1.
Weng L-C, Hall AW, Choi SH, et al. Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation. Circ Genom Precis Med. 2020;13(5):387-395. doi:10.1161/CIRCGEN.119.002874.
1.
Ye CJ, Chen J, Villani A-C, et al. Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of transcripts under balancing selection. Genome Res. 2018;28(12):1812-1825. doi:10.1101/gr.240390.118.
1.
Davenport EE, Amariuta T, Gutierrez-Arcelus M, et al. Discovering in vivo cytokine-eQTL interactions from a lupus clinical trial. Genome Biol. 2018;19(1):168. doi:10.1186/s13059-018-1560-8.
1.
Galván-Femenía I, Obón-Santacana M, Piñeyro D, et al. Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. J Med Genet. 2018;55(11):765-778. doi:10.1136/jmedgenet-2018-105437.
1.
Raj T, Li YI, Wong G, et al. Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer’s disease susceptibility. Nat Genet. 2018;50(11):1584-1592. doi:10.1038/s41588-018-0238-1.
1.
Went M, Sud A, Försti A, et al. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Nat Commun. 2018;9(1):3707. doi:10.1038/s41467-018-04989-w.
1.
Westra H-J, Martínez-Bonet M, Onengut-Gumuscu S, et al. Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes. Nat Genet. 2018;50(10):1366-1374. doi:10.1038/s41588-018-0216-7.
1.
Evangelou E, Warren HR, Mosen-Ansorena D, et al. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat Genet. 2018;50(10):1412-1425. doi:10.1038/s41588-018-0205-x.
1.
Hormozdiari F, Zhu A, Kichaev G, et al. Widespread Allelic Heterogeneity in Complex Traits. Am J Hum Genet. 2017;100(5):789-802. doi:10.1016/j.ajhg.2017.04.005.
1.
Gillies CE, Putler R, Menon R, et al. An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome. Am J Hum Genet. 2018;103(2):232-244. doi:10.1016/j.ajhg.2018.07.004.