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251 related items for PubMed ID: 21068433

  • 21. Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.
    Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A.
    Blood Cells Mol Dis; 2013 Jun; 51(1):22-6. PubMed ID: 23465615
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  • 22. A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.
    Adeyemo TA, Ojewunmi OO, Oyetunji IA, Rooks H, Rees DC, Akinsulie AO, Akanmu AS, Thein SL, Menzel S.
    PLoS One; 2018 Jun; 13(6):e0197927. PubMed ID: 29879141
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  • 23. The role of BCL11A and HMIP-2 polymorphisms on endogenous and hydroxyurea induced levels of fetal hemoglobin in sickle cell anemia patients from southern Brazil.
    Friedrisch JR, Sheehan V, Flanagan JM, Baldan A, Summarell CC, Bittar CM, Friedrisch BK, Wilke II, Ribeiro CB, Daudt LE, da Rocha Silla LM.
    Blood Cells Mol Dis; 2016 Nov; 62():32-37. PubMed ID: 27838552
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  • 24. Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia.
    Sales RR, Nogueira BL, Belisário AR, Faria G, Mendes F, Viana MB, Luizon MR.
    J Hum Genet; 2022 Dec; 67(12):701-709. PubMed ID: 36167770
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  • 26. Discovering the genetics underlying foetal haemoglobin production in adults.
    Thein SL, Menzel S.
    Br J Haematol; 2009 May; 145(4):455-67. PubMed ID: 19344402
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  • 31. Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children.
    Ginete C, Delgadinho M, Santos B, Miranda A, Silva C, Guerreiro P, Chimusa ER, Brito M.
    Genes (Basel); 2024 Apr 08; 15(4):. PubMed ID: 38674403
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  • 32. The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease.
    Al-Allawi N, Qadir SMA, Puehringer H, Chui DHK, Farrell JJ, Oberkanins C.
    Int J Lab Hematol; 2019 Feb 08; 41(1):87-93. PubMed ID: 30216683
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  • 36. Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
    Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer LA, Garrett ME, Ashley-Koch A, Telen MJ, Fucharoen S, Ha SY, Li CK, Chui DH, Baldwin CT, Steinberg MH.
    Blood; 2010 Mar 04; 115(9):1815-22. PubMed ID: 20018918
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  • 37. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.
    Sedgewick AE, Timofeev N, Sebastiani P, So JCC, Ma ESK, Chan LC, Fucharoen G, Fucharoen S, Barbosa CG, Vardarajan BN, Farrer LA, Baldwin CT, Steinberg MH, Chui DHK.
    Blood Cells Mol Dis; 2008 Mar 04; 41(3):255-258. PubMed ID: 18691915
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  • 38. Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.
    Pereira C, Relvas L, Bento C, Abade A, Ribeiro ML, Manco L.
    Blood Cells Mol Dis; 2015 Apr 04; 54(4):315-20. PubMed ID: 25842369
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  • 39. Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 loci.
    Leonardo FC, Brugnerotto AF, Domingos IF, Fertrin KY, de Albuquerque DM, Bezerra MA, Araújo AS, Saad ST, Costa FF, Menzel S, Conran N, Thein SL.
    Br J Haematol; 2016 May 04; 173(3):456-60. PubMed ID: 26888013
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  • 40. The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease.
    Adekile A.
    Med Princ Pract; 2021 May 04; 30(3):201-211. PubMed ID: 32892201
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