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BMC Medicine|March 18, 2021
Investigating the relationships between unfavourable habitual sleep and metabolomic traits: evidence from multi-cohort multivariable regression and Mendelian randomization analysesMaxime M Bos, Neil J Goulding, Matthew A Lee, et al.
Diabetes Care|January 27, 2022
Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 CohortsDaniel DiCorpo, Jessica LeClair, Joanne B Cole, et al.
Blood|July 26, 2018
DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysisCavin K Ward-Caviness, Jennifer E Huffman, Karl Everett, et al.
Plos One|May 8, 2020
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucosePeitao Wu, Denis Rybin, Lawrence F Bielak, et al.
Circulation. Genomic and Precision Medicine|July 16, 2021
Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride ConcentrationsDanielle E Haslam, Gina M Peloso, Melanie Guirette, et al.
Nature Communications|June 29, 2021
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipidsMin-A Jhun, Michael Mendelson, Rory Wilson, et al.
Alzheimer'S Research & Therapy|January 20, 2024
Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performanceHao Mei, Jeannette Simino, Lianna Li, et al.
Diabetes Care|April 23, 2024
Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People With Type 2 DiabetesSoo Heon Kwak, Ryan B Hernandez-Cancela, Daniel A DiCorpo, et al.
Medrxiv : the Preprint Server for Health Sciences|August 7, 2023
Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes MellitusSoo Heon Kwak, Ryan B Hernandez-Cancela, Daniel A DiCorpo, et al.
Nature Genetics|February 4, 2022
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk allelesHeidi Hautakangas, Bendik S Winsvold, Sanni E Ruotsalainen, et al.
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