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CDC-Authored Genomics and Precision Health Publications Database|Home|PHGKB

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Jan 23, 2020. (Total: 2739 publications since 2011)
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Records 1-5 (of 5 Records)
Query Trace: all>>Amanda B Payne[CDC Author]
The CDC Hemophilia B mutation project mutation list: a new online resource.
Tengguo Li, Connie H Miller, Amanda B Payne, and W Craig Hooper
Mol Genet Genomic Med 2013 Nov 1(4) 238-45
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
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
The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource.
Amanda B Payne, Connie H Miller, Fiona M Kelly, J Michael Soucie, and W Craig Hooper
Hum. Mutat. 2013 Feb 34(2) E2382-91
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
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