CDC-Authored Genomics and Precision Health Publications Database

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Last data update: Jul 18, 2025. (Total: 6743 publications)

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Records 1-7 (of 7 Records)

Query Trace: all>>Amanda B Payne[CDC Author]
The CDC Hemophilia B mutation project mutation list: a new online resource. Li T , Miller CH , Payne AB , Craig Hooper W . Mol Genet Genomic Med 2013 1 (4) 238-45
Occurrence rates of von Willebrand disease among people receiving care in specialized treatment centres in the United States. Michael Soucie J , Miller CH , Byams VR , Payne AB , Abe K , Sidonio RF Jr , Kouides PA . Haemophilia 2021 27 (3) 445-453
Coronavirus Disease among Persons with Sickle Cell Disease, United States, March 20-May 21, 2020. Panepinto JA , Brandow A , Mucalo L , Yusuf F , Singh A , Taylor B , Woods K , Payne AB , Peacock G , Schieve LA . Emerg Infect Dis 2020 26 (10) 2473-2476
Mutation analysis of a cohort of US patients with hemophilia B. Li T , Miller CH , Driggers J , Payne AB , Ellingsen D , Hooper WC . Am J Hematol 2013 89 (4) 375-9
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
The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource. Payne AB , Miller CH , Kelly FM , Soucie JM , Hooper WC . Hum Mutat 2012 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. 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