Jochen Kinter

1.2k total citations
21 papers, 895 citations indexed

About

Jochen Kinter is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Jochen Kinter has authored 21 papers receiving a total of 895 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 8 papers in Molecular Biology and 4 papers in Neurology. Recurrent topics in Jochen Kinter's work include Genetic Neurodegenerative Diseases (4 papers), Protease and Inhibitor Mechanisms (4 papers) and Muscle Physiology and Disorders (3 papers). Jochen Kinter is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Protease and Inhibitor Mechanisms (4 papers) and Muscle Physiology and Disorders (3 papers). Jochen Kinter collaborates with scholars based in Switzerland, United States and Germany. Jochen Kinter's co-authors include P. Sonderegger, Renato Frischknecht, Virginia Meskenaïte, Paolo Cinelli, Luigi Tornillo, Alexander Akhmedov, David P Wolfer, Hans‐Peter Lipp, Rime Madani and Markus H. Heim and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Hepatology.

In The Last Decade

Jochen Kinter

20 papers receiving 880 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jochen Kinter Switzerland	12	454	271	177	171	146	21	895
Myrna A.R. Dent Mexico	15	500 1.1×	115 0.4×	138 0.8×	314 1.8×	79 0.5×	29	858
Konstantin Adamsky Israel	17	681 1.5×	116 0.4×	166 0.9×	171 1.0×	101 0.7×	25	1.3k
Zofia M. Lasiecka United States	11	564 1.2×	367 1.4×	148 0.8×	287 1.7×	206 1.4×	14	968
Jonathan D. Leslie United Kingdom	12	1.0k 2.3×	571 2.1×	134 0.8×	301 1.8×	92 0.6×	13	1.5k
Marie Wattenhofer‐Donzé France	16	779 1.7×	158 0.6×	50 0.3×	305 1.8×	126 0.9×	19	1.1k
Sachiko Kamakura Japan	16	1.2k 2.7×	338 1.2×	164 0.9×	173 1.0×	122 0.8×	33	1.7k
Shalom Guy Slutsky Israel	7	663 1.5×	160 0.6×	105 0.6×	147 0.9×	335 2.3×	8	1.1k
Anastasia P. Grigorenko Russia	18	664 1.5×	124 0.5×	222 1.3×	120 0.7×	172 1.2×	34	1.1k
Filip A. Konopacki United Kingdom	15	681 1.5×	173 0.6×	293 1.7×	430 2.5×	96 0.7×	17	1.1k
T. Norene O’Sullivan United States	9	1.1k 2.4×	544 2.0×	84 0.5×	484 2.8×	129 0.9×	15	1.6k

Countries citing papers authored by Jochen Kinter

Since Specialization

Citations

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

Fields of papers citing papers by Jochen Kinter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jochen Kinter

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

All Works

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20 of 20 papers shown

Lin, Shuo, Lionel Tintignac, Robert Ivánek, et al.. (2024). CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I. Skeletal Muscle. 14(1). 11–11. 5 indexed citations

Ashley, Jon, Ke Shi, Michael Kyba, et al.. (2020). DNA aptamers against the DUX4 protein reveal novel therapeutic implications for FSHD. The FASEB Journal. 34(3). 4573–4590. 24 indexed citations

Erne, Beat, Frances Kern, Matthias Hamburger, et al.. (2016). Identification of Plant-derived Alkaloids with Therapeutic Potential for Myotonic Dystrophy Type I. Journal of Biological Chemistry. 291(33). 17165–17177. 15 indexed citations

Kinter, Jochen, et al.. (2015). Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf tm1Kcam. Skeletal Muscle. 5(1). 32–32. 4 indexed citations

Kinter, Jochen & Michael Sinnreich. (2014). Molecular targets to treat muscular dystrophies. Swiss Medical Weekly. 144(708). w13916–w13916. 7 indexed citations

Kinter, Jochen, Jürgen Hench, Stephan Frank, et al.. (2012). Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia. Neuromuscular Disorders. 23(2). 149–154. 10 indexed citations

Kinter, Jochen, Thomas Zeis, Beat Erne, et al.. (2012). An essential role of MAG in mediating axon–myelin attachment in Charcot–Marie–Tooth 1A disease. Neurobiology of Disease. 49. 221–231. 30 indexed citations

Steck, Andreas, Jochen Kinter, & Susanne Renaud. (2011). Neuropathies des vascularites : l’apport des techniques à puces d’ADN dans les biopsies de nerf. Revue Neurologique. 167(12). 927–929.

Steck, Andreas, Jochen Kinter, & Susanne Renaud. (2011). Differential gene expression in nerve biopsies of inflammatory neuropathies. Journal of the Peripheral Nervous System. 16(s1). 30–33. 12 indexed citations

10.

Kinter, Jochen, Laura Broglio, Andreas Steck, et al.. (2010). Gene expression profiling in nerve biopsy of vasculitic neuropathy. Journal of Neuroimmunology. 225(1-2). 184–189. 9 indexed citations

11.

Kinter, Jochen, Igor Allaman, Kate Schroder, et al.. (2009). Cellular Immunity And Pathological Alterations In Ms Grey Matter. Glia. 57. 1 indexed citations

12.

Tchorz, Jan S., Jochen Kinter, Mathias Müller, et al.. (2009). Notch2 signaling promotes biliary epithelial cell fate specification and tubulogenesis during bile duct development in mice #. Hepatology. 50(3). 871–879. 90 indexed citations

13.

Zeis, Thomas, et al.. (2008). Gene expression analysis of normal appearing brain tissue in an animal model for multiple sclerosis revealed grey matter alterations, but only minor white matter changes. Journal of Neuroimmunology. 205(1-2). 10–19. 19 indexed citations

14.

Kinter, Jochen, Thomas Zeis, & Nicole Schaeren‐Wiemers. (2008). RNA profiling of MS brain tissues.. PubMed. 15(2). 51–8. 18 indexed citations

15.

Galliciotti, Giovanna, Markus Glatzel, Jochen Kinter, et al.. (2007). Accumulation of Mutant Neuroserpin Precedes Development of Clinical Symptoms in Familial Encephalopathy with Neuroserpin Inclusion Bodies. American Journal Of Pathology. 170(4). 1305–1313. 31 indexed citations

16.

Madani, Rime, Serguei Kozlov, Alexander Akhmedov, et al.. (2003). Impaired explorative behavior and neophobia in genetically modified mice lacking or overexpressing the extracellular serine protease inhibitor neuroserpin. Molecular and Cellular Neuroscience. 23(3). 473–494. 120 indexed citations

17.

Vogt, Lorenz, Sabine Schrimpf, Virginia Meskenaïte, et al.. (2001). Calsyntenin-1, a Proteolytically Processed Postsynaptic Membrane Protein with a Cytoplasmic Calcium-Binding Domain. Molecular and Cellular Neuroscience. 17(1). 151–166. 90 indexed citations

18.

Kozlov, Serguei, Mariluce Riegel, Jochen Kinter, et al.. (1999). Assignment<footref rid="foot01"><sup>1</sup></footref> of the gene encoding the neuronal multidomain serine protease neurotrypsin (PRSS12) to human chromosome band 4q25→q26 by in situ hybridization. Cytogenetic and Genome Research. 84(1-2). 107–108. 3 indexed citations

19.

Davis, Richard L., Antony E. Shrimpton, P D Holohan, et al.. (1999). Familial dementia caused by polymerization of mutant neuroserpin. Nature. 401(6751). 376–379. 283 indexed citations

20.

Davis, Richard L., P D Holohan, Charles R. Bradshaw, et al.. (1999). Familial dementia caused by polymerization of mutant neuroserpin. Nature. 401(6751). 376–379. 5 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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