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MD, University of Minnesota Medical School




Boston University Clinical and Translational Science Award (CTSA) Program KL2
05/01/2012 - 04/30/2014 (Co-Investigator of Sub-Project / SP)
PI: David M. Center, MD
NIH/National Center for Health Research Resources
3KL2TR000158-05S1



Title


Yr Title Project-Sub Proj Pubs

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

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  1. Ngo DA, Steinberg MH. Genomic approaches to identifying targets for treating ß hemoglobinopathies. BMC Med Genomics. 2015; 8:44.View Related Profiles. PMID: 26215470; PMCID: PMC4517356; DOI: 10.1186/s12920-015-0120-2;
     
  2. 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. BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia. Blood Cells Mol Dis. 2015 Mar; 54(3):224-30.View Related Profiles. PMID: 25703683; PMCID: PMC4341902; DOI: 10.1016/j.bcmd.2015.01.001;
     
  3. Ngo D, Steinberg M. Hematology clinic. Sickle cell disease. Hematology. 2014 Jun; 19(4):244-5.View Related Profiles. PMID: 24666152; DOI: 10.1179/1024533214Z.000000000276;
     
  4. Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK. Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-ß(0) thalassemia. Am J Hematol. 2013 Jun; 88(6):531-2.View Related Profiles. PMID: 23483609; DOI: 10.1002/ajh.23434;
     
  5. 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. Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype. Blood Cells Mol Dis. 2013 Jun; 51(1):22-6.View Related Profiles. PMID: 23465615; PMCID: PMC3647015; DOI: 10.1016/j.bcmd.2012.12.005;
     
  6. Alsultan A, Ngo DA, Farrell JJ, Akinsheye I, Solovieff N, Ghabbour HA, Al-Ali A, Alsuliman A, Al-Baghshi M, Albu-Ali W, Alabdulaali M, Baldwin CT, Farrer LA, Luo H, Melista E, Safaya S, Nwaru M, Chui DH, Steinberg MH. A functional promoter polymorphism of the d-globin gene is a specific marker of the Arab-Indian haplotype. Am J Hematol. 2012 Aug; 87(8):824-6.View Related Profiles. PMID: 22641479; DOI: 10.1002/ajh.23239;
     
  7. Akinsheye I, Solovieff N, Ngo D, Malek A, Sebastiani P, Steinberg MH, Chui DH. Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans. Am J Hematol. 2012 Feb; 87(2):217-9.View Related Profiles. PMID: 22139998; PMCID: PMC3302931; DOI: 10.1002/ajh.22221;
     
  8. Ngo DA, Aygun B, Akinsheye I, Hankins JS, Bhan I, Luo HY, Steinberg MH, Chui DH. Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin. Br J Haematol. 2012 Jan; 156(2):259-64.View Related Profiles. PMID: 22017641; PMCID: PMC6605093; DOI: 10.1111/j.1365-2141.2011.08916.x;
     
  9. Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia. Blood. 2011 Jul 7; 118(1):19-27.View Related Profiles. PMID: 21490337; PMCID: PMC3139383; DOI: 10.1182/blood-2011-03-325258;
     
  10. Dai Y, Ngo D, Jacob J, Forman LW, Faller DV. Prohibitin and the SWI/SNF ATPase subunit BRG1 are required for effective androgen antagonist-mediated transcriptional repression of androgen receptor-regulated genes. Carcinogenesis. 2008 Sep; 29(9):1725-33.View Related Profiles. PMID: 18487222; PMCID: PMC2722849; DOI: 10.1093/carcin/bgn117;
     
Showing 10 of 12 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.




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