Last data update: Aug 05, 2020. (Total: 2888 publications since 2011)
|Query Trace: all>>Christopher J Bean[CDC Author]|
| Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.
Mary M Jenkins, Lynn M Almli, Faith Pangilinan, Jessica X Chong, Elizabeth E Blue, Stuart K Shapira, Janson White, Daniel McGoldrick, Joshua D Smith, James C Mullikin, Christopher J Bean, Wendy N Nembhard, Xiang-Yang Lou, Gary M Shaw, Paul A Romitti, Kim Keppler-Noreuil, Mahsa M Yazdy, Denise M Kay, Tonia C Carter, Andrew F Olshan, Kristin J Moore, Nanette Nascone-Yoder, Richard H Finnell, Philip J Lupo, Marcia L Feldkamp, , Deborah A Nickerson, Michael J Bamshad, Lawrence C Brody, Jennita Reefhuis,
Birth defects research 2019 Jul
| 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
| Genome-wide association study to identify variants associated with vaso-occlusive pain in sickle cell anemia.
Shruti Chaturvedi, Pallav Bhatnagar, Christopher J Bean, Martin H Steinberg, Jaqueline N Milton, James F Casella, Emily Barron-Casella, Dan E Arking, and Michael R Debaun
Blood 2017 Jun
| 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
| 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
| 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
| 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
| 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
| 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