Marius Kuhn

558 total citations
16 papers, 207 citations indexed

About

Marius Kuhn is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Marius Kuhn has authored 16 papers receiving a total of 207 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 4 papers in Genetics. Recurrent topics in Marius Kuhn's work include Neurogenetic and Muscular Disorders Research (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Ion channel regulation and function (3 papers). Marius Kuhn is often cited by papers focused on Neurogenetic and Muscular Disorders Research (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Ion channel regulation and function (3 papers). Marius Kuhn collaborates with scholars based in Germany, United States and Switzerland. Marius Kuhn's co-authors include Dieter Gläser, Benedikt Schoser, Marcus Deschauer, Stephan Wenninger, Karin Jurkat‐Rott, Pushpa Raj Joshi, Stephan Zierz, Wolfgang Müller‐Felber, Frank Lehmann‐Horn and B. Wüthrich and has published in prestigious journals such as The Journal of Immunology, Journal of Neurology Neurosurgery & Psychiatry and Journal of Clinical Pathology.

In The Last Decade

Marius Kuhn

16 papers receiving 201 citations

Peers

Marius Kuhn

CMN

PHYSI

GENET

CCM

Fılız Hazan Türkiye

Chris Esapa United Kingdom

Lenka Mrázová Czechia

Giuseppina Di Fruscio Italy

Pascal Laforêt France

Vedrana Milić Rašić Serbia

Frédéric Tran Mau‐Them France

Adrian G. Todd United States

Nicola Carboni Italy

Amina Chaouch United Kingdom

Fılız Hazan Türkiye

Marius Kuhn

183 ×1.7

24 ×0.5

CMN

32 ×0.8

PHYSI

18 ×0.5

GENET

18 ×0.5

CCM

Citations per year, relative to Marius Kuhn Marius Kuhn (= 1×) peers Fılız Hazan

Countries citing papers authored by Marius Kuhn

Since Specialization

Citations

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

Fields of papers citing papers by Marius Kuhn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marius Kuhn

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

All Works

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16 of 16 papers shown

Vill, Katharina, Wolfgang Müller‐Felber, Dieter Gläser, et al.. (2018). SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy. Human Genetics. 137(11-12). 911–919. 15 indexed citations

Kuhn, Marius, James R. Groome, Vern Winston, et al.. (2018). Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis.. PubMed. 37(3). 193–203. 3 indexed citations

Vill, Katharina, Astrid Blaschek, Dieter Gläser, et al.. (2017). Early-Onset Myopathies: Clinical Findings, Prevalence of Subgroups and Diagnostic Approach in a Single Neuromuscular Referral Center in Germany. Journal of Neuromuscular Diseases. 4(4). 315–325. 12 indexed citations

Kuhn, Marius, Dieter Gläser, Pushpa Raj Joshi, et al.. (2016). Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophy. Journal of Neurology. 263(4). 743–750. 42 indexed citations

Kuhn, Marius, Karin Jurkat‐Rott, & Frank Lehmann‐Horn. (2015). RareKCNJ18variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients: Table 1. Journal of Neurology Neurosurgery & Psychiatry. 87(1). jnnp–2014. 11 indexed citations

Musumeci, Olimpia, Andrea Thieme, Kristl G. Claeys, et al.. (2015). Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrum. Neuromuscular Disorders. 25(9). 719–724. 29 indexed citations

Vill, Katharina, Marius Kuhn, Dieter Gläser, Maggie C. Walter, & Wolfgang Müller‐Felber. (2015). Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene. Neuropediatrics. 46(4). 282–286. 4 indexed citations

Kuhn, Marius, Dieter Gläser, Wolfgang Müller‐Felber, & Katharina Vill. (2014). Overlap Phenotype between CMT1A and Hereditary Neuropathy with Liability to Pressure Palsies Caused by the Novel Small In-frame Deletion c.407_418del12 in PMP22 Gene. Neuropediatrics. 46(1). 44–48. 4 indexed citations

Blaschek, Astrid, Dieter Gläser, Marius Kuhn, et al.. (2013). Early infantile sensory-motor neuropathy with late onset respiratory distress. Neuromuscular Disorders. 24(3). 269–271. 10 indexed citations

10.

Benet‐Pagès, Anna, Sebastian Eck, Marius Kuhn, et al.. (2013). Applications and data analysis of next-generation sequencing. LaboratoriumsMedizin. 37(6). 305–315. 4 indexed citations

11.

Eck, Sebastian, Anna Benet‐Pagès, Philipp A. Greif, et al.. (2012). Diagnostic applications of next generation sequencing: working towards quality standards/Diagnostische Anwendung von Next Generation Sequencing: Auf dem Weg zu Qualitätsstandards. LaboratoriumsMedizin. 36(4). 227–239. 5 indexed citations

12.

Lehmann‐Horn, F., Michael Orth, Marius Kuhn, & Karin Jurkat‐Rott. (2011). A novel N440K sodium channel mutation causes myotonia with exercise-induced weakness--exclusion of CLCN1 exon deletion/duplication by MLPA.. PubMed. 30(2). 133–7. 12 indexed citations

13.

Minić, Snežana, Dušan Trpinac, M Obradović, et al.. (2010). Incontinentia pigmenti with ultrastructurally disordered leucocytes. Journal of Clinical Pathology. 63(7). 657–659. 3 indexed citations

14.

Schuster, Christian, B. Wüthrich, Katrin Hartmann, & Marius Kuhn. (2000). Anaphylaxis to E466. Allergy. 55(3). 303–304. 13 indexed citations

15.

Kuhn, Marius, et al.. (1999). Ondine’s Curse. Respiration. 66(3). 265–265. 20 indexed citations

16.

Rosloniec, Edward F., et al.. (1984). Aggressiveness of SJL/J lymphomas correlates with absence of H-2Ds antigens.. The Journal of Immunology. 132(2). 945–952. 20 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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