Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data - Karen Y. He; Xiaoyin Li; Tanika N. Kelly; Jingjing Liang; Brian E. Cade; Themistocles L. Assimes; Lewis C. Becker; Amber L. Beitelshees; Adam P. Bress; Yen-Pei Christy Chang; Yii-Der Ida Chen; Paul S. de Vries; et al. (Human Genetics, 2019)

A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss - Hui-Mei Hong; Jiann-Jou Yang; Ching-Chyuan Su; Juan-Yu Chang; Tung-Cheng Li; Shuan-Yow Li (Human Genetics, 2010)