1. A 1204-single nucleotide polymorphism and insertion–deletion polymorphism panel for massively parallel sequencing analysis of DNA mixtures. (January 2018) Authors: Hwa, Hsiao-Lin; Chung, Wan-Chia; Chen, Pei-Lung; Lin, Chih-Peng; Li, Huei-Ying; Yin, Hsiang-I; Lee, James Chun-I Journal: Forensic science international Issue: Volume 32(2018) Page Start: 94 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration. (April 2023) Authors: Chen, Huan-Yun; Lin, Han-I; Hsu, Chia-Lang; Chen, Pei-Lung; Huang, Cheng-Yen; Teng, Shu-Chun; Lin, Chin-Hsien Journal: Parkinsonism & related disorders Issue: Volume 109(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association Between Serum Levels of Adipocyte Fatty Acid-binding Protein and Free Thyroxine. Issue 41 (October 2015) Authors: Tseng, Fen-Yu; Chen, Pei-Lung; Chen, Yen-Ting; Chi, Yu-Chao; Shih, Shyang-Ron; Wang, Chih-Yuan; Chen, Chi-Ling; Yang, Wei-Shiung Editors: Schaller., Bernhard Journal: Medicine Issue: Volume 94:Issue 41(2015) Page Start: e1798 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical heterogeneity of LRRK2 p.I2012T mutation. (December 2016) Authors: Fan, Tian-Sin; Wu, Ruey-Meei; Chen, Pei-Lung; Chen, Ta-Fu; Li, Huei-Ying; Lin, Yin-Hung; Chen, Chien-Yu; Chen, Meng-Ling; Tai, Chun-Hwei; Lin, Hang-I.; Lin, Chin-Hsien Journal: Parkinsonism & related disorders Issue: Volume 33(2016) Page Start: 36 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer–Rokitansky–Küster–Hauser syndrome. Issue 7 (29th April 2015) Authors: Chen, Mei-Jou; Wei, Shin-Yi; Yang, Wei-Shiung; Wu, Tsai-Tzu; Li, Huei-Ying; Ho, Hong-Nerng; Yang, Yu-Shih; Chen, Pei-Lung Journal: Human reproduction Issue: Volume 30:Issue 7(2015) Page Start: 1732 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. First step towards precision medicine for antithyroid drug-induced agranulocytosis. Issue 6 (June 2016) Authors: Chen, Pei-Lung; Fann, Cathy Shen-Jang; Shih, Shyang-Rong; Yang, Wei-Shiung; Chang, Tien-Chun Journal: Lancet Issue: Volume 4:Issue 6(2016) Page Start: 473 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good 131I treatment response. (1st January 2016) Authors: Lu, Jin-Ying; Hung, Po-Ju; Chen, Pei-Lung; Yen, Ruoh-Fang; Kuo, Kuan-Ting; Yang, Tsung-Lin; Wang, Chih-Yuan; Chang, Tien-Chun; Huang, Tien-Shang; Chang, Ching-Chung Journal: Endocrinology, diabetes & metabolism case reports Issue: (2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response. (November 2013) Authors: Hung, Chin-Chuan; Chen, Pei-Lung; Huang, Wan-Min; Tai, John Jen; Hsieh, Tsung-Jen; Ding, Shih-Torng; Hsieh, Yow-Wen; Liou, Horng-Huei Journal: Pharmacogenomics Issue: Volume 14:Number 15(2013) Page Start: 1849 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response. (November 2013) Authors: Hung, Chin-Chuan; Chen, Pei-Lung; Huang, Wan-Min; Tai, John Jen; Hsieh, Tsung-Jen; Ding, Shih-Torng; Hsieh, Yow-Wen; Liou, Horng-Huei Journal: Pharmacogenomics Issue: Volume 14:Number 15(2013) Page Start: 1849 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study. Issue 4 (29th December 2021) Authors: Chen, Pey-Yu; Tsai, Cheng-Yu; Wu, Jiunn-Liang; Li, Yi-Lu; Wu, Che-Ming; Chen, Kuang-Chao; Hwang, Chung-Feng; Wu, Hung-Pin; Lin, Hung-Ching; Cheng, Yen-Fu; Lo, Ming-Yu; Liu, Tien-Chen; Yang, Ting-Hua; Chen, Pei-Lung; Hsu, Chuan-Jen; Wu, Chen-Chi Journal: Ear and hearing Issue: Volume 43:Issue 4(2022) Page Start: 1198 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗