| 中山醫學大學 |
2021 |
Haploidentical peripheral blood stem cell transplantation with posttransplant cyclophosphamide in a child with neuroblastoma relapse after autologous peripheral blood stem cell transplantation
|
Weng, TF; Wu, KH |
| 國家衛生研究院 |
2024-03-04 |
Haploinsufficiency of adenomatous polyposis coli coupled with kirsten rat sarcoma viral oncogene homologue activation and P53 loss provokes high-grade glioblastoma formation in mice
|
Fang, KT;Su, CS;Layos, JJ;Lau, NYS;Cheng, KH |
| 國家衛生研究院 |
2016-04 |
Haploinsufficiency of RCBTB1 is associated with coats disease and familial exudative vitreoretinopathy
|
Wu, JH;Liu, JH;Ko, YC;Wang, CT;Chung, YC;Chu, KC;Liu, TT;Chao, HM;Jiang, YJ;Chen, SJ;Chung, MY |
| 中國醫藥大學 |
2001 |
Haplotype analysis in patients with velopharyngeal insufficiency (VPI) minimizes one VPI locus in 2.8Mb region of 22q11.
|
Tsai, LP; Tsou, KS; Shi, YR; Wu, JY; Tsai, FJ |
| 國立臺灣大學 |
2006 |
Haplotype Analysis of Endothelial Nitric Oxide Synthase (Nos3) Genetic Variants and Tardive Dyskinesia in Patients with Schizophrenia
|
白雅美; 林朝誠; 林知遠; BAI, YA-MEI; LIN, CHAO-CHENG; LIN, CHIH-YUAN |
| 國立臺灣大學 |
2009 |
Haplotype Analysis of Lrrk2 R1441h Carriers with Parkinsonism
|
林靜嫻; 吳瑞美; LIN, CHIN-HSIEN; WU, RUEY-MEEI |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
|
Ross, O.A. and Spanaki, C. and Griffith, A. and Lin, C.-H. and Kachergus, J. and Haugarvoll, K. and Latsoudis, H. and Plaitakis, A. and Ferreira, J.J. and Sampaio, C. and Bonifati, V. and Wu, R.-M. and Zabetian, C.P. and Farrer, M.J.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2009 |
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
|
Ross O.A; Spanaki C; Griffith A; Lin C.-H; Kachergus J; Haugarvoll K; Latsoudis H; Plaitakis A; Ferreira J.J; Sampaio C; Bonifati V; RUEY-MEEI WU; Zabetian C.P; Farrer M.J. |
| 臺大學術典藏 |
2020-03-04T07:45:27Z |
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
|
Ross O.A.; Spanaki C.; Griffith A.; CHIN-HSIEN LIN; Kachergus J.; Haugarvoll K.; Latsoudis H.; Plaitakis A.; Ferreira J.J.; Sampaio C.; Bonifati V.; Wu R.-M.; Zabetian C.P.; Farrer M.J. |
| 臺大學術典藏 |
2020-11-03T12:12:56Z |
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
|
Ross O.A.;Spanaki C.;Griffith A.;Chin-Hsien Lin;Kachergus J.;Haugarvoll K.;Latsoudis H.;Plaitakis A.;Ferreira J.J.;Sampaio C.;Bonifati V.;Wu R.-M.;Zabetian C.P.;Farrer M.J.; Ross O.A.; Spanaki C.; Griffith A.; CHIN-HSIEN LIN; Kachergus J.; Haugarvoll K.; Latsoudis H.; Plaitakis A.; Ferreira J.J.; Farrer M.J.; Zabetian C.P.; Sampaio C.; Bonifati V.; Wu R.-M. |
| 義守大學 |
2009-09 |
Haplotype analysis of single nucleotide polymorphisms in the vascular endothelial growth factor (VEGFA) gene and antidepressant treatment response in major depressive disorder
|
Shih-Jen Tsai; Chen-Jee Hong; Ying-Jay Liou; Tai-Jui Chen; Mao-Liang Chen; Sheue-Jane Hou; Feng-Chang Yen;Younger W.-Y. Yu |
| 亞洲大學 |
2022-01-01 |
Haplotype distribution of SARS-CoV-2 variants in low and high vaccination rate countries during ongoing global COVID-19 pandemic in early 2021
|
Bu, Ngoc-Niem;Bui, Ngoc-Niem;Lin, Yu-Tzu;Lin, Yu-Tzu;黃素華;Huang, Su-Hua;林振文 |
| 臺大學術典藏 |
2020-07-03T08:28:35Z |
Haplotype frequencies of nine Y-chromosome STR loci in the Taiwanese Han population
|
Tsai L.-C.;Yuen T.-Y.;Hsieh H.-M.;Lin M.;Tzeng C.-H.;Huang N.-E.;Linacre A.;James Chun-I Lee; Tsai L.-C.; Yuen T.-Y.; Hsieh H.-M.; Lin M.; Tzeng C.-H.; Huang N.-E.; Linacre A.; JAMES CHUN-I LEE |
| 國立臺灣大學 |
2013 |
Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants
|
Lin, Wan-Yu; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞 |
| 臺大學術典藏 |
2018-09-10T09:41:02Z |
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants
|
Lin, Wan-Yu;Yi, Nengjun;Lou, Xiang-Yang;Zhi, Degui;Zhang, Kui;Gao, Guimin;Tiwari, Hemant K.;Liu, Nianjun; Lin, Wan-Yu; WAN-YU LIN; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun |
| 臺大學術典藏 |
2022-05-04T09:10:39Z |
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants
|
WAN-YU LIN; Yi N.; Lou X.-Y.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N. |
| 中國醫藥大學 |
2010-06 |
Haplotype of BAK1 (BCL2 antagonist killer 1) polymorphisms associated with the risk of developing Kawasaki disease in Taiwanese children
|
黃毓銓(Yu-Chuen Huang);林應如(Ying-Ju Lin);張正成(Jeng-Sheng Chang);陳世殷(Shih-Yin, Chen);萬磊(Lei Wan);許晉銓(Jinn-Chyuan Sheu);賴志河(Chih-Ho Lai);林振文(Lin Cheng Wen);劉詩平(Shih-Ping Liu);蔡輔仁(Fuu-Jen Tsai)* |
| 高雄醫學大學 |
2007 |
Haplotype Tag SNP Selection using Hybrid Algorithms
|
Yang, Cheng-Hong;Ho, Chang-Hsuan;谷德倫;張學偉 |
| 高雄醫學大學 |
2008 |
Haplotype Tagging SNPs Selection Using Particle Swarm Optimization
|
Yang, Cheng-Hong;Ho, Chang-Hsuan;張學偉;Chuang , Li-Yeh |
| 國立臺灣大學 |
2012 |
Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs
|
Lin, Wan-Yu; Yi, Nengjun; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞 |
| 臺大學術典藏 |
2022-05-04T09:10:40Z |
Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs
|
WAN-YU LIN; Yi N.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N. |
| 國家衛生研究院 |
2019-07 |
Haplotypes constructed by Whole exome sequencing to map and identify a novel disease-causing RP2 gene variant from a recessive X linked Retinities Pigmentosa family
|
Ching, Y;Fan, W;Lin, W;Tsai, W;Hu, L;Huang, S;Chung, R |
| 國家衛生研究院 |
2011-11 |
Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia
|
Chokkalingam, AP;Bartley, K;Wiemels, JL;Metayer, C;Barcellos, LF;Hansen, HM;Aldrich, MC;Guha, N;Urayama, KY;Scelo, G;Chang, JS;Month, SR;Wiencke, JK;Buffler, PA |
| 國立臺灣大學 |
2016 |
Haplotypes of the D-Amino Acid Oxidase Gene Are Significantly Associated with Schizophrenia and Its Neurocognitive Deficits
|
Liu, Yu-Li; Wang, Sheng-Chang; Hwu, Hai-Gwo; Fann, Cathy Shen-Jang; Yang, Ueng-Cheng; Yang, Wei-Chih; Hsu, Pei-Chun; Chang, Chien-Ching; Wen, Chun-Chiang; Tsai-Wu, Jyy-Jih; Hwang, Tzung-Jeng; Hsieh, Ming H.; Liu, Chen-Chung; Chien, Yi-Ling; Fang, Chiu-Ping; Faraone, Stephen V.; Tsuang, Ming T.; Chen, Wei J.; Liu, Chih-Min; 謝明憲; 蔡芷季; 黃宗正; 簡意玲; 劉智民; 劉震鐘; 陳為堅; 胡海國 |
| 臺大學術典藏 |
2021-08-13T03:35:09Z |
Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits
|
Liu Y.-L.; Wang S.-C.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C.; Chang C.-C.; Wen C.-C.; Tsai-Wu J.-J.; Hwang T.-J.; Hsieh M.H.; CHEN-CHUNG LIU; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Liu C.-M. |
