CDC-Authored Genomics and Precision Health Publications Database

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Last data update: Oct 07, 2024. (Total: 6342 publications)

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Records 1-14 (of 14 Records)

Query Trace: Bean CJ[original query]
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
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Jenkins MM , Almli LM , Pangilinan F , Chong JX , Blue EE , Shapira SK , White J , McGoldrick D , Smith JD , Mullikin JC , Bean CJ , Nembhard WN , Lou XY , Shaw GM , Romitti PA , Keppler-Noreuil K , Yazdy MM , Kay DM , Carter TC , Olshan AF , Moore KJ , Nascone-Yoder N , Finnell RH , Lupo PJ , Feldkamp ML , Nickerson DA , Bamshad MJ , Brody LC , Reefhuis J . Birth Defects Res 2019 111 (20) 1618-1632
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
Genome-wide association study to identify variants associated with vaso-occlusive pain in sickle cell anemia. Chaturvedi S , Bhatnagar P , Bean CJ , Steinberg MH , Milton JN , Casella JF , Barron-Casella E , Arking DE , DeBaun MR . Blood 2017 130 (5) 686-688
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
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
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
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