Katrin Voß

2.6k total citations
9 papers, 1.1k citations indexed

About

Katrin Voß is a scholar working on Neurology, Hematology and Immunology. According to data from OpenAlex, Katrin Voß has authored 9 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Neurology, 3 papers in Hematology and 3 papers in Immunology. Recurrent topics in Katrin Voß's work include Platelet Disorders and Treatments (3 papers), Intracerebral and Subarachnoid Hemorrhage Research (3 papers) and Immune Cell Function and Interaction (3 papers). Katrin Voß is often cited by papers focused on Platelet Disorders and Treatments (3 papers), Intracerebral and Subarachnoid Hemorrhage Research (3 papers) and Immune Cell Function and Interaction (3 papers). Katrin Voß collaborates with scholars based in Germany, United Kingdom and United States. Katrin Voß's co-authors include Dietmar Todt, Henrik Brumm, Ireen Köllmer, Sonja Stahl, Ute Felbor, Alfredo Ramı́rez, Franz Rüschendorf, Khalid Al Aboud, Ivar von Kügelgen and Young‐Ae Lee and has published in prestigious journals such as Nature Genetics, Blood and Genome Research.

In The Last Decade

Katrin Voß

9 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Katrin Voß Germany	9	365	213	204	204	147	9	1.1k
Kazuko Koshiba‐Takeuchi Japan	19	1.9k 5.1×	119 0.6×	65 0.3×	159 0.8×	18 0.1×	27	2.2k
Tohru Tsukui Japan	18	2.2k 6.0×	68 0.3×	119 0.6×	181 0.9×	20 0.1×	28	2.6k
Juliette Albuisson France	14	975 2.7×	31 0.1×	34 0.2×	99 0.5×	46 0.3×	44	1.9k
Paul Scherz United States	11	2.0k 5.5×	39 0.2×	175 0.9×	466 2.3×	13 0.1×	36	2.6k
Eric B. Johnson United States	17	911 2.5×	38 0.2×	27 0.1×	84 0.4×	31 0.2×	25	1.5k
Christine Vincent France	19	1.5k 4.0×	104 0.5×	37 0.2×	196 1.0×	6 0.0×	27	2.0k
Giorgio Bernardi France	11	1.3k 3.4×	73 0.3×	14 0.1×	79 0.4×	24 0.2×	11	2.1k
Nicole Van Regemorter Belgium	24	1.2k 3.2×	135 0.6×	23 0.1×	96 0.5×	6 0.0×	57	2.0k
Mark C. Hanks United States	15	1.9k 5.2×	10 0.0×	104 0.5×	189 0.9×	20 0.1×	18	2.5k
Ruijin Huang Germany	28	1.7k 4.7×	12 0.1×	92 0.5×	277 1.4×	16 0.1×	61	2.2k

Countries citing papers authored by Katrin Voß

Since Specialization

Citations

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

Fields of papers citing papers by Katrin Voß

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Voß

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

All Works

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9 of 9 papers shown

Paul, Dirk S., Cornelis A. Albers, Augusto Rendon, et al.. (2013). Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci. Genome Research. 23(7). 1130–1141. 25 indexed citations

Nürnberg, Sylvia, Augusto Rendon, Peter A. Smethurst, et al.. (2012). A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site. Blood. 120(24). 4859–4868. 31 indexed citations

Albers, Cornelis A., Ana Cvejic, Rémi Favier, et al.. (2011). Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. Nature Genetics. 43(8). 735–737. 160 indexed citations

Voß, Katrin, Sonja Stahl, Benjamin M. Hogan, et al.. (2009). Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 protein. Human Mutation. 30(6). 1003–1011. 58 indexed citations

Stahl, Sonja, Katrin Voß, Oǧuzkan Sürücü, et al.. (2008). Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex. Human Mutation. 29(5). 709–717. 87 indexed citations

Pasternack, Sandra M., Ivar von Kügelgen, Khalid Al Aboud, et al.. (2008). G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. Nature Genetics. 40(3). 329–334. 298 indexed citations

Voß, Katrin, et al.. (2007). CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations. Neurogenetics. 8(4). 249–256. 134 indexed citations

Brandt, Jens van den, Katrin Voß, Melanie Schott, et al.. (2004). Inhibition of Notch signaling biases rat thymocyte development towards the NK cell lineage. European Journal of Immunology. 34(5). 1405–1413. 32 indexed citations

Brumm, Henrik, Katrin Voß, Ireen Köllmer, & Dietmar Todt. (2003). Acoustic communication in noise: regulation of call characteristics in a New World monkey. Journal of Experimental Biology. 207(3). 443–448. 227 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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