Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia

por Bean, Christopher J., Boulet, Sheree L., Yang, Genyan, Payne, Amanda B., Ghaji, Nafisa, Pyle, Meredith E., Hooper, W. Craig, Bhatnagar, Pallav, Keefer, Jeffrey, Barron-Casella, Emily A., Casella, James F., DeBaun, Michael R.
Publicado 2013

Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism()

por Lewis, Deborah A., Suchindran, Sunil, Beckman, Michele G., Hooper, W. Craig, Grant, Althea M., Heit, John A., Manco-Johnson, Marilyn, Moll, Stephan, Philipp, Claire S., Kenney, Kristy, De Staercke, Christine, Pyle, Meredith E., Chi, Jen-Tsan, Ortel, Thomas L.
Publicado en Thromb Res (2015)

Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease

por Bean, Christopher J., Boulet, Sheree L., Ellingsen, Dorothy, Pyle, Meredith E., Barron-Casella, Emily A., Casella, James F., Payne, Amanda B., Driggers, Jennifer, Trau, Heidi A., Yang, Genyan, Jones, Kimberly, Ofori-Acquah, Solomon F., Hooper, W. Craig, DeBaun, Michael R.
Publicado 2012

Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle...

por Thangarajh, Mathula, Yang, Genyan, Fuchs, Dana, Ponisio, Maria R., McKinstry, Robert C., Jaju, Alok, Noetzel, Michael J., Casella, James F., Barron-Casella, Emily, Hooper, W. Craig, Boulet, Sheree L., Bean, Christopher J., Pyle, Meredith E., Payne, Amanda B., Driggers, Jennifer, Trau, Heidi A., Vendt, Bruce A., Rodeghier, Mark, DeBaun, Michael R.
Publicado 2012