Christopher J Bean

Christopher J Bean

UNVERIFIED PROFILE

Are you Christopher J Bean?   Register this Author

Register author
Christopher J Bean

Christopher J Bean

Publications by authors named "Christopher J Bean"

Are you Christopher J Bean?   Register this Author

22Publications

443Reads

49Profile Views

Reagent substitution in the chromogenic Bethesda assay for factor VIII inhibitors.

Haemophilia 2019 Sep 29;25(5):e342-e344. Epub 2019 Jul 29.

Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/hae.13827DOI Listing
September 2019

A significant proportion of children of African descent with HbSβ thalassaemia are inaccurately diagnosed based on phenotypic analyses alone.

Br J Haematol 2019 Apr 24;185(1):153-156. Epub 2018 May 24.

Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, TN, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/bjh.15400DOI Listing
April 2019

Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.

Public Health Genomics 2014 28;17(3):169-72. Epub 2014 Mar 28.

Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Ga., USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000360260DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394647PMC
February 2015

Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.

PLoS One 2013 13;8(9):e74193. Epub 2013 Sep 13.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0074193PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772989PMC
June 2014

Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.

Stroke 2014 Apr 11;45(4):961-7. Epub 2014 Mar 11.

From the Departments of Neurology (B.J., A.H., M.J.S., M.A.W., B.J.S., S.J.K., J.W.C.), Medicine (K.A.R., Y.C., P.F.M., J.R.O., B.D.M.), and Epidemiology and Public Health (O.C.S.), University of Maryland School of Medicine, Baltimore; Centers for Disease Control and Prevention, Atlanta, GA (D.K., C.J.B., M.G., W.C.H.); Department of Veterans Affairs, Veterans Affairs Medical Center Baltimore, MD (Y.C., M.A.W., B.J.S., S.J.K., J.W.C.); and Department of Veterans Affairs and Veterans Affairs Medical Center Baltimore, Geriatric Research, Education and Clinical Center, MD (B.D.M., S.J.K.).

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/STROKEAHA.113.004063DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049002PMC
April 2014

Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia.

Pediatr Blood Cancer 2013 Oct 15;60(10):E125-7. Epub 2013 May 15.

McKusick-Nathans Institute of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.24588DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387562PMC
October 2013

Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.

Br J Haematol 2013 Oct 16;163(2):268-76. Epub 2013 Aug 16.

Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/bjh.12507DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026174PMC
October 2013

Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks.

Thromb Res 2012 Dec 7;130(6):942-7. Epub 2012 Sep 7.

Clinical and Molecular Hemostasis Laboratory Branch, Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, United States.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S00493848120067
Publisher Site
http://dx.doi.org/10.1016/j.thromres.2012.08.300DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388034PMC
December 2012

Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.

Blood 2012 Nov 10;120(18):3822-8. Epub 2012 Sep 10.

Clinical and Molecular Hemostasis Laboratory Branch, Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/blood-2011-06-361642DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488892PMC
November 2012

RNA helicase A is important for germline transcriptional control, proliferation, and meiosis in C. elegans.

Mech Dev 2005 May 25;122(5):707-20. Epub 2004 Dec 25.

Division of Natural Sciences, New College of Florida, 5700 N. Tamiami Trail, Sarasota, FL 34243, USA.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S092547730400282
Publisher Site
http://dx.doi.org/10.1016/j.mod.2004.12.002DOI Listing
May 2005

Comment on "Diffusion of epicenters of earthquake aftershocks, Omori's law, and generalized continuous-time random walk models".

Phys Rev E Stat Nonlin Soft Matter Phys 2004 Jun 10;69(6 Pt 1):063101; discussion 063102. Epub 2004 Jun 10.

Laboratoire de Géophysique Interne et Tectonophysique, Université de Savoie, 73376 Le Bourget du Lac, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1103/PhysRevE.69.063101DOI Listing
June 2004

Meiotic pairing and imprinted X chromatin assembly in Caenorhabditis elegans.

Nat Genet 2004 Jan 21;36(1):100-5. Epub 2003 Dec 21.

Biology Department, 1510 Clifton Road, Rollins Research Center, Emory University, Atlanta, Georgia 30322, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/ng1283DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098868PMC
January 2004

Fertilization in vitro increases non-disjunction during early cleavage divisions in a mouse model system.

Hum Reprod 2002 Sep;17(9):2362-7

Department of Genetics and the Center for Human Genetics, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, OH 44106, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/humrep/17.9.2362DOI Listing
September 2002