academic article

• Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 2019
• Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity..  Nature communications.  10:-. 2019
• Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. 2019
• Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions..  American journal of epidemiology.  188:1033-1054. 2019
• A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure..  Human molecular genetics.  :-. 2019
• A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure..  American journal of human genetics.  102:375-400. 2018
• Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 2018
• Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 2018
• Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 2018
• Rare and low-frequency coding variants alter human adult height..  Nature.  542:186-190. 2017
• KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference. 2016
• Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. 2014
• Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci..  American journal of human genetics.  94:349-360. 2014
• Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. 2014
• Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error..  Human molecular genetics.  22:2754-2764. 2013