Stephan Züchner

21.9k total citations
177 papers, 6.6k citations indexed

About

Stephan Züchner is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Stephan Züchner has authored 177 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 108 papers in Cellular and Molecular Neuroscience, 84 papers in Molecular Biology and 38 papers in Cell Biology. Recurrent topics in Stephan Züchner's work include Hereditary Neurological Disorders (75 papers), Genetic Neurodegenerative Diseases (43 papers) and Neurological diseases and metabolism (29 papers). Stephan Züchner is often cited by papers focused on Hereditary Neurological Disorders (75 papers), Genetic Neurodegenerative Diseases (43 papers) and Neurological diseases and metabolism (29 papers). Stephan Züchner collaborates with scholars based in United States, Germany and United Kingdom. Stephan Züchner's co-authors include Jeffery M. Vance, Eden R. Martin, Michael Gonzalez, William K. Scott, Gaofeng Wang, Allison E. Ashley‐Koch, Peter De Jonghe, Yi‐Ju Li, Margaret A. Pericak‐Vance and Rebecca Schüle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neuron.

In The Last Decade

Stephan Züchner

170 papers receiving 6.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephan Züchner United States 46 3.2k 2.4k 1.1k 1.1k 1.0k 177 6.6k
Christian Kubisch Germany 37 4.6k 1.5× 2.2k 0.9× 1.1k 1.0× 694 0.6× 785 0.8× 144 7.3k
Robert G. Kalb United States 49 4.0k 1.3× 4.2k 1.7× 1.6k 1.4× 574 0.5× 1.5k 1.5× 112 8.4k
Yunjuan Sun United States 31 3.2k 1.0× 2.3k 0.9× 537 0.5× 1.6k 1.4× 1.2k 1.2× 55 7.4k
John Kamholz United States 45 2.8k 0.9× 2.1k 0.9× 862 0.8× 774 0.7× 600 0.6× 138 5.5k
Avi Orr‐Urtreger Israel 47 4.7k 1.5× 1.5k 0.6× 1.9k 1.7× 835 0.8× 905 0.9× 194 8.6k
Peter G. Noakes Australia 39 3.1k 1.0× 1.7k 0.7× 1.2k 1.0× 611 0.6× 925 0.9× 102 5.6k
Giuseppe De Michele Italy 43 3.0k 0.9× 3.9k 1.6× 3.2k 2.9× 1.2k 1.1× 537 0.5× 208 6.8k
Enza Maria Valente Italy 44 4.1k 1.3× 2.9k 1.2× 3.6k 3.2× 986 0.9× 753 0.7× 233 9.3k
Antonella Consiglio Italy 31 4.9k 1.5× 2.5k 1.0× 1.8k 1.6× 968 0.9× 705 0.7× 57 8.9k

Countries citing papers authored by Stephan Züchner

Since Specialization
Citations

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

Fields of papers citing papers by Stephan Züchner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephan Züchner

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Züchner. A scholar is included among the top collaborators of Stephan Züchner 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 Stephan Züchner. Stephan Züchner 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.
Laššuthová, Petra, et al.. (2025). Biallelic variants in the RFC4 gene cause a rapidly progressive congenital myopathy with severe hypotonia and axial weakness. Neuromuscular Disorders. 51. 105366–105366.
2.
Jensen, Tanner, Bohan Ni, Chloe M. Reuter, et al.. (2025). Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease. Genome Research. 35(4). 914–928. 2 indexed citations
3.
Record, Christopher J., Menelaos Pipis, Mariola Skorupinska, et al.. (2024). Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease. Brain. 147(9). 3144–3156. 13 indexed citations
4.
Pellerin, David, Matt C. Danzi, Stephan Züchner, et al.. (2024). Assessment of the Clinical Interactions of GAA Repeat Expansions in FGF14 and FXN. Neurology Genetics. 10(6). e200210–e200210. 1 indexed citations
5.
Forghani, Irman, Stephanie Bivona, Alejo A. Morales, et al.. (2024). EFEMP1 haploinsufficiency causes a Marfan‐like hereditary connective tissue disorder. American Journal of Medical Genetics Part A. 194(6). e63556–e63556. 1 indexed citations
6.
Indelicato, Elisabetta, David Pellerin, Matt C. Danzi, et al.. (2023). Spinocerebellar ataxia 27B: episodic symptoms and acetazolamide response in 34 patients. Brain Communications. 5(5). fcad239–fcad239. 12 indexed citations
7.
Bis‐Brewer, Dana M., Amy E. Sheehan, Daniel C. Maddison, et al.. (2021). TSG101 negatively regulates mitochondrial biogenesis in axons. Proceedings of the National Academy of Sciences. 118(20). 18 indexed citations
8.
Kozol, Robert A., et al.. (2021). Restoring Shank3 in the rostral brainstem of shank3ab−/− zebrafish autism models rescues sensory deficits. Communications Biology. 4(1). 1411–1411. 13 indexed citations
9.
Morani, Federica, Stefano Doccini, Giovanna Chiorino, et al.. (2021). Functional Network Profiles in ARSACS Disclosed by Aptamer-Based Proteomic Technology. Frontiers in Neurology. 11. 603774–603774. 10 indexed citations
10.
Buglo, Elena, David Sant, Matt C. Danzi, et al.. (2020). Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease. PLoS ONE. 15(3). e0230566–e0230566. 36 indexed citations
11.
Hirst, Jennifer, Marianna Madeo, Katrien Smets, et al.. (2016). Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48). Neurology Genetics. 2(5). e98–e98. 24 indexed citations
12.
Grosz, Zoltán, Michael Gonzalez, Anikó Gál, et al.. (2016). Genetic background of the hereditary spastic paraplegia phenotypes in Hungary — An analysis of 58 probands. Journal of the Neurological Sciences. 364. 116–121. 24 indexed citations
13.
Jerath, Nivedita U., Steven A. Moore, Michael E. Shy, et al.. (2015). Rare Manifestation of a c.290 C>T, p.Gly97GluVCPMutation. SHILAP Revista de lepidopterología. 2015. 1–5. 16 indexed citations
14.
Kennerson, Marina, Eppie M. Yiu, David Chuang, et al.. (2013). A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene. Human Molecular Genetics. 22(7). 1404–1416. 56 indexed citations
15.
Daftarian, Pirouz, Changli Wei, Alan King, et al.. (2011). In vivo Electroporation and Non-protein Based Screening Assays to Identify Antibodies Against Native Protein Conformations. Hybridoma. 30(5). 409–418. 6 indexed citations
16.
Choi, Byung‐Ok, Young Se Hyun, Heasoo Koo, et al.. (2011). A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14. Human Mutation. 32(6). 669–677. 41 indexed citations
17.
Taylor, Warren D., Stephan Züchner, Douglas R. McQuoid, et al.. (2008). Social support in older individuals: The role of the BDNF Val66Met polymorphism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1205–1212. 18 indexed citations
18.
Züchner, Stephan, et al.. (2007). Update on psychiatric genetics. Genetics in Medicine. 9(6). 332–340. 11 indexed citations
19.
Timmerman, Vincent, et al.. (2005). Mutations in Mitofusin 2 are a major cause for autosomal dominant axonal Charcot-Marie-Tooth neuropathy. Journal of the Peripheral Nervous System. 10. 16–17. 1 indexed citations
20.
Haubrich, C., Timo Krings, Jan Senderek, et al.. (2002). Hypertrophic nerve roots in a case of Roussy-Lévy syndrome. Neuroradiology. 44(11). 933–937. 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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