臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Showing items 211-220 of 539 (54 Page(s) Totally)
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Institution	Date	Title	Author
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	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	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	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.

Showing items 211-220 of 539 (54 Page(s) Totally)
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