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Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
Diabetes|September 5, 2014
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East AsiansJoo-Yeon Hwang, Xueling Sim, Ying Wu, et al.
European Journal of Preventive Cardiology|August 16, 2022
Including measures of chronic kidney disease to improve cardiovascular risk prediction by SCORE2 and SCORE2-OPKunihiro Matsushita, Stephen Kaptoge, Steven H J Hageman, et al.
Genetic Epidemiology|April 28, 2012
Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25Li-Shiun Chen, Nancy L Saccone, Robert C Culverhouse, et al.
Scientific Reports|January 21, 2016
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumferenceWanqing Wen, Norihiro Kato, Joo-Yeon Hwang, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing StudyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
American Journal of Human Genetics|October 6, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing studyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
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