Orah S. Platt

9.6k total citations · 3 hit papers
36 papers, 6.0k citations indexed

About

Orah S. Platt is a scholar working on Genetics, Hematology and Genetics. According to data from OpenAlex, Orah S. Platt has authored 36 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Hematology and 8 papers in Genetics. Recurrent topics in Orah S. Platt's work include Hemoglobinopathies and Related Disorders (20 papers), Iron Metabolism and Disorders (11 papers) and Erythrocyte Function and Pathophysiology (6 papers). Orah S. Platt is often cited by papers focused on Hemoglobinopathies and Related Disorders (20 papers), Iron Metabolism and Disorders (11 papers) and Erythrocyte Function and Pathophysiology (6 papers). Orah S. Platt collaborates with scholars based in United States, France and Italy. Orah S. Platt's co-authors include Wendell F. Rosse, Donald Brambilla, Paul Milner, Panpit Klug, Martin H. Steinberg, Oswaldo Castro, Thomas R. Kinney, Elliott Vichinsky, Mark A. Espeland and Bai-Lin Wu and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Orah S. Platt

36 papers receiving 5.8k citations

Hit Papers

Mortality In Sickle Cell Disease -- Life Expectancy and R... 1991 2026 2002 2014 1994 1991 2008 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Orah S. Platt United States 19 4.2k 3.2k 1.5k 1.2k 1.1k 36 6.0k
Lynn R. Goldin United States 54 2.6k 0.6× 2.0k 0.6× 110 0.1× 2.7k 2.3× 2.4k 2.1× 192 8.6k
Michael J. Noetzel United States 29 783 0.2× 614 0.2× 765 0.5× 498 0.4× 576 0.5× 71 3.0k
Steven G. Pavlakis United States 32 752 0.2× 677 0.2× 564 0.4× 1.7k 1.5× 196 0.2× 89 4.1k
Jane Worthington United Kingdom 56 819 0.2× 1.1k 0.3× 104 0.1× 1.8k 1.5× 1.9k 1.7× 215 9.7k
Giulio Genovese United States 33 859 0.2× 305 0.1× 242 0.2× 2.6k 2.2× 1.8k 1.6× 67 6.8k
Josué Feingold France 34 336 0.1× 262 0.1× 438 0.3× 1.3k 1.1× 791 0.7× 89 3.8k
Sandra J. Hasstedt United States 41 407 0.1× 522 0.2× 292 0.2× 1.3k 1.1× 1.5k 1.3× 120 4.7k
Peter Clark United Kingdom 31 260 0.1× 1.8k 0.6× 616 0.4× 371 0.3× 164 0.1× 74 4.0k
Walter Hader Canada 36 574 0.1× 191 0.1× 852 0.6× 616 0.5× 253 0.2× 101 5.4k
Martin O. Savage United Kingdom 57 447 0.1× 261 0.1× 1.5k 1.0× 2.7k 2.2× 3.4k 3.0× 268 12.8k

Countries citing papers authored by Orah S. Platt

Since Specialization
Citations

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

Fields of papers citing papers by Orah S. Platt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Orah S. Platt. 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 Orah S. Platt. The network helps show where Orah S. Platt may publish in the future.

Co-authorship network of co-authors of Orah S. Platt

This figure shows the co-authorship network connecting the top 25 collaborators of Orah S. Platt. A scholar is included among the top collaborators of Orah S. Platt 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 Orah S. Platt. Orah S. Platt 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.
Bao, Erik L., Caleb A. Lareau, Carlo Brugnara, et al.. (2019). Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort. American Journal of Hematology. 94(5). 522–527. 4 indexed citations
2.
Yu, Yongguo, Haitao Zhu, David T. Miller, et al.. (2011). Age- and gender-dependent obesity in individuals with 16p11.2 deletion. Journal of genetics and genomics. 38(9). 403–409. 14 indexed citations
3.
Dai, Pu, Qi Li, Deliang Huang, et al.. (2008). SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss. Genetics in Medicine. 10(8). 586–592. 51 indexed citations
4.
Weiss, Lauren A., Yiping Shen, Joshua M. Korn, et al.. (2008). Association between Microdeletion and Microduplication at 16p11.2 and Autism. New England Journal of Medicine. 358(7). 667–675. 1100 indexed citations breakdown →
5.
Platt, Orah S.. (2006). Prevention and Management of Stroke in Sickle Cell Anemia. Hematology. 2006(1). 54–57. 31 indexed citations
6.
Peters, Luanne L., Weidong Zhang, Amy J. Lambert, et al.. (2005). Quantitative trait loci for baseline white blood cell count, platelet count, and mean platelet volume. Mammalian Genome. 16(10). 749–763. 23 indexed citations
7.
Sonis, Andrew L., et al.. (2005). Acquisition of mutans streptococci and caries prevalence in pediatric sickle cell anemia patients receiving long-term antibiotic therapy.. PubMed. 27(3). 186–90. 37 indexed citations
8.
Wu, Bai‐Lin, Margaret A. Kenna, Va Lip, Mira Irons, & Orah S. Platt. (2003). Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness. American Journal of Medical Genetics Part A. 121A(2). 102–108. 29 indexed citations
9.
Zhang, Yuxun, et al.. (2003). Human Erythrocyte Membrane Band 3 Protein Influences Hemoglobin Cooperativity. Journal of Biological Chemistry. 278(41). 39565–39571. 16 indexed citations
10.
Wu, Bai-Lin, Neal I. Lindeman, Va Lip, et al.. (2002). Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing. Genetics in Medicine. 4(4). 279–288. 57 indexed citations
11.
Brugnara, Carlo, David Zelmanovic, Martin Sorette, Samir K. Ballas, & Orah S. Platt. (1997). Reticulocyte Hemoglobin:An Integrated Parameter for Evaluation of Erythropoietic Activity. American Journal of Clinical Pathology. 108(2). 133–142. 60 indexed citations
12.
Platt, Orah S.. (1995). Sickle cell paths converge on hydroxyurea. Nature Medicine. 1(4). 307–308. 9 indexed citations
13.
Rifai, Nader, Masayuki Sakamoto, Orah S. Platt, & Carlo Brugnara. (1995). A High-Performance Liquid Chromatographic Assay for the Determination of Itraconazole Concentration Using Solid-Phase Extraction and Small Sample Volume. Therapeutic Drug Monitoring. 17(5). 522–525. 18 indexed citations
14.
Brugnara, Carlo, Lucia De Franceschi, C. C. Armsby, et al.. (1995). A New Therapeutic Approach for Sickle Cell Disease. Annals of the New York Academy of Sciences. 763(1). 262–271. 20 indexed citations
15.
Platt, Orah S., Donald Brambilla, Wendell F. Rosse, et al.. (1994). Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death. New England Journal of Medicine. 330(23). 1639–1644. 2458 indexed citations breakdown →
16.
Platt, Orah S., Donald Brambilla, Paul Milner, et al.. (1991). Pain in Sickle Cell Disease. New England Journal of Medicine. 325(1). 11–16. 1213 indexed citations breakdown →
17.
Espeland, Mark A., et al.. (1990). Reliability of Tanner stage assessments in a multi‐center study. American Journal of Human Biology. 2(5). 503–510. 8 indexed citations
18.
Espeland, Mark A., Orah S. Platt, & Dianne Gallagher. (1989). Joint Estimation of Incidence and Diagnostic Error Rates from Irregular Longitudinal Data. Journal of the American Statistical Association. 84(408). 972–979. 26 indexed citations
19.
Sosenko, Jay M., Rudolf Flückiger, Orah S. Platt, & Kenneth H. Gabbay. (1980). Glycosylation of Variant Hemoglobins in Normal and Diabetic Subjects. Diabetes Care. 3(5). 590–593. 29 indexed citations
20.
Glader, Bertil & Orah S. Platt. (1978). Haemolytic Disorders of Infancy. Clinics in Haematology. 7(1). 35–61. 9 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.

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