Last data update: Feb 20, 2020. (Total: 2767 publications since 2011)
|Query Trace: all>>Meredith E Pyle[CDC Author]|
| Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism.
Deborah A Lewis, Sunil Suchindran, Michele G Beckman, W Craig Hooper, Althea M Grant, John A Heit, Marilyn Manco-Johnson, Stephan Moll, Claire S Philipp, Kristy Kenney, Christine De Staercke, Meredith E Pyle, Jen-Tsan Chi, and Thomas L Ortel
Thromb. Res. 2015 Apr 135(4) 659-65
| Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.
Christopher J Bean, Sheree L Boulet, Genyan Yang, Amanda B Payne, Nafisa Ghaji, Meredith E Pyle, W Craig Hooper, Pallav Bhatnagar, Jeffrey Keefer, Emily A Barron-Casella, James F Casella, and Michael R Debaun
Br. J. Haematol. 2013 Oct 163(2) 268-76
| Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.
Christopher J Bean, Sheree L Boulet, Dorothy Ellingsen, Meredith E Pyle, Emily A Barron-Casella, James F Casella, Amanda B Payne, Jennifer Driggers, Heidi A Trau, Genyan Yang, Kimberly Jones, Solomon F Ofori-Acquah, W Craig Hooper, and Michael R Debaun
Blood 2012 Nov 1. 120(18) 3822-8