Stefan Eber

3.9k total citations
96 papers, 2.6k citations indexed

About

Stefan Eber is a scholar working on Physiology, Pediatrics, Perinatology and Child Health and Hematology. According to data from OpenAlex, Stefan Eber has authored 96 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Physiology, 30 papers in Pediatrics, Perinatology and Child Health and 26 papers in Hematology. Recurrent topics in Stefan Eber's work include Erythrocyte Function and Pathophysiology (48 papers), Neonatal Health and Biochemistry (20 papers) and Blood properties and coagulation (17 papers). Stefan Eber is often cited by papers focused on Erythrocyte Function and Pathophysiology (48 papers), Neonatal Health and Biochemistry (20 papers) and Blood properties and coagulation (17 papers). Stefan Eber collaborates with scholars based in Germany, United States and France. Stefan Eber's co-authors include W. Schröter, Samuel E. Lux, Arnulf Pekrun, Wolfgang K.G. Krietsch, Manfred Gahr, M. Lakomek, Alberto Zanella, Peter A. Lane, Gordon W. Stewart and Brian D. Smith and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Stefan Eber

91 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefan Eber Germany 29 1.4k 733 640 631 596 96 2.6k
Rina Zaizov Israel 33 676 0.5× 740 1.0× 935 1.5× 668 1.1× 357 0.6× 185 3.5k
Ruth Andrea Seeler United States 25 302 0.2× 611 0.8× 813 1.3× 377 0.6× 434 0.7× 93 2.3k
Linda R. Bressler United States 18 386 0.3× 516 0.7× 502 0.8× 288 0.5× 247 0.4× 38 2.6k
Paul Martin United States 27 407 0.3× 432 0.6× 985 1.5× 225 0.4× 262 0.4× 109 3.1k
Bertil Glader United States 30 674 0.5× 694 0.9× 1.4k 2.2× 239 0.4× 365 0.6× 131 4.6k
Stephen H. Embury United States 28 652 0.5× 3.7k 5.1× 2.9k 4.5× 273 0.4× 850 1.4× 52 4.7k
Kenichi Koike Japan 28 302 0.2× 314 0.4× 789 1.2× 171 0.3× 178 0.3× 158 2.5k
Wolf W. Zuelzer United States 30 398 0.3× 760 1.0× 1.0k 1.6× 223 0.4× 751 1.3× 101 2.6k
Peter Soothill United Kingdom 36 259 0.2× 203 0.3× 666 1.0× 473 0.7× 2.7k 4.6× 133 4.2k
J. Lawrence Naiman United States 20 333 0.2× 197 0.3× 443 0.7× 171 0.3× 325 0.5× 56 1.6k

Countries citing papers authored by Stefan Eber

Since Specialization
Citations

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

Fields of papers citing papers by Stefan Eber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefan Eber

This figure shows the co-authorship network connecting the top 25 collaborators of Stefan Eber. A scholar is included among the top collaborators of Stefan Eber 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 Stefan Eber. Stefan Eber 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.
Koenig, Mary Dawn, et al.. (2025). Anemia, Growth Impairment, and Micronutrients Status in Syrian Children Aged 12–60 Months. International Journal of Pediatrics. 2025(1). 6172527–6172527.
2.
3.
Boscoe, Audra, Elizabeth Hedgeman, Eduard J. van Beers, et al.. (2020). Comorbidities and complications in adults with pyruvate kinase deficiency. European Journal Of Haematology. 106(4). 484–492. 17 indexed citations
4.
Andrés, Oliver, Stefan Eber, & Christian P. Speer. (2015). Early postnatal diagnosis of hereditary spherocytosis by combining light microscopy, acidified glycerol lysis test and eosin-5′-maleimide binding assay. Annals of Hematology. 94(12). 1959–1964. 6 indexed citations
5.
Eber, Stefan, Ulrich Germing, H. Heimpel, et al.. (2013). Prävention von Infektionen und Thrombosen nach Splenektomie oder funktioneller Asplenie. Kinder- und Jugendmedizin. 13(3). 197–205. 2 indexed citations
6.
Mittler, U., et al.. (2006). Near‐total splenectomy for hereditary spherocytosis: clinical prospects in relation to disease severity. British Journal of Haematology. 132(6). 791–793. 22 indexed citations
7.
8.
Eber, Stefan, et al.. (2001). Infektionsprophylaxe bei Asplenie. Klinische Pädiatrie. 213(S1). A84–A87. 6 indexed citations
9.
Neerman‐Arbez, Marguerite, Philippe de Moerloose, Christine A. Biron, et al.. (2001). Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. Human Genetics. 108(3). 237–240. 56 indexed citations
10.
Jäckel, Martin C., Olaf Witt, Stefan Eber, Helmut Eiffert, & Rainer Laskawi. (1999). Die postoperative antibiotische Therapie von zervikalen Lymphadenitiden durch nichttuberkulöse, atypische Mykobakterien*. Laryngo-Rhino-Otologie. 78(8). 450–454. 2 indexed citations
11.
Willig, Thiébaut-Noël, Thierry Leblanc, Christian Tiemann, et al.. (1999). Identification of New Prognosis Factors from the Clinical and Epidemiologic Analysis of a Registry of 229 Diamond-Blackfan Anemia Patients. Pediatric Research. 46(5). 553–553. 129 indexed citations
12.
Roth, Christian, Arnulf Pekrun, Hubertus Jarry, et al.. (1997). Short stature and failure of pubertal development in thalassaemia major: evidence for hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotropin secretion. European Journal of Pediatrics. 156(10). 777–783. 82 indexed citations
13.
Pekrun, Arnulf, Bernd A. Neubauer, Stefan Eber, et al.. (1995). Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosis. Clinical Genetics. 47(4). 175–179. 15 indexed citations
14.
Eber, Stefan, et al.. (1992). Prevalence of increased osmotic fragility of erythrocytes in German blood donors: Screening using a modified glycerol lysis test. Annals of Hematology. 64(2). 88–92. 73 indexed citations
15.
Eber, Stefan, et al.. (1992). Absence of phosphorylation-induced gelation of erythrocyte membrane skeletons: A diagnostic tool for hereditary spherocytosis. Annals of Hematology. 64(2). 93–96. 1 indexed citations
16.
Eber, Stefan, et al.. (1991). Saethre‐Chotzen syndrome (ACS III) in four generations. Clinical Genetics. 40(4). 271–276. 8 indexed citations
17.
Eber, Stefan, et al.. (1990). Variable clinical severity of hereditary spherocytosis: Relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis. The Journal of Pediatrics. 117(3). 409–416. 105 indexed citations
18.
Pekrun, Arnulf, Stefan Eber, & W. Schr�ter. (1989). G6PD Avenches and G6PD Moosburg: biochemical and erythrocyte membrane characterization. Annals of Hematology. 58(1). 11–14. 4 indexed citations
19.
Eber, Stefan, Stephen Morris, W. Schröter, & Walter Gratzer. (1988). Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.. Journal of Clinical Investigation. 81(2). 523–530. 23 indexed citations
20.
Krietsch, Wolfgang K.G., et al.. (1979). Multiple forms of human phosphoglycerate kinase. Archives of Biochemistry and Biophysics. 193(2). 415–421. 7 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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