CDC-Authored Genomics and Precision Health Publications Database

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Last data update: Dec 09, 2024. (Total: 6442 publications)

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Records 1-13 (of 13 Records)

Query Trace: Miller CH[original query]
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
Genetic causes of haemophilia in women and girls. Miller CH , Bean CJ . Haemophilia 2020 27 (2) e164-e179
Evaluation of CDC's Hemophilia Surveillance Program - Universal Data Collection (1998-2011) and Community Counts (2011-2019), United States. Schieve LA , Byams VR , Dupervil B , Oakley MA , Miller CH , Soucie JM , Abe K , Bean CJ , Hooper WC . MMWR Surveill Summ 2020 69 (5) 1-18
Game, set, match for factor VIII mismatch? Miller CH . Blood 2015 126 (7) 829-30
Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations. Boylan B , Rice AS , De Staercke C , Eyster ME , Yaish HM , Knoll CM , Bean CJ , Miller CH . J Thromb Haemost 2015 13 (6) 1036-42
High factor VIII, von Willebrand factor, and fibrinogen levels and risk of venous thromboembolism in blacks and whites Payne AB , Miller CH , Hooper WC , Lally C , Austin HD . Ethn Dis 2014 24 (2) 169-74
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
A study of prospective surveillance for inhibitors among persons with haemophilia in the United States Soucie JM , Miller CH , Kelly FM , Payne AB , Creary M , Bockenstedt PL , Kempton CL , Manco-Johnson MJ , Neff AT . Haemophilia 2013 20 (2) 230-7
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
F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis. Gouw SC , van den Berg HM , Oldenburg J , Astermark J , de Groot PG , Margaglione M , Thompson AR , van Heerde W , Boekhorst J , Miller CH , le Cessie S , van der Bom JG . Blood 2012 119 (12) 2922-34
F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity. Miller CH , Benson J , Ellingsen D , Driggers J , Payne A , Kelly FM , Soucie JM , Hooper WC . Haemophilia 2011 18 (3) 375-82
Complications associated with carrier status among people with blood disorders: a commentary Hooper WC , Miller CH , Key NS . Am J Prev Med 2010 38 S456-8