Thein, Swee Lay
National Institutes of Health · National Heart, Lung, and Blood Institute
11 papers on CoChatORCID 0000-0002-9835-6501
Most cited papers
- Verified
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
Menzel, S., Garner, C., Gut, I., Matsuda, F., Yamaguchi, M., Heath, S., Foglio, M., Zelenika, D., Boland, A., Rooks, H., et al. (2007) · Nature Genetics
Hemoglobinopathies and Related DisordersGenetic Associations and Epidemiology
Cited by 529
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Control of fetal hemoglobin: new insights emerging from genomics and clinical implications
Thein, S. L., Menzel, S., Lathrop, M., & Garner, C. (2009) · Human Molecular Genetics
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 250
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Pathophysiology of β Thalassemia—A Guide to Molecular Therapies
Thein, S. L. (2005) · Hematology
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 103
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Molecular therapies in β‐thalassaemia
Quek, L., & Thein, S. L. (2007) · British Journal of Haematology
Hemoglobinopathies and Related DisordersIron Metabolism and Disorders
Cited by 88
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Allosteric control of hemoglobin S fiber formation by oxygen and its relation to the pathophysiology of sickle cell disease
Henry, E. R., Cellmer, T., Dunkelberger, E. B., Metaferia, B., Hofrichter, J., Li, Q., Ostrowski, D., Ghirlando, R., Louis, J. M., Moutereau, S., et al. (2020) · Proceedings of the National Academy of Sciences
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 65
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Binding patterns of BCL11A in the globin and GATA1 loci and characterization of the BCL11A fetal hemoglobin locus
Jawaid, K., Wahlberg, K., Thein, S. L., & Best, S. (2010) · Blood Cells, Molecules, and Diseases
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 64
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Genetic modifiers of fetal haemoglobin in sickle cell disease
Menzel, S., & Thein, S. L. (2019) · Molecular Diagnosis & Therapy
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 50
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g(HbF): a genetic model of fetal hemoglobin in sickle cell disease
Gardner, K., Fulford, T., Silver, N., Rooks, H., Angelis, N., Allman, M., Nkya, S., Makani, J., Howard, J., Kesse-Adu, R., et al. (2018) · Blood Advances
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 43
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Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya Syndrome
Birkeland, P., Gardner, K., Kesse-Adu, R., Davies, J., Lauritsen, J., Rom Poulsen, F., Tolias, C. M., & Thein, S. L. (2016) · Stroke
Hemoglobinopathies and Related DisordersIntracranial Aneurysms: Treatment and Complications
Cited by 37
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Fetal hemoglobin is associated with peripheral oxygen saturation in sickle cell disease in Tanzania
Nkya, S., Mgaya, J., Urio, F., Makubi, A., Thein, S. L., Menzel, S., Cox, S. E., Newton, C. R., Kirkham, F. J., Mmbando, B. P., et al. (2017) · EBioMedicine
Hemoglobinopathies and Related DisordersHemoglobin structure and function
Cited by 13
- Verified
Erythrocytosis and the Chuvash von Hippel-Lindau mutation
Percy, M. J., Beard, M. E. J., Carter, C., & Thein, S. L. (2003) · British Journal of Haematology
Ear and Head TumorsErythropoietin and Anemia Treatment
Cited by 8
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