Andreas Hermann

11.0k total citations · 1 hit paper
241 papers, 5.8k citations indexed

About

Andreas Hermann is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Andreas Hermann has authored 241 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Neurology, 80 papers in Molecular Biology and 71 papers in Genetics. Recurrent topics in Andreas Hermann's work include Amyotrophic Lateral Sclerosis Research (78 papers), Neurogenetic and Muscular Disorders Research (60 papers) and Parkinson's Disease Mechanisms and Treatments (34 papers). Andreas Hermann is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (78 papers), Neurogenetic and Muscular Disorders Research (60 papers) and Parkinson's Disease Mechanisms and Treatments (34 papers). Andreas Hermann collaborates with scholars based in Germany, United States and Switzerland. Andreas Hermann's co-authors include Alexander Storch, Martina Maisel, Johannes Schwarz, Stefan Liebau, René Günther, Holger Lerche, Albert C. Ludolph, Regina Gastl, Jörg Fiedler and Kevin Peikert and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Andreas Hermann

231 papers receiving 5.7k citations

Hit Papers

Direct Reprogramming of F... 2012 2026 2016 2021 2012 100 200 300 400

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Andreas Hermann 2.6k 1.7k 1.7k 1.3k 845 241 5.8k
Stefania Corti 4.6k 1.8× 2.7k 1.5× 1.9k 1.1× 1.4k 1.1× 742 0.9× 256 7.7k
Kevin D. Foust 3.0k 1.1× 1.7k 1.0× 1.2k 0.7× 825 0.7× 608 0.7× 47 5.4k
Siddharthan Chandran 4.4k 1.7× 2.3k 1.3× 3.4k 2.0× 1.6k 1.3× 1.1k 1.4× 204 9.0k
Linda Greensmith 3.7k 1.4× 2.0k 1.2× 3.3k 2.0× 2.6k 2.1× 919 1.1× 152 7.8k
Eugenio Parati 4.5k 1.7× 2.2k 1.3× 939 0.6× 1.6k 1.3× 483 0.6× 188 9.6k
Brent T. Harris 2.4k 0.9× 1.2k 0.7× 1.1k 0.6× 848 0.7× 730 0.9× 138 6.4k
Nicholas M. Boulis 1.7k 0.7× 1.2k 0.7× 1.8k 1.0× 1.5k 1.2× 533 0.6× 206 4.8k
Guido Nikkhah 2.7k 1.0× 2.5k 1.4× 2.1k 1.2× 2.8k 2.3× 271 0.3× 165 7.9k
Brian J. Wainger 2.9k 1.1× 648 0.4× 927 0.5× 1.4k 1.1× 947 1.1× 38 4.8k
Wilfred F.A. den Dunnen 2.9k 1.1× 806 0.5× 1.5k 0.9× 2.9k 2.3× 816 1.0× 177 7.6k

Countries citing papers authored by Andreas Hermann

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Hermann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Hermann

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Hermann. A scholar is included among the top collaborators of Andreas Hermann 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 Andreas Hermann. Andreas Hermann 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.
Müller, Katharina, Sonja Schönecker, Katharina Kamm, et al.. (2024). Diagnostic accuracy and confounders of vagus nerve ultrasound in amyotrophic lateral sclerosis—a single-center case series and pooled individual patient data meta-analysis. Journal of Neurology. 271(9). 6255–6263. 1 indexed citations
2.
Freischmidt, Axel, et al.. (2024). An integrative miRNA-mRNA expression analysis identifies miRNA signatures associated with SOD1 and TARDBP patient-derived motor neurons. Human Molecular Genetics. 33(15). 1300–1314. 4 indexed citations
3.
Peikert, Kevin, Gábriel Miltenberger-Miltényi, Hannes Glaß, et al.. (2024). Phosphatidylethanolamines are the Main Lipid Class Altered in Red Blood Cells from Patients with VPS13A Disease/Chorea‐Acanthocytosis. Movement Disorders. 40(3). 544–549. 2 indexed citations
4.
Seifert, Michael, et al.. (2024). Comparative analysis of neurofilaments and biomarkers of muscular damage in amyotrophic lateral sclerosis. Brain Communications. 6(5). fcae288–fcae288. 5 indexed citations
5.
Bickle, Marc, Kathrin Brockmann, Lydia Reinhardt, et al.. (2024). Axonal Lysosomal Assays for Characterizing the Effects of LRRK2 G2019S. Biology. 13(1). 58–58. 1 indexed citations
6.
Scheveneels, Wendy, Katarina Stoklund Dittlau, Arun Pal, et al.. (2024). PP2A and GSK3 act as modifiers of FUS-ALS by modulating mitochondrial transport. Acta Neuropathologica. 147(1). 41–41. 5 indexed citations
7.
Zimyanin, Vitaly, Hannes Glaß, Julia Japtok, et al.. (2023). Live Cell Imaging of ATP Levels Reveals Metabolic Compartmentalization within Motoneurons and Early Metabolic Changes in FUS ALS Motoneurons. Cells. 12(10). 1352–1352. 3 indexed citations
8.
Walker, Ruth H., Kevin Peikert, Hans H. Jung, Andreas Hermann, & Adrian Danek. (2023). Neuroacanthocytosis Syndromes: The Clinical Perspective. SHILAP Revista de lepidopterología. 6. 3090220387–3090220387. 5 indexed citations
9.
Walter, Uwe, et al.. (2023). Ultrasonic detection of vagus, accessory, and phrenic nerve atrophy in amyotrophic lateral sclerosis: Relation to impairment and mortality. European Journal of Neurology. 31(2). e16127–e16127. 6 indexed citations
10.
Yin, Xiaoke, Barbka Repič Lampret, Manuela Neumann, et al.. (2023). Phenylalanine-tRNA aminoacylation is compromised by ALS/FTD-associated C9orf72 C4G2 repeat RNA. Nature Communications. 14(1). 5764–5764. 5 indexed citations
11.
Renger, Roman, José A. Morín, Régis Lemaitre, et al.. (2022). Co-condensation of proteins with single- and double-stranded DNA. Proceedings of the National Academy of Sciences. 119(10). e2107871119–e2107871119. 38 indexed citations
12.
Völkner, Manuela, Felix Wagner, Madalena Carido, et al.. (2022). HBEGF-TNF induce a complex outer retinal pathology with photoreceptor cell extrusion in human organoids. Nature Communications. 13(1). 6183–6183. 32 indexed citations
13.
Kasper, Elisabeth, Judith Machts, Stefan Vielhaber, et al.. (2022). Cognitive reserve protects ALS‐typical cognitive domains: A longitudinal study.. Annals of Clinical and Translational Neurology. 9(8). 1212–1223. 16 indexed citations
14.
Kasper, Elisabeth, Stefan Vielhaber, Judith Machts, et al.. (2021). Loss of “insight” into behavioral changes in ALS: Differences across cognitive profiles. Brain and Behavior. 12(1). e2439–e2439. 8 indexed citations
15.
Hermann, Andreas, et al.. (2021). Pathophysiological In Vitro Profile of Neuronal Differentiated Cells Derived from Niemann-Pick Disease Type C2 Patient-Specific iPSCs Carrying the NPC2 Mutations c.58G>T/c.140G>T. International Journal of Molecular Sciences. 22(8). 4009–4009. 3 indexed citations
16.
Federti, Enrica, Alessandro Mattè, Kevin Peikert, et al.. (2021). Adaptative Up-Regulation of PRX2 and PRX5 Expression Characterizes Brain from a Mouse Model of Chorea-Acanthocytosis. Antioxidants. 11(1). 76–76. 8 indexed citations
17.
Prudlo, Johannes, Stefan Vielhaber, Judith Machts, et al.. (2021). Cognitive reserve and regional brain volume in amyotrophic lateral sclerosis. Cortex. 139. 240–248. 20 indexed citations
18.
Naumann, Marcel, et al.. (2020). Genome Wide Analysis Points towards Subtype-Specific Diseases in Different Genetic Forms of Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences. 21(18). 6938–6938. 12 indexed citations
19.
Beyer, Léon, René Günther, Jan Christoph Koch, et al.. (2020). TDP‐43 as structure‐based biomarker in amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 8(1). 271–277. 20 indexed citations
20.
Lottaz, Claudio, Dagmar Beier, Katharina Meyer, et al.. (2010). Transcriptional Profiles of CD133+ and CD133− Glioblastoma-Derived Cancer Stem Cell Lines Suggest Different Cells of Origin. Cancer Research. 70(5). 2030–2040. 207 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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