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Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine.
Juang JJ, Lu TP, Su MW, Lin CW, Yang JH, Chu HW, Chen CH, Hsiao YW, Lee CY, Chiang LM, Yu QY, Hsiao CK, Chen CJ, Wu PE, Pai CH, Chuang EY, Shen CY. Juang JJ, et al. Among authors: lin cw. J Adv Res. 2020 Dec 7;30:147-158. doi: 10.1016/j.jare.2020.12.003. eCollection 2021 May. J Adv Res. 2020. PMID: 34026292 Free PMC article.
Association of ADH1B and ALDH2 genotypes with the risk of lung adenocarcinoma.
Pan TY, Lee JY, Chen JJ, Liu YW, Abishaw AN, Su MW, Lin CW, Hsieh TJ, Peng CY, Turesky RJ, Bellamri M, Kwan AL, Wu CF, Wu MT. Pan TY, et al. Among authors: lin cw. Pharmacogenet Genomics. 2024 Dec 10. doi: 10.1097/FPC.0000000000000555. Online ahead of print. Pharmacogenet Genomics. 2024. PMID: 39641391
SAQC: SNP array quality control.
Yang HC, Lin HC, Kang M, Chen CH, Lin CW, Li LH, Wu JY, Chen YT, Pan WH. Yang HC, et al. Among authors: lin cw, lin hc. BMC Bioinformatics. 2011 Apr 18;12:100. doi: 10.1186/1471-2105-12-100. BMC Bioinformatics. 2011. PMID: 21501472 Free PMC article.
2,123 results