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American Journal of Human Genetics|December 21, 2021
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomesGeorge Hindy, Peter Dornbos, Mark D Chaffin, et al.
Nature Communications|August 2, 2023
Genetic insights into resting heart rate and its role in cardiovascular diseaseYordi J van de Vegte, Ruben N Eppinga, M Yldau van der Ende, et al.
Nature Genetics|November 10, 2015
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociKyle J Gaulton, Teresa Ferreira, Yeji Lee, et al.
Nature Genetics|September 13, 2016
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertensionPraveen Surendran, Fotios Drenos, Robin Young, et al.
Nature Communications|January 30, 2015
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityJennifer Wessel, Audrey Y Chu, Sara M Willems, et al.
Nature Genetics|April 11, 2018
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetesAnubha Mahajan, Jennifer Wessel, Sara M Willems, et al.
Nature Genetics|October 31, 2017
Exome-wide association study of plasma lipids in >300,000 individualsDajiang J Liu, Gina M Peloso, Haojie Yu, et al.
Nature Genetics|May 3, 2019
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factorsNicole M Warrington, Robin N Beaumont, Momoko Horikoshi, et al.
Nature Genetics|September 7, 2022
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease preventionZhe Wang, Andrew Emmerich, Nicolas J Pillon, et al.
Diabetes|March 26, 2017
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes RiskAlisa Manning, Heather M Highland, Jessica Gasser, et al.
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