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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Institution Date Title Author
亞洲大學 1997 Rare mutations and no hypermethylation at the CDKN2A locus in epithelial ovarian tumors. International Journal of Cancer Shih, Yang-Chia;J. Kerr;J. Liu;T. Hurst;S-K. Khoo; B. Ward; B. Wainwright;G. Chenevix-Trench
中國醫藥大學 2014-12-14 Rare neoplasm located at cerebellopontine angle with unique imaging presentation. 陳哲圃(Paul J. Chen);陳春忠(CHUN-CHUNG CHEN);陳哲圃(Paul J. Chen)
國立中山大學 2003 Rare northward flow in the Taiwan Strait in winter: a note C.T.A. Chen
國立成功大學 2017-10-13 Rare occurrence of inflammatory bowel disease in a cohort of Han Chinese ankylosing spondylitis patients-a single institute study Wang;Chrong-Reen;Weng;Chia-Tse;Lee;Chung-Ta;Huang;Kuo-Yuan;Hsu;Sheng-Min;Liu;Ming-Fei
國立臺灣大學 2005 Rare Presentation of Endocrine Pancreatic Tumor: A Case of Diffuse Glucagonoma without Metastasis and Necrolytic Migratory Erythema 陳煥武; 陳煥文; 蘇登煌; 孫家棟; 劉高郎; CHEN, HUAN-WU; CHEN, HUAN-WEN; SU, DENG- HUANG; SHUN, CHIA-TUNG; LIU, KAO-LANG
臺大學術典藏 2018-09-10T05:13:04Z Rare presentation of endocrine pancreatic tumor: A case of diffuse glucagonoma without metastasis and necrolytic migratory erythema Chen, H.-W. and Chen, H.-W. and Su, D.-H. and Shun, C.-T. and Liu, K.-L.; KAO-LANG LIU
臺大學術典藏 2020-03-27T02:03:57Z Rare presentation of endocrine pancreatic tumor: A case of diffuse glucagonoma without metastasis and necrolytic migratory erythema Chen H.-W.;Chen H.-W.;Su D.-H.;Shun C.-T.;Kao-Lang Liu; Chen H.-W.; Chen H.-W.; Su D.-H.; Shun C.-T.; KAO-LANG LIU
臺大學術典藏 2021-03-18T02:03:16Z Rare presentation of endocrine pancreatic tumor: A case of diffuse glucagonoma without metastasis and necrolytic migratory erythema Chen H.-W.;Chen H.-W.;Su D.-H.;Chia-Tung Shun;Liu K.-L.; Chen H.-W.; Chen H.-W.; Su D.-H.; CHIA-TUNG SHUN; Liu K.-L.
國立成功大學 2019 Rare Presentation of Giant Isolated Enteric Cyst in Anterior Mediastinum Huang, W.-L.;Tseng, Y.-L.
國立成功大學 2024--JUN Rare Presentation of Monkeypox: Initial Tonsillitis Symptoms Leading to Diagnostic Challenges Huang;Chien-Wei;Liao;Jyun-Yi;Lin;Sheng-Chiao
中國醫藥大學 2011-01 Rare Presentation of Pulmonary Cryptococcosis as Calcified Nodule 陳碩爵(Shuo-Chueh Chen); 劉峻成(Juhn-Cherng Liu); 曾冠欽(Guan-Chin Teseng); 陳志毅(Chih-Yi Chen)*
國立成功大學 2022-01-29 Rare presentations of primary amyloidosis as ptosis: a case report Lee;Peng-Hsuan;Liao;I-Chuang;Lee;Annabelle, Wan-Ju
中國醫藥大學 2008-11-10 Rare Rearrangement: Familial Jumping Satellite and YSRY+;Autosome Translocation in XX Male 林齊強(Chyi-Chyang Lin); 簡淑錦(Shu-Chin Chien); 何銘(Ming- Ho); 許佩菁; 鄧如琇(Ru-Hsiou Teng); 蔡輔仁(Fuu-Jen Tsai); 李月君(Y.-C. LIN)
中國醫藥大學 2009-12 Rare Rearrangements: A ‘‘Jumping Satellite’’ in One Family and Autosomal Location of the SRY Gene in an XX Male 簡淑錦(Shu-Chin Chien); 李月君(Y.-C LI); 何銘(Ming- Ho); 許佩菁; 鄧如琇(Ru-Hsiou Teng); 林瑋德(Wei-De Lin); 蔡輔仁(Fuu-Jen Tsai)*; 林齊強(Chyi-Chyang Lin)*
臺大學術典藏 2018-09-10T09:18:12Z Rare solvent annealing effective benzo(1,2-b:4,5-b′)dithiophene-based low band-gap polymer for bulk heterojunction organic photovoltaics Chen, H.-Y.;Wu, J.-L.;Chen, C.-T.;Chen, C.-T.; Chen, H.-Y.; Wu, J.-L.; Chen, C.-T.; Chen, C.-T.; CHAO-TSEN CHEN
國立成功大學 2024-04-02 Rare top-quark decays in scotogenic models 陳泉宏
臺大學術典藏 2018-09-10T14:50:56Z Rare variant association testing by adaptive combination of P-values Lin, W.-Y. ; Lou, X.-Y. ; Gao, G. ; Liu, N.; WAN-YU LIN
臺大學術典藏 2022-05-04T09:10:38Z Rare variant association testing by adaptive combination of P-values WAN-YU LIN; Lou X.-Y.; Gao G.; Liu N.
國家衛生研究院 2015-11 Rare variant association tests for longitudinal family studies Chien, LC;Chiu, YF;Hsu, FC;Bowden, D
國家衛生研究院 2018-10 Rare variant association tests for pleiotropy in longitudinal family studies Yu, J;Chiu, Y
國家衛生研究院 2024-10-09 Rare variant contribution to the heritability of coronary artery disease Rocheleau, G;Clarke, SL;Auguste, G;Hasbani, NR;Morrison, AC;Heath, AS;Bielak, LF;Iyer, KR;Young, EP;Stitziel, NO;Jun, G;Laurie, C;Broome, JG;Khan, AT;Arnett, DK;Becker, LC;Bis, JC;Boerwinkle, E;Bowden, DW;Carson, AP;Ellinor, PT;Fornage, M;Franceschini, N;Freedman, BI;Heard-Costa, NL;Hou, LF;Chen, YDI;Kenny, EE;Kooperberg, C;Kral, BG;Loos, RJF;Lutz, SM;Manson, JE;Martin, LW;Mitchell, BD;Nassir, R;Palmer, ND;Post, WS;Preuss, MH;Psaty, BM;Raffield, LM;Regan, EA;Rich, SS;Smith, JA;Taylor, KD;Yanek, LR;Young, KA;Anugu, P;Arnett, DK;Assimes, TL;Auer, P;Barwick, L;Becker, D;Becker, LC;Bielak, LF;Bis, JC;Boerwinkle, E;Bowden, DW;Broome, JG;Carson, AP;Carty, C;Castaldi, P;Chaffin, M;Chang, YC;Choi, SH;Chung, RH;Clarke, SL;Crandall, C;David, S;de las Fuentes, L;Deka, R;DeMeo, D;de Vries, PS;Do, R;Duan, Q;Eaton, C;Eaton, C;El Boueiz, A;Ellinor, PT;Fornage, M;Franceschini, N;Freedman, BI;Gao, SS;Gao, Y;Gass, M;Ghosh, A;Grine, D;Hall, M;Hasbani, NR;Heard-Costa, NL;Heath, AS;Hersh, C;Hobbs, B;Hou, LF;Hsiung, CA;Hung, YJ;Huston, H;Hwu, CM;Chen, YDI;Iyer, KR;Jackson, R;Johnsen, J;Jun, G;Kenny, EE;Khan, AT;Kooperberg, C;Kral, BG;Lange, C;Lange, E;Laurie, C;LeBoff, M;Lee, WJ;Li, Y;Liu, S;Liu, Y;Loos, RJF;Lutz, SM;Manson, JE;Martin, LW;Mathai, S;Mei, H;Miller, CL;Mitchell, BD;Morrison, AC;Naik, R;Naseri, T;Nassir, R;Neltner, B;Ochs-Balcom, H;Paik, DT;Palmer, ND;Parker, C;Perez, M;Peters, U;Peyser, PA;Phillips, LS;Post, WS;Becker, JP;Preuss, MH;Psaty, BM;Raffield, LM;Regan, EA;Reupena, MS;Rich, SS;Rocheleau, G;Roselli, C;Rotter, JI;Russell, P;Sabino, EC;Sandow, K;Schwander, K;Sciurba, F;Silver, B;Smith, JA;Smoller, S;Snively, B;Stitziel, NO;Storm, G;Sung, YJ;Tang, H;Taub, M;Taylor, KD;Tinker, L;Tirschwell, D;Tiwari, H;Vaidya, D;Vasan, RS;Walker, T;Wallace, R;Walts, A;Weng, LC;Yanek, LR;Yang, I;Young, EP;Young, KA;Zhao, SX;Hilliard, AT;Tcheandjieu, C;Peyser, PA;Vasan, RS;Rotte, JI;Miller, CL;Assimes, TL;de Vries, PS;Do, R
國立成功大學 2016-06 Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level Jeng, Xinge Jessie; Daye, Zhongyin John; Lu, Wenbin; Tzeng, Jung-Ying
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 2021-09-02T00:09:10Z 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 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.

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