| 臺大學術典藏 |
2020-12-28T12:04:07Z |
Next-generation sequencing in the genetics of human atrial fibrillation
|
Hsieh C.-S.; Chuang E.Y.; Juang J.-M.J.; HWANG, JUEY-JEN; Tseng C.-D.; Chiang F.-T.; Lai L.-P.; Lin J.-L.; Tsai C.-T. |
| 臺大學術典藏 |
2020-12-28T12:04:03Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
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, JUEY-JEN; 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 |
2020-12-28T12:03:59Z |
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, JUEY-JEN; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:54Z |
Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation
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Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Ueng K.-C.; Tsai C.-F.; Lin T.-H.; Wu C.-K.; Lee J.-K.; Lin L.-Y.; Wang Y.-C.; Yu C.-C.; Lai L.-P.; Tseng C.-D.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:19Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
|
Lin J.-L.; Yang D.-H.; Chuang J.-Y.; Sherri Yeh S.-F.; Chen J.-J.; Liao M.-T.; Jyh-Ming J.-J.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; HWANG, JUEY-JEN; Lin T.-T.; Lu T.-P.; Chuang E.Y.; Ackerman M.J. |
| 臺大學術典藏 |
2020-12-28T12:03:16Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
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Antzelevitch C.; Rivolta I.; Chuang E.Y.; Lai L.-P.; Yeh S.-F.S.; Lai L.-C.; Lu T.-P.; Huang H.-C.; Chen C.-Y.J.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Liu Y.-B.; Juang J.-M.J.; Binda A.; Lee S.-J.; HWANG, JUEY-JEN; Chen W.-J. |
| 臺大學術典藏 |
2020-12-28T12:03:15Z |
Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence
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Chiu F.-C.; Wu C.-K.; HWANG, JUEY-JEN; Chuang E.Y.; Tsai C.-T.; Huang P.-S.; Hsieh C.-S.; Chang S.-N.; Chen J.-J. |
| 臺大學術典藏 |
2020-12-28T10:52:55Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
|
Liu Y.-B.; Jyh-Ming J.-J.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; HUI-CHUN HUANG; Ho L.-T.; Lai L.-P.; Hwang J.-J.; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y.; Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J. |
| 臺大學術典藏 |
2020-12-28T10:52:54Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Binda A.; Juang J.-M.J.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; HUI-CHUN HUANG; 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 |
2020-12-28T10:02:42Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; CHIH-CHIEH YU; 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. |
| 臺大學術典藏 |
2020-12-28T10:02:41Z |
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.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; CHIH-CHIEH YU; 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 |
2020-12-28T08:14:22Z |
SLCO3A1, a novel Crohn's disease-associated gene, regulates NF-κB activity and associates with intestinal perforation
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Wei S.-C.; Podolsky D.K.; Wong J.-M.; Tan Y.-Y.; Weng M.-T.; Lai L.-C.; Hsiao J.-H.; Chuang E.Y.; Shun C.-T.; Wu D.-C.; Kao A.-W.; Chuang C.-S.; YEN-HSUAN NI; Shieh M.-J.; Tung C.-C.; Chen Y.; Wang C.-Y.; Xavier R.J. |
| 臺大學術典藏 |
2020-12-28T08:14:12Z |
SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway
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Shun C.-T.; YEN-HSUAN NI; Chuang E.Y.; Hsiao J.-H.; Lai L.-C.; Yu L.C.H.; Wei S.-C.; Yang-Yen H.-F.; Tsao P.-N.; Weng M.-T.; Tung C.-C.; Xavier R.J.; Podolsky D.K.; Yen J.J.Y.; Wong J.-M. |
| 臺大學術典藏 |
2020-12-28T07:56:49Z |
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation
|
Lin L.-Y.; JYH-MING JIMMY JUANG; Chuang E.Y.; Chang S.-N.; Hsieh C.-S.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T07:56:42Z |
An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases
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Huang S.-H.; Chang Y.-S.; JYH-MING JIMMY JUANG; Chang K.-W.; Tsai M.-H.; Lu T.-P.; Lai L.-C.; Chuang E.Y.; Huang N.-T. |
| 臺大學術典藏 |
2020-12-28T07:56:41Z |
VariED: The first integrated database of gene annotation and expression profiles for variants related to human diseases
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Tsai M.-H.; Lai L.-C.; Chiang L.-M.; JYH-MING JIMMY JUANG; Chattopadhyay A.; Lee C.-Y.; Lu T.-P.; Chuang E.Y. |
| 臺大學術典藏 |
2020-12-28T07:56:37Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Huang H.-C.; Yu C.-C.; Ho L.-T.; Liu Y.-B.; Lin L.-Y.; Chen W.-J.; Hwang J.-J.; JYH-MING JIMMY JUANG; Binda A.; Lee S.-J.; 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 |
2020-12-22T03:29:15Z |
SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway
|
Ni Y.-H.; Shun C.-T.; Chuang E.Y.; Hsiao J.-H.; Yu L.C.H.; Lai L.-C.; Tung C.-C.; Weng M.-T.; PO-NIEN TSAO; Yang-Yen H.-F.; Wei S.-C.; Wei S.-C.;Yang-Yen H.-F.;Po-Nien Tsao;Weng M.-T.;Tung C.-C.;Yu L.C.H.;Lai L.-C.;Hsiao J.-H.;Chuang E.Y.;Shun C.-T.;Ni Y.-H.;Xavier R.J.;Podolsky D.K.;Yen J.J.Y.;Wong J.-M.; Xavier R.J.; Podolsky D.K.; Yen J.J.Y.; Wong J.-M. |
| 臺大學術典藏 |
2020-12-21T08:16:30Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Lin J.-L.; 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. |
| 臺大學術典藏 |
2020-12-04T07:44:55Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; LIAN-YU LIN; 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 |
2020-12-04T07:44:54Z |
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.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; LIAN-YU LIN; 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 |
2020-12-04T07:44:53Z |
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.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-04T07:44:49Z |
Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation
|
Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Ueng K.-C.; Tsai C.-F.; Lin T.-H.; Wu C.-K.; Lee J.-K.; LIAN-YU LIN; Wang Y.-C.; Yu C.-C.; Lai L.-P.; Tseng C.-D.; Hwang J.-J.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-04T07:44:31Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
|
Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.; Jyh-Ming J.-J.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; LIAN-YU LIN; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; Hwang J.-J.; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y. |
| 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. |
