1. 7th Drug hypersensitivity meeting: part two. Issue 3 (August 2016) Authors: Elera, Javier; Boteanu, Cosmin; Blanco, Maria; Gonzalez-Mendiola, Rosario; García, Irene; Alvarez, Antonio; Martinez, Jose; Garrido, Jaume; Barona, Carla; Chorda, Carolina; Salgueiro, Ramón; Palacios, Miguel; Rojas, Dolores; Acar, Emre; Aktas, Ayse; Ermertcan, Aylin; Temiz, Peyker; Lin, Chien-Yio... Journal: Clinical and translational allergy Issue: Volume 6:Issue 3(2016) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect. Issue 10 (17th May 2006) Authors: Niu, Dau-Ming; Hwang, Betau; Hwang, Han-Wei; Wang, Nana H; Wu, Jer-Yuarn; Lee, Pi-Chang; Chien, Jen-Chung; Shieh, Ru-Chi; Chen, Yuan-Tsong Journal: Journal of medical genetics Issue: Volume 43:Issue 10(2006) Page Start: 817 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A genome-wide association study links small-vessel ischemic stroke to autophagy. Issue 1 (December 2017) Authors: Lee, Tsong-Hai; Ko, Tai-Ming; Chen, Chien-Hsiun; Chang, Yeu-Jhy; Lu, Liang-Suei; Chang, Chien-Hung; Huang, Kuo-Lun; Chang, Ting-Yu; Lee, Jiann-Der; Chang, Ku-Chou; Yang, Jen-Tsung; Wen, Ming-Shien; Wang, Chao-Yung; Chen, Ying-Ting; Chen, Tsai-Chuan; Chou, Shu-Yu; Lee, Ming-Ta; Chen, Yuan-Tsong; W... Journal: Scientific reports Issue: Volume 7:Issue 1(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays. (December 2016) Authors: Huang, Mei-Chu; Chuang, Tzu-Po; Chen, Chien-Hsiun; Wu, Jer-Yuarn; Chen, Yuan-Tsong; Li, Ling-Hui; Yang, Hsin-Chou Journal: BMC genomics Issue: Volume 17:Number 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. CXCL10/IP-10 Is a Biomarker and Mediator for Kawasaki Disease. Issue 5 (27th February 2015) Authors: Ko, Tai-Ming; Kuo, Ho-Chang; Chang, Jeng-Sheng; Chen, Shih-Ping; Liu, Yi-Min; Chen, Hui-Wen; Tsai, Fuu-Jen; Lee, Yi-Ching; Chen, Chien-Hsiun; Wu, Jer-Yuarn; Chen, Yuan-Tsong Journal: Circulation research Issue: Volume 116:Issue 5(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. CXCL10/IP-10 Is a Biomarker and Mediator for Kawasaki Disease. Issue 5 (27th February 2015) Authors: Ko, Tai-Ming; Kuo, Ho-Chang; Chang, Jeng-Sheng; Chen, Shih-Ping; Liu, Yi-Min; Chen, Hui-Wen; Tsai, Fuu-Jen; Lee, Yi-Ching; Chen, Chien-Hsiun; Wu, Jer-Yuarn; Chen, Yuan-Tsong Journal: Circulation research Issue: Volume 116:Issue 5(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic determinants of warfarin dosing in the Han-Chinese population. (December 2009) Authors: Lee, MT Michael; Chen, Chien-Hsiun; Chou, Ching-Heng; Lu, Liang-Suei; Chuang, Hui-Ping; Chen, Ying-Ting; Saleem, Amir N; Wen, Ming-Shien; Chen, Jin-Jer; Wu, Jer-Yuarn; Chen, Yuan-Tsong Journal: Pharmacogenomics Issue: Volume 10:Number 12(2009) Page Start: 1905 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder. Issue 1 (December 2016) Authors: Yin, Chia-Lin; Chen, Hsin-I; Li, Ling-Hui; Chien, Yi-Ling; Liao, Hsiao-Mei; Chou, Miao; Chou, Wen-Jiun; Tsai, Wen-Che; Chiu, Yen-Nan; Wu, Yu-Yu; Lo, Chen-Zen; Wu, Jer-Yuarn; Chen, Yuan-Tsong; Gau, Susan Journal: Molecular autism Issue: Volume 7:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan. (March 2018) Authors: Chen, Shih-Pin; Fuh, Jong-Ling; Chung, Ming-Yi; Lin, Ying-Chao; Liao, Yi-Chu; Wang, Yen-Feng; Hsu, Chia-Lin; Yang, Ueng-Cheng; Lin, Ming-Wei; Chiou, Jen-Jie; Wang, Po-Jen; Chen, Ping-Kun; Fan, Pi-Chuan; Wu, Jer-Yuan; Chen, Yuan-Tsong; Kao, Lung-Sen; Shen-Jang Fann, Cathy; Wang, Shuu-Jiun Journal: Cephalalgia Issue: Volume 38:Number 3(2018) Page Start: 466 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations. (November 2013) Authors: Cornejo-García, José Antonio; Liou, Lieh-Bang; Blanca-López, Natalia; Doña, Inmaculada; Chen, Chien-Hsiun; Chou, Yi-Chun; Chuang, Hui-Ping; Wu, Jer-Yuarn; Chen, Yuan-Tsong; Plaza-Serón, María del Carmen; Mayorga, Cristobalina; Guéant-Rodríguez, Rosa María; Lin, Shih-Chang; Torres, María José; Cam... Journal: Pharmacogenomics Issue: Volume 14:Number 15(2013) Page Start: 1857 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗