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List of works by Christopher Bean

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia

scientific article

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

scientific article published on 24 May 2018

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

scientific article published on August 16, 2013

Alphoid variant-specific FISH probes can distinguish autosomal meiosis I from meiosis II non-disjunction in human sperm ⬇️

scientific article published on November 1, 1997

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

scientific article published on May 15, 2013

Current research in preterm birth.

scientific article published on December 2008

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

scientific article

Evaluation of pre-analytic heat treatment protocol used in the CDC Nijmegen-Bethesda assay for heat inactivation of extended half-life haemophilia treatment products

scientific article published on 06 December 2019

Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations

scientific article published on 9 May 2015

Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data

scientific article published on 21 July 2019

Genetic causes of haemophilia in women and girls

scientific article published on 13 December 2020

Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia

scientific article published on 5 June 2017

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

scientific article

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

scientific article

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

scientific article

Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.

scientific article published on 07 September 2012

Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans

scientific article published on August 2012

Parvovirus B19 infection in sickle cell disease: An analysis from the Centers for Disease Control haemoglobinopathy blood surveillance project

scientific article published on 04 March 2020

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

scientific article

Reagent substitution in the chromogenic Bethesda assay for factor VIII inhibitors

scientific article published on 29 July 2019

Reagent substitutions in the Centers for Disease Control and Prevention Nijmegen-Bethesda assay for factor VIII inhibitors

scientific article published on 24 March 2018

Utility of multiplex ligation-dependent probe amplification (MLPA) for hemophilia mutation screening.

scientific article published in September 2012

VKORC1-1639A allele influences warfarin maintenance dosage among Blacks receiving warfarin anticoagulation: a retrospective cohort study.

scientific article published on 8 December 2017

Validation of the chromogenic Bethesda assay for factor VIII inhibitors in hemophilia a patients receiving Emicizumab

scientific article published on 10 November 2020

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