F. Schunter

1.5k total citations
39 papers, 1.0k citations indexed

About

F. Schunter is a scholar working on Hematology, Immunology and Physiology. According to data from OpenAlex, F. Schunter has authored 39 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Hematology, 11 papers in Immunology and 10 papers in Physiology. Recurrent topics in F. Schunter's work include Blood groups and transfusion (14 papers), Erythrocyte Function and Pathophysiology (8 papers) and Blood disorders and treatments (7 papers). F. Schunter is often cited by papers focused on Blood groups and transfusion (14 papers), Erythrocyte Function and Pathophysiology (8 papers) and Blood disorders and treatments (7 papers). F. Schunter collaborates with scholars based in Germany, United States and Austria. F. Schunter's co-authors include Thomas Müller, Christoph Gassner, Willy A. Flegel, Franz F. Wagner, Diether Schönitzer, Peter Wernet, Nicole I. Eicher, S. Bissbort, Hans Wigzell and Andreas Ziegler and has published in prestigious journals such as Blood, Journal of Clinical Microbiology and Human Genetics.

In The Last Decade

F. Schunter

36 papers receiving 976 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. Schunter Germany	12	799	571	326	195	148	39	1.0k
G.L. Daniels United Kingdom	17	644 0.8×	535 0.9×	229 0.7×	179 0.9×	157 1.1×	36	949
M.A.M. Overbeeke Netherlands	23	1.3k 1.6×	825 1.4×	329 1.0×	291 1.5×	152 1.0×	54	1.5k
Christine Lomas‐Francis United States	18	1.3k 1.7×	1.1k 1.9×	287 0.9×	531 2.7×	121 0.8×	98	1.6k
Kenichi Ogasawara Japan	17	869 1.1×	580 1.0×	208 0.6×	283 1.5×	60 0.4×	61	1.0k
H.‐H. Sonneborn Germany	15	321 0.4×	298 0.5×	97 0.3×	73 0.4×	125 0.8×	43	786
Joseph J. Burge United States	11	234 0.3×	134 0.2×	48 0.1×	116 0.6×	553 3.7×	17	798
Britt Thuresson Sweden	12	276 0.3×	197 0.3×	55 0.2×	68 0.3×	82 0.6×	23	412
Benoît Vingert France	17	224 0.3×	151 0.3×	60 0.2×	164 0.8×	460 3.1×	39	916
T Shibuya Japan	12	235 0.3×	37 0.1×	129 0.4×	116 0.6×	183 1.2×	30	568
M. Alcorn United Kingdom	14	420 0.5×	27 0.0×	130 0.4×	139 0.7×	144 1.0×	23	678

Countries citing papers authored by F. Schunter

Since Specialization

Citations

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

Fields of papers citing papers by F. Schunter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Schunter

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

All Works

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20 of 20 papers shown

1.

Petershofen, Eduard K., et al.. (2002). RHCE‐D‐CEhybrid genes can cause false‐negative DNA typing of the Rh e antigen. Vox Sanguinis. 83(3). 268–272. 3 indexed citations

2.

Metzner, Bernd, Wolfgang Gebauer, Thomas Müller, et al.. (2002). Späte infektiöse Komplikationen nach Hochdosistherapie und autologer Blutstammzelltransplantation. Medizinische Klinik. 97(11). 650–658. 2 indexed citations

3.

Müller, Thomas, Franz F. Wagner, Nicole I. Eicher, et al.. (2001). PCR screening for common weak D types shows different distributions in three Central European populations. Transfusion. 41(1). 45–52. 83 indexed citations

4.

Gassner, Christoph, et al.. (2000). Fy ^x is associated with two missense point mutations in its gene and can be detected by PCR–SSP. Immunohematology. 16(2). 61–67. 19 indexed citations

5.

Wagner, Franz F., Christoph Gassner, Thomas Müller, et al.. (1999). Molecular Basis of Weak D Phenotypes. Blood. 93(1). 385–393. 258 indexed citations

6.

Wagner, Franz F., Christoph Gassner, Thomas Müller, et al.. (1998). Three Molecular Structures Cause Rhesus D Category VI Phenotypes With Distinct Immunohematologic Features. Blood. 91(6). 2157–2168. 92 indexed citations

7.

Wagner, Franz F., Christoph Gassner, Thomas Müller, et al.. (1998). Three Molecular Structures Cause Rhesus D Category VI Phenotypes With Distinct Immunohematologic Features. Blood. 91(6). 2157–2168. 28 indexed citations

8.

Müller, Thomas, et al.. (1997). Genotyping of the Human Platelet Antigen‐1 by ELISA Detection of Allele – Specific Amplicons. Vox Sanguinis. 73(3). 185–188. 6 indexed citations

9.

Müller, Thomas, et al.. (1997). Manual and automated methods for the determination of leukocyte counts at extreme low levels: Comparative evaluation of the Nageotte chamber and the abbott cell dyn 3500 analyser. Transfusion Science. 18(4). 505–515. 12 indexed citations

10.

Sonneborn, H.‐H., Willy A. Flegel, P. Kühnl, et al.. (1992). Results of the DGTI Workshop on the Evaluation of the Reactivity of Monoclonal Anti-D. Transfusion Medicine and Hemotherapy. 19(1). 12–16. 6 indexed citations

11.

Kloor, Doris, et al.. (1988). Human factor H (?1H-globulin): linkage analysis. Human Genetics. 79(2). 181–182. 1 indexed citations

12.

Caspari, G., et al.. (1987). HIV-specific antibody among voluntary blood donors in lower saxony (FRG). Annals of Hematology. 55(3). 181–187. 6 indexed citations

13.

Schunter, F., et al.. (1985). Linkage between the loci for mitochondrial malic enzyme (ME2) and coagulation factor XIIIA subunit (F13A). Human Genetics. 70(1). 43–44. 9 indexed citations

14.

Wilms, K., H. Link, Philippe Meyer, et al.. (1982). Knochenmarktransplantation bei Patienten mit Leukämien. Journal of Molecular Medicine. 60(20). 1279–1287. 12 indexed citations

15.

Schunter, F., et al.. (1978). Mapping of the linkage group GLO-Bf-HLA-B, C, A-PGM3. Human Genetics. 44(3). 321–331. 3 indexed citations

16.

Bissbort, S., et al.. (1978). Mapping of the linkage group GLO-Bf-HLA-B,C,A-PGM3. Human Genetics. 44(3). 313–319. 4 indexed citations

17.

Schunter, F., et al.. (1977). Apparent Lack of Gene Dosage Effect in the PLT Assay. Scandinavian Journal of Immunology. 6(5). 529–532. 3 indexed citations

18.

Bissbort, S., et al.. (1976). Confirmation of linkage between the loci for HL-A and glyoxalase I. Human Genetics. 32(2). 197–198. 22 indexed citations

19.

Schunter, F., et al.. (1974). [HL-A antigens in common psoriasis].. PubMed. 25(2). 82–3. 6 indexed citations

20.

Schneider, Wilhelm, et al.. (1972). [Extension of survival time of washed erythrocyte sediments in vivo by using an adequate washing solution].. PubMed. 23(11). 368–9. 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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