Genetic modifiers of sickle cell diseaseSTEINBERG, Martin H; SEBASTIANI, Paola.American journal of hematology. 2012, Vol 87, Num 8, pp 795-803, issn 0361-8609, 9 p.Article

Modifier genes and sickle cell anemia : Erythrold system and its diseasesSTEINBERG, Martin H; ADEWOYE, Adeboye H.Current opinion in hematology. 2006, Vol 13, Num 3, pp 131-136, issn 1065-6251, 6 p.Article

Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African AmericansAKINSHEYE, Idowu; SOLOVIEFF, Nadia; NGO, Duyen et al.American journal of hematology. 2012, Vol 87, Num 2, pp 217-219, issn 0361-8609, 3 p.Article

Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong KongGIBNEY, Geoffrey T; PANHUYSEN, Carolien I. M; JOHNSON, David M et al.American journal of hematology. 2008, Vol 83, Num 6, pp 458-464, issn 0361-8609, 7 p.Article

Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1 BNOLAN, Vikki G; QIANLI MA; NAGEL, Ronald L et al.American journal of hematology. 2007, Vol 82, Num 3, pp 179-184, issn 0361-8609, 6 p.Article

Deconstructing sickle cell disease : Reappraisal of the role of hemolysis in the development of clinical subphenotypesKATO, Gregory J; GLADWIN, Mark T; STEINBERG, Martin H et al.Blood reviews. 2007, Vol 21, Num 1, pp 37-47, issn 0268-960X, 11 p.Article

In the Clinic: Sickle Cell DiseaseCOTTON, Deborah; TAICHMAN, Darren; WILLIAMS, Sankey et al.Annals of internal medicine. 2011, Vol 155, Num 5, issn 0003-4819, ITC3.1-ITC3.14Article

The paradox of hemoglobin SC diseaseNAGEL, Ronald L; FABRY, Mary E; STEINBERG, Martin H et al.Blood reviews. 2003, Vol 17, Num 3, pp 167-178, issn 0268-960X, 12 p.Article

An Official American Thoracic Society Clinical Practice Guideline: Diagnosis, Risk Stratification, and Management of Pulmonary Hypertension of Sickle Cell DiseaseKLINGS, Elizabeth S; MACHADO, Roberto F; ROSENZWEIG, Erika B et al.American journal of respiratory and critical care medicine. 2014, Vol 189, Num 6, pp 727-740, issn 1073-449X, 14 p.Article

Hypoxic Response Contributes to Altered Gene Expression and Precapillary Pulmonary Hypertension in Patients With Sickle Cell DiseaseXU ZHANG; WEI ZHANG; ABBASI, Taimur et al.Circulation (New York, N.Y.). 2014, Vol 129, Num 16, pp 1650-1658, issn 0009-7322, 9 p.Article

Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1DWORKIS, Daniel A; KLINGS, Elizabeth S; BALDWIN, Clinton T et al.American journal of hematology. 2011, Vol 86, Num 2, pp 220-223, issn 0361-8609, 4 p.Article

The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-upSTEINBERG, Martin H; MCCARTHY, William F; WACLAWIW, Myron A et al.American journal of hematology. 2010, Vol 85, Num 6, pp 403-408, issn 0361-8609, 6 p.Article

Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: A systematic reviewVERHOVSEK, Madeleine; HENDERSON, Matthew P. A; COX, Gerard et al.American journal of hematology. 2010, Vol 85, Num 11, pp 882-885, issn 0361-8609, 4 p.Article

Hemoglobin Kenya composed of α-and (^Aγβ)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobinWILCOX, Ibifiri; BOETTGER, Kevin; GREENE, Lance et al.American journal of hematology. 2009, Vol 84, Num 1, pp 55-58, issn 0361-8609, 4 p.Article

Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern Province have similar HBB haplotypes but higher HbF levels than African AmericansALSULTAN, Abdulrahman; SOLOVIEFF, Nadia; CHUI, David H. K et al.American journal of hematology. 2011, Vol 86, Num 7, pp 612-614, issn 0361-8609, 3 p.Article

Fetal hemoglobin in sickle cell anemiaAKINSHEYE, Idowu; ALSULTAN, Abdulrahman; SOLOVIEFF, Nadia et al.Blood. 2011, Vol 118, Num 1, pp 19-27, issn 0006-4971, 9 p.Article

Genome-wide association studies and the genetic dissection of complex traitsSEBASTIANI, Paola; TIMOFEEV, Nadia; DWORKIS, Daniel A et al.American journal of hematology. 2009, Vol 84, Num 8, pp 504-515, issn 0361-8609, 12 p.Article

Fetal hemoglobin in sickle cell anemia : Bayesian modeling of genetic associationsSEBASTIANI, Paola; LING WANG; NOLAN, Vikki G et al.American journal of hematology. 2008, Vol 83, Num 3, pp 189-195, issn 0361-8609, 7 p.Article

Sickle cell bone disease : Response to vitamin D and calciumADEWOYE, Adeboye H; CHEN, Tai C; QIANLI MA et al.American journal of hematology. 2008, Vol 83, Num 4, pp 271-274, issn 0361-8609, 4 p.Article

Association of polymorphisms of IGF1R and genes in the transforming growth factor-β/bone morphogenetic protein pathway with bacteremia in sickle cell anemiaADEWOYE, Adeboye H; NOLAN, Vikki G; QIANLI MA et al.Clinical infectious diseases. 2006, Vol 43, Num 5, pp 593-598, issn 1058-4838, 6 p.Article

Hemoglobinopathies mimicking Hb S/β-thalassemia : Hb S/S with α-thalassemia and Hb S/volgaLUO, Hong-Yuan; HEENEY, Matthew; WANG, Winfred C et al.American journal of hematology. 2006, Vol 81, Num 5, pp 361-365, issn 0361-8609, 5 p.Article

Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemiaNOLAN, Vikki G; BALDWIN, Clinton; QIANLI MA et al.British journal of haematology. 2005, Vol 128, Num 2, pp 266-272, issn 0007-1048, 7 p.Article

Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell diseaseSTEINBERG, Martin H; VOSKARIDOU, Ersi; KUTLAR, Abdullah et al.American journal of hematology. 2003, Vol 72, Num 2, pp 121-126, issn 0361-8609, 6 p.Article

Genetic determinants of haemolysis in sickle cell anaemiaMILTON, Jacqueline N; ROOKS, Helen; TAYLOR, James et al.British journal of haematology. 2013, Vol 161, Num 2, pp 270-278, issn 0007-1048, 9 p.Article

Climatic and geographic temporal patterns of pain in the Multicenter Study of HydroxyureaSMITH, Wally R; BAUSERMAN, Robert L; BALLAS, Samir K et al.Pain (Amsterdam). 2009, Vol 146, Num 1-2, pp 91-98, issn 0304-3959, 8 p.Article