CDC-Authored Genomics and Precision Health Publications Database

Last data update: Feb 24, 2021. (Total: 3169 publications since 2011)

All HLBS Cancer Rare Diabetes FHH Equity COVID-19 RCH Environmental PGx dataset

Filtered By: Select to fine-tune your search CDC Author Year CDC Organization

Records 1-10 (of 10 Records)

Query Trace: Hemophilia A[original query]
Genetic causes of haemophilia in women and girls. Connie H Miller, and Christopher J Bean Haemophilia : the official journal of the World Federation of Hemophilia 2020 Dec Similar articles in PubMed
Evaluation of CDC's Hemophilia Surveillance Program - Universal Data Collection (1998-2011) and Community Counts (2011-2019), United States. Laura A Schieve, Vanessa R Byams, Brandi Dupervil, Meredith A Oakley, Connie H Miller, J Michael Soucie, Karon Abe, Christopher J Bean, and W Craig Hooper Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C. : 2002) 2020 Sep 69(5) 1-18 Similar articles in PubMed
Origins and organization of the NHLBI State of the Science Workshop: Generating a national blueprint for future research on factor VIII inhibitors. Denise E Sabatino, Steven W Pipe, Diane J Nugent, J Michael Soucie, W Craig Hooper, W Keith Hoots, and Donna M DiMichele Haemophilia : the official journal of the World Federation of Hemophilia 2019 Jul 25(4) 575-580 Similar articles in PubMed
Achievements, challenges and unmet needs for haemophilia patients with inhibitors: Report from a symposium in Paris, France on 20 November 2014. Y Dargaud, A Pavlova, S Lacroix-Desmazes, K Fischer, M Soucie, S Claeyssens, D W Scott, R D'Oiron, G Lavigne-Lissalde, G Kenet, C Escuriola Ettingshausen, A Borel-Derlon, T Lambert, G Pasta, and C Négrier Haemophilia : the official journal of the World Federation of Hemophilia 2016 Jan 22 Suppl 11-24 Similar articles in PubMed
Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations. B Boylan, A S Rice, C De Staercke, M E Eyster, H M Yaish, C M Knoll, C J Bean, C H Miller, and J. Thromb. Haemost. 2015 Jun 13(6) 1036-42 Similar articles in PubMed
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
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
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
Utility of multiplex ligation-dependent probe amplification (MLPA) for hemophilia mutation screening. A B Payne, C J Bean, W C Hooper, and C H Miller J. Thromb. Haemost. 2012 Sep 10(9) 1951-4 Similar articles in PubMed
F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis. Samantha C Gouw, H Marijke van den Berg, Johannes Oldenburg, Jan Astermark, Philip G de Groot, Maurizio Margaglione, Arthur R Thompson, Waander van Heerde, Jorien Boekhorst, Connie H Miller, Saskia le Cessie, and Johanna G van der Bom Blood 2012 Mar 22. 119(12) 2922-34 Similar articles in PubMed