R. D. Koler

1.3k total citations
25 papers, 1.0k citations indexed

About

R. D. Koler is a scholar working on Physiology, Genetics and Molecular Biology. According to data from OpenAlex, R. D. Koler has authored 25 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 8 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in R. D. Koler's work include Erythrocyte Function and Pathophysiology (10 papers), Hemoglobinopathies and Related Disorders (8 papers) and Neonatal Health and Biochemistry (5 papers). R. D. Koler is often cited by papers focused on Erythrocyte Function and Pathophysiology (10 papers), Hemoglobinopathies and Related Disorders (8 papers) and Neonatal Health and Biochemistry (5 papers). R. D. Koler collaborates with scholars based in United States, Czechia and Hungary. R. D. Koler's co-authors include Richard T. Jones, R. Bigley, James F. Fitzgibbons, J. R. Samples, Mary K. Wirtz, Ted S. Acott, P. L. Kramer, Demetrios A. Rigas, J. Rick Topinka and Susan R. Hollán and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

R. D. Koler

25 papers receiving 923 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. D. Koler United States 15 366 255 250 236 207 25 1.0k
R.S. Sparkes United States 16 484 1.3× 373 1.5× 84 0.3× 85 0.4× 48 0.2× 32 978
Michele R. Filling‐Katz United States 13 294 0.8× 99 0.4× 369 1.5× 61 0.3× 88 0.4× 22 908
Leena Peltonen Finland 8 295 0.8× 311 1.2× 155 0.6× 43 0.2× 76 0.4× 9 935
Kyung Chin United States 17 480 1.3× 77 0.3× 266 1.1× 408 1.7× 64 0.3× 28 1.3k
Kiyoko Tanaka Japan 20 514 1.4× 114 0.4× 116 0.5× 41 0.2× 65 0.3× 40 1.2k
Adriano Angioni Italy 21 739 2.0× 435 1.7× 51 0.2× 115 0.5× 60 0.3× 56 1.3k
Marjolein Kriek Netherlands 19 773 2.1× 607 2.4× 59 0.2× 133 0.6× 55 0.3× 31 1.4k
Sophie Valleix France 19 603 1.6× 253 1.0× 147 0.6× 33 0.1× 82 0.4× 50 1.0k
Géraldine Mollet France 15 538 1.5× 377 1.5× 54 0.2× 82 0.3× 99 0.5× 24 1.0k
S.A. Whitmore Australia 18 536 1.5× 255 1.0× 153 0.6× 46 0.2× 114 0.6× 26 1.3k

Countries citing papers authored by R. D. Koler

Since Specialization
Citations

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

Fields of papers citing papers by R. D. Koler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. D. Koler. 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 R. D. Koler. The network helps show where R. D. Koler may publish in the future.

Co-authorship network of co-authors of R. D. Koler

This figure shows the co-authorship network connecting the top 25 collaborators of R. D. Koler. A scholar is included among the top collaborators of R. D. Koler 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 R. D. Koler. R. D. Koler 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.
Wirtz, Mary K., J. R. Samples, P. L. Kramer, et al.. (1997). Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.. PubMed. 60(2). 296–304. 168 indexed citations
2.
Wirtz, Mary K., J. R. Samples, P. L. Kramer, et al.. (1996). Weill-Marchesani syndrome - possible linkage of the autosomal dominant form to 15q21.1. American Journal of Medical Genetics. 65(1). 68–75. 31 indexed citations
3.
Coetzer, Thérèsa L., Kenneth E. Sahr, Josef T. Prchal, et al.. (1991). Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.. Journal of Clinical Investigation. 88(3). 743–749. 46 indexed citations
4.
Godfrey, Maurice, Victor Menashe, Richard G. Weleber, et al.. (1990). Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families.. PubMed. 46(4). 652–60. 71 indexed citations
5.
Weatherall, D. J., Douglas R. Higgs, C Bunch, et al.. (1981). Hemoglobin H Disease and Mental Retardation. New England Journal of Medicine. 305(11). 607–612. 109 indexed citations
6.
Jones, Gail, Jan S. Peterson, John M. Bissonnette, et al.. (1980). Postnatal regulation of canine oxygen delivery: erythrocyte components affecting Hb function. American Journal of Physiology-Heart and Circulatory Physiology. 238(1). H73–H79. 6 indexed citations
7.
Koler, R. D., et al.. (1980). Physiologic and Genetic Alterations in Human Red Cell DPGM. Hemoglobin. 4(5-6). 593–600. 1 indexed citations
8.
Black, J.A., Marvin B. Rittenberg, R. Bigley, & R. D. Koler. (1979). Hemolytic anemia due to pyruvate kinase deficiency: characterization of the enzymatic activity from eight patients.. PubMed. 31(3). 300–10. 16 indexed citations
9.
Fitzgibbons, James F., R. D. Koler, & Richard T. Jones. (1976). Red cell age-related changes of hemoglobins AIa+b and AIc in normal and diabetic subjects.. Journal of Clinical Investigation. 58(4). 820–824. 140 indexed citations
10.
Dhindsa, Dharam S., J.A. Black, R. D. Koler, et al.. (1976). Respiratory characteristics of blood from Basenji dogs with classical erythrocyte pyruvate kinase deficiency. Respiration Physiology. 26(1). 65–75. 9 indexed citations
11.
Magenis, R.E., et al.. (1975). Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2.. Proceedings of the National Academy of Sciences. 72(11). 4526–4530. 34 indexed citations
12.
Bigley, R., R. D. Koler, & R. Richterich. (1974). Regulatory Properties of Three Human Pyruvate Kinases. Enzyme. 17(5). 297–306. 3 indexed citations
13.
Hollán, Susan R., Richard T. Jones, & R. D. Koler. (1972). Duplication of haemoglobin genes. Biochimie. 54(5-6). 639–648. 10 indexed citations
14.
Koler, R. D., et al.. (1971). Genetics of haemoglobin H and α‐thalassaemia. Annals of Human Genetics. 34(4). 371–377. 11 indexed citations
15.
Bigley, R. & R. D. Koler. (1968). Liver pyruvate kinase (PK) isozymes in a PK‐deficient patient*. Annals of Human Genetics. 31(4). 383–388. 45 indexed citations
16.
Hecht, Frederick, Richard T. Jones, & R. D. Koler. (1968). Newborn infants with Hb Portland 1, an indicator of α‐chain deficiency. Annals of Human Genetics. 31(3). 215–218. 21 indexed citations
17.
Bigley, R., et al.. (1968). Tissue Distribution of Human Pyruvate Kinase Isozymes. Enzymologia biologica et clinica. 9(1). 10–20. 61 indexed citations
18.
Koler, R. D., et al.. (1964). Pyruvate Kinase: Molecular Differences Between Human Red Cell and Leukocyte Enzyme. Cold Spring Harbor Symposia on Quantitative Biology. 29(0). 213–221. 32 indexed citations
19.
Donnell, George N., R. D. Koler, & Susan M. Smith. (1963). Studies on linkage between Galactosaemia and the blood groups. Annals of Human Genetics. 27(2). 125–142. 1 indexed citations
20.
Rigas, Demetrios A. & R. D. Koler. (1961). Erythrocyte enzymes and reduced glutathione (GSH) in hemoglobin H disease: relation to cell age and denaturation of hemoglobin H.. PubMed. 58. 417–24. 33 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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