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Martin H. Steinberg

Martin H. Steinberg

D-Index & Metrics

Medicine

D-Index
101
Citations
44696
World Ranking
7875
National Ranking
4102

Research.com Recognitions

  • 1989 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

Martin H. Steinberg is affiliated with Boston University in the United States. Their research primarily focuses on medicine, with significant work in the subfields of genetics, hematology, pediatrics, perinatology and child health, molecular biology, and physiology. The main topics Steinberg covers include hemoglobinopathies and related disorders, iron metabolism and disorders, prenatal screening and diagnostics, blood groups and transfusion, erythrocyte function and pathophysiology, parvovirus B19 infection studies, and RNA modifications and cancer.

The scientist has published extensively in venues such as Blood, the American Journal of Hematology, Expert Review of Hematology, British Journal of Haematology, and Transplantation and Cellular Therapy. Blood stands out as a frequent publication venue, featuring twelve of their works, followed by nine publications in the American Journal of Hematology.

Some of the recent papers authored or co-authored by Martin H. Steinberg include:

  • Fetal hemoglobin in sickle cell anemia, 2020, Blood
  • Fetal Hemoglobin in Sickle Hemoglobinopathies: High HbF Genotypes and Phenotypes, 2020, Journal of Clinical Medicine

Additionally, Steinberg has collaborated on several papers with collaborator Haydar Frangoul, such as "CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia" (2020, New England Journal of Medicine), and "Exagamglogene Autotemcel for Severe Sickle Cell Disease" (2024, New England Journal of Medicine), though Steinberg is not listed as author on these.

Frequent co-authors working with Martin H. Steinberg include:

  • Haydar Frangoul
  • Franco Locatelli
  • Stephan A. Grupp
  • Markus Y. Mapara
  • Mariane de Montalembert

Martin H. Steinberg was awarded the Fellow of the American Association for the Advancement of Science (AAAS) in 1989.

Best Publications

  • Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death

    Orah S. Platt;Donald J. Brambilla;Wendell F. Rosse;Paul F. Milner

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

    Haydar Frangoul;David Altshuler;M. Domenica Cappellini;Yi-Shan Chen

  • Mental and Behavioral Disturbances in Dementia: Findings from the Cache County Study on Memory in Aging

    Constantine G. Lyketsos;Martin Steinberg;Jo Ann T. Tschanz;Maria C. Norton

  • Effect of Hydroxyurea on Mortality and Morbidity in Adult Sickle Cell Anemia: Risks and Benefits Up to 9 Years of Treatment

    Martin H. Steinberg;Martin H. Steinberg;Franca Barton;Oswaldo Castro;Charles H. Pegelow

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

    Gregory J. Kato;Mark T. Gladwin;Martin H. Steinberg

  • Sickle Cell Disease.

    Frédéric B Piel;Martin H Steinberg;David C Rees

  • Management of Sickle Cell Disease

    Martin H. Steinberg

  • Point and 5-year period prevalence of neuropsychiatric symptoms in dementia: The Cache county study

    Martin Steinberg;Huibo Shao;Peter Zandi;Constantine G. Lyketsos

  • Intravascular hemolysis and the pathophysiology of sickle cell disease

    Gregory J. Kato;Martin H. Steinberg;Mark T. Gladwin

  • Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severity.

    Robert P. Hebbel;Marc A. B. Boogaerts;John W. Eaton;Martin H. Steinberg

  • Fetal hemoglobin in sickle cell anemia

    Idowu Akinsheye;Abdulrahman Alsultan;Nadia Solovieff;Duyen Ngo

  • Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management

    Martin H. Steinberg;Bernard G. Forget;Douglas R. Higgs;David J. Weatherall

  • Genetic signatures of exceptional longevity in humans.

    Paola Sebastiani;Nadia Solovieff;Andrew T. DeWan;Kyle M. Walsh

  • Spontaneous oxygen radical generation by sickle erythrocytes.

    Robert P. Hebbel;John W. Eaton;M. Balasingam;Martin H. Steinberg

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

    Martin H. Steinberg;William F. McCarthy;Oswaldo Castro;Samir K. Ballas

  • Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms

    Maya Saleh;John P. Vaillancourt;Rona K. Graham;Matthew Huyck

  • Treating depression in Alzheimer disease: Efficacy and safety of sertraline therapy, and the benefits of depression reduction: The DIADS

    Constantine G. Lyketsos;Lourdes DelCampo;Martin Steinberg;Quincy Miles

  • Do statins reduce risk of incident dementia and Alzheimer disease? The Cache county study

    Peter P. Zandi;D. Larry Sparks;Ara S. Khachaturian;JoAnn T. Tschanz

  • Hydroxyurea and Sickle Cell Anemia: Clinical Utility of a Myelosuppressive "Switching" Agent

    Samuel Charache;Franca B. Barton;Richard D. Moore;Michael L. Terrin

  • Effect of Hydroxyurea on Mortality and Morbidity in Adult Sickle Cell Anemia

    Martin H. Steinberg;Franca Barton;Oswaldo Castro;Charles H. Pegelow

Frequent Co-Authors

David H.K. Chui
David H.K. Chui Boston University
Clinton T. Baldwin
Clinton T. Baldwin Boston University
Constantine G. Lyketsos
Constantine G. Lyketsos Johns Hopkins University
Lindsay A. Farrer
Lindsay A. Farrer Boston University
Mark T. Gladwin
Mark T. Gladwin University of Pittsburgh
John C.S. Breitner
John C.S. Breitner Douglas Mental Health University Institute
Gregory J. Kato
Gregory J. Kato CSL Behring
JoAnn T. Tschanz
JoAnn T. Tschanz Utah State University
Victor R. Gordeuk
Victor R. Gordeuk University of Illinois at Chicago

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