Erick W. Loomis, Ph.D.
Affiliations: | 2013 | Genetics | University of California, Davis, Davis, CA |
Area:
Genetics, Molecular Biology, General BiologyGoogle:
"Erick Loomis"Parents
Sign in to add mentorPaul J. Hagerman | grad student | 2013 | UC Davis | |
(Molecular Consequences of Expanded CGG Repeats in the Human FMR1 Gene: R-loops, Methylation, and DNA Sequencing.) |
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Publications
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Gallon J, Loomis E, Martin N, et al. (2018) Abstract 4326: The chromatin context and consequence of cisplatin-adduct DNA damage Cancer Research. 78: 4326-4326 |
Simmonds P, Loomis E, Curry E. (2017) DNA methylation-based chromatin compartments and ChIP-seq profiles reveal transcriptional drivers of prostate carcinogenesis. Genome Medicine. 9: 54 |
Flanagan JM, Wilson A, Koo C, et al. (2016) Platinum-based chemotherapy induces methylation changes in blood DNA associated with overall survival in ovarian cancer patients. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research |
Pham TT, Yin J, Eid JS, et al. (2016) Single-locus enrichment without amplification for sequencing and direct detection of epigenetic modifications. Molecular Genetics and Genomics : Mgg |
Pretto DI, Eid JS, Yrigollen CM, et al. (2015) Differential increases of specific FMR1 mRNA isoforms in premutation carriers. Journal of Medical Genetics. 52: 42-52 |
Loomis EW, Sanz LA, Chédin F, et al. (2014) Transcription-associated R-loop formation across the human FMR1 CGG-repeat region. Plos Genetics. 10: e1004294 |
Loomis EW, Eid JS, Peluso P, et al. (2013) Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene. Genome Research. 23: 121-8 |
Hagerman PJ, Eid J, Peluso P, et al. (2013) Sequencing the Unsequenceable: Expanded CGG Repeats in the Human FMR1 Gene Biophysical Journal. 104: 377a |