| 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. |
| 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
|
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
|
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. |
