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American Journal of Human Genetics|January 11, 2016
An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between VariantsJoe R Davis, Laure Fresard, David A Knowles, et al.Nature Communications|January 3, 2025
regionalpcs improve discovery of DNA methylation associations with complex traitsTiffany Eulalio, Min Woo Sun, Olivier Gevaert, et al.American Journal of Human Genetics|July 3, 2021
Nonsense-mediated decay is highly stable across individuals and tissuesNicole A Teran, Daniel C Nachun, Tiffany Eulalio, et al.Briefings in Bioinformatics|November 6, 2024
siRNADiscovery: a graph neural network for siRNA efficacy prediction via deep RNA sequence analysisRongzhuo Long, Ziyu Guo, Da Han, et al.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.Proceedings of the National Academy of Sciences of the United States of America|May 22, 2013
Systematic functional regulatory assessment of disease-associated variantsKonrad J Karczewski, Joel T Dudley, Kimberly R Kukurba, et al.Nucleic Acids Research|April 8, 2025
DragonRNA: Generality of DNA-primed RNA-extension activities by DNA-directed RNA polymerasesEmily Greenwald, Drew Galls, Joon Park, et al.Plos Genetics|April 7, 2010
Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associationsAlexandra C Nica, Stephen B Montgomery, Antigone S Dimas, et al.Nucleic Acids Research|July 4, 2025
Toward optimizing diversifying base editors for high-throughput mutational scanning studiesCarley I Schwartz, Nathan S Abell, Amy Li, et al.Biorxiv : the Preprint Server for Biology|November 28, 2024
Towards optimizing diversifying base editors for high-throughput studies of single- nucleotide variantsCarley I Schwartz, Nathan S Abell, Amy Li, et al.Pageof 22