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机构 日期 题名 作者
臺大學術典藏 2022-09-20T06:48:30Z Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry Jimmy Juang J.-M.; 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.; 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 2022-09-06T02:41:46Z Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry Jimmy Juang J.-M.; 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.; Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.
臺大學術典藏 2022-05-03T08:28:07Z An Integrative Co-localization (INCO) Analysis for SNV and CNV Genomic Features With an Application to Taiwan Biobank Data Yu Q.-Y.; TZU-PIN LU; Hsiao T.-H.; Lin C.-H.; Wu C.-Y.; Tzeng J.-Y.; Hsiao C.K.
臺大學術典藏 2022-04-20T07:19:09Z Probabilistic prioritization of candidate pathway association with pathway score Lin S.-J.; Lu T.-P.; Yu Q.-Y.; CHUHSING KATE HSIAO
臺大學術典藏 2022-04-20T07:19:08Z Association test using copy number profile curves (CONCUR) enhances power in rare copy number variant analysis Brucker A.; Lu W.; West R.M.; Yu Q.-Y.; CHUHSING KATE HSIAO; Hsiao T.-H.; Lin C.-H.; Magnusson P.K.E.; Sullivan P.F.; Szatkiewicz J.P.; Lu T.-P.; Tzeng J.-Y.
臺大學術典藏 2022-04-20T07:19:07Z Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine Juang J.-M.J.; Lu T.-P.; Su M.-W.; Lin C.-W.; Yang J.-H.; Chu H.-W.; Chen C.-H.; Hsiao Y.-W.; Lee C.-Y.; Chiang L.-M.; Yu Q.-Y.; CHUHSING KATE HSIAO; Chen C.-Y.J.; Wu P.-E.; Pai C.-H.; Chuang E.Y.; Shen C.-Y.
臺大學術典藏 2022-04-20T07:19:06Z An Integrative Co-localization (INCO) Analysis for SNV and CNV Genomic Features With an Application to Taiwan Biobank Data Yu Q.-Y.; Lu T.-P.; Hsiao T.-H.; Lin C.-H.; Wu C.-Y.; Tzeng J.-Y.; CHUHSING KATE HSIAO
臺大學術典藏 2022-02-23T08:10:42Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry 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.; 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 2022-02-15T06:22:55Z Adenylate Kinase 4 Promotes Inflammatory Gene Expression via Hif1α and AMPK in Macrophages Chin W.-Y.; He C.-Y.; Chow T.W.; Yu Q.-Y.; Liang-Chuan Lai; Miaw S.-C.
臺大學術典藏 2022-02-15T03:21:42Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry 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 J.-J.; Lin T.-T.; Liao M.-T.; JIEN-JIUN CHEN; 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 2021-09-09T07:52:41Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry Jyh-Ming J.-J.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; CHIH-CHIEH YU; 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.; Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.
臺大學術典藏 2021-09-02T00:09:10Z Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine Juang J.-M.J;Lu T.-P;Su M.-W;Lin C.-W;Yang J.-H;Chu H.-W;Chen C.-H;Hsiao Y.-W;Lee C.-Y;Chiang L.-M;Yu Q.-Y;Hsiao C.K;Chen C.-Y.J;Wu P.-E;Pai C.-H;Chuang E.Y;Shen C.-Y.; Juang J.-M.J; ERIC YAO-YU CHUANG et al.
臺大學術典藏 2021-05-21T07:46:16Z Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine Juang J.-M.J.;Tzu-Pin Lu;Su M.-W.;Lin C.-W.;Yang J.-H.;Chu H.-W.;Chen C.-H.;Hsiao Y.-W.;Lee C.-Y.;Chiang L.-M.;Yu Q.-Y.;Hsiao C.K.;Chen C.-Y.J.;Wu P.-E.;Pai C.-H.;Chuang E.Y.;Shen C.-Y.; Juang J.-M.J.; TZU-PIN LU; Su M.-W.; Lin C.-W.; Yang J.-H.; Chu H.-W.; Chen C.-H.; Hsiao Y.-W.; Lee C.-Y.; Chiang L.-M.; Yu Q.-Y.; Hsiao C.K.; Chen C.-Y.J.; Wu P.-E.; Pai C.-H.; Chuang E.Y.; Shen C.-Y.
臺大學術典藏 2021-05-21T07:46:16Z Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine Juang J.-M.J.;Tzu-Pin Lu;Su M.-W.;Lin C.-W.;Yang J.-H.;Chu H.-W.;Chen C.-H.;Hsiao Y.-W.;Lee C.-Y.;Chiang L.-M.;Yu Q.-Y.;Hsiao C.K.;Chen C.-Y.J.;Wu P.-E.;Pai C.-H.;Chuang E.Y.;Shen C.-Y.; Juang J.-M.J.; TZU-PIN LU; Su M.-W.; Lin C.-W.; Yang J.-H.; Chu H.-W.; Chen C.-H.; Hsiao Y.-W.; Lee C.-Y.; Chiang L.-M.; Yu Q.-Y.; Hsiao C.K.; Chen C.-Y.J.; Wu P.-E.; Pai C.-H.; Chuang E.Y.; Shen C.-Y.
臺大學術典藏 2021-03-29T06:08:19Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry 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, 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.; ERIC YAO-YU CHUANG
臺大學術典藏 2020-12-30T07:47:46Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry Jyh-Ming J.-J.; YEN BIN LIU; 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 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 2020-12-28T12:03:19Z 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 2020-12-28T10:52:55Z 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 2020-12-04T07:44:31Z 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 2020-11-17T02:45:23Z Probabilistic prioritization of candidate pathway association with pathway score Lin S.-J.;Tzu-Pin Lu;Yu Q.-Y.;Hsiao C.K.; Lin S.-J.; TZU-PIN LU; Yu Q.-Y.; Hsiao C.K.
臺大學術典藏 2020-11-17T02:45:23Z Probabilistic prioritization of candidate pathway association with pathway score Lin S.-J.;Tzu-Pin Lu;Yu Q.-Y.;Hsiao C.K.; Lin S.-J.; TZU-PIN LU; Yu Q.-Y.; Hsiao C.K.
臺大學術典藏 2020-11-17T02:45:19Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry 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 J.-J.; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y.; Yang D.-H.; Lin J.-L.; TZU-PIN LU; Chuang E.Y.; Ackerman M.J.
臺大學術典藏 2020-11-17T02:45:18Z Association test using copy number profile curves (CONCUR) enhances power in rare copy number variant analysis West R.M.; Lu W.; Brucker A.; Brucker A.;Lu W.;West R.M.;Yu Q.-Y.;Hsiao C.K.;Hsiao T.-H.;Lin C.-H.;Magnusson P.K.E.;Sullivan P.F.;Szatkiewicz J.P.;Tzu-Pin Lu;Tzeng J.-Y.; Tzeng J.-Y.; TZU-PIN LU; Szatkiewicz J.P.; Sullivan P.F.; Magnusson P.K.E.; Yu Q.-Y.; Hsiao C.K.; Hsiao T.-H.; Lin C.-H.
臺大學術典藏 2020-11-17T02:45:18Z Association test using copy number profile curves (CONCUR) enhances power in rare copy number variant analysis West R.M.; Lu W.; Brucker A.; Brucker A.;Lu W.;West R.M.;Yu Q.-Y.;Hsiao C.K.;Hsiao T.-H.;Lin C.-H.;Magnusson P.K.E.;Sullivan P.F.;Szatkiewicz J.P.;Tzu-Pin Lu;Tzeng J.-Y.; Tzeng J.-Y.; TZU-PIN LU; Szatkiewicz J.P.; Sullivan P.F.; Magnusson P.K.E.; Yu Q.-Y.; Hsiao C.K.; Hsiao T.-H.; Lin C.-H.
臺大學術典藏 2020 Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry Ackerman M.J.; Chuang E.Y.; Lu T.-P.; Jyh-Ming J.-J.;Liu Y.-B.;Julius Chen C.-Y.;Yu Q.-Y.;Chattopadhyay A.;Lin L.-Y.;Wen-Jone Chen;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.;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.; Lin L.-Y.; WEN-JONE CHEN; 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.; Yang D.-H.; Lin J.-L.

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