Peter Bauer

8.9k total citations · 1 hit paper
113 papers, 4.6k citations indexed

About

Peter Bauer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Peter Bauer has authored 113 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 34 papers in Cellular and Molecular Neuroscience and 22 papers in Neurology. Recurrent topics in Peter Bauer's work include Genetic Neurodegenerative Diseases (29 papers), Studies on Chitinases and Chitosanases (25 papers) and Mitochondrial Function and Pathology (22 papers). Peter Bauer is often cited by papers focused on Genetic Neurodegenerative Diseases (29 papers), Studies on Chitinases and Chitosanases (25 papers) and Mitochondrial Function and Pathology (22 papers). Peter Bauer collaborates with scholars based in Japan, Germany and United States. Peter Bauer's co-authors include Lüdger Schöls, Olaf Rieß, Thorsten Schulte, Nobuyuki Nukina, Thorsten Schmidt, Fumitaka Oyama, Haruko Miyazaki, Arndt Rolfs, Silvia Weissgram and Susanne Jungwirth and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Peter Bauer

108 papers receiving 4.5k citations

Hit Papers

Autosomal dominant cerebellar ataxias: clinical features,... 2004 2026 2011 2018 2004 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Bauer Japan 36 2.4k 1.7k 1.4k 688 462 113 4.6k
Stephan von Hörsten Germany 46 2.0k 0.8× 3.1k 1.8× 972 0.7× 864 1.3× 292 0.6× 192 6.8k
Paola Lenzi Italy 33 1.3k 0.6× 1.3k 0.8× 1.2k 0.9× 675 1.0× 699 1.5× 183 4.1k
Masayuki Sasaki Japan 34 3.3k 1.3× 1.8k 1.1× 1.2k 0.9× 822 1.2× 387 0.8× 303 6.4k
Masanori Nakagawa Japan 48 3.0k 1.2× 1.7k 1.0× 2.4k 1.7× 1.3k 1.9× 567 1.2× 324 8.3k
Christine Tranchant France 39 2.0k 0.8× 1.5k 0.9× 2.3k 1.6× 407 0.6× 196 0.4× 209 5.2k
Yves Robitaille Canada 41 2.4k 1.0× 1.7k 1.0× 877 0.6× 1.1k 1.7× 350 0.8× 127 5.3k
Antonio Paparelli Italy 31 868 0.4× 1.2k 0.7× 1.5k 1.1× 517 0.8× 583 1.3× 114 3.5k
Arnulf H. Koeppen United States 46 3.2k 1.3× 3.1k 1.8× 2.1k 1.5× 511 0.7× 374 0.8× 129 5.7k
Anna E. King Australia 32 1.0k 0.4× 651 0.4× 1.3k 0.9× 781 1.1× 333 0.7× 125 3.2k
Jian Feng United States 47 4.8k 2.0× 2.9k 1.7× 1.1k 0.8× 784 1.1× 494 1.1× 124 8.5k

Countries citing papers authored by Peter Bauer

Since Specialization
Citations

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

Fields of papers citing papers by Peter Bauer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Bauer

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Bauer. A scholar is included among the top collaborators of Peter Bauer 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 Peter Bauer. Peter Bauer 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.
Beetz, Christian, Krishna Kumar Kandaswamy, Peter Bauer, et al.. (2025). Plasma Glucosylceramide Levels Are Regulated by ATP10D and Are Not Involved in Parkinson's Disease Pathogenesis. Annals of Neurology. 97(5). 873–878. 1 indexed citations
2.
Chaichoompu, Kridsadakorn, Franco Valzania, Francesco Cavallieri, et al.. (2024). Genetic and Epidemiological Insights into RAB32‐Linked Parkinson's Disease. Movement Disorders. 40(1). 147–151. 2 indexed citations
3.
Suzuki, Keita W., et al.. (2024). Evolutionary insights into sequence modifications governing chitin recognition and chitinase inactivity in YKL-40 (HC-gp39, CHI3L1). Journal of Biological Chemistry. 300(6). 107365–107365. 6 indexed citations
4.
Havlas, Vojtěch, et al.. (2022). Treatment of knee cartilage by cultured stem cells and three dimensional scaffold: a phase I/IIa clinical trial. International Orthopaedics. 47(10). 2375–2382. 3 indexed citations
5.
Tabata, Eri, Akinori Kashimura, Satoshi Wakita, et al.. (2017). Protease resistance of porcine acidic mammalian chitinase under gastrointestinal conditions implies that chitin-containing organisms can be sustainable dietary resources. Scientific Reports. 7(1). 12963–12963. 31 indexed citations
6.
Wakita, Satoshi, Masahiro Kimura, Naoki Kato, et al.. (2017). Improved fluorescent labeling of chitin oligomers: Chitinolytic properties of acidic mammalian chitinase under somatic tissue pH conditions. Carbohydrate Polymers. 164. 145–153. 23 indexed citations
7.
Matthijs, Gert, Mariëlle Alders, Peter Bauer, et al.. (2014). EuroGentest guidelines for diagnostic next generation sequencing. European Journal of Human Genetics. 22. 566–566. 3 indexed citations
8.
Reetz, Kathrin, Ana Sofia Costa, Shahram Mirzazade, et al.. (2013). Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6. Brain. 136(3). 905–917. 109 indexed citations
9.
Lee, Chris W., Sandra Almeida, Mercedes Prudencio, et al.. (2013). Targeted manipulation of the sortilin–progranulin axis rescues progranulin haploinsufficiency. Human Molecular Genetics. 23(6). 1467–1478. 78 indexed citations
10.
Belzil, Véronique, Peter Bauer, Mercedes Prudencio, et al.. (2013). Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood. Acta Neuropathologica. 126(6). 895–905. 236 indexed citations
11.
Kim, Hong Sug, Kevin Woolard, Chen Lai, et al.. (2012). Gliomagenesis Arising from Pten- and Ink4a/Arf-Deficient Neural Progenitor Cells Is Mediated by the p53-Fbxw7/Cdc4 Pathway, Which Controls c-Myc. Cancer Research. 72(22). 6065–6075. 29 indexed citations
12.
Bauer, Peter, Roman Hudec, Anand Goswami, et al.. (2012). ROCK-phosphorylated vimentin modifies mutant huntingtin aggregation via sequestration of IRBIT. Molecular Neurodegeneration. 7(1). 43–43. 24 indexed citations
13.
Brüggemann, Norbert, J. Hagenah, Peter Bauer, et al.. (2011). Autosomal dominant Parkinson’s disease in a large German pedigree. Acta Neurologica Scandinavica. 126(2). 129–137. 2 indexed citations
14.
Munkert, Jennifer, Peter Bauer, Edyta Burda, Frieder Müller‐Uri, & Wolfgang Kreis. (2011). Progesterone 5β-reductase of Erysimum crepidifolium: cDNA cloning, expression in Escherichia coli, and reduction of enones with the recombinant protein. Phytochemistry. 72(14-15). 1710–1717. 17 indexed citations
15.
Bauer, Peter, Hon Kit Wong, Fumitaka Oyama, et al.. (2009). Inhibition of Rho Kinases Enhances the Degradation of Mutant Huntingtin. Journal of Biological Chemistry. 284(19). 13153–13164. 83 indexed citations
16.
Meyer, Chris, G. Schmid, Peter H. Kraus, et al.. (2007). Cardiomyopathy in Friedreich's ataxia‐assessment by cardiac MRI. Movement Disorders. 22(11). 1615–1622. 37 indexed citations
17.
Khan, Liakot A., Peter Bauer, Haruko Miyazaki, et al.. (2006). Expanded polyglutamines impair synaptic transmission and ubiquitin–proteasome system in Caenorhabditis elegans. Journal of Neurochemistry. 98(2). 576–587. 45 indexed citations
18.
Rolfs, Arndt, Tobias Böttcher, Peter J. Morris, et al.. (2005). Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study. The Lancet. 366(9499). 1794–1796. 321 indexed citations
19.
Grundmann, Kathrin, Ulrike Laubis‐Herrmann, Ingrid Bauer, et al.. (2003). Frequency and Phenotypic Variability of the GAG Deletion of the DYT1 Gene in an Unselected Group of Patients With Dystonia. Archives of Neurology. 60(9). 1266–70. 70 indexed citations
20.
Bauer, Peter, et al.. (1976). Zu den Beziehungen zwischen Standardmerkmalen von Mutter und Neugeborenem. Archives of Gynecology and Obstetrics. 220(4). 307–317. 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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