S. Krey

568 total citations
7 papers, 395 citations indexed

About

S. Krey is a scholar working on Hematology, Genetics and Immunology. According to data from OpenAlex, S. Krey has authored 7 papers receiving a total of 395 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Hematology, 2 papers in Genetics and 2 papers in Immunology. Recurrent topics in S. Krey's work include Platelet Disorders and Treatments (5 papers), Blood groups and transfusion (3 papers) and Hemophilia Treatment and Research (3 papers). S. Krey is often cited by papers focused on Platelet Disorders and Treatments (5 papers), Blood groups and transfusion (3 papers) and Hemophilia Treatment and Research (3 papers). S. Krey collaborates with scholars based in Germany, United States and Switzerland. S. Krey's co-authors include Reinhard Schneppenheim, Ulrich Budde, Frauke Bergmann, E. Drewke, T J Kunicki, Jerry Ware, Jacqueline Brassard, Andreas Gal, Lars Holmberg and Michael J. Denton and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and Thrombosis and Haemostasis.

In The Last Decade

S. Krey

7 papers receiving 376 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Krey Germany	7	325	64	63	63	59	7	395
Paula M. Jacobi United States	10	316 1.0×	103 1.6×	85 1.3×	62 1.0×	49 0.8×	18	427
S.J. Shattil United States	6	198 0.6×	16 0.3×	75 1.2×	38 0.6×	72 1.2×	7	356
Annika de Jong Netherlands	9	158 0.5×	34 0.5×	120 1.9×	38 0.6×	49 0.8×	16	294
Nicola Hellen United Kingdom	9	89 0.3×	15 0.2×	199 3.2×	51 0.8×	46 0.8×	13	340
Akio Kanzaki Japan	14	120 0.4×	60 0.9×	150 2.4×	30 0.5×	78 1.3×	34	547
Rosanne Rabinowitz United States	5	285 0.9×	67 1.0×	20 0.3×	41 0.7×	46 0.8×	5	387
Scott W. Boyer United States	8	238 0.7×	19 0.3×	154 2.4×	267 4.2×	25 0.4×	10	482
Martijn A. van der Ent United States	5	46 0.1×	11 0.2×	93 1.5×	35 0.6×	11 0.2×	7	194
Katsuyoshi Kanemoto Japan	10	49 0.2×	66 1.0×	203 3.2×	22 0.3×	22 0.4×	21	362
Alberto Del Monte-Monge Spain	6	132 0.4×	10 0.2×	130 2.1×	191 3.0×	16 0.3×	9	361

Countries citing papers authored by S. Krey

Since Specialization

Citations

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

Fields of papers citing papers by S. Krey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Krey

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

All Works

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7 of 7 papers shown

1.

Federici, Augusto B., Ulrich Budde, Giancarlo Castaman, et al.. (2000). Von Willebrand Disease Type 2M “Vicenza” in Italian and German Patients: Identification of the First Candidate Mutation (G3864A; R1205H) in 8 Families. Thrombosis and Haemostasis. 83(1). 136–140. 53 indexed citations

2.

Aumann, V., Frauke Bergmann, U. Budde, et al.. (1996). Prevalence of factor V Leiden in children with thrombo-embolism. European Journal of Pediatrics. 155(12). 1009–1014. 52 indexed citations

3.

Schneppenheim, Reinhard, Ulrich Budde, S. Krey, et al.. (1996). Results of a Screening for von Willebrand Disease Type 2N in Patients with Suspected Haemophilia A or von Willebrand Disease Type 1. Thrombosis and Haemostasis. 76(4). 598–602. 55 indexed citations

4.

Schneppenheim, Reinhard, Jacqueline Brassard, S. Krey, et al.. (1996). Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.. Proceedings of the National Academy of Sciences. 93(8). 3581–3586. 62 indexed citations

5.

Schneppenheim, Reinhard, et al.. (1995). Identification of a candidate missense mutation in a family with von Willebrand disease type IIC. Human Genetics. 95(6). 681–6. 41 indexed citations

6.

Schneppenheim, Reinhard, S. Krey, Frauke Bergmann, et al.. (1994). Genetic heterogeneity of severe von Willebrand disease type III in the German population. Human Genetics. 94(6). 640–52. 77 indexed citations

7.

Denton, Michael J., et al.. (1993). Autosomal dominant ‘sector’ retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin. Human Molecular Genetics. 2(6). 813–814. 55 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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