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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Biallelic variants in the RFC4 gene cause a rapidly progressive congenital myopathy with severe hypotonia and axial weakness 2025 ·Neuromuscular Disorders ·(unknown), (unknown), Petra Laššuthová, (unknown), (unknown), Marie Morimoto, Stephan Züchner, (unknown), Adriana Rebelo, Jana Haberlová	0
2	Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease 2025 ·Genome Research ·Tanner Jensen, Bohan Ni, Chloe M. Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner, (unknown), Pagé C. Goddard, Archana N. Raja, Euan A. Ashley, Jonathan A. Bernstein, Stephan Züchner, (unknown), Michael D. Greicius, Stephen B. Montgomery, Michael C. Schatz, Matthew T. Wheeler, Alexis Battle	2
3	Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease 2024 ·Brain ·Christopher J. Record, Menelaos Pipis, Mariola Skorupinska, Julian Blake, Roy Poh, James M. Polke, (unknown), Tina Nanji, Stephan Züchner, Andrea Cortese, Henry Houlden, Alexander M. Rossor, Matilde Laurá, Mary M. Reilly	13
4	Assessment of the Clinical Interactions of GAA Repeat Expansions in FGF14 and FXN 2024 ·Neurology Genetics ·(unknown), David Pellerin, Matt C. Danzi, Stephan Züchner, Bernard Brais, Gabriel Matos‐Rodrigues, André Nussenzweig, Karen Usdin, (unknown), Jill S. Napierala, David R. Lynch, Марек Напиерала	1
5	EFEMP1 haploinsufficiency causes a Marfan‐like hereditary connective tissue disorder 2024 ·American Journal of Medical Genetics Part A ·Irman Forghani, (unknown), (unknown), Stephanie Bivona, (unknown), Alejo A. Morales, Stephan Züchner, Güney Bademci, Mustafa Tekin	1
6	Spinocerebellar ataxia 27B: episodic symptoms and acetazolamide response in 34 patients 2023 ·Brain Communications ·(unknown), Elisabetta Indelicato, David Pellerin, (unknown), Matt C. Danzi, Marie‐Josée Dicaire, Céline Bonnet, Henry Houlden, Stephan Züchner, Matthis Synofzik, Phillipa J. Lamont, M. Renaud, Sylvia Boesch, Bernard Brais	12
7	TSG101 negatively regulates mitochondrial biogenesis in axons 2021 ·Proceedings of the National Academy of Sciences ·(unknown), Dana M. Bis‐Brewer, Amy E. Sheehan, (unknown), Daniel C. Maddison, Stephan Züchner, Gaynor A. Smith, Marc Freeman	18
8	Restoring Shank3 in the rostral brainstem of shank3ab−/− zebrafish autism models rescues sensory deficits 2021 ·Communications Biology ·Robert A. Kozol, David M. James, (unknown), (unknown), Stephan Züchner, Julia E. Dallman	13
9	Functional Network Profiles in ARSACS Disclosed by Aptamer-Based Proteomic Technology 2021 ·Frontiers in Neurology ·Federica Morani, Stefano Doccini, Giovanna Chiorino, Fabiana Fattori, Daniele Galatolo, (unknown), Federica Gemignani, Stephan Züchner, Enrico Bertini, Filippo M. Santorelli	10
10	Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease 2020 ·PLoS ONE ·Elena Buglo, (unknown), (unknown), David Sant, Matt C. Danzi, Alexander J. Abrams, Julia E. Dallman, Stephan Züchner	36
11	Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48) 2016 ·Neurology Genetics ·Jennifer Hirst, Marianna Madeo, Katrien Smets, James R. Edgar, Lüdger Schöls, Jun Li, (unknown), Tine Deconinck, Jonathan Baets, Elisabeth Van Aken, Jan De Bleecker, Manuel B. Datiles, Ricardo H. Roda, Joachim Liepert, Stephan Züchner, Caterina Mariotti, Peter De Jonghe, Craig Blackstone, Michael C. Kruer	24
12	Genetic background of the hereditary spastic paraplegia phenotypes in Hungary — An analysis of 58 probands 2016 ·Journal of the Neurological Sciences ·(unknown), Zoltán Grosz, Michael Gonzalez, (unknown), (unknown), Anikó Gál, Edina Varga, Péter Klivènyi, Júlia Koller, Stephan Züchner, Mária Judit Molnár	24
13	Rare Manifestation of a c.290 C>T, p.Gly97GluVCPMutation 2015 ·SHILAP Revista de lepidopterología ·Nivedita U. Jerath, (unknown), Steven A. Moore, Michael E. Shy, Conrad C. Weihl, Tsui‐Fen Chou, Tiffany Grider, Michael Gonzalez, Stephan Züchner, Andrea Swenson	16
14	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 2013 ·Human Molecular Genetics ·Marina Kennerson, Eppie M. Yiu, David Chuang, (unknown), Shih-Chia Tso, (unknown), Rama Chaudhry, Alexander P. Drew, Gary Rance, Martin B. Delatycki, Stephan Züchner, Monique M. Ryan, Garth A. Nicholson	56
15	In vivo Electroporation and Non-protein Based Screening Assays to Identify Antibodies Against Native Protein Conformations 2011 ·Hybridoma ·Pirouz Daftarian, (unknown), (unknown), Changli Wei, Alan King, Juan Pablo de Rivero Vaccari, Lloye M. Dillon, Justin Price, Howard J. Leung, Brittany M. Ashlock, Enrique A. Mesri, Víctor Pérez, Stephan Züchner, Jochen Reiser, Vance Lemmon, Robert W. Keane	6
16	A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14 2011 ·Human Mutation ·Byung‐Ok Choi, (unknown), Young Se Hyun, (unknown), (unknown), Heasoo Koo, (unknown), Young‐Chul Choi, Jeong Hyun Yoo, Jong‐Won Kim, Kee Duk Park, Kyoung‐Gyu Choi, Song Ja Kim, Stephan Züchner, Ki Wha Chung	41
17	Social support in older individuals: The role of the BDNF Val66Met polymorphism 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Warren D. Taylor, Stephan Züchner, Douglas R. McQuoid, David C. Steffens, Dan G. Blazer, K. Ranga Krishnan	18
18	Update on psychiatric genetics 2007 ·Genetics in Medicine ·Stephan Züchner, (unknown), Marcy C. Speer, Jean C. Beckham	11
19	Mutations in Mitofusin 2 are a major cause for autosomal dominant axonal Charcot-Marie-Tooth neuropathy 2005 ·Journal of the Peripheral Nervous System ·Vincent Timmerman, Kristl G. Claeys, K. Verhoeven, Stephan Züchner, (unknown), (unknown), Peter De Jonghe	1
20	Hypertrophic nerve roots in a case of Roussy-Lévy syndrome 2002 ·Neuroradiology ·C. Haubrich, Timo Krings, Jan Senderek, Stephan Züchner, J. M. Schröder, J. Noth, Rudolf Töpper	5

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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