Olivia Corradin
Affiliations: | 2017 | Biology | Whitehead Institute (MIT), Cambridge, MA, United States |
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Children
Sign in to add traineeOrian Stapleton | research assistant | Whitehead Institute (MIT) | |
An Hoang | research assistant | 2018- | Whitehead Institute (MIT) |
Fatir Qureshi | research scientist | 2022- | Whitehead Institute (MIT) (MathTree) |
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Publications
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Hoang AT, Corradin O. (2023) Epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid overdose. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology |
Corradin O, Sallari R, Hoang AT, et al. (2022) Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid overdose. Molecular Psychiatry |
Factor DC, Barbeau AM, Allan KC, et al. (2020) Cell Type-Specific Intralocus Interactions Reveal Oligodendrocyte Mechanisms in MS. Cell |
Bailey SD, Zhang X, Desai K, et al. (2018) Publisher Correction: ZNF143 provides sequence specificity to secure chromatin interactions at gene promoters. Nature Communications. 9: 16194 |
Cohen AJ, Saiakhova A, Corradin O, et al. (2017) Hotspots of aberrant enhancer activity punctuate the colorectal cancer epigenome. Nature Communications. 8: 14400 |
Corradin O, Cohen AJ, Luppino JM, et al. (2016) Modeling disease risk through analysis of physical interactions between genetic variants within chromatin regulatory circuitry. Nature Genetics |
Bailey SD, Zhang X, Desai K, et al. (2015) ZNF143 provides sequence specificity to secure chromatin interactions at gene promoters. Nature Communications. 2: 6186 |
Vučićević D, Corradin O, Ntini E, et al. (2015) Long ncRNA expression associates with tissue-specific enhancers. Cell Cycle (Georgetown, Tex.). 14: 253-60 |
Corradin O, Scacheri PC. (2014) Enhancer variants: evaluating functions in common disease. Genome Medicine. 6: 85 |
Factor DC, Corradin O, Zentner GE, et al. (2014) Epigenomic comparison reveals activation of "seed" enhancers during transition from naive to primed pluripotency. Cell Stem Cell. 14: 854-63 |