David Hing-Kwei Chui, MD
Professor
Boston University School of Medicine
Dept of Medicine
Hematology & Medical Oncology Section

MD, McGill University



Expertise includes: Globin gene mutations; Hemoglobin diseases; Thalassmeias; and Regulation of fetal hemoglobin expression.

Professor
Boston University School of Medicine
Pathology & Laboratory Medicine


Active Staff Hospital Privileges
Boston Medical Center
Pathology & Laboratory Medicine



2011 McGill University Alumni Association: D. Lorne Gales Award
2007-2016 The Best Doctors in America
2002 The Thalassemia Foundation of Canada: Hour Glass Award
2000-2002 The Thalassemia Foundation of Canada: Chair, Medical Advisory Board
1991 Association of American Physicians: elected to membership
1987-1991 NIH: Hematology Study Section
1980-1984 BLOOD: Editorial Board member
1980 American Society for Clinical Investigation: elected to membership
1971-1976 Medical Research Council of Canada: Scholar
1970 Royal College of Physicians of Canada: Fellow


Globin Gene Expression in Sickle Cell Genotype-Specific iPS cells
07/05/2011 - 06/30/2017 (Co-PI)
PI: Martin H. Steinberg, MD
NIH/National Heart, Lung, and Blood Institute
5U01HL107443-05

Globin Gene Expression in Sickle Cell Genotype-Specific iPS cells
07/05/2011 - 06/30/2012 (Co-PI)
PI: Martin H. Steinberg, MD
NIH/National Heart, Lung, and Blood Institute
1U01HL107443-01


Sickle Cell - Research Scholar
04/01/2003 - 03/31/2008 (PI)
NIH-NHLBI
5 U54 HL070819-05 (A)



Yr Title Project-Sub Proj Pubs
2014 Globin Gene Expression in Sickle Cell Genotype-Specific iPS cells 5U01HL107443-04 6
2013 Globin Gene Expression in Sickle Cell Genotype-Specific iPS cells 5U01HL107443-03 6
2012 Globin Gene Expression in Sickle Cell Genotype-Specific iPS cells 5U01HL107443-02 6
2011 Globin Gene Expression in Sickle Cell Genotype-Specific iPS cells 1U01HL107443-01 6
2009 Genetic Modulation of HbF in Beta Thalassemia 5R01DK069646-05 16
2008 AUTOMATED ID OF PROTEINS, VARIANTS &POST-TRANSLATIONAL MODIFICATIONS 5P41RR010888-12-5180 236
2008 Genetic Modulation of HbF in Beta Thalassemia 5R01DK069646-04 16
2007 AUTOMATED ID OF PROTEINS, VARIANTS &POST-TRANSLATIONAL MODIFICATIONS 2P41RR010888-11-8001 236
2007 Genetic Modulation of HbF in Beta Thalassemia 5R01DK069646-03 16
2006 AUTOMATED ID OF PROTEINS, VARIANTS &POST-TRANSLATIONAL MODIFICATIONS 5P41RR010888-10-7080 236
Showing 10 of 14 results. Show All Results
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.

  1. Cancio MI, Aygun B, Chui DHK, Rothman JA, Scott JP, Estepp JH, Hankins JS. The clinical severity of hemoglobin S/Black (A ?dß)0 -thalassemia. Pediatr Blood Cancer. 2017 Apr 28. PMID: 28453928; DOI: 10.1002/pbc.26596;.
  2. Jiang Z, Luo HY, Farrell JJ, Zhang Z, Schulz VP, Albarawi D, Steinberg MH, Al-Allawi NA, Gallagher PG, Forget BG, Chui DH. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in ß0 -thalassaemia homozygotes. Br J Haematol. 2017 Feb 27.View Related Profiles. PMID: 28240767; DOI: 10.1111/bjh.14445;.
  3. Luo HY, Chui DH. Diverse hematological phenotypes of ß-thalassemia carriers. Ann N Y Acad Sci. 2016 Mar; 1368(1):49-55.View Related Profiles. PMID: 27123947; DOI: 10.1111/nyas.13056;.
  4. 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, Basak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH. The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) ß(0) -thalassaemia homozygotes. Br J Haematol. 2016 Mar; 172(6):958-65.View Related Profiles. PMID: 26771086; DOI: 10.1111/bjh.13909;.
  5. Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH. Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease. Hemoglobin. 2016; 40(1):64-5.View Related Profiles. PMID: 26372199; DOI: 10.3109/03630269.2015.1080725;.
  6. Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH. Hb Youngstown [ß101(G3)Glu???Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia. Hemoglobin. 2014; 38(6):381-4.View Related Profiles. PMID: 25347256; DOI: 10.3109/03630269.2014.971960;.
  7. Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH. The genetics of hemoglobin A2 regulation in sickle cell anemia. Am J Hematol. 2014 Nov; 89(11):1019-23.View Related Profiles. PMID: 25042611; PMCID: PMC4298130; DOI: 10.1002/ajh.23811;.
  8. Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign. Br J Haematol. 2014 Feb; 164(4):597-604.View Related Profiles. PMID: 24224700; PMCID: PMC4094128; DOI: 10.1111/bjh.12650;.
  9. Steinberg MH, Chui DH, Dover GJ, Sebastiani P, Alsultan A. Fetal hemoglobin in sickle cell anemia: a glass half full? Blood. 2014 Jan 23; 123(4):481-5.View Related Profiles. PMID: 24222332; DOI: 10.1182/blood-2013-09-528067;.
  10. Croteau SE, Luo HY, Lehmann LE, Chui DH, Neufeld EJ. Novel dominant ß-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)]. Pediatr Blood Cancer. 2013 Oct; 60(10):E131-4. PMID: 23776097; DOI: 10.1002/pbc.24611;.
Showing 10 of 92 results. Show More

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

Bar chart showing 87 publications over 30 distinct years, with a maximum of 9 publications in 2011

YearPublications
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In addition to these self-described keywords below, a list of MeSH based concepts is available here.

Genetics
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75 E. Newton St Evans Building
Boston MA 02118
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