A. Buschmann

2.3k total citations
44 papers, 1.7k citations indexed

About

A. Buschmann is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, A. Buschmann has authored 44 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 16 papers in Neurology and 11 papers in Nutrition and Dietetics. Recurrent topics in A. Buschmann's work include Prion Diseases and Protein Misfolding (34 papers), Neurological diseases and metabolism (16 papers) and Trace Elements in Health (11 papers). A. Buschmann is often cited by papers focused on Prion Diseases and Protein Misfolding (34 papers), Neurological diseases and metabolism (16 papers) and Trace Elements in Health (11 papers). A. Buschmann collaborates with scholars based in Germany, France and Poland. A. Buschmann's co-authors include Martin H. Groschup, Martin Eiden, G. Erhardt, Gesine Lühken, Cristina Casalone, Anne-Gaëlle Biacabé, Jan Langeveld, Ute Ziegler, Christine Hoffmann and Bjoern Seidel and has published in prestigious journals such as PLoS ONE, Journal of Virology and Biochemical and Biophysical Research Communications.

In The Last Decade

A. Buschmann

40 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Buschmann Germany 22 1.6k 810 649 153 117 44 1.7k
Marion M. Simmons United Kingdom 22 1.5k 0.9× 750 0.9× 548 0.8× 156 1.0× 170 1.5× 74 1.6k
D. Drummond United Kingdom 7 1.5k 0.9× 660 0.8× 436 0.7× 68 0.4× 105 0.9× 9 1.6k
M. E. W. Vromans Serbia 8 1.1k 0.7× 474 0.6× 463 0.7× 148 1.0× 76 0.6× 8 1.1k
David Parnham United Kingdom 11 880 0.5× 306 0.4× 298 0.5× 111 0.7× 80 0.7× 14 947
J Chatelain France 13 773 0.5× 433 0.5× 328 0.5× 93 0.6× 33 0.3× 36 824
Timm Konold United Kingdom 18 932 0.6× 429 0.5× 374 0.6× 132 0.9× 106 0.9× 50 1.0k
Jean E. Jewell United States 14 1.1k 0.7× 367 0.5× 261 0.4× 68 0.4× 149 1.3× 23 1.1k
M. M. Simmons United Kingdom 17 896 0.6× 407 0.5× 411 0.6× 116 0.8× 76 0.6× 29 952
Cristina Acín Spain 17 591 0.4× 272 0.3× 336 0.5× 111 0.7× 51 0.4× 40 680
S. Jo Moore United Kingdom 18 661 0.4× 217 0.3× 263 0.4× 66 0.4× 82 0.7× 41 767

Countries citing papers authored by A. Buschmann

Since Specialization
Citations

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

Fields of papers citing papers by A. Buschmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Buschmann

This figure shows the co-authorship network connecting the top 25 collaborators of A. Buschmann. A scholar is included among the top collaborators of A. Buschmann 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 A. Buschmann. A. Buschmann 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.
Sachse, Steffi & A. Buschmann. (2016). (Sprach-)Diagnostische Möglichkeiten bei 2-Jährigen. Sprache · Stimme · Gehör. 40(2). 68–75. 1 indexed citations
2.
Polak, Mirosław P., Magdalena Larska, Jan Langeveld, et al.. (2009). Diagnosis of the first cases of scrapie in Poland. The Veterinary Journal. 186(1). 47–52. 14 indexed citations
3.
Ramljak, Sanja, Abdul R. Asif, Victor W. Armstrong, et al.. (2008). Physiological Role of the Cellular Prion Protein (PrPc): Protein Profiling Study in Two Cell Culture Systems. Journal of Proteome Research. 7(7). 2681–2695. 33 indexed citations
4.
Groschup, Martin H., Thomas Selhorst, A. Buschmann, Thomas C. Mettenleiter, & Franz J. Conraths. (2008). Bovine Spongiforme Enzephalopathie – gesundheitlicher Verbraucherschutz beginnt beim Tier. Journal of Consumer Protection and Food Safety. 3(2). 152–158.
5.
Lühken, Gesine, et al.. (2007). Microsatellites MCMA53 and MCMA16 on OAR15 are associated with susceptibility to atypical scrapie. Animal Genetics. 38(1). 88–89. 4 indexed citations
6.
Seidel, Bjoern, Achim Thomzig, A. Buschmann, et al.. (2007). Scrapie Agent (Strain 263K) Can Transmit Disease via the Oral Route after Persistence in Soil over Years. PLoS ONE. 2(5). e435–e435. 118 indexed citations
7.
Hoffmann, Christine, et al.. (2007). Prions spread via the autonomic nervous system from the gut to the central nervous system in cattle incubating bovine spongiform encephalopathy. Journal of General Virology. 88(3). 1048–1055. 97 indexed citations
8.
Seitz, Rainer, Johannes Blümel, Reinhard Bürger, et al.. (2007). Impact of vCJD on blood supply. Biologicals. 35(2). 79–97. 12 indexed citations
9.
Lühken, Gesine, et al.. (2006). Microsatellite CTSBJ12 is located distal to the ovine prion protein gene on OAR13 and is not associated with scrapie susceptibility. Animal Genetics. 37(4). 426–427. 2 indexed citations
10.
Lühken, Gesine, et al.. (2006). Epidemiological and genetical differences between classical and atypical scrapie cases. Veterinary Research. 38(1). 65–80. 84 indexed citations
11.
Eiden, Martin, et al.. (2006). Synthetic Prions. Journal of Veterinary Medicine Series B. 53(6). 251–256. 5 indexed citations
12.
Buschmann, A., Martin Eiden, Ute Ziegler, et al.. (2005). Strain Typing of German Transmissible Spongiform Encephalopathies Field Cases in Small Ruminants by Biochemical Methods. Journal of Veterinary Medicine Series B. 52(2). 55–63. 41 indexed citations
13.
Kuczius, Thorsten, A. Buschmann, Wenlan Zhang, et al.. (2004). Cellular prion protein acquires resistance to proteolytic degradation following copper ion binding. Biological Chemistry. 385(8). 739–47. 33 indexed citations
14.
Buschmann, A., et al.. (2003). [First description of scrapie in the free state of Bavaria--a case report].. PubMed. 116(3-4). 142–3. 1 indexed citations
15.
Vilotte, Jean-Luc, Solange Soulier, Daniel Vaiman, et al.. (2001). Markedly Increased Susceptibility to Natural Sheep Scrapie of Transgenic Mice Expressing Ovine PrP. Journal of Virology. 75(13). 5977–5984. 152 indexed citations
16.
Buschmann, A., et al.. (2000). Detection of cattle-derived BSE prions using transgenic mice overexpressing bovine PrPc. PubMed. 75–86. 44 indexed citations
17.
Vorberg, Ina, A. Buschmann, Silke S. Harmeyer, et al.. (1999). A Novel Epitope for the Specific Detection of Exogenous Prion Proteins in Transgenic Mice and Transfected Murine Cell Lines. Virology. 255(1). 26–31. 41 indexed citations
18.
Madec, Jean‐Yves, et al.. (1998). Sensitivity of the Western blot detection of prion protein PrPres in natural sheep scrapie. Journal of Virological Methods. 75(2). 169–177. 21 indexed citations
19.
Buschmann, A., et al.. (1998). Cellular Prion Proteins of Mammalian Species Display an Intrinsic Partial Proteinase K Resistance. Biochemical and Biophysical Research Communications. 253(3). 693–702. 25 indexed citations
20.
Buschmann, A., et al.. (1967). [On the problem of early arthrodesis in the management of calcaneal fractures].. PubMed. 38(10). 468–71. 1 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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