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Public Health Genomics and Precision Health Knowledge Base (v7.7)
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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: May 20, 2022
. (Total: 3839 publications since 2011)
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Records 1-7 (of 7 Records)
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 7 (10) 2473-2476
Similar articles in PubMed
DOI:
10.3201/EID2610.202792
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
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
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
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
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
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Page last reviewed:
Oct 1, 2021
Page last updated:
May 20, 2022
Content source:
Office of Genomics and Precision Public Health
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