Christoph Hotzy

2.1k total citations
18 papers, 641 citations indexed

About

Christoph Hotzy is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Christoph Hotzy has authored 18 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Christoph Hotzy's work include Bacteriophages and microbial interactions (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Christoph Hotzy is often cited by papers focused on Bacteriophages and microbial interactions (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Christoph Hotzy collaborates with scholars based in Austria, Germany and United Kingdom. Christoph Hotzy's co-authors include Uwe B. Sleytr, Alexander Zimprich, Margit Sára, William L. Ries, Eva M. Egelseer, M Sára, Fritz Zimprich, Elisabeth Stögmann, Thomas Brücke and Tim M. Strom and has published in prestigious journals such as Neurology, Biochemical Journal and Journal of Bacteriology.

In The Last Decade

Christoph Hotzy

18 papers receiving 618 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christoph Hotzy Austria 14 294 172 161 130 96 18 641
Richa Tyagi United States 9 465 1.6× 69 0.4× 133 0.8× 58 0.4× 14 0.1× 13 812
Eva Wagner Germany 14 538 1.8× 148 0.9× 18 0.1× 87 0.7× 93 1.0× 21 1.0k
Xue Gong China 15 260 0.9× 90 0.5× 238 1.5× 12 0.1× 39 0.4× 42 628
Jessica M. Jones United States 21 756 2.6× 246 1.4× 208 1.3× 57 0.4× 11 0.1× 26 1.2k
Antonia Martín-Gallardo United States 14 379 1.3× 306 1.8× 53 0.3× 28 0.2× 14 0.1× 21 757
Núria Andreu Spain 15 276 0.9× 131 0.8× 55 0.3× 14 0.1× 9 0.1× 27 579
Josué O. Ramírez‐Jarquín Mexico 13 249 0.8× 82 0.5× 38 0.2× 33 0.3× 8 0.1× 27 572
Shuyan Yang China 12 1.4k 4.8× 146 0.8× 69 0.4× 24 0.2× 9 0.1× 29 1.5k
Holger Hengel Germany 13 180 0.6× 64 0.4× 106 0.7× 16 0.1× 33 0.3× 34 481
Francesca Macchi Italy 18 252 0.9× 91 0.5× 217 1.3× 6 0.0× 27 0.3× 29 782

Countries citing papers authored by Christoph Hotzy

Since Specialization
Citations

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

Fields of papers citing papers by Christoph Hotzy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christoph Hotzy

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

All Works

18 of 18 papers shown
1.
König, Theresa, Raphael Wurm, Evelyn Berger–Sieczkowski, et al.. (2023). Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes. Human Genomics. 17(1). 55–55. 1 indexed citations
2.
König, Theresa, Raphael Wurm, Christoph Hotzy, et al.. (2022). C9orf72 repeat length might influence clinical sub-phenotypes in dementia patients. Neurobiology of Disease. 175. 105927–105927. 6 indexed citations
3.
Pichler, Peter, Alexander Zimprich, Christoph Hotzy, et al.. (2020). The urinary microbiome shows different bacterial genera in renal transplant recipients and non-transplant patients at time of acute kidney injury – a pilot study. BMC Nephrology. 21(1). 117–117. 16 indexed citations
4.
Krenn, Martin, Matias Wagner, Christoph Hotzy, et al.. (2020). Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes. Journal of Medical Genetics. 57(9). 624–633. 18 indexed citations
5.
Winnicki, Wolfgang, Alexander Zimprich, Christoph Hotzy, et al.. (2019). FP247The urinary microbiome during acute kidney injury in renal transplant recipients versus non-transplant recipients. Nephrology Dialysis Transplantation. 34(Supplement_1). 1 indexed citations
6.
Mir, Rafeeq, Francesca Tonelli, Paweł Lis, et al.. (2018). The Parkinson's disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human. Biochemical Journal. 475(11). 1861–1883. 141 indexed citations
7.
Krenn, Martin, Gudrun Zulehner, Christoph Hotzy, et al.. (2017). Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene. European Journal of Neurology. 24(5). 741–747. 17 indexed citations
8.
Hilger, Eva, Eva M. Reinthaler, Elisabeth Stögmann, et al.. (2012). Lack of Association Between ABCC2 Gene Variants and Treatment Response in Epilepsy. Pharmacogenomics. 13(2). 185–190. 32 indexed citations
9.
Schlachter, Kurt, U Gruber‐Sedlmayr, Elisabeth Stögmann, et al.. (2009). A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures. Neurology. 72(11). 974–978. 41 indexed citations
10.
Haubenberger, Dietrich, Christoph Hotzy, Walter Pirker, et al.. (2009). Role of LINGO1 polymorphisms in Parkinson's disease. Movement Disorders. 24(16). 2404–2407. 22 indexed citations
11.
Haubenberger, Dietrich, Silvia Bonelli, Christoph Hotzy, et al.. (2007). A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease. Movement Disorders. 22(11). 1640–1643. 17 indexed citations
12.
Stögmann, Elisabeth, Peter Lichtner, Christian Baumgärtner, et al.. (2006). Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations. Neurology. 67(11). 2029–2031. 51 indexed citations
13.
Stögmann, Elisabeth, Peter Lichtner, M. Schmied, et al.. (2006). Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes. Neurogenetics. 7(4). 265–268. 19 indexed citations
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Ries, William L., et al.. (1997). Evidence that the N-terminal part of the S-layer protein from Bacillus stearothermophilus PV72/p2 recognizes a secondary cell wall polymer. Journal of Bacteriology. 179(12). 3892–3898. 99 indexed citations
18.
Hotzy, Christoph, et al.. (1996). Regulation of S-layer protein synthesis of Bacillus stearothermophilus PV72 through variation of continuous cultivation conditions. Journal of Biotechnology. 50(2-3). 189–200. 11 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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