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机构 日期 题名 作者
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.
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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