Katrin Bürk

6.8k total citations
73 papers, 3.7k citations indexed

About

Katrin Bürk is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Katrin Bürk has authored 73 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Cellular and Molecular Neuroscience, 49 papers in Molecular Biology and 43 papers in Neurology. Recurrent topics in Katrin Bürk's work include Genetic Neurodegenerative Diseases (61 papers), Mitochondrial Function and Pathology (43 papers) and Parkinson's Disease Mechanisms and Treatments (21 papers). Katrin Bürk is often cited by papers focused on Genetic Neurodegenerative Diseases (61 papers), Mitochondrial Function and Pathology (43 papers) and Parkinson's Disease Mechanisms and Treatments (21 papers). Katrin Bürk collaborates with scholars based in Germany, Netherlands and France. Katrin Bürk's co-authors include J. Dichgans, Christine Zühlke, Lüdger Schöls, Thomas Klockgether, Michael Abele, Jörg B. Schulz, Alexis Brice, Udo Rüb, Irene Daum and Franco Laccone and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Katrin Bürk

71 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrin Bürk Germany 37 2.8k 2.4k 1.6k 477 206 73 3.7k
Hajime Tanaka Japan 31 2.6k 0.9× 2.5k 1.0× 1.5k 0.9× 294 0.6× 474 2.3× 138 4.4k
Kleopas A. Kleopa Cyprus 33 2.1k 0.8× 2.1k 0.9× 2.5k 1.6× 562 1.2× 568 2.8× 120 5.2k
S. H. Subramony United States 34 4.6k 1.6× 4.5k 1.9× 2.4k 1.5× 628 1.3× 397 1.9× 123 6.5k
Christine Zühlke Germany 29 1.5k 0.5× 1.5k 0.6× 635 0.4× 235 0.5× 221 1.1× 67 2.1k
Sylvia Boesch Austria 34 2.3k 0.8× 1.8k 0.8× 1.8k 1.1× 311 0.7× 313 1.5× 127 3.6k
Lawrence J. Schut United States 25 2.6k 0.9× 2.3k 1.0× 1.1k 0.7× 564 1.2× 315 1.5× 50 3.6k
E. R. Brunt Netherlands 35 2.6k 0.9× 2.7k 1.1× 1.2k 0.8× 291 0.6× 209 1.0× 55 3.7k
Fatima Memic Sweden 11 567 0.2× 1.3k 0.5× 211 0.1× 427 0.9× 172 0.8× 15 2.5k
M. Ben Hamida Tunisia 22 1.3k 0.5× 1.2k 0.5× 681 0.4× 492 1.0× 182 0.9× 43 2.4k
Angelo C. Lepore United States 34 1.5k 0.5× 990 0.4× 776 0.5× 534 1.1× 80 0.4× 80 3.5k

Countries citing papers authored by Katrin Bürk

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Bürk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Bürk

This figure shows the co-authorship network connecting the top 25 collaborators of Katrin Bürk. A scholar is included among the top collaborators of Katrin Bürk 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 Bürk. Katrin Bürk 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.
Schmidt‐Samoa, Carsten, Kathleen A. Williams, Igor Kagan, et al.. (2019). Aberrant functional connectivity of resting state networks related to misperceptions and intra-individual variability in Parkinson‘s disease. NeuroImage Clinical. 25. 102076–102076. 10 indexed citations
2.
Bürk, Katrin. (2017). Friedreich Ataxia: current status and future prospects. SHILAP Revista de lepidopterología. 4(1). 4–4. 104 indexed citations
3.
Zühlke, Christine, Barbara Mikat, Dagmar Timmann, et al.. (2015). Spinocerebellar ataxia 28: a novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowing. PubMed. 2(1). 19–19. 18 indexed citations
4.
Bürk, Katrin, Frank J. Kaiser, Stephanie Tennstedt, et al.. (2014). A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression. European Journal of Medical Genetics. 57(5). 207–211. 17 indexed citations
5.
Bürk, Katrin. (2011). Antineuronal autoantibodies in neurological disorders. BioMolecular Concepts. 2(3). 149–157.
6.
Bernard, Veronica, Martina Minnerop, Katrin Bürk, et al.. (2009). Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2. BMC Medical Genetics. 10(1). 87–87. 17 indexed citations
7.
Schulz, Jörg B., Sylvia Boesch, Katrin Bürk, et al.. (2009). Diagnosis and treatment of Friedreich ataxia: a European perspective. Nature Reviews Neurology. 5(4). 222–234. 178 indexed citations
8.
Bürk, Katrin, Irene Daum, & Udo Rüb. (2006). Cognitive function in multiple system atrophy of the cerebellar type. Movement Disorders. 21(6). 772–776. 53 indexed citations
9.
Bauer, Peter, Friedmar R. Kreuz, Katrin Bürk, et al.. (2006). Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause. Movement Disorders. 21(10). 1734–1737. 10 indexed citations
10.
Reimold, Matthias, Christoph Globas, Marc Gleichmann, et al.. (2006). Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: Striatal dopamine D2 receptor status investigated by [11C]raclopride positron emission tomography. Movement Disorders. 21(10). 1667–1673. 30 indexed citations
11.
Wüllner, Ullrich, Michael Abele, Katrin Bürk, et al.. (2005). Dopamine Transporter Positron Emission Tomography in Spinocerebellar Ataxias Type 1, 2, 3, and 6. Archives of Neurology. 62(8). 1280–1280. 70 indexed citations
12.
Healy, Daniel G., Patrick M. Abou‐Sleiman, Tetsutaro Ozawa, et al.. (2004). A functional polymorphism regulating dopamine β‐hydroxylase influences against Parkinson's disease. Annals of Neurology. 55(3). 443–446. 40 indexed citations
13.
Zühlke, Christine, et al.. (2003). Phenotypical variability of expanded alleles in the TATA-binding protein gene. Journal of Neurology. 250(2). 161–163. 42 indexed citations
14.
Bürk, Katrin, Sylvia Bösch, Christoph Globas, et al.. (2001). Executive Dysfunction in Spinocerebellar Ataxia Type 1. European Neurology. 46(1). 43–48. 49 indexed citations
15.
Schocke, Michael, et al.. (2001). Proton magnetic resonance spectroscopic imaging reveals differences in spinocerebellar ataxia types 2 and 6. Journal of Magnetic Resonance Imaging. 13(4). 553–559. 32 indexed citations
16.
Abele, Michael, Jörg B. Schulz, Katrin Bürk, et al.. (2000). Nerve Conduction Studies in Multiple System Atrophy. European Neurology. 43(4). 221–223. 13 indexed citations
17.
Bürk, Katrin. (1999). Cognitive deficits in spinocerebellar ataxia 2. Brain. 122(4). 769–777. 101 indexed citations
18.
Bürk, Katrin, Thomas Klockgether, & J. Dichgans. (1999). Neue Erkenntnisse zur Molekulargenetik und Pathophysiologie der hereditären Ataxien. Der Nervenarzt. 70(6). 491–495. 1 indexed citations
19.
Bürk, Katrin, Giovanni Stévanin, Olivier Didierjean, et al.. (1997). Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus. Journal of Neurology. 244(4). 256–261. 27 indexed citations
20.
Klockgether, Thomas, Jörg B. Schulz, Katrin Bürk, et al.. (1996). Friedreich's ataxia with retained tendon reflexes. Neurology. 46(1). 118–121. 36 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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