Ryan S. Tewhey, Ph.D.

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Siraj L, Castro RI, Dewey H, et al. (2024) Functional dissection of complex and molecular trait variants at single nucleotide resolution. Biorxiv : the Preprint Server For Biology
Kotliar D, Raju S, Tabrizi S, et al. (2024) Genome-wide association study identifies human genetic variants associated with fatal outcome from Lassa fever. Nature Microbiology
Brown EA, Kales S, Boyle MJ, et al. (2023) Three linked variants have opposing regulatory effects on isovaleryl-CoA dehydrogenase gene expression. Human Molecular Genetics
Xue JR, Mackay-Smith A, Mouri K, et al. (2023) The functional and evolutionary impacts of human-specific deletions in conserved elements. Science (New York, N.Y.). 380: eabn2253
Mouri K, Guo MH, de Boer CG, et al. (2022) Prioritization of autoimmune disease-associated genetic variants that perturb regulatory element activity in T cells. Nature Genetics
Lagerborg KA, Normandin E, Bauer MR, et al. (2021) Synthetic DNA spike-ins (SDSIs) enable sample tracking and detection of inter-sample contamination in SARS-CoV-2 sequencing workflows. Nature Microbiology
Griesemer D, Xue JR, Reilly SK, et al. (2021) Genome-wide functional screen of 3'UTR variants uncovers causal variants for human disease and evolution. Cell
Ray JP, de Boer CG, Fulco CP, et al. (2020) Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features. Nature Communications. 11: 1237
Tewhey R, Kotliar D, Park DS, et al. (2018) Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay. Cell. 172: 1132-1134
Grossman SR, Zhang X, Wang L, et al. (2017) Systematic dissection of genomic features determining transcription factor binding and enhancer function. Proceedings of the National Academy of Sciences of the United States of America