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Scientific Reports|August 23, 2016
A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck diseaseJingcan Hao, Wenyu Wang, Yan Wen, et al.
New Biotechnology|December 25, 2025
The GigaAssay: A combined high throughput and highly accurate platform for variant classificationChristopher J Giacoletto, Liz J Valente, Lancer Brown, et al.
Genomics|October 4, 2025
High-throughput characterization of 5886 HER2 variants identifies 112 new in cellulo gain-of-function mutationsChristopher J Giacoletto, Liz J Valente, Lancer Brown, et al.
Frontiers in Genetics|May 28, 2019
Causal Effects of Genetically Predicted Cardiovascular Risk Factors on Chronic Kidney Disease: A Two-Sample Mendelian Randomization StudyHui-Min Liu, Qin Hu, Qiang Zhang, et al.
The Journal of Clinical Endocrinology and Metabolism|July 13, 2006
Assessment of genetic linkage and parent-of-origin effects on obesityYan-Fang Guo, Hui Shen, Yong-jun Liu, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|April 22, 2016
Analysis of Diagnostic Value of YKL-40 in Ovarian CancerJie Chen, Xian Liu, Yu-Qin Pan, et al.
The Journal of Clinical Endocrinology and Metabolism|August 28, 2015
Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at MenarcheLi-Jun Tan, Zhuo-Er Wang, Ke-Hao Wu, et al.
Annals of Human Genetics|April 18, 2018
Genome-wide association study of lncRNA polymorphisms with bone mineral densityQin Zeng, Ke-Hao Wu, Kun Liu, et al.
The Journal of Clinical Endocrinology and Metabolism|August 23, 2020
Gene Expression and RNA Splicing Imputation Identifies Novel Candidate Genes Associated with OsteoporosisYong Liu, Hui Shen, Jonathan Greenbaum, et al.
Epilepsy Research|July 21, 2005
Absence of linkage to 8q23.3-q24.1 and 2p11.1-q12.2 in a new BAFME pedigree in China: indication of a third locus for BAFMEFei-Yan Deng, Jian Gong, Yun-Ci Zhang, et al.
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