W. Schröter

2.5k total citations
121 papers, 1.8k citations indexed

About

W. Schröter is a scholar working on Physiology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, W. Schröter has authored 121 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Physiology, 40 papers in Pediatrics, Perinatology and Child Health and 27 papers in Genetics. Recurrent topics in W. Schröter's work include Erythrocyte Function and Pathophysiology (76 papers), Neonatal Health and Biochemistry (36 papers) and Hemoglobinopathies and Related Disorders (25 papers). W. Schröter is often cited by papers focused on Erythrocyte Function and Pathophysiology (76 papers), Neonatal Health and Biochemistry (36 papers) and Hemoglobinopathies and Related Disorders (25 papers). W. Schröter collaborates with scholars based in Germany, United States and France. W. Schröter's co-authors include Stefan Eber, Arnulf Pekrun, M. Lakomek, Wolfgang Tillmann, Christian Roth, Manfred Gahr, H. Winkler, F. Hanefeld, U. Leonhardt and B. Wilken and has published in prestigious journals such as Nature, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

W. Schröter

111 papers receiving 1.7k citations

Peers

W. Schröter

PHYSI

PPCH

GENET

PRM

HEMAT

K. G. Blume Germany

F.L.A. Willekens Netherlands

Cheryl A. Hillery United States

Ernst R. Jaffé United States

EA Rachmilewitz Israel

G Sansone Italy

O Platt United States

Melissa Wasserstein United States

J C Dreyfus France

Margaret M. McGovern United States

K. G. Blume Germany

W. Schröter

678 ×0.6

PHYSI

314 ×0.6

PPCH

140 ×0.3

GENET

166 ×0.5

PRM

199 ×0.5

HEMAT

Citations per year, relative to W. Schröter W. Schröter (= 1×) peers K. G. Blume

Countries citing papers authored by W. Schröter

Since Specialization

Citations

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

Fields of papers citing papers by W. Schröter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W. Schröter

This figure shows the co-authorship network connecting the top 25 collaborators of W. Schröter. A scholar is included among the top collaborators of W. Schröter 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 W. Schröter. W. Schröter 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

Pekrun, Arnulf, et al.. (2008). Diagnostik des Pyruvatkinase-Mangels bei erhöhter Retikulozytenzahl. DMW - Deutsche Medizinische Wochenschrift. 120(47). 1620–1624. 7 indexed citations

Eber, Stefan, et al.. (1999). Frequency of very late fatal sepsis after splenectomy for hereditary spherocytosis: impact of insufficient antibody response to pneumococcal infection. Annals of Hematology. 78(11). 524–528. 41 indexed citations

Reinhardt, Dirk, Dagmar Haase, Claudia Schoch, et al.. (1998). Hemoglobin F in myelodysplastic syndrome. Annals of Hematology. 76(3-4). 135–138. 21 indexed citations

Braun, Felix, Ekkehard Schütz, Uwe Christians, et al.. (1997). Pitfalls in Monitoring Tacrolimus (FK 506). Therapeutic Drug Monitoring. 19(6). 628–631. 18 indexed citations

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

Eber, Stefan, Jennifer M. Reingle González, Marcia L. Lux, et al.. (1996). Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nature Genetics. 13(2). 214–218. 169 indexed citations

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

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

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

10.

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

11.

Ullrich, D., et al.. (1990). Low Fractions of Mono- and Diconjugated Bilirubin in Patients with β-Thalassemia. Journal of Pediatric Gastroenterology and Nutrition. 11(1). 21–26. 2 indexed citations

12.

Neubauer, Bernd A., Stefan Eber, M. Lakomek, Manfred Gahr, & W. Schröter. (1990). Combination of Congenital Nonspherocytic Haemolytic Anaemia and Impairment of Granulocyte Function in Severe Glucosephosphate Isomerase Deficiency. Acta Haematologica. 83(4). 206–210. 11 indexed citations

13.

Schröter, W., et al.. (1989). [Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia].. PubMed. 137(7). 368–79.

14.

Lakomek, M., et al.. (1989). Erythrocyte pyruvate kinase deficiency: A kinetic method for differentiation between heterozygosity and compound‐heterozygosity. American Journal of Hematology. 31(4). 225–232. 7 indexed citations

15.

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

16.

Schröter, W., et al.. (1983). Diagnosis of hereditary spherocytosis in newborn infants. The Journal of Pediatrics. 103(3). 460–463. 29 indexed citations

17.

Schröter, W., et al.. (1977). [Pyrivate kinase deficiency. II. Biochemical studies (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 125(7). 713–9. 2 indexed citations

18.

Schröter, W.. (1972). [Intracellular bilirubin transport and the membrane of the hepatic endoplasmic reticulum: new aspects in the development of transitory bilirubinemia of the newborn].. PubMed. 120(3). 119–22.

19.

Schröter, W., et al.. (1970). Membrane-bound 2,3-diphosphoglycerate phosphatase of human erythrocytes. The Journal of Membrane Biology. 2(1). 31–40. 7 indexed citations

20.

Schröter, W.. (1970). 2,3-Diphosphoglyceratstoffwechsel und 2,3-diphosphoglyceratmutase-mangel in erythrozyten. Annals of Hematology. 20(5). 311–316. 3 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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