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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 30, 2023. (Total: 4301 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.
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
Origins and organization of the NHLBI State of the Science Workshop: Generating a national blueprint for future research on factor VIII inhibitors.
Sabatino DE , Pipe SW , Nugent DJ , Soucie JM , Hooper WC , Hoots WK , DiMichele DM .
Haemophilia 2019 25 (4) 575-580
VKORC1-1639A allele influences warfarin maintenance dosage among Blacks receiving warfarin anticoagulation: a retrospective cohort study.
Mili FD , Allen T , Wadell PW , Hooper WC , Staercke C , Bean CJ , Lally C , Austin H , Wenger NK .
Future Cardiol 2018 14 (1) 15-26
Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism.
Lewis Deborah A, Suchindran Sunil, Beckman Michele G, Hooper W Craig, Grant Althea M, Heit John A, Manco-Johnson Marilyn, Moll Stephan, Philipp Claire S, Kenney Kristy, De Staercke Christine, Pyle Meredith E, Chi Jen-Tsan, Ortel Thomas L. Thromb. Res. 2015 Apr 135(4) 659-65 .
Thromb. Res. 2015 Apr 135(4) 659-65
Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.
Bean Christopher J, Hooper W Craig, Ellingsen Dorothy, DeBaun Michael R, Sonderman Jennifer, Blot William J. Public Health Genomics 2014 17(3) 169-72 .
Public Health Genomics 2014 17(3) 169-72
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Jiang Baijia, Ryan Kathleen A, Hamedani Ali, Cheng Yuching, Sparks Mary J, Koontz Deborah, Bean Christopher J, Gallagher Margaret, Hooper W Craig, McArdle Patrick F, O'Connell Jeffrey R, Stine O Colin, Wozniak Marcella A, Stern Barney J, Mitchell Braxton D, Kittner Steven J, Cole John W. Stroke 2014 Apr 45(4) 961-7 .
Stroke 2014 Apr 45(4) 961-7
Mutation analysis of a cohort of US patients with hemophilia B.
Li Tengguo, Miller Connie H, Driggers Jennifer, Payne Amanda B, Ellingsen Dorothy, Hooper W Craig. Am. J. Hematol. 2014 Apr 89(4) 375-9 .
Am. J. Hematol. 2014 Apr 89(4) 375-9
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.
Bean Christopher J, Boulet Sheree L, Yang Genyan, Payne Amanda B, Ghaji Nafisa, Pyle Meredith E, Hooper W Craig, Bhatnagar Pallav, Keefer Jeffrey, Barron-Casella Emily A, Casella James F, Debaun Michael R. Br. J. Haematol. 2013 Oct 163(2) 268-76 .
Br. J. Haematol. 2013 Oct 163(2) 268-76
Relationships between selected gene polymorphisms and blood pressure sensitivity to weight loss in elderly persons with hypertension.
Kostis William J, Cabrera Javier, Hooper W Craig, Whelton Paul K, Espeland Mark A, Cosgrove Nora M, Cheng Jerry Q, Deng Yingzi, De Staerck Christine, Pyle Meredith, Maruthur Nisa, Reyes Ingrid, Anderson Cheryl A M, Liu Jie, Kostis John B. Hypertension 2013 Apr 61(4) 857-63 .
Hypertension 2013 Apr 61(4) 857-63
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.
Soucie J Michael, De Staercke Christine, Monahan Paul E, Recht Michael, Chitlur Meera B, Gruppo Ralph, Hooper W Craig, Kessler Craig, Kulkarni Roshni, Manco-Johnson Marilyn J, Powell Jerry, Pyle Meredith, Riske Brenda, Sabio Hernan, Trimble Sean, . Transfusion 2013 Jun 53(6) 1217-25 .
Transfusion 2013 Jun 53(6) 1217-25
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.
Bean Christopher J, Boulet Sheree L, Ellingsen Dorothy, Pyle Meredith E, Barron-Casella Emily A, Casella James F, Payne Amanda B, Driggers Jennifer, Trau Heidi A, Yang Genyan, Jones Kimberly, Ofori-Acquah Solomon F, Hooper W Craig, DeBaun Michael R. Blood 2012 Nov 1. 120(18) 3822-8 .
Blood 2012 Nov 1. 120(18) 3822-8
Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks.
Bean Christopher J, Boulet Sheree L, Ellingsen Dorothy, Trau Heidi, Ghaji Nafisa, Hooper W Craig, Austin Harland. Thromb. Res. 2012 Dec 130(6) 942-7 .
Thromb. Res. 2012 Dec 130(6) 942-7
Family history of myocardial infarction is a risk factor for venous thromboembolism among whites but not among blacks.
Mili Fatima D, Hooper W Craig, Lally Cathy, Austin Harland. Clin. Appl. Thromb. Hemost. 19(4) 410-7 .
Clin. Appl. Thromb. Hemost. 19(4) 410-7
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Milton Jacqueline N, Sebastiani Paola, Solovieff Nadia, Hartley Stephen W, Bhatnagar Pallav, Arking Dan E, Dworkis Daniel A, Casella James F, Barron-Casella Emily, Bean Christopher J, Hooper W Craig, DeBaun Michael R, Garrett Melanie E, Soldano Karen, Telen Marilyn J, Ashley-Koch Allison, Gladwin Mark T, Baldwin Clinton T, Steinberg Martin H, Klings Elizabeth S. PLoS ONE 2012 7(4) e34741 .
PLoS ONE 2012 7(4) e34741
The impact of co-morbid conditions on family history of venous thromboembolism in Whites and Blacks.
Mili Fatima D, Hooper W Craig, Lally Cathy, Austin Harland. Thrombosis research 2011 Apr 127(4) 309-16 .
Thrombosis research 2011 Apr 127(4) 309-16
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