Steinberg, Martin H.

Mortality in sickle cell disease. Life expectancy and risk factors for early death

Platt, O. S., Brambilla, D. J., Rosse, W. F., Milner, P. F., Castro, O., Steinberg, M. H., & Klug, P. P. (1994) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersMalaria Research and Control

Cited by 3,320

CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia

Frangoul, H., Altshuler, D., Cappellini, M. D., Chen, Y.-S., Domm, J., Eustace, B. K., Foell, J., de la Fuente, J., Grupp, S., Handgretinger, R., et al. (2021) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersCRISPR and Genetic Engineering

Cited by 1,962

Sickle cell disease

Piel, F. B., Steinberg, M. H., & Rees, D. C. (2017) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersMalaria Research and Control

Cited by 1,488

Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes

Kato, G. J., Gladwin, M. T., & Steinberg, M. H. (2007) · Blood Reviews

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 876

Intravascular hemolysis and the pathophysiology of sickle cell disease

Kato, G. J., Steinberg, M. H., & Gladwin, M. T. (2017) · Journal of Clinical Investigation

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 748

Fetal hemoglobin in sickle cell anemia

Akinsheye, I., Alsultan, A., Solovieff, N., Ngo, D., Baldwin, C. T., Sebastiani, P., Chui, D. H. K., & Steinberg, M. H. (2011) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 553

Exagamglogene Autotemcel for Severe Sickle Cell Disease

Frangoul, H., Locatelli, F., Sharma, A., Bhatia, M., Mapara, M., Molinari, L., Wall, D., Liem, R. I., Telfer, P., Shah, A. J., et al. (2024) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersVirus-based gene therapy research

Cited by 493

The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: a 17.5 year follow-up

Steinberg, M. H., McCarthy, W. F., Castro, O., Ballas, S. K., Armstrong, F. D., Smith, W., Ataga, K., Swerdlow, P., Kutlar, A., DeCastro, L., et al. (2010) · American Journal of Hematology

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 486

Genetic signatures of exceptional longevity in humans

Sebastiani, P., Solovieff, N., DeWan, A. T., Walsh, K. M., Puca, A., Hartley, S. W., Melista, E., Andersen, S., Dworkis, D. A., Wilk, J. B., et al. (2012) · PLoS ONE

Genetic Associations and EpidemiologyGenetics, Aging, and Longevity in Model Organisms

Cited by 464

Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea

Steinberg, M. H., Lu, Z.-H., Barton, F. B., Terrin, M. L., Charache, S., Dover, G. J., & Hydroxyurea, T. M. S. O. (1997) · Blood

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 407

Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions

Kato, G. J., Hebbel, R. P., Steinberg, M. H., & Gladwin, M. T. (2009) · American Journal of Hematology

Hemoglobinopathies and Related DisordersBlood properties and coagulation

Cited by 349

Genetic modifiers of sickle cell disease

Steinberg, M. H., & Sebastiani, P. (2012) · American Journal of Hematology

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 315

Fetal hemoglobin in sickle cell anemia: a glass half full?

Steinberg, M. H., Chui, D. H. K., Dover, G. J., Sebastiani, P., & Alsultan, A. (2014) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 267

N-Terminal Pro-Brain Natriuretic Peptide Levels and Risk of Death in Sickle Cell Disease

Machado, R. F., Anthi, A., Steinberg, M. H., Bonds, D., Sachdev, V., Kato, G. J., Taveira-DaSilva, A. M., Ballas, S. K., Blackwelder, W., Xu, X., et al. (2006) · JAMA

Hemoglobinopathies and Related DisordersPulmonary Hypertension Research and Treatments

Cited by 197

BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies

Sedgewick, A. E., Timofeev, N., Sebastiani, P., So, J. C. C., Ma, E. S. K., Chan, L. C., Fucharoen, G., Fucharoen, S., Barbosa, C. G., Vardarajan, B. N., et al. (2008) · Blood Cells, Molecules, and Diseases

Hemoglobinopathies and Related DisordersGenetic Associations and Epidemiology

Cited by 172

Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin

Ngo, D. A., Aygun, B., Akinsheye, I., Hankins, J. S., Bhan, I., Luo, H. Y., Steinberg, M. H., & Chui, D. H. K. (2012) · British Journal of Haematology

Hemoglobinopathies and Related DisordersIron Metabolism and Disorders

Cited by 142

Genetic Signatures of Exceptional Longevity in Humans

Sebastiani, P., Solovieff, N., Puca, A., Hartley, S. W., Melista, E., Andersen, S., Dworkis, D. A., Wilk, J. B., Myers, R. H., Steinberg, M. H., et al. (2010) · Science

Genetic Associations and EpidemiologyGenetics, Aging, and Longevity in Model Organisms

Cited by 141

Fetal hemoglobin in sickle cell anemia

Steinberg, M. H. (2020) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 136

Ascorbic Acid-Induced Hemolysis in G-6-PD Deficiency

CAMPBELL, G. D., STEINBERG, M. H., & BOWER, J. D. (1975) · Annals of Internal Medicine

Neonatal Health and BiochemistryMethemoglobinemia and Tumor Lysis Syndrome

Cited by 134

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

Alsultan, A., Alabdulaali, M. K., Griffin, P. J., AlSuliman, A. M., Ghabbour, H. A., Sebastiani, P., Albuali, W. H., Al‐Ali, A. K., Chui, D. H. K., & Steinberg, M. H. (2014) · British Journal of Haematology

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 95

Genome-wide association studies and the genetic dissection of complex traits

Sebastiani, P., Timofeev, N., Dworkis, D. A., Perls, T. T., & Steinberg, M. H. (2009) · American Journal of Hematology

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 67

Safety and Efficacy of CTX001 in Patients with Transfusion-Dependent β-Thalassemia and Sickle Cell Disease: Early Results from the Climb THAL-111 and Climb SCD-121 Studies of Autologous CRISPR-CAS9-Modified CD34+ Hematopoietic Stem and Progenitor Cells

Frangoul, H., Bobruff, Y., Cappellini, M. D., Corbacioglu, S., Fernandez, C. M., de la Fuente, J., Grupp, S. A., Handgretinger, R., Ho, T. W., Imren, S., et al. (2020) · Blood

Hemoglobinopathies and Related DisordersVirus-based gene therapy research

Cited by 54

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

Park, S., Gianotti-Sommer, A., Molina-Estevez, F. J., Vanuytsel, K., Skvir, N., Leung, A., Rozelle, S. S., Shaikho, E. M., Weir, I., Jiang, Z., et al. (2017) · Stem Cell Reports

Hemoglobinopathies and Related DisordersPluripotent Stem Cells Research

Cited by 50

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

Sebastiani, P., Farrell, J. J., Alsultan, A., Wang, S., Edward, H. L., Shappell, H., Bae, H., Milton, J. N., Baldwin, C. T., Al-Rubaish, A. M., et al. (2015) · Blood Cells, Molecules, and Diseases

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 41