Journal article
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster
Abstract
In a genome-wide association study of 848 blacks with sickle cell anemia, we identified single nucleotide polymorphisms (SNPs) associated with fetal hemoglobin concentration. The most significant SNPs in a discovery sample were tested in a replication set of 305 blacks with sickle cell anemia and in subjects with hemoglobin E or beta thalassemia trait from Thailand and Hong Kong. A novel region on chromosome 11 containing olfactory receptor …
Authors
Solovieff N; Milton JN; Hartley SW; Sherva R; Sebastiani P; Dworkis DA; Klings ES; Farrer LA; Garrett ME; Ashley-Koch A
Journal
Blood, Vol. 115, No. 9, pp. 1815–1822
Publisher
American Society of Hematology
Publication Date
March 4, 2010
DOI
10.1182/blood-2009-08-239517
ISSN
0006-4971
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AdolescentAdultBlack or African AmericanAnemia, Sickle CellCarrier ProteinsChildChild, PreschoolChromosomes, Human, Pair 11Chromosomes, Human, XFemaleFetal HemoglobinGenome-Wide Association StudyHemoglobin EHong KongHumansMaleMultigene FamilyNuclear ProteinsPolymorphism, Single NucleotideReceptors, OdorantRegulatory Sequences, Nucleic AcidRepressor ProteinsThailandYoung Adultbeta-Thalassemia