal of Neurodevelopmental Disorders | 16 | 15 | |
2019 | Newly diagnosed and growing subependymal giant cell astrocytoma in adults with tuberous sclerosis complex: Results from the International TOSCA Study | PEI-LUNG CHEN | Frontiers in Neurology | 19 | 18 | |
2016 | Next generation sequencing yields the complete mitochondrial genome of the flathead mullet, Mugil cephalus cryptic species NWP2 (Teleostei: Mugilidae) | Shen K.-N.; Yen T.-C.; Chen C.-H.; Li H.-Y.; PEI-LUNG CHEN ; Hsiao C.-D. | Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis | 33 | 32 | |
2021 | Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermia | HUEI-MING YEH ; Liao M.-H.; Chu C.-L.; Lin Y.-H.; WEI-ZEN SUN ; LING-PING LAI ; PEI-LUNG CHEN | Journal of the Formosan Medical Association | 7 | 3 | |
2023 | A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration | Chen, Huan-Yun; Lin, Han-I; Hsu, Chia-Lang; PEI-LUNG CHEN ; Huang, Cheng-Yen; SHU-CHUN TENG ; CHIN-HSIEN LIN | Parkinsonism & Related Disorders | 0 | 0 | |
2017 | A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss | Lin Y.-H.; Lin Y.-H.; Lu Y.-C.; TIEN-CHEN LIU ; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN ; CHIEN-YU CHEN ; CHEN-CHI WU | Scientific Reports | 20 | 19 | |