Last data update: Sep 16, 2021. (Total: 3468 publications since 2011)
|Query Trace: all>>Dorothy Ellingsen[CDC Author]|
| Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.
Christopher J Bean, W Craig Hooper, Dorothy Ellingsen, Michael R Debaun, Jennifer Sonderman, and William J Blot
Public Health Genomics 2014 17(3) 169-72
Similar articles in PubMed DOI:10.1159/000360260
| Mutation analysis of a cohort of US patients with hemophilia B.
Tengguo Li, Connie H Miller, Jennifer Driggers, Amanda B Payne, Dorothy Ellingsen, and W Craig Hooper
Am. J. Hematol. 2014 Apr 89(4) 375-9
Similar articles in PubMed DOI:10.1002/ajh.23645
| 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
Similar articles in PubMed DOI:10.1182/blood-2011-06-361642
| Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks.
Christopher J Bean, Sheree L Boulet, Dorothy Ellingsen, Heidi Trau, Nafisa Ghaji, W Craig Hooper, and Harland Austin
Thromb. Res. 2012 Dec 130(6) 942-7
Similar articles in PubMed DOI:10.1016/j.thromres.2012.08.300