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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: Nov 23, 2021. (Total: 3579 publications since 2011)
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Records 1-15 (of 15 Records)
Query Trace: all>>W Craig Hooper[CDC Author]
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
VKORC1-1639A allele influences warfarin maintenance dosage among Blacks receiving warfarin anticoagulation: a retrospective cohort study.
Fatima Donia Mili, Tenecia Allen, Paula Weinstein Wadell, W Craig Hooper, Christine De Staercke, Christopher J Bean, Cathy Lally, Harland Austin, and Nanette K Wenger
Future cardiology 2018 14(1) 15-26
Evidence for the transmission of parvovirus B19 in patients with bleeding disorders treated with plasma-derived factor concentrates in the era of nucleic acid test screening.
J Michael Soucie, Christine De Staercke, Paul E Monahan, Michael Recht, Meera B Chitlur, Ralph Gruppo, W Craig Hooper, Craig Kessler, Roshni Kulkarni, Marilyn J Manco-Johnson, Jerry Powell, Meredith Pyle, Brenda Riske, Hernan Sabio, Sean Trimble, and
Transfusion 2013 Jun 53(6) 1217-25
The impact of co-morbid conditions on family history of venous thromboembolism in Whites and Blacks.
Fatima D Mili, W Craig Hooper, Cathy Lally, and Harland Austin
Thrombosis research 2011 Apr 127(4) 309-16
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
Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism.
Deborah A Lewis, Sunil Suchindran, Michele G Beckman, W Craig Hooper, Althea M Grant, John A Heit, Marilyn Manco-Johnson, Stephan Moll, Claire S Philipp, Kristy Kenney, Christine De Staercke, Meredith E Pyle, Jen-Tsan Chi, and Thomas L Ortel
Thromb. Res. 2015 Apr 135(4) 659-65
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
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Baijia Jiang, Kathleen A Ryan, Ali Hamedani, Yuching Cheng, Mary J Sparks, Deborah Koontz, Christopher J Bean, Margaret Gallagher, W Craig Hooper, Patrick F McArdle, Jeffrey R O'Connell, O Colin Stine, Marcella A Wozniak, Barney J Stern, Braxton D Mitchell, Steven J Kittner, and John W Cole
Stroke 2014 Apr 45(4) 961-7
Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.
Christopher J Bean, W Craig Hooper, Dorothy Ellingsen, Michael R Debaun, Jennifer Sonderman, and William J Blot
Public Health Genomics 2014 17(3) 169-72
Family history of myocardial infarction is a risk factor for venous thromboembolism among whites but not among blacks.
Fatima D Mili, W Craig Hooper, Cathy Lally, and Harland Austin
Clin. Appl. Thromb. Hemost. 19(4) 410-7
Relationships between selected gene polymorphisms and blood pressure sensitivity to weight loss in elderly persons with hypertension.
William J Kostis, Javier Cabrera, W Craig Hooper, Paul K Whelton, Mark A Espeland, Nora M Cosgrove, Jerry Q Cheng, Yingzi Deng, Christine De Staerck, Meredith Pyle, Nisa Maruthur, Ingrid Reyes, Cheryl A M Anderson, Jie Liu, and John B Kostis
Hypertension 2013 Apr 61(4) 857-63
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
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Jacqueline N Milton, Paola Sebastiani, Nadia Solovieff, Stephen W Hartley, Pallav Bhatnagar, Dan E Arking, Daniel A Dworkis, James F Casella, Emily Barron-Casella, Christopher J Bean, W Craig Hooper, Michael R Debaun, Melanie E Garrett, Karen Soldano, Marilyn J Telen, Allison Ashley-Koch, Mark T Gladwin, Clinton T Baldwin, Martin H Steinberg, and Elizabeth S Klings
PLoS ONE 2012 7(4) e34741
Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks.
Christopher J Bean, Sheree L Boulet, Dorothy Ellingsen, Heidi Trau, Nafisa Ghaji, W Craig Hooper, and Harland Austin
Thromb. Res. 2012 Dec 130(6) 942-7
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
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