S
Simon G. Gregory
Researcher at Duke University
Publications - 216
Citations - 50384
Simon G. Gregory is an academic researcher from Duke University. The author has contributed to research in topics: Single-nucleotide polymorphism & Gene. The author has an hindex of 54, co-authored 198 publications receiving 47130 citations. Previous affiliations of Simon G. Gregory include University of Helsinki & Wellcome Trust.
Papers
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Journal ArticleDOI
Single Cell RNA-Seq Analysis of Human Red Cells
TL;DR: Single cell RNA-Seq is performed to analyze the transcriptional heterogeneity of RBCs from three adult healthy donors which have been stored in the blood bank conditions and assayed at day 1 and day 15 to indicate the power of single RBC RNA- Seq to capture and discover known and unexpected heterogeneity ofRBC population.
Development of Biomarkers to Assess Fumonisin Exposure and Birth Defects
Waes Gelineau-van,Ronald T. Riley,Kenneth A. Voss,Jency L. Showker,Olga Torres,J. Matutue,Joyce R. Maddox,Mark A. Rainey,Nicole M. Gardner,Andrew J. Sachs,Simon G. Gregory,Allison E. Ashley-Koch,D. Krupp +12 more
Journal ArticleDOI
U2AF2 binds IL7R exon 6 ectopically and represses its inclusion.
Geraldine Schott,Gaddiel Galarza-Muñoz,Noe Trevino,Xiaoting Chen,Matthew T. Weirauch,Simon G. Gregory,Shelton S. Bradrick,Mariano A. Garcia-Blanco +7 more
TL;DR: In this paper, a competition between PTBP1 and U2AF2 at the polypyrimidine tract (PPT) of intron 5 was found to increase skipping of the exon, resulting in elevated levels of sIL7R.
Patent
Methods and compositions for correlating genetic markers with cardiovascular disease
Jeffery M. Vance,Pascal J. Goldschmidt,Simon G. Gregory,William E. Kraus,Elizabeth R. Hauser +4 more
TL;DR: In this paper, the authors presented methods of identifying a subject having an increased or decreased risk of developing cardiovascular disease, comprising of correlating the presence of one or more genetic markers in chromosome 3q13.31 with an increased risk of cardiovascular disease; and detecting the one or multiple genetic markers of step (a) in the subject.
Journal ArticleDOI
Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.
Jennifer R. Dungan,Xuejun Qin,Benjamin D. Horne,Benjamin D. Horne,John F. Carlquist,John F. Carlquist,Abanish Singh,Melissa Hurdle,Elizabeth Grass,Carol Haynes,Simon G. Gregory,Svati H. Shah,Elizabeth R. Hauser,William E. Kraus +13 more
TL;DR: Evaluated LSAMP SNP-specific hazards for all-cause mortality post-catheterization in a larger cohort of the authors' CAD cases and performed additional replication in an independent dataset suggest that genetic effects of rs1462845 on survival are unique to CAD presence.