Helmut Fuchs

19.5k total citations
185 papers, 5.4k citations indexed

About

Helmut Fuchs is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Helmut Fuchs has authored 185 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Molecular Biology, 34 papers in Genetics and 22 papers in Cell Biology. Recurrent topics in Helmut Fuchs's work include Connexins and lens biology (14 papers), Hearing, Cochlea, Tinnitus, Genetics (12 papers) and Adipose Tissue and Metabolism (10 papers). Helmut Fuchs is often cited by papers focused on Connexins and lens biology (14 papers), Hearing, Cochlea, Tinnitus, Genetics (12 papers) and Adipose Tissue and Metabolism (10 papers). Helmut Fuchs collaborates with scholars based in Germany, United States and United Kingdom. Helmut Fuchs's co-authors include Martin Hrabě de Angelis, Valérie Gailus‐Durner, Eckhard Wolf, Birgit Rathkolb, Rudi Balling, Gregory S. Barsh, Wolfgang Wurst, Karen B. Avraham, Karen P. Steel and Sabine M. Hölter and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Helmut Fuchs

178 papers receiving 5.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Helmut Fuchs Germany 40 2.8k 912 643 643 582 185 5.4k
Roberto Ravazzolo Italy 39 3.6k 1.3× 936 1.0× 451 0.7× 422 0.7× 609 1.0× 206 6.5k
Janine Altmüller Germany 48 3.4k 1.2× 1.3k 1.5× 570 0.9× 640 1.0× 773 1.3× 213 6.5k
Hossein Najmabadi Iran 41 3.5k 1.3× 1.7k 1.9× 1.0k 1.6× 494 0.8× 386 0.7× 292 6.5k
Vincenzo Sorrentino Italy 53 6.7k 2.4× 991 1.1× 772 1.2× 754 1.2× 784 1.3× 203 9.1k
Kazuo Katoh Japan 33 2.0k 0.7× 706 0.8× 291 0.5× 971 1.5× 939 1.6× 222 5.4k
Andreas F. Mack Germany 44 2.6k 0.9× 276 0.3× 406 0.6× 530 0.8× 467 0.8× 160 5.7k
Gudrun Nürnberg Germany 44 2.9k 1.1× 1.6k 1.7× 424 0.7× 895 1.4× 275 0.5× 93 5.1k
Klaus Addicks Germany 50 3.7k 1.3× 686 0.8× 293 0.5× 941 1.5× 1.1k 1.9× 199 8.4k
Rainer Schreiber Germany 57 5.8k 2.1× 562 0.6× 888 1.4× 431 0.7× 1.1k 1.8× 188 8.2k
Shigeru Kobayashi Japan 48 2.2k 0.8× 481 0.5× 253 0.4× 708 1.1× 1.1k 1.9× 387 9.1k

Countries citing papers authored by Helmut Fuchs

Since Specialization
Citations

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

Fields of papers citing papers by Helmut Fuchs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helmut Fuchs

This figure shows the co-authorship network connecting the top 25 collaborators of Helmut Fuchs. A scholar is included among the top collaborators of Helmut Fuchs 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 Helmut Fuchs. Helmut Fuchs 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.
Karnebeek, Clara D.M. van, Valérie Gailus‐Durner, Udo F. H. Engelke, et al.. (2025). New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouse. Brain Communications. 7(6). fcaf397–fcaf397. 1 indexed citations
2.
Hönes, Georg Sebastian, Elen Tolstik, Nadine Spielmann, et al.. (2024). Canonical and Noncanonical Contribution of Thyroid Hormone Receptor Isoforms Alpha and Beta to Cardiac Hypertrophy and Heart Rate in Male Mice. Thyroid. 34(6). 785–795. 3 indexed citations
3.
Nichtová, Zuzana, Nathalia Romanelli Vicente Dragano, David Pajuelo Reguera, et al.. (2023). A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice. Mammalian Genome. 34(2). 107–122. 2 indexed citations
4.
Garrett, Lillian, Martin Irmler, Angela Baljuls, et al.. (2023). GPR101 loss promotes insulin resistance and diet-induced obesity risk. Neuroscience Applied. 2. 101126–101126. 1 indexed citations
5.
Milenkovic, Dusanka, Adrián Sanz‐Moreno, Julia Calzada‐Wack, et al.. (2022). Mice lacking the mitochondrial exonuclease MGME1 develop inflammatory kidney disease with glomerular dysfunction. PLoS Genetics. 18(5). e1010190–e1010190. 10 indexed citations
6.
Spielmann, Nadine, Patricia da Silva‐Buttkus, Oana V. Amarie, et al.. (2022). Knockout of the Complex III subunit Uqcrh causes bioenergetic impairment and cardiac contractile dysfunction. Mammalian Genome. 34(2). 229–243. 6 indexed citations
7.
Keipert, Susanne, Dominik Lutter, Bjoern O. Schroeder, et al.. (2021). Author Correction: Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice. Nature Communications. 12(1). 1804–1804. 1 indexed citations
8.
Tomar, Archana, David Corujo, Raffaele Gerlini, et al.. (2021). Disruption of paternal circadian rhythm affects metabolic health in male offspring via nongerm cell factors. Science Advances. 7(22). 21 indexed citations
9.
Auffenberg, Eva, Ulrike B. S. Hedrich, Raffaella Barbieri, et al.. (2021). Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model. Journal of Clinical Investigation. 131(21). 39 indexed citations
10.
Keipert, Susanne, Dominik Lutter, Bjoern O. Schroeder, et al.. (2020). Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice. Nature Communications. 11(1). 624–624. 62 indexed citations
11.
Aguilar‐Pimentel, Juan Antonio, Raffaele Gerlini, Julia Calzada‐Wack, et al.. (2020). Increased estrogen to androgen ratio enhances immunoglobulin levels and impairs B cell function in male mice. Scientific Reports. 10(1). 18334–18334. 23 indexed citations
12.
Tiso, Natascia, Martin Irmler, Marion Horsch, et al.. (2019). Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmia. Experimental Eye Research. 188. 107632–107632. 6 indexed citations
13.
Baumann, Peter, Sonja C. Schriever, Stephanie Kullmann, et al.. (2019). Dusp8 affects hippocampal size and behavior in mice and humans. Scientific Reports. 9(1). 19483–19483. 11 indexed citations
14.
Sabrautzki, Sibylle, Bettina Lorenz‐Depiereux, Julia Calzada‐Wack, et al.. (2013). An ENU Mutagenesis-Derived Mouse Model with a Dominant Jak1 Mutation Resembling Phenotypes of Systemic Autoimmune Disease. American Journal Of Pathology. 183(2). 352–368. 19 indexed citations
15.
Thiele, Frank, Christian M. Cohrs, Thomas S. Lisse, et al.. (2012). Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms. Human Molecular Genetics. 21(16). 3535–3545. 54 indexed citations
16.
Deussing, Jan M., Christian Kühne, Magdalena Kallnik, et al.. (2010). Urocortin 3 Modulates Social Discrimination Abilities via Corticotropin-Releasing Hormone Receptor Type 2. Journal of Neuroscience. 30(27). 9103–9116. 73 indexed citations
17.
Grzmil, Paweł, J Konietzko, Alicia Aguilar, et al.. (2009). Targeted Disruption of the Mouse <i>Npal3</i> Gene Leads to Deficits in Behavior, Increased IgE Levels, and Impaired Lung Function. Cytogenetic and Genome Research. 125(3). 186–200. 7 indexed citations
18.
Puk, Oliver, Claudia Dalke, Dian Soewarto, et al.. (2008). Mutation in a Novel Connexin-like Gene ( Gjf1 ) in the Mouse Affects Early Lens Development and Causes a Variable Small-Eye Phenotype. Investigative Ophthalmology & Visual Science. 49(4). 1525–1525. 23 indexed citations
19.
Reinhard, Claudia, Bernhard Meyer, Helmut Fuchs, et al.. (2005). Genomewide Linkage Analysis Identifies Novel Genetic Loci for Lung Function in Mice. American Journal of Respiratory and Critical Care Medicine. 171(8). 880–888. 31 indexed citations
20.
Austria, et al.. (2002). Wiener Kommentar zur Strafprozessordnung. 2 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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