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Items: 1 to 50 of 327

1.

Airlie House Legend.

Steinberg MH, Schechter AN.

Am J Hematol. 2018 Sep 22. doi: 10.1002/ajh.25293. [Epub ahead of print] No abstract available.

PMID:
30242871
2.

A New Trans-Acting Modulator of Fetal Hemoglobin?

Steinberg MH.

Acta Haematol. 2018 Sep 18;140(2):112-113. doi: 10.1159/000492147. [Epub ahead of print] No abstract available.

3.

Induced pluripotent stem cell-based mapping of β-globin expression throughout human erythropoietic development.

Vanuytsel K, Matte T, Leung A, Naing ZH, Morrison T, Chui DHK, Steinberg MH, Murphy GJ.

Blood Adv. 2018 Aug 14;2(15):1998-2011. doi: 10.1182/bloodadvances.2018020560.

4.

Biomarker signatures of sickle cell disease severity.

Du M, Van Ness S, Gordeuk V, Nouraie SM, Nekhai S, Gladwin M, Steinberg MH, Sebastiani P.

Blood Cells Mol Dis. 2018 Sep;72:1-9. doi: 10.1016/j.bcmd.2018.05.001. Epub 2018 May 16.

PMID:
29778312
5.

Notch and Aryl Hydrocarbon Receptor Signaling Impact Definitive Hematopoiesis from Human Pluripotent Stem Cells.

Leung A, Zulick E, Skvir N, Vanuytsel K, Morrison TA, Naing ZH, Wang Z, Dai Y, Chui DHK, Steinberg MH, Sherr DH, Murphy GJ.

Stem Cells. 2018 Mar 23. doi: 10.1002/stem.2822. [Epub ahead of print]

6.

A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy.

Akinbami AO, Sobota AE, Luo HY, Chui DHK, Steinberg MH.

J Pediatr Hematol Oncol. 2018 Apr;40(3):e145-e147. doi: 10.1097/MPH.0000000000001068.

PMID:
29309373
7.

A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression.

Morrison TA, Wilcox I, Luo HY, Farrell JJ, Kurita R, Nakamura Y, Murphy GJ, Cui S, Steinberg MH, Chui DHK.

Blood Cells Mol Dis. 2018 Mar;69:1-9. doi: 10.1016/j.bcmd.2017.11.003. Epub 2017 Nov 29.

PMID:
29227829
8.

A phased SNP-based classification of sickle cell anemia HBB haplotypes.

Shaikho EM, Farrell JJ, Alsultan A, Qutub H, Al-Ali AK, Figueiredo MS, Chui DHK, Farrer LA, Murphy GJ, Mostoslavsky G, Sebastiani P, Steinberg MH.

BMC Genomics. 2017 Aug 11;18(1):608. doi: 10.1186/s12864-017-4013-y.

9.

SIRT1 activates the expression of fetal hemoglobin genes.

Dai Y, Chen T, Ijaz H, Cho EH, Steinberg MH.

Am J Hematol. 2017 Nov;92(11):1177-1186. doi: 10.1002/ajh.24879. Epub 2017 Aug 28.

10.

Fetal hemoglobin in sickle cell anemia: The Arab-Indian haplotype and new therapeutic agents.

Habara AH, Shaikho EM, Steinberg MH.

Am J Hematol. 2017 Nov;92(11):1233-1242. doi: 10.1002/ajh.24872. Epub 2017 Aug 17. Review.

PMID:
28736939
11.

Sickle Cell Disease.

Piel FB, Steinberg MH, Rees DC.

N Engl J Med. 2017 Jul 20;377(3):305. doi: 10.1056/NEJMc1706325. No abstract available.

PMID:
28723338
12.

Genetic determinants of HbF in Saudi Arabian and African Benin haplotype sickle cell anemia.

Shaikho EM, Farrell JJ, Alsultan A, Sebastiani P, Steinberg MH.

Am J Hematol. 2017 Sep;92(9):E555-E557. doi: 10.1002/ajh.24822. Epub 2017 Jul 19. No abstract available.

13.

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

Chaturvedi S, Bhatnagar P, Bean CJ, Steinberg MH, Milton JN, Casella JF, Barron-Casella E, Arking DE, DeBaun MR.

Blood. 2017 Aug 3;130(5):686-688. doi: 10.1182/blood-2017-02-769661. Epub 2017 Jun 5. No abstract available.

14.

Sickle Cell Disease.

Piel FB, Steinberg MH, Rees DC.

N Engl J Med. 2017 Apr 20;376(16):1561-1573. doi: 10.1056/NEJMra1510865. Review. No abstract available.

15.

Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi β-Thalassemia Patients.

Cyrus C, Vatte C, Borgio JF, Al-Rubaish A, Chathoth S, Nasserullah ZA, Jarrash SA, Sulaiman A, Qutub H, Alsaleem H, Alzahrani AJ, Steinberg MH, Ali AK.

Biomed Res Int. 2017;2017:1972429. doi: 10.1155/2017/1972429. Epub 2017 Feb 9.

16.

Intravascular hemolysis and the pathophysiology of sickle cell disease.

Kato GJ, Steinberg MH, Gladwin MT.

J Clin Invest. 2017 Mar 1;127(3):750-760. doi: 10.1172/JCI89741. Epub 2017 Mar 1. Review.

17.

A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0 -thalassaemia homozygotes.

Jiang Z, Luo HY, Farrell JJ, Zhang Z, Schulz VP, Albarawi D, Steinberg MH, Al-Allawi NAS, Gallagher PG, Forget BG, Chui DHK.

Br J Haematol. 2018 Mar;180(5):755-757. doi: 10.1111/bjh.14445. Epub 2017 Feb 27. No abstract available.

PMID:
28240767
18.

Genetic modulation of fetal hemoglobin in hydroxyurea-treated sickle cell anemia.

Aleluia MM, Santiago RP, da Guarda CC, Fonseca TC, Neves FI, Quinto RS, Figueiredo CV, Yahouédéhou SC, Oliveira RM, Ferreira JR, Cerqueira BA, Barbosa CG, Milton JN, Steinberg MH, de Souza Gonçalves M.

Am J Hematol. 2017 May;92(5):E70-E72. doi: 10.1002/ajh.24680. Epub 2017 Mar 10. No abstract available.

19.

Go with the Flow.

Steinberg MH.

N Engl J Med. 2017 Feb 2;376(5):485-487. doi: 10.1056/NEJMe1615651. No abstract available.

PMID:
28146663
20.

A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells.

Park S, Gianotti-Sommer A, Molina-Estevez FJ, Vanuytsel K, Skvir N, Leung A, Rozelle SS, Shaikho EM, Weir I, Jiang Z, Luo HY, Chui DHK, Figueiredo MS, Alsultan A, Al-Ali A, Sebastiani P, Steinberg MH, Mostoslavsky G, Murphy GJ.

Stem Cell Reports. 2017 Apr 11;8(4):1076-1085. doi: 10.1016/j.stemcr.2016.12.017. Epub 2017 Jan 19.

21.

A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.

Vathipadiekal V, Farrell JJ, Wang S, Edward HL, Shappell H, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Simkin I, Farrer LA, Jiang Z, Luo HY, Huang S, Mostoslavsky G, Murphy GJ, Patra PK, Chui DH, Alsultan A, Al-Ali AK, Sebastiani P, Steinberg MH.

Am J Hematol. 2016 Nov;91(11):1118-1122. doi: 10.1002/ajh.24527. Epub 2016 Aug 22.

22.

Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia.

Shaikho EM, Habara AH, Alsultan A, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Patra PK, Sebastiani P, Baltrusaitis K, Farrell JJ, Jiang Z, Luo HY, Chui DH, Al-Ali AK, Steinberg MH.

Blood Cells Mol Dis. 2016 Jul;59:49-51. doi: 10.1016/j.bcmd.2016.04.001. Epub 2016 Apr 13. No abstract available.

PMID:
27282567
23.

Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.

Vathipadiekal V, Alsultan A, Baltrusaitis K, Farrell JJ, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Suliman A, Patra PK, Milton JN, Farrer LA, Chui DH, Al-Ali AK, Sebastiani P, Steinberg MH.

Am J Hematol. 2016 Jun;91(6):E308-11. doi: 10.1002/ajh.24368. Epub 2016 Apr 28. No abstract available.

24.

Learning Bayesian Networks from Correlated Data.

Bae H, Monti S, Montano M, Steinberg MH, Perls TT, Sebastiani P.

Sci Rep. 2016 May 5;6:25156. doi: 10.1038/srep25156.

25.

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. doi: 10.1177/1535370216642047. Epub 2016 Mar 27.

26.

Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.

Habara A, Steinberg MH.

Exp Biol Med (Maywood). 2016 Apr;241(7):689-96. doi: 10.1177/1535370216636726. Epub 2016 Mar 1. Review.

27.

Mutations in the β-globin gene from a Saudi population: an update.

Borgio JF, AbdulAzeez S, Naserullah ZA, Al-Jarrash S, Al-Ali RA, Al-Madan MS, Al-Muhanna F, Al-Suliman AM, Al-Nafie A, Steinberg MH, Al-Ali AK.

Int J Lab Hematol. 2016 Apr;38(2):e38-40. doi: 10.1111/ijlh.12463. Epub 2016 Jan 29. No abstract available.

PMID:
26822801
28.

The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.

Jiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Başak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH.

Br J Haematol. 2016 Mar;172(6):958-65. doi: 10.1111/bjh.13909. Epub 2016 Jan 13.

29.

Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 14: Sickle Cell Trait: A Scientific Statement From the American Heart Association and American College of Cardiology.

Maron BJ, Harris KM, Thompson PD, Eichner ER, Steinberg MH.

J Am Coll Cardiol. 2015 Dec 1;66(21):2444-2446. doi: 10.1016/j.jacc.2015.09.046. Epub 2015 Nov 2. No abstract available.

30.

Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 14: Sickle Cell Trait: A Scientific Statement From the American Heart Association and American College of Cardiology.

Maron BJ, Harris KM, Thompson PD, Eichner ER, Steinberg MH; American Heart Association Electrocardiography and Arrhythmias Committee of Council on Clinical Cardiology, Council on Cardiovascular Disease in Young, Council on Cardiovascular and Stroke Nursing, Council on Functional Genomics and Translational Biology, and American College of Cardiology.

Circulation. 2015 Dec 1;132(22):e343-5. doi: 10.1161/CIR.0000000000000250. Epub 2015 Nov 2. Review. No abstract available.

PMID:
26527715
31.

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.

Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH.

Hemoglobin. 2016;40(1):64-5. doi: 10.3109/03630269.2015.1080725. Epub 2015 Sep 15.

PMID:
26372199
32.

Genomic approaches to identifying targets for treating β hemoglobinopathies.

Ngo DA, Steinberg MH.

BMC Med Genomics. 2015 Jul 29;8:44. doi: 10.1186/s12920-015-0120-2. Review.

33.

HbA2 : biology, clinical relevance and a possible target for ameliorating sickle cell disease.

Steinberg MH, Rodgers GP.

Br J Haematol. 2015 Sep;170(6):781-7. doi: 10.1111/bjh.13570. Epub 2015 Jun 24. Review.

PMID:
26104837
34.

Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease.

Zhang X, Zhang W, Saraf SL, Nouraie M, Han J, Gowhari M, Hassan J, Miasnikova G, Sergueeva A, Nekhai S, Kittles R, Machado RF, Garcia JG, Gladwin MT, Steinberg MH, Sebastiani P, McClain DA, Gordeuk VR.

Hum Genet. 2015 Aug;134(8):895-904. doi: 10.1007/s00439-015-1572-3. Epub 2015 May 30.

35.

Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.

Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK.

Blood Cells Mol Dis. 2015 Jun;55(1):27-9. doi: 10.1016/j.bcmd.2015.03.008. Epub 2015 Mar 30.

PMID:
25976463
36.

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.

Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, Ngo D, Vathipadiekal V, Chui DH, Al-Ali AK, Steinberg MH.

Blood Cells Mol Dis. 2015 Mar;54(3):224-30. doi: 10.1016/j.bcmd.2015.01.001. Epub 2015 Jan 30.

37.

Evaluation of an ensemble of genetic models for prediction of a quantitative trait.

Milton JN, Steinberg MH, Sebastiani P.

Front Genet. 2015 Jan 13;5:474. doi: 10.3389/fgene.2014.00474. eCollection 2014.

38.

Nitric oxide-based treatment for sickle cell leg ulcers?

Steinberg MH.

Lancet Haematol. 2014 Dec;1(3):e86-7. doi: 10.1016/S2352-3026(14)00020-9. Epub 2014 Nov 13. No abstract available.

PMID:
27029231
39.

Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.

Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH.

Hemoglobin. 2014;38(6):381-4. doi: 10.3109/03630269.2014.971960. Epub 2014 Oct 27.

PMID:
25347256
40.

More blood for sickle cell anemia?

Steinberg MH.

N Engl J Med. 2014 Aug 21;371(8):775-6. doi: 10.1056/NEJMe1405776. No abstract available.

PMID:
25140964
41.

A novel HBA2 gene conversion in cis or trans: "α12 allele" in a Saudi population.

Borgio JF, AbdulAzeez S, Al-Nafie AN, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Muhanna F, Steinberg MH, Al-Ali AK.

Blood Cells Mol Dis. 2014 Dec;53(4):199-203. doi: 10.1016/j.bcmd.2014.07.001. Epub 2014 Jul 25.

PMID:
25065854
42.

The genetics of hemoglobin A2 regulation in sickle cell anemia.

Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH.

Am J Hematol. 2014 Nov;89(11):1019-23. doi: 10.1002/ajh.23811. Epub 2014 Aug 4.

43.

Reply: Practice guideline for pulmonary hypertension in sickle cell: direct evidence needed before universal adoption.

Klings ES, Machado RF, Morris CR, Gordeuk VR, Kato GJ, Ataga KI, Castro O, Hsu L, Telen MJ, Krishnamurti L, Steinberg MH, Gladwin MT; ATS Clinical Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension in Sickle Cell Disease Committee.

Am J Respir Crit Care Med. 2014 Jul 15;190(2):238-40. doi: 10.1164/rccm.201404-0733LE. No abstract available.

44.

Quantitative magnetic resonance imaging analysis of the lacrimal gland in sickle cell disease.

Buch K, Watanabe M, Elias EJ, Liao JH, Jara H, Nadgir RN, Saito N, Steinberg MH, Sakai O.

J Comput Assist Tomogr. 2014 Sep-Oct;38(5):674-80. doi: 10.1097/RCT.0000000000000104.

PMID:
24834886
45.

Deferiprone versus deferoxamine in sickle cell disease: results from a 5-year long-term Italian multi-center randomized clinical trial.

Calvaruso G, Vitrano A, Di Maggio R, Ballas S, Steinberg MH, Rigano P, Sacco M, Telfer P, Renda D, Barone R, Maggio A; Investigators of the Multicenter Randomized Clinical Trial of Deferiprone versus Deferoxamine in Sickle-Cell-Disease.

Blood Cells Mol Dis. 2014 Dec;53(4):265-71. doi: 10.1016/j.bcmd.2014.04.004. Epub 2014 May 9.

PMID:
24814618
46.

An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell disease.

Klings ES, Machado RF, Barst RJ, Morris CR, Mubarak KK, Gordeuk VR, Kato GJ, Ataga KI, Gibbs JS, Castro O, Rosenzweig EB, Sood N, Hsu L, Wilson KC, Telen MJ, Decastro LM, Krishnamurti L, Steinberg MH, Badesch DB, Gladwin MT; American Thoracic Society Ad Hoc Committee on Pulmonary Hypertension of Sickle Cell Disease.

Am J Respir Crit Care Med. 2014 Mar 15;189(6):727-40. doi: 10.1164/rccm.201401-0065ST.

47.

Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models.

Milton JN, Gordeuk VR, Taylor JG 6th, Gladwin MT, Steinberg MH, Sebastiani P.

Circ Cardiovasc Genet. 2014 Apr;7(2):110-5. doi: 10.1161/CIRCGENETICS.113.000387. Epub 2014 Mar 1.

48.

Hypoxic response contributes to altered gene expression and precapillary pulmonary hypertension in patients with sickle cell disease.

Zhang X, Zhang W, Ma SF, Desai AA, Saraf S, Miasniakova G, Sergueeva A, Ammosova T, Xu M, Nekhai S, Abbasi T, Casanova NG, Steinberg MH, Baldwin CT, Sebastiani P, Prchal JT, Kittles R, Garcia JG, Machado RF, Gordeuk VR.

Circulation. 2014 Apr 22;129(16):1650-8. doi: 10.1161/CIRCULATIONAHA.113.005296. Epub 2014 Feb 10.

49.

HbC disorders.

Steinberg MH, Chui DH.

Blood. 2013 Nov 21;122(22):3698. doi: 10.1182/blood-2013-09-526764. No abstract available.

50.

Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.

Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH.

Br J Haematol. 2014 Feb;164(4):597-604. doi: 10.1111/bjh.12650. Epub 2013 Nov 13.

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