Jan Senderek

11.2k citations

133 papers · 8.7k · 1 hit paper · h-index 51

Impact in

Cellular and Molecular Neuroscience top 0.5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 1%
- Neurological diseases and metabolism

Papers in

Cellular and Molecular Neuroscience 62
- Hereditary Neurological Disorders 54
- Genetic Neurodegenerative Diseases 22
Cell Biology 45
- Cellular transport and secretion 18
- Cellular Mechanics and Interactions 12
- Endoplasmic Reticulum Stress and Disease 9

Co-authors: Carsten Bergmann (29 shared papers)Klaus Zerres (31 shared papers)Sabine Rudnik-Schöneborn (21 shared papers)Thomas Eggermann (12 shared papers)Laszlo Furu (5 shared papers)Luiz F. Onuchic (5 shared papers)Stefan Somlo (5 shared papers)Lisa M. Guay‐Woodford (5 shared papers)
Journals: Brain (14 papers)The American Journal of Human Genetics (10 papers)Neurology (7 papers)Clinical Genetics (6 papers)Nature Genetics (6 papers)
Partner nations: Germany United Kingdom United States

In The Last Decade

Jan Senderek

132 papers receiving 8.4k citations

Jan Senderek's Hit Papers

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A 2004 · 1.3k citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2004 Nature Genetics

Peers

Countries citing papers authored by Jan Senderek

Since Specialization

Citations

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

Fields of papers citing papers by Jan Senderek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jan Senderek, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jan Senderek Line = papers co-authored together Jan Senderek links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 133 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A Nature Genetics ·Stephan L. Zuchner, Irina Mersiyanova, Maria Muglia, Nisrine Bissar‐Tadmouri, Julie M. Rochelle, Elena L. Dadali, Mario Zappia, Eva Nelis Hit paper breakdown →	2004	1324
2	PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats The American Journal of Human Genetics ·Luiz F. Onuchic, Laszlo Furu, Yasuyuki Nagasawa, Xiaoying Hou, Thomas Eggermann, Zhiyong Ren, Carsten Bergmann, Jan Senderek	2002	418
3	Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia The American Journal of Human Genetics ·Carsten Bergmann, Manfred Fliegauf, Nadina Ortiz‐Brüchle, Valeska Frank, Heike Olbrich, Janbernd Kirschner, Bernhard Schermer, Ingolf Schmedding	2008	263
4	Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD) Kidney International ·Carsten Bergmann, Jan Senderek, Ellen Windelen, Fabian Küpper, Iris Middeldorf, Frank W. Schneider, Christian Dornia, Sabine Rudnik-Schöneborn	2005	256
5	Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C Nature Genetics ·Michaela Auer‐Grumbach, Andrea Olschewski, Lea Papić, Hannie Kremer, Meriel McEntagart, Sabine Uhrig, Carina Fischer, Eleonore Fröhlich	2009	222
6	Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15 Human Molecular Genetics ·Jan Senderek	2003	217
7	Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy Nature Genetics ·Ingo Kurth, Torsten Pamminger, J. Christopher Hennings, Désirée Soehendra, Antje K. Huebner, Annelies Rotthier, Jonathan Baets, Jan Senderek	2009	214
8	Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration Nature Genetics ·Jijun Wan, Michael Yourshaw, Hafsa Mamsa, Sabine Rudnik-Schöneborn, Manoj P. Menezes, Ji Eun Hong, Derek W. Leong, Jan Senderek	2012	207
9	Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy Nature Genetics ·Jan Senderek, Michael J. B. Krieger, Claudia Stendel, Carsten Bergmann, Markus Moser, Nico Breitbach‐Faller, Sabine Rudnik-Schöneborn, Astrid Blaschek	2005	198
10	Spectrum of Mutations in the Gene for Autosomal Recessive Polycystic Kidney Disease (ARPKD/PKHD1) Journal of the American Society of Nephrology ·Carsten Bergmann, Jan Senderek, Beate Sedlacek, Ioannis Pegiazoglou, Patricia Puglia, Thomas Eggermann, Sabine Rudnik-Sch�neborn, Laszlo Furu	2003	177
11	Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy The American Journal of Human Genetics ·Jan Senderek, Carsten Bergmann, Claudia Stendel, Jutta Kirfel, Nathalie Verpoorten, Peter De Jonghe, Vincent Timmerman, Roman Chrast	2003	168
12	Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum Orphanet Journal of Rare Diseases ·Matthis Synofzik, Anne S. Soehn, Janina Gburek‐Augustat, Julia Schicks, Kathrin N. Karle, Rebecca Schüle, Tobias B. Haack, Martin Schöning	2013	147
13	Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect The American Journal of Human Genetics ·Jan Senderek, Juliane S. Müller, Marina Dusl, Tim Matthias Strom, Velina Guergueltcheva, Irmgard Diepolder, Steven H. Laval, Susan Maxwell	2011	138
14	Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3 The American Journal of Human Genetics ·Jan Senderek, Sean M. Garvey, Michael J. B. Krieger, Velina Guergueltcheva, Andoni Urtizberea, Andreas Roos, Miriam Elbracht, Claudia Stendel	2009	137
15	PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD) Human Mutation ·Carsten Bergmann, Jan Senderek, Fabian Küpper, Frank W. Schneider, Christian Dornia, Ellen Windelen, Thomas Eggermann, Sabine Rudnik-Schöneborn	2004	133
16	Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome Human Mutation ·Valeska Frank, Anneke I. den Hollander, Nadina Ortiz‐Brüchle, Marijke N. Zonneveld, Gudrun Nürnberg, Christian Becker, Gabriele du Bois, Heide Kendziorra	2007	127
17	Transcriptional regulator PRDM12 is essential for human pain perception Nature Genetics ·Ya-Chun Chen, Michaela Auer‐Grumbach, Shinya Matsukawa, Manuela Zitzelsberger, Andreas C. Themistocleous, Tim Matthias Strom, Chrysanthi Samara, Adrian Walton Moore	2015	127
18	Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4 The American Journal of Human Genetics ·Claudia Stendel, Andreas Roos, Tine Deconinck, Jorge A. Pereira, François Castagner, Axel Niemann, Janbernd Kirschner, Rudolf Korinthenberg	2007	115
19	Milder Presentation of Recessive Polycystic Kidney Disease Requires Presence of Amino Acid Substitution Mutations Journal of the American Society of Nephrology ·Laszlo Furu, Luiz F. Onuchic, Ali Gharavi, Xiaoying Hou, Ernie L. Esquivel, Yasuyuki Nagasawa, Carsten Bergmann, Jan Senderek	2003	110
20	Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration The EMBO Journal ·Vandana Shashi, Maria M. Magiera, Dennis Klein, Maha Saad Zaki, Kelly Schoch, Sabine Rudnik-Schöneborn, Andrew M. Norman, Osório Lopes Abath Neto	2018	106

About Jan Senderek

Jan Senderek is a scholar working on Cellular and Molecular Neuroscience, Cell Biology, Neurology, Neurology and Genetics, having authored 133 papers that have together received 8.7k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (54 papers), Genetic Neurodegenerative Diseases (22 papers), Cellular transport and secretion (18 papers), Neurological diseases and metabolism (17 papers), Genetic and Kidney Cyst Diseases (16 papers), Cellular Mechanics and Interactions (12 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Endoplasmic Reticulum Stress and Disease (9 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.7k citations), Neurology (868 citations), Cell Biology (1.4k citations), Neurology (1.2k citations) and Genetics (2.3k citations). Jan Senderek has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Carsten Bergmann, Klaus Zerres, Sabine Rudnik-Schöneborn, Thomas Eggermann, Laszlo Furu, Luiz F. Onuchic, Stefan Somlo, Lisa M. Guay‐Woodford, Gregory George Germino and Markus Moser. Their work appears in journals such as Brain, The American Journal of Human Genetics, Neurology, Clinical Genetics and Nature Genetics.

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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Jan Senderek

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In The Last Decade

Jan Senderek

Jan Senderek's Hit Papers

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Fields of papers citing papers by Jan Senderek

All Works

About Jan Senderek

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