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Science (New York, N.Y.)|March 17, 2022
Multiple causal variants underlie genetic associations in humansNathan S Abell, Marianne K DeGorter, Michael J Gloudemans, et al.Communications Biology|May 25, 2019
Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanismsBoxiang Liu, Melissa A Calton, Nathan S Abell, et al.Genome Medicine|March 16, 2022
Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genesMichael J Gloudemans, Brunilda Balliu, Daniel Nachun, et al.Nature|August 3, 2022
RNA editing underlies genetic risk of common inflammatory diseasesQin Li, Michael J Gloudemans, Jonathan M Geisinger, et al.American Journal of Human Genetics|September 28, 2021
An integrated approach to identify environmental modulators of genetic risk factors for complex traitsBrunilda Balliu, Ivan Carcamo-Orive, Michael J Gloudemans, et al.American Journal of Physiology. Cell Physiology|July 24, 2023
A single-cell CRISPRi platform for characterizing candidate genes relevant to metabolic disorders in human adipocytesEwa Bielczyk-Maczynska, Disha Sharma, Montgomery Blencowe, et al.Genome Biology|November 6, 2019
Genetic regulation of gene expression and splicing during a 10-year period of human agingBrunilda Balliu, Matthew Durrant, Olivia de Goede, et al.American Journal of Physiology. Endocrinology and Metabolism|February 16, 2026
Colocalization and functional analyses identify GBE1 as a gene linking muscle strength and cardiometabolic fitnessTheresia M Schnurr, Miranda Lee Johnson, Christopher Jin, et al.Nature Genetics|October 27, 2020
Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseasesM Ryan Corces, Anna Shcherbina, Soumya Kundu, et al.American Journal of Human Genetics|May 19, 2022
Integration of rare expression outlier-associated variants improves polygenic risk predictionCraig Smail, Nicole M Ferraro, Qin Hui, et al.Pageof 2