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機構 日期 題名 作者
臺大學術典藏 2020-12-04T07:44:49Z Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy Chen P.-C.; Chung Y.-W.; Yang Y.-H.; Wu C.-K.; Yu C.-C.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏 2020-12-04T07:44:48Z Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study LIAN-YU LIN; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Tseng W.-Y.I.; Lin J.-L.
臺大學術典藏 2020-12-04T07:44:42Z Genome-wide methylation profiles in coronary artery ectasia Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; LIAN-YU LIN; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.
臺大學術典藏 2020-12-04T07:44:40Z Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study Chen C.-Y.J.; Juang J.-M.J.; Chen Y.-H.; Wu I.-C.; Hsu C.-C.; Wu R.-C.; Chen K.-C.; Liaw W.-J.; Tsai T.-L.; LIAN-YU LIN; Hwang J.-J.; Ho L.-T.; Yu C.-C.; Lee J.-K.; Wu C.-K.; Yeh S.-F.S.; Yang D.-H.; Chang I.-S.; Lai L.-P.; Chiang F.-T.; Lin J.-L.; Hsiung C.A.
臺大學術典藏 2020-12-04T07:44:36Z Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry Chen C.-Y.J.; Lu T.-P.; LIAN-YU LIN; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏 2020-12-04T07:44:29Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Juang J.-M.J.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; LIAN-YU LIN; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C.
臺大學術典藏 2020-12-02T11:04:36Z Effects of angiotensin converting enzyme inhibition or angiotensin receptor blockade in dialysis patients: A nationwide data survey and propensity analysis CHO-KAI WU; Yang Y.-H.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.; Lin L.-Y.
臺大學術典藏 2020-12-02T11:04:34Z Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease Yang Y.-H.; CHO-KAI WU; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.; Chen P.-C.; Ho L.-T.; Lin L.-Y.
臺大學術典藏 2020-12-02T11:04:33Z Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study Lin L.-Y.; CHO-KAI WU; Juang J.-M.J.; Wang Y.-C.; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Tseng W.-Y.I.; Lin J.-L.
臺大學術典藏 2020-12-02T11:04:31Z Genome-wide methylation profiles in coronary artery ectasia Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; CHO-KAI WU; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.
臺大學術典藏 2020-12-02T11:04:29Z Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry Chen C.-Y.J.; Lu T.-P.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; CHO-KAI WU; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏 2020-12-02T11:04:29Z Metabolomic analysis of platelets of patients with aspirin non-response Chiang J.-Y.; Lee S.-H.; Chen Y.-C.; CHO-KAI WU; Chuang J.-Y.; Lo S.-C.; Yeh H.-M.; Yeh S.-F.; Hsu C.-A.; Lin B.-B.; Chang P.-C.; Chang C.-H.; Liang H.-J.; Chiang F.-T.; Lin C.-Y.; Juang J.-M.J.
臺大學術典藏 2020-12-02T11:04:29Z Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study Chen C.-Y.J.; Juang J.-M.J.; Chen Y.-H.; Wu I.-C.; Hsu C.-C.; Wu R.-C.; Chen K.-C.; Liaw W.-J.; Tsai T.-L.; Lin L.-Y.; Hwang J.-J.; Ho L.-T.; Yu C.-C.; Lee J.-K.; CHO-KAI WU; Yeh S.-F.S.; Yang D.-H.; Chang I.-S.; Lai L.-P.; Chiang F.-T.; Lin J.-L.; Hsiung C.A.
臺大學術典藏 2020-12-02T11:04:24Z Application of the newest European Association of Cardiovascular Imaging Recommendation regarding the long-term prognostic relevance of left ventricular diastolic function in heart failure with preserved ejection fraction Lin T.-T.; Wang Y.-C.; Juang J.-M.J.; Hwang J.-J.; CHO-KAI WU
臺大學術典藏 2020-12-02T09:15:20Z Effects of angiotensin converting enzyme inhibition or angiotensin receptor blockade in dialysis patients: A nationwide data survey and propensity analysis Wu C.-K.; Yang Y.-H.; Juang J.-M.J.; YI-CHIH WANG; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.; Lin L.-Y.
臺大學術典藏 2020-12-02T09:15:19Z Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy Lin L.-Y.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.; Chung Y.-W.; Yang Y.-H.; Wu C.-K.; Yu C.-C.; Juang J.-M.J.; YI-CHIH WANG; Tsai C.-T.
臺大學術典藏 2020-12-02T09:15:18Z Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study Lin J.-L.; Lin L.-Y.; Wu C.-K.; Juang J.-M.J.; YI-CHIH WANG; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Tseng W.-Y.I.
臺大學術典藏 2020-12-02T09:15:17Z Genome-wide methylation profiles in coronary artery ectasia Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; YI-CHIH WANG; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.
臺大學術典藏 2020-12-02T09:15:11Z Application of the newest European Association of Cardiovascular Imaging Recommendation regarding the long-term prognostic relevance of left ventricular diastolic function in heart failure with preserved ejection fraction Wu C.-K.; Hwang J.-J.; Juang J.-M.J.; YI-CHIH WANG; Lin T.-T.
臺大學術典藏 2020-12-01T08:29:26Z Trans-Ethnic Fine-Mapping of Lipid Loci Identifies Population-Specific Signals and Allelic Heterogeneity That Increases the Trait Variance Explained Feranil A.B.; Ho L.-T.; Hung Y.-J.; Hunt S.C.; Hveem K.; Juang J.-M.J.; Kesäniemi A.Y.; Kuusisto J.; Laakso M.; Lakka T.A.; Lee I.-T.; Leppert M.F.; Matise T.C.; Moilanen L.; Njølstad I.; Peters U.; Quertermous T.; Rauramaa R.; Rotter J.I.; Saramies J.; Tuomilehto J.; Uusitupa M.; TZUNG-DAU WANG; Boehnke M.; Haiman C.A.; Chen Y.-D.I.; Kooperberg C.; Assimes T.L.; Crawford D.C.; Hsiung C.A.; North K.E.; Mohlke K.L.; Wu Y.; Waite L.L.; Jackson A.U.; Sheu W.-H.H.; Buyske S.; Absher D.; Arnett D.K.; Boerwinkle E.; Bonnycastle L.L.; Carty C.L.; Cheng I.; Cochran B.; Croteau-Chonka D.C.; Dumitrescu L.; Eaton C.B.; Franceschini N.; Guo X.; Henderson B.E.; Hindorff L.A.; Kim E.; Kinnunen L.; Komulainen P.; Lee W.-J.; Le Marchand L.; Lin Y.; Lindström J.; Lingaas-Holmen O.; Mitchell S.L.; Narisu N.; Robinson J.G.; Schumacher F.; Stančáková A.; Sundvall J.; Sung Y.-J.; Swift A.J.; Wang W.-C.; Wilkens L.; Wilsgaard T.; Young A.M.; Adair L.S.; Duggan D.; Collins F.S.; Chakravarti A.; Bůžková P.; Ballantyne C.M.
臺大學術典藏 2020-12-01T08:29:25Z Trans-ethnic fine mapping identifies a novel independent locus at the 3′ end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population Goodarzi M.O.; Lee I.-T.; Knowles J.W.; Miller B.E.; Lee W.-J.; Juang J.-M.J.; TZUNG-DAU WANG; Guo X.; Taylor K.D.; Chuang L.-M.; Hsiung C.A.; Quertermous T.; Rotter J.I.; Chen Y.-D.I.; Kuo J.Z.; Sheu W.H.-H.; Assimes T.L.; Hung Y.-J.; Absher D.; Chiu Y.-F.; Mak J.; Wang J.-S.; Kwon S.; Hsu C.-C.
臺大學術典藏 2020-12-01T08:29:18Z Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci Zubair N.; Graff M.; Ambite J.L.; Bush W.S.; Kichaev G.; Lu Y.; Manichaikul A.; Sheu W.H.-H.; Absher D.; Assimes T.L.; Bielinski S.J.; Bottinger E.P.; Buzkova P.; Chuang L.-M.; Chung R.-H.; Cochran B.; Dumitrescu L.; Gottesman O.; Haessler J.W.; Haiman C.; Heiss G.; Hsiung C.A.; Hung Y.-J.; Hwu C.-M.; Juang J.-m.J.; Marchand L.L.; Lee I.-T.; Lee W.-J.; Lin L.-A.; Lin D.; Lin S.-Y.; Mackey R.H.; Martin L.W.; Pasaniuc B.; Peters U.; Predazzi I.; Quertermous T.; Reiner A.P.; Robinson J.; Rotter J.I.; Ryckman K.K.; Schreiner P.J.; Stahl E.; Tao R.; Tsai M.Y.; Waite L.L.; TZUNG-DAU WANG; Buyske S.; Chen Y.-D.I.; Cheng I.; Crawford D.C.; Loos R.J.F.; Rich S.S.; Fornage M.; North K.E.; Kooperberg C.; Carty C.L.
臺大學術典藏 2020-12-01T08:29:13Z Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci Taylor K.D.; Lee I.-T.; Liu Y.; TZUNG-DAU WANG; Quertermous T.; Juang J.-M.J.; Rotter J.I.; Assimes T.; Hsiung C.A.; Chen Y.-D.I.; Prentice R.; Kuller L.H.; Manson J.A.E.; Kooperberg C.; Smokowski P.; Robinson W.R.; Gordon-Larsen P.; Li R.; Hindorff L.; Buyske S.; Matise T.C.; Peters U.; North K.E.; Tao R.; Isasi C.; Avilés-Santa L.; Daviglus M.; Mackey R.H.; Houston D.; Gu C.C.; Ehret G.; Nguyen K.-D.H.; Lewis C.E.; Leppert M.; Irvin M.R.; Lim U.; Haiman C.A.; Le Marchand L.; Schumacher F.; Wilkens L.; Lu Y.; Bottinger E.P.; Loos R.J.L.; Sheu W.H.-H.; Guo X.; Lee W.-J.; Hai Y.; Hung Y.-J.; Absher D.; Wu I.-C.; Buzkova P.; Fernández-Rhodes L.; Gong J.; Haessler J.; Franceschini N.; Graff M.; Nishimura K.K.; Wang Y.; Highland H.M.; Yoneyama S.; Bush W.S.; Goodloe R.; Ritchie M.D.; Crawford D.; Gross M.; Fornage M.
臺大學術典藏 2020-12-01T08:29:12Z Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms Howson J.M.M.; Zhao W.; Barnes D.R.; Ho W.-K.; Young R.; Paul D.S.; Waite L.L.; Freitag D.F.; Fauman E.B.; Salfati E.L.; Sun B.B.; Eicher J.D.; Johnson A.D.; Sheu W.H.H.; Nielsen S.F.; Lin W.-Y.; Surendran P.; Malarstig A.; Wilk J.B.; Tybjærg-Hansen A.; Rasmussen K.L.; Kamstrup P.R.; Deloukas P.; Erdmann J.; Kathiresan S.; Samani N.J.; Schunkert H.; Watkins H.; Do R.; Rader D.J.; Johnson J.A.; Hazen S.L.; Quyyumi A.A.; Spertus J.A.; Pepine C.J.; Franceschini N.; Justice A.; Reiner A.P.; Buyske S.; Hindorff L.A.; Carty C.L.; North K.E.; Kooperberg C.; Boerwinkle E.; Young K.; Graff M.; Peters U.; Absher D.; Hsiung C.A.; Lee W.-J.; Taylor K.D.; Chen Y.-H.; Lee I.-T.; Guo X.; Chung R.-H.; Hung Y.-J.; Rotter J.I.; Juang J.-M.J.; Quertermous T.; TZUNG-DAU WANG; Rasheed A.; Frossard P.; Alam D.S.; Majumder A.A.S.; Di Angelantonio E.; Chowdhury R.; Chen Y.-D.I.; Nordestgaard Bø.G.; Assimes T.L.; Danesh J.; Butterworth A.S.; Saleheen D.; CARDIoGRAMplusC4D, EPIC-CVD
臺大學術典藏 2020-12-01T08:29:11Z Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease Hussain Qureshi I.; Tanveer-Us-Salam, Iqbal W.; Malik U.; Mehra N.; Kuo J.Z.; Sheu W.H.-H.; Guo X.; Hsiung C.A.; Juang J.-M.J.; Taylor K.D.; Hung Y.-J.; Lee W.-J.; Quertermous T.; Lee I.-T.; Hsu C.-C.; Bottinger E.P.; Ralhan S.; Teo Y.Y.; TZUNG-DAU WANG; Alam D.S.; Di Angelantonio E.; Epstein S.; Nielsen S.F.; Nordestgaard B.G.; Tybjaerg-Hansen A.; Young R.; Benn M.; Frikke-Schmidt R.; Kamstrup P.R.; Jukema J.W.; Sattar N.; Smit R.; Chung R.-H.; Liang K.-W.; Anand S.; Sanghera D.K.; Ripatti S.; Loos R.J.F.; Kooner J.S.; Tai E.S.; Rotter J.I.; Ida Chen Y.-D.; Frossard P.; Maeda S.; Kadowaki T.; Reilly M.; Pare G.; Melander O.; Salomaa V.; Rader D.J.; Danesh J.; Voight B.F.; Saleheen D.; Zhao W.; Rasheed A.; Tikkanen E.; Lee J.-J.; Butterworth A.S.; Howson J.M.M.; Assimes T.L.; Chowdhury R.; Orho-Melander M.; Damrauer S.; Small A.; Asma S.; Imamura M.; Yamauch T.; Chambers J.C.; Chen P.; Sapkota B.R.; Shah N.; Jabeen S.; Surendran P.; Lu Y.; Zhang W.; Imran A.; Abbas S.; Majeed F.; Trindade K.; Qamar N.; Mallick N.H.; Yaqoob Z.; Saghir T.; Hasan Rizvi S.N.; Memon A.; Rasheed S.Z.; Memon F.-U.-R.; Mehmood K.; Ahmed N.
臺大學術典藏 2020-12-01T08:29:03Z Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids Bentley A.R.; Sung Y.J.; Brown M.R.; Winkler T.W.; Kraja A.T.; Ntalla I.; Schwander K.; Chasman D.I.; Lim E.; Deng X.; Guo X.; Liu J.; Lu Y.; Cheng C.-Y.; Sim X.; Vojinovic D.; Huffman J.E.; Musani S.K.; Li C.; Feitosa M.F.; Richard M.A.; Noordam R.; Baker J.; Chen G.; Aschard H.; Bartz T.M.; Ding J.; Dorajoo R.; Manning A.K.; Rankinen T.; Smith A.V.; Tajuddin S.M.; Zhao W.; Graff M.; Alver M.; Boissel M.; Chai J.F.; Chen X.; Divers J.; Evangelou E.; Gao C.; Goel A.; Hagemeijer Y.; Harris S.E.; Hartwig F.P.; He M.; Horimoto A.R.V.R.; Hsu F.-C.; Hung Y.-J.; Jackson A.U.; Kasturiratne A.; Komulainen P.; Kühnel B.; Leander K.; Lin K.-H.; Luan J.; Lyytikäinen L.-P.; Matoba N.; Nolte I.M.; Pietzner M.; Prins B.; Riaz M.; Robino A.; Said M.A.; Schupf N.; Scott R.A.; Sofer T.; Stancáková A.; Takeuchi F.; Tayo B.O.; van der Most P.J.; Varga T.V.; TZUNG-DAU WANG; Wang Y.; Ware E.B.; Wen W.; Xiang Y.-B.; Yanek L.R.; Zhang W.; Zhao J.H.; Adeyemo A.; Afaq S.; Amin N.; Amini M.; Arking D.E.; Arzumanyan Z.; Aung T.; Ballantyne C.; Barr R.G.; Bielak L.F.; Boerwinkle E.; Bottinger E.P.; Broeckel U.; Brown M.; Cade B.E.; Campbell A.; Canouil M.; Charumathi S.; Chen Y.-D.I.; Christensen K.; Concas M.P.; Connell J.M.; de las Fuentes L.; de Silva H.J.; de Vries P.S.; Doumatey A.; Duan Q.; Eaton C.B.; Eppinga R.N.; Faul J.D.; Floyd J.S.; Forouhi N.G.; Forrester T.; Friedlander Y.; Gandin I.; Gao H.; Ghanbari M.; Gharib S.A.; Gigante B.; Giulianini F.; Grabe H.J.; Gu C.C.; Harris T.B.; Heikkinen S.; Heng C.-K.; Hirata M.; Hixson J.E.; Ikram M.A.; Jia Y.; Joehanes R.; Johnson C.; Jonas J.B.; Justice A.E.; Katsuya T.; Khor C.C.; Kilpeläinen T.O.; Koh W.-P.; Kolcic I.; Kooperberg C.; Krieger J.E.; Kritchevsky S.B.; Kubo M.; Kuusisto J.; Lakka T.A.; Langefeld C.D.; Langenberg C.; Launer L.J.; Lehne B.; Lewis C.E.; Li Y.; Liang J.; Lin S.; Liu C.-T.; Liu J.; Liu K.; Loh M.; Lohman K.K.; Louie T.; Luzzi A.; Mägi R.; Mahajan A.; Manichaikul A.W.; McKenzie C.A.; Meitinger T.; Metspalu A.; Milaneschi Y.; Milani L.; Mohlke K.L.; Momozawa Y.; Morris A.P.; Murray A.D.; Nalls M.A.; Nauck M.; Nelson C.P.; North K.E.; O’Connell J.R.; Palmer N.D.; Papanicolau G.J.; Pedersen N.L.; Peters A.; Peyser P.A.; Polasek O.; Poulter N.; Raitakari O.T.; Reiner A.P.; Renström F.; Rice T.K.; Rich S.S.; Robinson J.G.; Rose L.M.; Rosendaal F.R.; Rudan I.; Schmidt C.O.; Schreiner P.J.; Scott W.R.; Sever P.; Shi Y.; Sidney S.; Sims M.; Smith J.A.; Snieder H.; Starr J.M.; Strauch K.; Stringham H.M.; Tan N.Y.Q.; Tang H.; Taylor K.D.; Teo Y.Y.; Tham Y.C.; Tiemeier H.; Turner S.T.; Uitterlinden A.G.; van Heemst D.; Waldenberger M.; Wang H.; Wang L.; Wang L.; Wei W.B.; Williams C.A.; Wilson G.; Sr, Wojczynski M.K.; Yao J.; Young K.; Yu C.; Yuan J.-M.; Zhou J.; Zonderman A.B.; Becker D.M.; Boehnke M.; Bowden D.W.; Chambers J.C.; Cooper R.S.; de Faire U.; Deary I.J.; Elliott P.; Esko T.; Farrall M.; Franks P.W.; Freedman B.I.; Froguel P.; Gasparini P.; Gieger C.; Horta B.L.; Juang J.-M.J.; Kamatani Y.; Kammerer C.M.; Kato N.; Kooner J.S.; Laakso M.; Laurie C.C.; Lee I.-T.; Lehtimäki T.; Magnusson P.K.E.; Oldehinkel A.J.; Penninx B.W.J.H.; Pereira A.C.; Rauramaa R.; Redline S.; Samani N.J.; Scott J.; Shu X.-O.; van der Harst P.; Wagenknecht L.E.; Wang J.-S.; Wang Y.X.; Wareham N.J.; Watkins H.; Weir D.R.; Wickremasinghe A.R.; Wu T.; Zeggini E.; Zheng W.; Bouchard C.; Evans M.K.; Gudnason V.; Kardia S.L.R.; Liu Y.; Psaty B.M.; Ridker P.M.; van Dam R.M.; Mook-Kanamori D.O.; Fornage M.; Province M.A.; Kelly T.N.; Fox E.R.; Hayward C.; van Duijn C.M.; Tai E.S.; Wong T.Y.; Loos R.J.F.; Franceschini N.; Rotter J.I.; Zhu X.; Bierut L.J.; Gauderman W.J.; Rice K.; Munroe P.B.; Morrison A.C.; Rao D.C.; Rotimi C.N.; Cupples L.A.; COGENT-Kidney Consortium, EPIC-InterAct Consortium, Understanding Society Scientific Group, Lifelines Cohort
臺大學術典藏 2020-11-25T07:22:53Z Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry Chen, C-Y J; Juang, J-M J; Lin, L-Y; Liu, Y-B; Ho, L-T; Yu, C-C; Huang, H-C; Lin, T-T; Liao, M-C; Chen, J-J; Hwang, J-J; Chen, W-J; Yeh, S-F S; Yang, D-H; Chiang, F-T; Lin, J-L; Lai, L-P; Horie, M
臺大學術典藏 2020-11-17T02:45:34Z Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome Lin J.-L.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Hwang J.-J.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Hwang J.-J.;Chiang F.-T.;Yeh S.S.-F.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.
臺大學術典藏 2020-11-17T02:45:33Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Chuang E.Y.; Lin J.-L.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Ho C.-C.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Chiang F.-T.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.
臺大學術典藏 2020-11-17T02:45:26Z Genome-wide methylation profiles in coronary artery ectasia Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.; Tzu-Pin Lu;Chuang N.-C.;Cheng C.-Y.;Hsu C.-A.;Wang Y.-C.;Lin Y.-H.;Lee J.-K.;Wu C.-K.;Hwang J.-J.;Lin L.-Y.;Yeh S.-F.S.;Chien K.-L.;Juang J.-M.J.; TZU-PIN LU
臺大學術典藏 2020-11-17T02:45:24Z An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases Huang S.-H.;Chang Y.-S.;Juang J.-M.J.;Chang K.-W.;Tsai M.-H.;Tzu-Pin Lu;Lai L.-C.;Chuang E.Y.;Huang N.-T.; Huang S.-H.; Chang Y.-S.; Juang J.-M.J.; Chang K.-W.; Tsai M.-H.; TZU-PIN LU; Lai L.-C.; Chuang E.Y.; Huang N.-T.
臺大學術典藏 2020-11-17T02:45:22Z VariED: The first integrated database of gene annotation and expression profiles for variants related to human diseases Juang J.-M.J.; Lai L.-C.; Tsai M.-H.; TZU-PIN LU; Chuang E.Y.; Lee C.-Y.;Chattopadhyay A.;Chiang L.-M.;Juang J.-M.J.;Lai L.-C.;Tsai M.-H.;Tzu-Pin Lu;Chuang E.Y.; Lee C.-Y.; Chattopadhyay A.; Chiang L.-M.
臺大學術典藏 2020-11-17T02:45:22Z Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry Chen C.-Y.J.;Tzu-Pin Lu;Lin L.-Y.;Liu Y.-B.;Ho L.-T.;Huang H.-C.;Lai L.-P.;Hwang J.-J.;Yeh S.-F.S.;Wu C.-K.;Juang J.-M.J.;Antzelevitch C.; Chen C.-Y.J.; TZU-PIN LU; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏 2020-07-01T08:12:26Z Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome Juang J.-M.J.;Lu T.-P.;Liang-Chuan Lai;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Hwang J.-J.;Chiang F.-T.;Yeh S.S.-F.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; Juang J.-M.J.; Lu T.-P.; LIANG-CHUAN LAI; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏 2020-07-01T08:12:23Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Juang J.-M.J.;Lu T.-P.;Liang-Chuan Lai;Ho C.-C.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Chiang F.-T.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; Lu T.-P.; LIANG-CHUAN LAI; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L.
臺大學術典藏 2020-07-01T08:12:15Z An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases Huang S.-H.;Chang Y.-S.;Juang J.-M.J.;Chang K.-W.;Tsai M.-H.;Lu T.-P.;Liang-Chuan Lai;Chuang E.Y.;Huang N.-T.; Huang S.-H.; Chang Y.-S.; Juang J.-M.J.; Chang K.-W.; Tsai M.-H.; Lu T.-P.; LIANG-CHUAN LAI; Chuang E.Y.; Huang N.-T.
臺大學術典藏 2020-06-29T01:21:30Z An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases Huang, S.-H.;Chang, Y.-S.;Juang, J.-M.J.;Chang, K.-W.;Tsai, M.-H.;Lu, T.-P.;Lai, L.-C.;Chuang, E.Y.;Huang, N.-T.; Huang, S.-H.; Chang, Y.-S.; Juang, J.-M.J.; Chang, K.-W.; Tsai, M.-H.; Lu, T.-P.; Lai, L.-C.; Chuang, E.Y.; Huang, N.-T.; NIEN-TSU HUANG
臺大學術典藏 2020-04-16T02:34:27Z Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome Yeh, S.S.-F.; Chen, W.-P.; Chuang, E.Y.; Lai, L.-P.; Lin, J.-L.; ERIC YAO-YU CHUANG; Juang, J.-M.J.;Lu, T.-P.;Lai, L.-C.;Hsueh, C.-H.;Liu, Y.-B.;Tsai, C.-T.;Lin, L.-Y.;Yu, C.-C.;Hwang, J.-J.;Chiang, F.-T.;Yeh, S.S.-F.;Chen, W.-P.;Chuang, E.Y.;Lai, L.-P.;Lin, J.-L.; Juang, J.-M.J.; Lu, T.-P.; Lai, L.-C.; Hsueh, C.-H.; Liu, Y.-B.; Tsai, C.-T.; Lin, L.-Y.; Yu, C.-C.; Hwang, J.-J.; Chiang, F.-T.
臺大學術典藏 2020-04-16T02:34:24Z Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation Tsai, C.-T.;Hsieh, C.-S.;Chang, S.-N.;Chuang, E.Y.;Juang, J.-M.J.;Lin, L.-Y.;Lai, L.-P.;Hwang, J.-J.;Chiang, F.-T.;Lin, J.-L.; Tsai, C.-T.; Hsieh, C.-S.; Chang, S.-N.; Chuang, E.Y.; Juang, J.-M.J.; Lin, L.-Y.; Lai, L.-P.; Hwang, J.-J.; Chiang, F.-T.; Lin, J.-L.; ERIC YAO-YU CHUANG
臺大學術典藏 2020-03-03T03:06:30Z Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study Lin L.-Y.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; WEN-YIH TSENG; Lin J.-L.
臺大學術典藏 2020-02-27T07:42:50Z Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan Liu Y.B.; Lin L.-Y.; WEN-JONE CHEN; Lai L.-P.; Tsai C.-T.; Lin J.-L.; Lin J.-L.;Tsai C.-T.;Lai L.-P.;WEN-JONE CHEN;Lin L.-Y.;Liu Y.B.;Chen C.-Y.;Juang J.-M.J.; Juang J.-M.J.; Chen C.-Y.
臺大學術典藏 2020-02-27T07:42:47Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Lin J.-L.;Chuang E.Y.;Lai L.-P.;Yeh S.-F.S.;Chiang F.-T.;WEN-JONE CHEN;Yu C.-C.;Lin L.-Y.;Tsai C.-T.;Liu Y.-B.;Ho C.-C.;Lai L.-C.;Lu T.-P.;Juang J.-M.J.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; WEN-JONE CHEN; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L.
臺大學術典藏 2020-02-27T07:42:46Z Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan Lin J.-L.;Lai L.-P.;Sherri Yeh S.-F.;Yeh H.-M.;Chiang F.-T.;Tseng C.-D.;WEN-JONE CHEN;Chiu F.-C.;Chen J.-J.;Hwang J.-J.;Yu C.-C.;Liu Y.-B.;Lin L.-Y.;Tsai C.-T.;Juang J.M.J.; Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; WEN-JONE CHEN; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L.
臺大學術典藏 2020-02-10T09:00:12Z VariED: the first integrated database of gene annotation and expression profiles for variants related to human diseases Lee C.-Y.;Chattopadhyay A.;Chiang L.-M.;Juang J.-M.J.;Lai L.-C.;Tsai M.-H.;Lu T.-P.;Chuang E.Y.; Lee C.-Y.; Chattopadhyay A.; Chiang L.-M.; Juang J.-M.J.; Lai L.-C.; Tsai M.-H.; Lu T.-P.; Chuang E.Y.; MONG-HSUN TSAI
臺大學術典藏 2020 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Juang J.-M.J.; TZU-PIN LU; Chen C.-Y.J.; Huang H.-C.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Antzelevitch C.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Juang J.-M.J.;Binda A.;Lee S.-J.;Hwang J.-J.;Chen W.-J.;Liu Y.-B.;Lin L.-Y.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Tzu-Pin Lu;Lai L.-C.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.
臺大學術典藏 2020 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Binda A.; Juang J.-M.J.; Antzelevitch C.; Chuang E.Y.; Rivolta I.; Lee S.-J.; Hwang J.-J.; WEN-JONE CHEN; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.
臺大學術典藏 2020 Application of the newest European Association of Cardiovascular Imaging Recommendation regarding the long-term prognostic relevance of left ventricular diastolic function in heart failure with preserved ejection fraction Wu C.-K.; HWANG, JUEY-JEN; Juang J.-M.J.; Wang Y.-C.; Lin T.-T.
臺大學術典藏 2020 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Chen, W.-J.; Lee, S.-J.; Hwang, J.-J.; Binda, A.; Juang, J.-M.J.; Juang, J.-M.J.;Binda, A.;Lee, S.-J.;Hwang, J.-J.;Chen, W.-J.;Liu, Y.-B.;Lin, L.-Y.;Yu, C.-C.;Ho, L.-T.;Huang, H.-C.;Chen, C.-Y.J.;Lu, T.-P.;Lai, L.-C.;Yeh, S.-F.S.;Lai, L.-P.;Chuang, E.Y.;Rivolta, I.;Antzelevitch, C.; SHYH-JYE LEE; Liu, Y.-B.; Lin, L.-Y.; Yu, C.-C.; Ho, L.-T.; Huang, H.-C.; Chen, C.-Y.J.; Lu, T.-P.; Lai, L.-C.; Yeh, S.-F.S.; Lai, L.-P.; Chuang, E.Y.; Rivolta, I.; Antzelevitch, C.
臺大學術典藏 2019-11-27T06:54:13Z Fabry disease cardiac variant IVS4+919 G>A is associated with multiple cardiac gene variants in patients with severe cardiomyopathy and fatal arrhythmia Juang J.-M.J.;Shun C.-T.;Yih-Sharng Chen;Hwu W.-L.;Lee N.-C.;Tsai W.-H.;Chen N.-Q.;Chien Y.-H.; Juang J.-M.J.; Shun C.-T.; YIH-SHARNG CHEN; Hwu W.-L.; Lee N.-C.; Tsai W.-H.; Chen N.-Q.; Chien Y.-H.
臺大學術典藏 2019 Metabolomic analysis of platelets of patients with aspirin non-response Chuang J.-Y.; Wu C.-K.; Lee S.-H.; Chen Y.-C.; Chiang J.-Y.; Chiang J.-Y.;Lee S.-H.;Chen Y.-C.;Wu C.-K.;Chuang J.-Y.;Shyh-Chyi Lo;Yeh H.-M.;Yeh S.-F.;Hsu C.-A.;Lin B.-B.;Chang P.-C.;Chang C.-H.;Liang H.-J.;Chiang F.-T.;Lin C.-Y.;Juang J.-M.J.; SHYH-CHYI LO; Yeh H.-M.; Yeh S.-F.; Hsu C.-A.; Lin B.-B.; Chang P.-C.; Chang C.-H.; Liang H.-J.; Chiang F.-T.; Lin C.-Y.; Juang J.-M.J.

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