146 related articles for article (PubMed ID: 30680775)
1. Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.
Bao EL; Lareau CA; Brugnara C; Fulcher IR; Barau C; Moutereau S; Habibi A; Badaoui B; Berkenou J; Bartolucci P; Galactéros F; Platt OS; Mahaney M; Sankaran VG
Am J Hematol; 2019 May; 94(5):522-527. PubMed ID: 30680775
[TBL] [Abstract][Full Text] [Related]
2. Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania.
Mtatiro SN; Makani J; Mmbando B; Thein SL; Menzel S; Cox SE
Am J Hematol; 2015 Jan; 90(1):E1-4. PubMed ID: 25263325
[TBL] [Abstract][Full Text] [Related]
3. The proinflammatory cytokine GM-CSF downregulates fetal hemoglobin expression by attenuating the cAMP-dependent pathway in sickle cell disease.
Ikuta T; Adekile AD; Gutsaeva DR; Parkerson JB; Yerigenahally SD; Clair B; Kutlar A; Odo N; Head CA
Blood Cells Mol Dis; 2011 Dec; 47(4):235-42. PubMed ID: 21945571
[TBL] [Abstract][Full Text] [Related]
4. Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania.
Nkya S; Mwita L; Mgaya J; Kumburu H; van Zwetselaar M; Menzel S; Mazandu GK; Sangeda R; Chimusa E; Makani J
BMC Med Genet; 2020 Jun; 21(1):125. PubMed ID: 32503527
[TBL] [Abstract][Full Text] [Related]
5. Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease.
Liu L; Pertsemlidis A; Ding LH; Story MD; Steinberg MH; Sebastiani P; Hoppe C; Ballas SK; Pace BS
Exp Biol Med (Maywood); 2016 Apr; 241(7):706-18. PubMed ID: 27022141
[TBL] [Abstract][Full Text] [Related]
6. Variation and impact of polygenic hematologic traits in monogenic sickle cell disease.
Pincez T; Lo KS; D'Orengiani APHD; Garrett ME; Brugnara C; Ashley-Koch AE; Telen MJ; Galacteros F; Joly P; Bartolucci P; Lettre G
Haematologica; 2023 Mar; 108(3):870-881. PubMed ID: 36226494
[TBL] [Abstract][Full Text] [Related]
7. 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
[TBL] [Abstract][Full Text] [Related]
8. Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models.
Milton JN; Gordeuk VR; Taylor JG; Gladwin MT; Steinberg MH; Sebastiani P
Circ Cardiovasc Genet; 2014 Apr; 7(2):110-5. PubMed ID: 24585758
[TBL] [Abstract][Full Text] [Related]
9. Fetal hemoglobin in sickle cell anemia.
Akinsheye I; Alsultan A; Solovieff N; Ngo D; Baldwin CT; Sebastiani P; Chui DH; Steinberg MH
Blood; 2011 Jul; 118(1):19-27. PubMed ID: 21490337
[TBL] [Abstract][Full Text] [Related]
10. Implication of HMOX1 and CCR5 genotypes on clinical phenotype of Egyptian patients with sickle cell anemia.
Bakr S; Khorshied M; Talha N; Jaffer KY; Soliman N; Eid K; El-Ghamrawy M
Ann Hematol; 2019 Aug; 98(8):1805-1812. PubMed ID: 31030250
[TBL] [Abstract][Full Text] [Related]
11.
Gardner K; Fulford T; Silver N; Rooks H; Angelis N; Allman M; Nkya S; Makani J; Howard J; Kesse-Adu R; Rees DC; Stuart-Smith S; Yeghen T; Awogbade M; Sangeda RZ; Mgaya J; Patel H; Newhouse S; Menzel S; Thein SL
Blood Adv; 2018 Feb; 2(3):235-239. PubMed ID: 29437638
[TBL] [Abstract][Full Text] [Related]
12. Genetic Variation and Sickle Cell Disease Severity: A Systematic Review and Meta-Analysis.
Kirkham JK; Estepp JH; Weiss MJ; Rashkin SR
JAMA Netw Open; 2023 Oct; 6(10):e2337484. PubMed ID: 37851445
[TBL] [Abstract][Full Text] [Related]
13. Genetic Modifiers of Fetal Haemoglobin in Sickle Cell Disease.
Menzel S; Thein SL
Mol Diagn Ther; 2019 Apr; 23(2):235-244. PubMed ID: 30478714
[TBL] [Abstract][Full Text] [Related]
14. Hereditary persistence of hemoglobin F is protective against red cell sickling. A case report and brief review.
Sokolova A; Mararenko A; Rozin A; Podrumar A; Gotlieb V
Hematol Oncol Stem Cell Ther; 2019 Dec; 12(4):215-219. PubMed ID: 29079125
[TBL] [Abstract][Full Text] [Related]
15. Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease.
Marcus SJ; Kinney TR; Schultz WH; O'Branski EE; Ware RE
Am J Hematol; 1997 Jan; 54(1):40-6. PubMed ID: 8980259
[TBL] [Abstract][Full Text] [Related]
16. Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia.
Bhanushali AA; Patra PK; Pradhan S; Khanka SS; Singh S; Das BR
Transl Res; 2015 Jun; 165(6):696-703. PubMed ID: 25651163
[TBL] [Abstract][Full Text] [Related]
17. rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Chaouch L; Moumni I; Ouragini H; Darragi I; Kalai M; Chaouachi D; Boudrigua I; Hafsia R; Abbes S
Hematology; 2016 Aug; 21(7):425-9. PubMed ID: 27077760
[TBL] [Abstract][Full Text] [Related]
18. 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; 41(1):87-93. PubMed ID: 30216683
[TBL] [Abstract][Full Text] [Related]
19. Clinical variability and molecular characterization of Hbs/Gγ (Aγδβ)0-thal and Hbs/HPFH in Indian sickle cell disease patients: AIIMS experience.
Pandey H; Singh K; Ranjan R; Pandey SK; Sharma A; Kishor K; Seth T; Mahapatra M; Saxena R
Hematology; 2019 Dec; 24(1):349-352. PubMed ID: 30777489
[TBL] [Abstract][Full Text] [Related]
20. Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania.
Nkya S; Mgaya J; Urio F; Makubi A; Thein SL; Menzel S; Cox SE; Newton CR; Kirkham FJ; Mmbando BP; Makani J
EBioMedicine; 2017 Sep; 23():146-149. PubMed ID: 28844412
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]