公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
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 | |
2018 | Oncogenic Function of a KIF5B-MET Fusion Variant in Non-Small Cell Lung Cancer | Gow C.-H.; Liu Y.-N.; Li H.-Y.; MIN-SHU HSIEH ; Chang S.-H.; Luo S.-C.; TZU-HSIU TSAI ; PEI-LUNG CHEN ; Tsai M.-F.; JIN-YUAN SHIH | Neoplasia (United States) | 22 | 22 | |
2018 | Overview of the current status of familial hypercholesterolaemia care in over 60 countries - The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC) | Vallejo-Vaz A.J.; Marco M.D.; Stevens C.A.T.; Akram A.; Freiberger T.; Hovingh G.K.; Kastelein J.J.P.; Mata P.; Raal F.J.; Santos R.D.; Soran H.; Jambart S.; Khoury P.E.; Gargalskaite U.; Kutkiene S.; Al-Khateeb A.; An C.Y.; Ismail Z.; Kasim S.; Ibrahim K.S.; Al-Sarraf A.; Torlak V.A.; Radzi A.B.M.; Kasim N.A.; Nor N.S.M.; Ramli A.S.; Razak S.A.; Muid S.; Rosman A.; Sanusi A.R.; Razman A.Z.; Nazli S.A.; Jannes C.E.; Ashavaid T.F.; Kek T.L.; Azzopardi C.; Aguilar Salinas C.A.; Gal?n G.; Rubinstein A.; Maga?a-Torres M.T.; Martagon A.; Mehta R.; Wittekoek M.E.; Krieger J.E.; Isara A.R.; Binder C.J.; Obaseki D.E.; Ohenhen O.A.; Holven K.B.; Grucha?a M.; Baranowska M.; Borowiec-Wolny J.; Gilis-Malinowska N.; Michalska-Grzonkowska A.; Pereira A.C.; Pajkowski M.; Parczewska A.; Bogsrud M.P.; Romanowska-Kocejko M.; Str??yk A.; ?arczy?ska-Buchowiecka M.; Kleinschmidt M.; Alves A.C.; Medeiros A.M.; Ershova A.; Ruel I.; Korneva V.; Kuznetsova T.; Malyshev P.; Bourbon M.; Meshkov A.; Rozhkova T.; Popovic L.; Lukac S.S.; Stosic L.; Rasulic I.; Asenjo S.; Lalic N.M.; Chua T.S.J.; Ting S.P.L.; Raslova K.; Bruckert E.; Battelino T.; Cevc M.; Jug B.; Kovac J.; Podkrajsek K.T.; Cuevas A.; Sustar U.; Trontelj K.J.; Marais D.; Isla L.P.; Martin F.J.; Chlebus K.; Charng M.-J.; PEI-LUNG CHEN ; Kayik?ioglu M.; Dell’oca N.; Pe?in I.; Fern?ndez G.; Ressia A.; Reyes X.; Zelarayan M.; Alieva R.B.; Hoshimov S.U.; Corral P.; Nizamov U.I.; Kurbanov R.D.; Lima-Mart?nez M.M.; Miltiadous G.; Nguyen M.-N.T.; Do D.-L.; Kim N.-T.; Le T.-T.; Le H.-A.; Descamps O.; Durst R.; Ezhov M.; Fras Z.; Genest J.; Panayiotou A.G.; Groselj U.; Harada-Shiba M.; Kayikcioglu M.; Lalic K.; Lam C.S.P.; Latkovskis G.; Laufs U.; Liberopoulos E.; Lin J.; Maher V.; Watts G.F.; Majano N.; Marais A.D.; M?rz W.; Mirrakhimov E.; Miserez A.R.; Mitchenko O.; Nawawi H.M.; Nordestgaard B.G.; Paragh G.; Petrulioniene Z.; Vrablik M.; Pojskic B.; Postadzhiyan A.; Reda A.; Reiner ?.; Sadoh W.E.; Sahebkar A.; Shehab A.; Shek A.B.; Stoll M.; TA-CHEN SU ; Benn M.; Subramaniam T.; Susekov A.V.; Symeonides P.; Tilney M.; Tomlinson B.; Truong T.-H.; Tselepis A.D.; Tybj?rg-Hansen A.; V?zquez-C?rdenas A.; Viigimaa M.; Heinsar S.; Vohnout B.; Wid?n E.; Yamashita S.; Banach M.; Gaita D.; Jiang L.; Nilsson L.; Santos L.E.; Schunkert H.; Tokg?zo?lu L.; B?liard S.; Car J.; Catapano A.L.; Ray K.K.; Schreier L.; Pang J.; Dieplinger H.; Hanauer-Mader G.; Desutter J.; Langlois M.; Mertens A.; Gouni-Berthold I.; Rietzschel E.; Wallemacq C.; Isakovic D.; Dzankovic A.M.; Obralija J.; Pojskic L.; Sisic I.; Stimjanin E.; Hengstenberg W.; Julius U.; Kassner U.; Klose G.; K?nig C.; Abifadel M.; K?nig W.; Otte B.; Parhofer K.; Schatz U.; Schmidt N.; Steinhagen-Thiessen E.; Vogt A.; Antza C.; Athyros V.; Bilianou E.; Aguilar-Salinas C.A.; Boufidou A.; Chrousos G.; Elisaf M.; Garoufi A.; Katsiki N.; Kolovou G.; Kotsis V.; Rallidis L.; Rizos C.; Skalidis E.; Al-Khnifsawi M.; Skoumas I.; Tziomalos K.; Shawney J.P.S.; Abbaszadegan M.R.; Aminzadeh M.; Hosseini S.; Mobini M.; Vakili R.; Zaeri H.; Agar R.; Alkindi F.A.; Boran G.; Colwell N.; Crowley V.; Durkin M.; Griffin D.; Kelly M.; Rakovac-Tisdall A.; Bitzur R.; Cohen H.; Eliav O.; Alnouri F.; Ellis A.; Gavish D.; Harats D.; Henkin Y.; Knobler H.; Leavit L.; Leitersdorf E.; Schurr D.; Shpitzen S.; Szalat A.; Alonso R.; Arca M.; Averna M.; Bertolini S.; Calandra S.; Tarugi P.; Erglis A.; Gilis D.; Nesterovics G.; Saripo V.; Upena-Roze A.; Al-Rasadi K.; Elbitar S. | Atherosclerosis | 152 | 138 | |
2019 | P53 ICE CRIM mouse: A tool to generate mutant allelic series in somatic cells and germ lines for cancer studies | Fan H.-H.; Shing Yu I.; Lin Y.-H.; Wang S.-Y.; Liaw Y.-H.; PEI-LUNG CHEN ; TSUNG-LIN YANG ; SHU-WHA LIN ; YOU-TZUNG CHEN | FASEB Journal | 1 | 1 | |
2022 | Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes | Lee, Chia-Jung; Chen, Ting-Huei; Lim, Aylwin Ming Wee; Chang, Chien-Ching; Sie, Jia-Jyun; PEI-LUNG CHEN ; Chang, Su-Wei; Wu, Shang-Jung; Hsu, Chia-Lin; Hsieh, Ai-Ru; WEI-SHIUNG YANG ; Fann, Cathy S J | Acta Crystallographica Section F Structural Biology Communications | 7 | 8 | |
2019 | Plectin Mutations in Progressive Familial Intrahepatic Cholestasis | Wu S.-H.; Jacob Shujui Hsu ; HUEY-LING CHEN ; Chien M.-M.; JIA-FENG WU ; YEN-HSUAN NI ; Liou B.-Y.; MING-CHIH HO ; YUNG-MING JENG ; MEI-HWEI CHANG ; PEI-LUNG CHEN | Hepatology | 10 | 7 | |
2022 | PREDICTED PROTEIN STRUCTURE VARIATIONS INDICATE THE CLINICAL PRESENTATION OF CYP4V2 -RELATED BIETTI CRYSTALLINE DYSTROPHY | Chan, Li Wei; Sung, Yu Chi; Wu, Dung Chi; CHIEN-YU CHEN ; CHANG-HAO YANG ; CHUNG-MAY YANG ; PEI-LUNG CHEN ; TA-CHING CHEN | Retina | 4 | 3 | |