| 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. |
