CDC-Authored Genomics and Precision Health Publications Database

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Last data update: Nov 04, 2024. (Total: 6390 publications)

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Records 1-23 (of 23 Records)

Query Trace: Hooper WC[original query]
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 DA , Suchindran S , Beckman MG , Hooper WC , Grant AM , Heit JA , Manco-Johnson M , Moll S , Philipp CS , Kenney K , De Staercke C , Pyle ME , Chi JT , Ortel TL . Thromb Res 2015 135 (4) 659-65
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
Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults. Bean CJ , Hooper WC , Ellingsen D , Debaun MR , Sonderman J , Blot WJ . 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 B , Ryan KA , Hamedani A , Cheng Y , Sparks MJ , Koontz D , Bean CJ , Gallagher M , Hooper WC , McArdle PF , O'Connell JR , Stine OC , Wozniak MA , Stern BJ , Mitchell BD , Kittner SJ , Cole JW . Stroke 2014 45 (4) 961-7
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
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia. Bean CJ , Boulet SL , Yang G , Payne AB , Ghaji N , Pyle ME , Hooper WC , Bhatnagar P , Keefer J , Barron-Casella EA , Casella JF , Debaun MR . Br J Haematol 2013 163 (2) 268-76
Family history of myocardial infarction is a risk factor for venous thromboembolism among whites but not among blacks. Mili FD , Hooper WC , Lally C , Austin H . Clin Appl Thromb Hemost 2013 19 (4) 410-7
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 JM , De Staercke C , Monahan PE , Recht M , Chitlur MB , Gruppo R , Hooper WC , Kessler C , Kulkarni R , Manco-Johnson MJ , Powell J , Pyle M , Riske B , Sabio H , Trimble S . Transfusion 2013 53 (6) 1217-25
Relationships between selected gene polymorphisms and blood pressure sensitivity to weight loss in elderly persons with hypertension. Kostis WJ , Cabrera J , Hooper WC , Whelton PK , Espeland MA , Cosgrove NM , Cheng JQ , Deng Y , De Staerck C , Pyle M , Maruthur N , Reyes I , Anderson CA , Liu J , Kostis JB . Hypertension 2013 61 (4) 857-63
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
Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia Thangarajh M , Yang G , Fuchs D , Ponisio MR , McKinstry RC , Jaju A , Noetzel MJ , Casella JF , Barron-Casella E , Hooper WC , Boulet SL , Bean CJ , Pyle ME , Payne AB , Driggers J , Trau HA , Vendt BA , Rodeghier M , Debaun MR . Br J Haematol 2012 159 (3) 352-9
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans Bae HT , Baldwin CT , Sebastiani P , Telen MJ , Ashley-Koch A , Garrett M , Hooper WC , Bean CJ , Debaun MR , Arking DE , Bhatnagar P , Casella JF , Keefer JR , Barron-Casella E , Gordeuk V , Kato GJ , Minniti C , Taylor J , Campbell A , Luchtman-Jones L , Hoppe C , Gladwin MT , Zhang Y , Steinberg MH . Blood 2012 120 (9) 1961-2
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease. Bean CJ , Boulet SL , Ellingsen D , Pyle ME , Barron-Casella EA , Casella JF , Payne AB , Driggers J , Trau HA , Yang G , Jones K , Ofori-Acquah SF , Hooper WC , Debaun MR . Blood 2012 120 (18) 3822-8
Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks. Bean CJ , Boulet SL , Ellingsen D , Trau H , Ghaji N , Hooper WC , Austin H . Thromb Res 2012 130 (6) 942-7
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. Milton JN , Sebastiani P , Solovieff N , Hartley SW , Bhatnagar P , Arking DE , Dworkis DA , Casella JF , Barron-Casella E , Bean CJ , Hooper WC , Debaun MR , Garrett ME , Soldano K , Telen MJ , Ashley-Koch A , Gladwin MT , Baldwin CT , Steinberg MH , Klings ES . PLoS One 2012 7 (4) e34741
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
The impact of co-morbid conditions on family history of venous thromboembolism in Whites and Blacks. Mili FD , Hooper WC , Lally C , Austin H . Thromb Res 2011 127 (4) 309-16
New gene variants associated with venous thrombosis - a replication study in United States Whites and Blacks Austin H , De Staercke C , Lally C , Bezemer ID , Rosendaal FR , Hooper WC . J Thromb Haemost 2011 9 (3) 489-95
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
Venous thromboembolism in African-Americans: a literature-based commentary Hooper WC . Thromb Res 2010 125 (1) 12-8