| 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
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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
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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
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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
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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
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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
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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
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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
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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. |
| 臺大學術典藏 |
2019 |
VariED: the first integrated database of gene annotation and expression profiles for variants related to human diseases
|
ERIC YAO-YU CHUANG; Chuang, E.Y.; Tsai, M.-H.; Lu, T.-P.; Lai, L.-C.; Juang, J.-M.J.; Chiang, L.-M.; Chattopadhyay, A.; Lee, C.-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. |
| 臺大學術典藏 |
2019 |
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.; LIANG-CHUAN LAI; Tsai M.-H.; Lu T.-P.; Chuang E.Y.; Lee C.-Y.;Chattopadhyay A.;Chiang L.-M.;Juang J.-M.J.;Liang-Chuan Lai;Tsai M.-H.;Lu T.-P.;Chuang E.Y. |
| 臺大學術典藏 |
2019 |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
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Feng W.-J.; Chang S.-X.; Lei M.-H.; Ko W.-C.; Kong C.-W.; Kuo C.-T.; Huang B.-X.; Li K.-T.; Chen W.-D.; Luo J.-L.; Lin J.-Y.; Tsai T.-N.; Hsu C.-T.; Lin L.-R.; Chen R.-Y.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry; Chang J.-R.; Ye G.-H.; Chiu W.-R.; Liu Z.-Z.; Lin H.-H.; Liao Y.-C.; Li C.-H.; Hsieh Y.-C.; Chua S.-K.; Lin M.-T.; Chiu S.-N.; Horie M.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; Chang K.-C.; Feng A.-N.; Lin Y.-J.; Ueng K.-C.; Tsao H.-M.; Huang J.-L.; Tsai W.-C.; Tsai C.-F.; Chang S.-L.; Lo L.-W.; Hu Y.-F.; Chung F.-P.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; Chen C.-Y.J.; Juang J.-M.J.; LIAN-YU LIN; 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. |
| 臺大學術典藏 |
2019 |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
|
Lin L.-R.; Hsu C.-T.; Tsai T.-N.; Lin J.-Y.; Luo J.-L.; Chen W.-D.; Li K.-T.; Huang B.-X.; Kuo C.-T.; Hu Y.-F.; Chung F.-P.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; Chiu S.-N.; Lin M.-T.; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; Liao Y.-C.; Lin H.-H.; Liu Z.-Z.; Ye G.-H.; Chiu W.-R.; Chang J.-R.; Feng W.-J.; Chang S.-X.; Lei M.-H.; Ko W.-C.; Kong C.-W.; Chen C.-Y.J.; Juang J.-M.J.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Yu C.-C.; HUI-CHUN HUANG; 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.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; Chang K.-C.; Feng A.-N.; Lin Y.-J.; Ueng K.-C.; Tsao H.-M.; Huang J.-L.; Tsai W.-C.; Tsai C.-F.; Chang S.-L.; Lo L.-W.; Chen R.-Y.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry |
| 臺大學術典藏 |
2018 |
An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases
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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.; ERIC YAO-YU CHUANG; 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. |
| 臺大學術典藏 |
2018 |
The Taiwan Heart Registries: Its Influence on Cardiovascular Patient Care
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CHO-KAI WU; Juang J.-M.J.; Chiang J.-Y.; Li Y.-H.; Tsai C.-T.; Chiang F.-T. |
| 臺大學術典藏 |
2016 |
Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study
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Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Tseng W.-Y.I.; Lin J.-L.; MAO-YUAN SU; Wang Y.-C.; Lin L.-Y.; Wu C.-K.; Juang J.-M.J. |
| 臺大學術典藏 |
2016 |
Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy
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Chung Y.-W.; Yang Y.-H.; CHO-KAI WU; Yu C.-C.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lin L.-Y.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L. |
| 臺大學術典藏 |
2015 |
Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease
|
Ho L.-T.; Lin L.-Y.; Yang Y.-H.; Wu C.-K.; Juang J.-M.J.; YI-CHIH WANG; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.; Chen P.-C. |
| 臺大學術典藏 |
2015 |
Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease
|
Ho L.-T.; Lin L.-Y.; Yang Y.-H.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L.; Chen P.-C. |
| 國立臺灣大學 |
2014 |
THE RISK OF OSTEONECROSIS OF THE JAW IN TAIWANESE OSTEOPOROTIC PATIENTS TREATED WITH ORAL ALENDRONATE OR RALOXIFENE
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Chiu, W. -Y.; Chien, J. -Y.; Yang, W. -S.; Juang, J. -M J.; Lee, J. -J.; Tsai, K. -S.; 蔡克嵩; 李正?; 楊偉勛; 莊志明; 邱偉益; 簡榮彥 |
| 臺大學術典藏 |
2013 |
Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan
|
Juang J.-M.J.; Juang J.-M.J.;Chen C.-Y.;Liu Y.B.;Lin L.-Y.;Wen-Jone Chen;Lai L.-P.;Tsai C.-T.;Lin J.-L.; Chen C.-Y.; Liu Y.B.; Lin L.-Y.; WEN-JONE CHEN; Lai L.-P.; Tsai C.-T.; Lin J.-L. |
