Elias Schwartz

6.4k total citations · 1 hit paper
148 papers, 5.4k citations indexed

About

Elias Schwartz is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elias Schwartz has authored 148 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Genetics, 70 papers in Hematology and 34 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elias Schwartz's work include Hemoglobinopathies and Related Disorders (89 papers), Iron Metabolism and Disorders (39 papers) and Neonatal Health and Biochemistry (25 papers). Elias Schwartz is often cited by papers focused on Hemoglobinopathies and Related Disorders (89 papers), Iron Metabolism and Disorders (39 papers) and Neonatal Health and Biochemistry (25 papers). Elias Schwartz collaborates with scholars based in United States, Israel and Jamaica. Elias Schwartz's co-authors include Saul Surrey, Mortimer Poncz, Alan R. Cohen, Toshio Asakura, Joel Bennett, Shlomo Friedman, M Ballantine, Y Mory, K. Adachi and R Eisman and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Elias Schwartz

142 papers receiving 5.1k citations

Hit Papers

Construction of Human Gen... 1982 2026 1996 2011 1982 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elias Schwartz United States 35 2.7k 2.7k 1.3k 714 670 148 5.4k
Giovanni Migliaccio Italy 46 2.4k 0.9× 1.8k 0.7× 2.5k 1.9× 1.2k 1.7× 104 0.2× 190 7.2k
C Jasmin France 37 1.3k 0.5× 661 0.2× 1.7k 1.3× 428 0.6× 510 0.8× 242 6.7k
Leon W. Hoyer United States 42 4.8k 1.7× 1.2k 0.4× 1.5k 1.1× 298 0.4× 341 0.5× 105 6.9k
Russell P. Rother United States 34 2.4k 0.9× 2.0k 0.7× 989 0.7× 658 0.9× 88 0.1× 72 7.9k
Peter J. Lenting France 57 5.9k 2.1× 1.5k 0.6× 1.8k 1.4× 996 1.4× 505 0.8× 208 10.0k
Charles D. Scher United States 36 714 0.3× 628 0.2× 3.1k 2.4× 450 0.6× 172 0.3× 81 5.9k
Hideki Muramatsu Japan 38 1.6k 0.6× 750 0.3× 2.5k 1.9× 255 0.4× 302 0.5× 274 5.9k
B Furie United States 36 2.6k 1.0× 790 0.3× 1.6k 1.2× 220 0.3× 907 1.4× 59 5.4k
Margaret J. Polley United States 27 1.3k 0.5× 614 0.2× 839 0.6× 508 0.7× 597 0.9× 52 3.7k
Toshihiko Terao Japan 43 876 0.3× 414 0.2× 1.6k 1.2× 165 0.2× 468 0.7× 220 5.8k

Countries citing papers authored by Elias Schwartz

Since Specialization
Citations

This map shows the geographic impact of Elias Schwartz'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 Elias Schwartz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elias Schwartz more than expected).

Fields of papers citing papers by Elias Schwartz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elias Schwartz. 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 Elias Schwartz. The network helps show where Elias Schwartz may publish in the future.

Co-authorship network of co-authors of Elias Schwartz

This figure shows the co-authorship network connecting the top 25 collaborators of Elias Schwartz. A scholar is included among the top collaborators of Elias Schwartz 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 Elias Schwartz. Elias Schwartz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Rösch, Andreas, et al.. (2023). Accuracy Evaluation of 3D Pose Estimation with MediaPipe Pose for Physical Exercises. SHILAP Revista de lepidopterología. 9(1). 563–566. 14 indexed citations
3.
Keller, Michael A., Diana L. Cassel, Eric Rappaport, et al.. (1993). Fluorescence-based RT PCR analysis: determination of the ratio of soluble to membrane-bound forms of Fc gamma RIIA transcripts in hematopoietic cell lines.. Genome Research. 3(1). 32–38. 14 indexed citations
4.
McKenzie, Steven E., Margaret Keller, Diana L. Cassel, et al.. (1992). Characterization of the 5′-flanking transcriptional regulatory region of the human Fcγ receptor gene, Fcγ RIIA. Molecular Immunology. 29(10). 1165–1174. 20 indexed citations
5.
Month, Stacy, Robert W. Wood, Panayiota Trifillis, et al.. (1990). Analysis of 5' flanking regions of the gamma globin genes from major African haplotype backgrounds associated with sickle cell disease.. Journal of Clinical Investigation. 85(2). 364–370. 21 indexed citations
6.
Burk, Carol D., et al.. (1988). A Taq 1 polymorphism for the human platelet glycoprotein IIIa gene (GP3A). Nucleic Acids Research. 16(14). 7216–7216. 11 indexed citations
7.
Sosnoski, Donna M., B S Emanuel, Anita L. Hawkins, et al.. (1988). Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa.. Journal of Clinical Investigation. 81(6). 1993–1998. 68 indexed citations
8.
Zimrin, Ann B., R Eisman, Gaston Vilaire, et al.. (1988). Structure of platelet glycoprotein IIIa. A common subunit for two different membrane receptors.. Journal of Clinical Investigation. 81(5). 1470–1475. 94 indexed citations
9.
Schwartz, Elias, et al.. (1988). Overview of the β Thalassemias: Genetic and Clinical Aspects. Hemoglobin. 12(5-6). 551–564. 9 indexed citations
10.
Hoyt, Reed W., et al.. (1986). Pulmonary function abnormalities in homozygous β-thalassemia. The Journal of Pediatrics. 109(3). 452–455. 30 indexed citations
11.
Surrey, Saul, Kathleen Delgrosso, Padmini Malladi, & Elias Schwartz. (1985). Functional analysis of a beta-globin gene containing a TATA box mutation from a Kurdish Jew with beta thalassemia.. Journal of Biological Chemistry. 260(11). 6507–6510. 13 indexed citations
12.
Poncz, Mortimer, et al.. (1982). "Nonrandom" DNA sequence analysis in bacteriophage M13 by the dideoxy chain-termination method.. Proceedings of the National Academy of Sciences. 79(14). 4298–4302. 263 indexed citations
13.
Cohen, Alan R., Marie Martin, & Elias Schwartz. (1981). Response to long-term deferoxamine therapy in thalassemia. The Journal of Pediatrics. 99(5). 689–694. 30 indexed citations
14.
Poncz, Mortimer, Neville Colman, Victor Herbert, Elias Schwartz, & Alan R. Cohen. (1981). Therapy of congenital folate malabsorption. The Journal of Pediatrics. 98(1). 76–79. 29 indexed citations
15.
Cohen, Alan R., Alicejane L Markenson, & Elias Schwartz. (1980). Transfusion requirements and splenectomy in thalassemia major. The Journal of Pediatrics. 97(1). 100–102. 28 indexed citations
16.
Cohen, Alan R. & Elias Schwartz. (1978). Excretion of iron in response to deferoxamine in sickle cell anemia. The Journal of Pediatrics. 92(4). 659–662. 33 indexed citations
17.
Cohen, Alan R. & Elias Schwartz. (1978). Iron chelation therapy with deferoxamine in Cooley anemia. The Journal of Pediatrics. 92(4). 643–647. 23 indexed citations
18.
Kim, Haewon C., et al.. (1977). Globin biosynthesis in sickle cell, Hb SC, and Hb C diseases. The Journal of Pediatrics. 91(1). 13–18. 5 indexed citations
19.
Schwartz, Elias & Frances M. Gill. (1974). REGULATION OF HEMOGLOBIN SYNTHESIS IN β‐THALASSEMIA*. Annals of the New York Academy of Sciences. 232(1). 33–39. 1 indexed citations
20.
Schwartz, Elias, et al.. (1964). Treatment of painful crises of sickle cell disease. The Journal of Pediatrics. 64(1). 132–133. 12 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

Rankless by CCL
2026