Martin H. Steinberg

34.1k total citations · 6 hit papers
413 papers, 21.4k citations indexed

About

Martin H. Steinberg is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Martin H. Steinberg has authored 413 papers receiving a total of 21.4k indexed citations (citations by other indexed papers that have themselves been cited), including 300 papers in Genetics, 218 papers in Hematology and 74 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Martin H. Steinberg's work include Hemoglobinopathies and Related Disorders (296 papers), Iron Metabolism and Disorders (179 papers) and Blood groups and transfusion (76 papers). Martin H. Steinberg is often cited by papers focused on Hemoglobinopathies and Related Disorders (296 papers), Iron Metabolism and Disorders (179 papers) and Blood groups and transfusion (76 papers). Martin H. Steinberg collaborates with scholars based in United States, Saudi Arabia and Canada. Martin H. Steinberg's co-authors include Mark T. Gladwin, Gregory J. Kato, Oswaldo Castro, Paola Sebastiani, Wendell F. Rosse, Donald Brambilla, Orah S. Platt, Panpit Klug, Paul Milner and Robert P. Hebbel and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Martin H. Steinberg

402 papers receiving 20.6k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

1994 2.5k citations Oswaldo Castro, Martin H. Steinberg et al. profile →
Sickle Cell Disease

2017 749 citations Martin H. Steinberg et al. profile →
Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes

2006 587 citations Gregory J. Kato, Mark T. Gladwin et al. profile →
Point and 5‐year period prevalence of neuropsychiatric symptoms in dementia: the Cache County Study

2007 530 citations Martin H. Steinberg, Constantine G. Lyketsos et al. International Journal of Geriatric Psychiatry profile →
Intravascular hemolysis and the pathophysiology of sickle cell disease

2017 451 citations Gregory J. Kato, Martin H. Steinberg et al. profile →
Erythrocyte Adherence to Endothelium in Sickle-Cell Anemia

1980 437 citations Martin H. Steinberg et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Martin H. Steinberg United States	70	13.7k	10.7k	3.7k	3.7k	3.5k	413	21.4k
Piet L. C. M. van Riel Netherlands	69	2.6k 0.2×	6.3k 0.6×	934 0.3×	379 0.1×	1.9k 0.5×	328	24.1k
Avital Cnaan United States	59	2.0k 0.1×	1.3k 0.1×	690 0.2×	3.7k 1.0×	2.0k 0.6×	177	12.6k
Fenella J. Kirkham United Kingdom	60	3.8k 0.3×	5.3k 0.5×	652 0.2×	2.4k 0.7×	559 0.2×	324	12.7k
Philip J. Mease United States	90	955 0.1×	12.5k 1.2×	1.9k 0.5×	766 0.2×	1.4k 0.4×	800	39.2k
Frederick Wolfe United States	76	1.3k 0.1×	3.0k 0.3×	1.5k 0.4×	637 0.2×	918 0.3×	205	24.4k
Myron A. Waclawiw United States	56	2.2k 0.2×	1.6k 0.1×	3.2k 0.9×	863 0.2×	3.1k 0.9×	139	14.9k
Ronald L. Wilder United States	47	1.5k 0.1×	3.7k 0.4×	1.6k 0.4×	282 0.1×	3.8k 1.1×	113	27.1k
Elizabeth C. Wright United States	62	1.8k 0.1×	1.6k 0.1×	1.8k 0.5×	1.1k 0.3×	1.3k 0.4×	185	13.8k
Ernest Choy United Kingdom	68	1.1k 0.1×	3.2k 0.3×	1.4k 0.4×	377 0.1×	2.1k 0.6×	352	19.0k
Richard E. Harris United States	69	804 0.1×	1.5k 0.1×	3.0k 0.8×	982 0.3×	2.1k 0.6×	274	14.6k

Countries citing papers authored by Martin H. Steinberg

Since Specialization

Citations

This map shows the geographic impact of Martin H. Steinberg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Martin H. Steinberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martin H. Steinberg more than expected).

Fields of papers citing papers by Martin H. Steinberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martin H. Steinberg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Martin H. Steinberg. The network helps show where Martin H. Steinberg may publish in the future.

Co-authorship network of co-authors of Martin H. Steinberg

This figure shows the co-authorship network connecting the top 25 collaborators of Martin H. Steinberg. A scholar is included among the top collaborators of Martin H. Steinberg based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Martin H. Steinberg. Martin H. Steinberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Wilks, Andrew F., Martin H. Steinberg, & Haydar Frangoul. (2025). Gene therapy for HbSC disease and other compound heterozygous sickle hemoglobinopathies: a time for inclusion. Blood. 146(20). 2385–2391.

Weinberg, Joanne, et al.. (2024). P066 Treatment effects of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis heterozygous for 3849 + 10 kbC->T. Journal of Cystic Fibrosis. 23. S87–S87.

Williams, Christopher, Kiana Mahdaviani, Yuriy O. Alekseyev, et al.. (2024). PGC-1α agonism induces fetal hemoglobin and exerts antisickling effects in sickle cell disease. Science Advances. 10(31). eadn8750–eadn8750. 3 indexed citations

Ribeil, Jean‐Antoine, et al.. (2023). An integrated therapeutic approach to sickle cell disease management beyond infancy. American Journal of Hematology. 98(7). 1087–1096. 3 indexed citations

Cyrus, Cyril, Chittibabu Vatte, Shahanas Chathoth, et al.. (2022). miRNA Expression Associated with HbF in Saudi Sickle Cell Anemia. Medicina. 58(10). 1470–1470. 3 indexed citations

Steinberg, Martin H., et al.. (2019). Sickle cell disease in the era of precision medicine: looking to the future. Expert Review of Precision Medicine and Drug Development. 4(6). 357–367. 6 indexed citations

Vanuytsel, Kim, Taylor Matte, Amy Leung, et al.. (2018). Induced pluripotent stem cell–based mapping of β-globin expression throughout human erythropoietic development. Blood Advances. 2(15). 1998–2011. 14 indexed citations

Morrison, Tasha, John J. Farrell, Ryo Kurita, et al.. (2017). A Long Noncoding RNA from the HBS1L-MYB Intergenic Region on Chr6q23 Regulates Human Fetal Hemoglobin Expression. Blood. 130. 288–288. 2 indexed citations

Sebastiani, Paola, John J. Farrell, Heather M. Shappell, et al.. (2015). BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia. Blood Cells Molecules and Diseases. 54(3). 224–230. 32 indexed citations

10.

Klings, Elizabeth S., Roberto F. Machado, Robyn J. Barst, et al.. (2014). An Official American Thoracic Society Clinical Practice Guideline: Diagnosis, Risk Stratification, and Management of Pulmonary Hypertension of Sickle Cell Disease. American Journal of Respiratory and Critical Care Medicine. 189(6). 727–740. 155 indexed citations

11.

Bhatnagar, Pallav, Emily Barron‐Casella, Christopher J. Bean, et al.. (2013). Genome-Wide Meta-Analysis of Systolic Blood Pressure in Children with Sickle Cell Disease. PLoS ONE. 8(9). e74193–e74193. 17 indexed citations

12.

Nolan, Val, Yuqing Zhang, Timothy L. Lash, Paola Sebastiani, & Martin H. Steinberg. (2008). Association between wind speed and the occurrence of sickle cell acute painful episodes: results of a case‐crossover study. British Journal of Haematology. 143(3). 433–438. 44 indexed citations

13.

Adewoye, Adeboye H., et al.. (2006). Lacrimal gland enlargement in sickle cell disease. American Journal of Hematology. 81(11). 888–889. 9 indexed citations

14.

Munro, Cynthia A., Jason Brandt, Jeannie‐Marie E. Sheppard, et al.. (2004). Cognitive Response to Pharmacological Treatment for Depression in Alzheimer Disease: Secondary Outcomes From the Depression in Alzheimer's Disease Study (DIADS). American Journal of Geriatric Psychiatry. 12(5). 491–498. 32 indexed citations

15.

Steinberg, Martin H., Cynthia A. Munro, Quincy M. Samus, et al.. (2004). Patient predictors of response to treatment of depression in Alzheimer's disease: the DIADS study. International Journal of Geriatric Psychiatry. 19(2). 144–150. 18 indexed citations

16.

Charache, Samuel, Franca B. Barton, Richard D. Moore, et al.. (1996). Hydroxyurea and Sickle Cell Anemia Clinical Utility of a Myelosuppressive “Switching” Agent. Medicine. 75(6). 300–326. 268 indexed citations

17.

Steinberg, Martin H., et al.. (1996). 5′ Hypersensitive Site-2 and Fetal Hemogln in Brazilians. Hemoglobin. 20(4). 435–438. 4 indexed citations

18.

Steinberg, Martin H.. (1996). Modulation of the Phenotypic Diversity of Sickle Cell Anemia. Hemoglobin. 20(1). 1–19. 25 indexed citations

19.

Miale, Thomas D., et al.. (1987). Difficulty in establishing diagnosis from lung biopsies and bronchial washing analysis in children with leukemia following bone marrow transplantation.. PubMed. 1. 165–72. 3 indexed citations

20.

Steinberg, Martin H., et al.. (1986). A new gene deletion in the α-like globin gene cluster as the molecular basis for the rare α-thalassemia-1(−−/αα) in blacks: HbH disease in sickle cell trait. Blood. 67(2). 469–473. 14 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact