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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Apr 15, 2024. (Total: 5790 publications)
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Records 1-3 (of 3 Records)
Query Trace: all>>Meredith E Pyle[CDC Author]
Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism.
Lewis DA , Suchindran S , Beckman MG , Hooper WC , Grant AM , Heit JA , Manco-Johnson M , Moll S , Philipp CS , Kenney K , De Staercke C , Pyle ME , Chi JT , Ortel TL .
Thromb Res 2015 135 (4) 659-65
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.
Bean CJ , Boulet SL , Yang G , Payne AB , Ghaji N , Pyle ME , Hooper WC , Bhatnagar P , Keefer J , Barron-Casella EA , Casella JF , Debaun MR .
Br J Haematol 2013 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.
Bean CJ , Boulet SL , Ellingsen D , Pyle ME , Barron-Casella EA , Casella JF , Payne AB , Driggers J , Trau HA , Yang G , Jones K , Ofori-Acquah SF , Hooper WC , Debaun MR .
Blood 2012 120 (18) 3822-8
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