Andrew Sharp, Ph.D.

Genome Sciences University of Washington, Seattle, Seattle, WA 
"Andrew Sharp"
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Garg P, Martin-Trujillo A, Rodriguez OL, et al. (2021) Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression. American Journal of Human Genetics
Martin-Trujillo A, Patel N, Richter F, et al. (2020) Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles. Plos Genetics. 16: e1009189
Garg P, Jadhav B, Rodriguez OL, et al. (2020) A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions. American Journal of Human Genetics
Breen MS, Garg P, Tang L, et al. (2020) Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype. American Journal of Human Genetics
Seiden AH, Richter F, Patel N, et al. (2020) Elucidation of de novo small insertion/deletion biology with parent-of-origin phasing. Human Mutation
Do AN, Watson CT, Cohain AT, et al. (2019) Dual transcriptomic and epigenomic study of reaction severity in peanut allergic children. The Journal of Allergy and Clinical Immunology
Choudhury A, Garg S, Smith J, et al. (2019) Prospective evaluation of an ultrathin strut biodegradable polymer-coated sirolimus-eluting stent: 12 months' results from the S-FLEX UK registry. Bmj Open. 9: e026578
Richter F, Hoffman GE, Manheimer KB, et al. (2019) ORE Identifies Extreme Expression Effects Enriched for Rare Variants. Bioinformatics (Oxford, England)
Garg P, Sharp AJ. (2019) Screening for rare epigenetic variations in autism and schizophrenia. Human Mutation
Ntranos A, Ntranos V, Bonnefil V, et al. (2019) Fumarates target the metabolic-epigenetic interplay of brain-homing T cells in multiple sclerosis. Brain : a Journal of Neurology
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