Last data update: Sep 23, 2021. (Total: 3483 publications since 2011)
|Query Trace: all>>Amanda B Payne[CDC Author]|
| Occurrence rates of von Willebrand disease among people receiving care in specialized treatment centres in the United States.
John Michael Soucie, Connie H Miller, Vanessa R Byams, Amanda B Payne, Karon Abe, Robert F Sidonio, and Peter A Kouides
Haemophilia : the official journal of the World Federation of Hemophilia 2021
Similar articles in PubMed DOI:10.1111/hae.14263
| Coronavirus Disease among Persons with Sickle Cell Disease, United States, March 20-May 21, 2020.
Julie A Panepinto, Amanda Brandow, Lana Mucalo, Fouza Yusuf, Ashima Singh, Bradley Taylor, Katherine Woods, Amanda B Payne, Georgina Peacock, and Laura A Schieve
Emerging infectious diseases 2020 26(10) 2473-2476
Similar articles in PubMed DOI:10.3201/eid2610.202792
| 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
Similar articles in PubMed DOI:10.1002/mgg3.30
| 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
| 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
Similar articles in PubMed DOI:10.1111/bjh.12507
| 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
Similar articles in PubMed DOI:10.1002/humu.22247
| 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