Jan Senderek

10.9k total citations
92 papers, 3.9k citations indexed

About

Jan Senderek is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Jan Senderek has authored 92 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cellular and Molecular Neuroscience, 46 papers in Molecular Biology and 35 papers in Cell Biology. Recurrent topics in Jan Senderek's work include Hereditary Neurological Disorders (43 papers), Genetic Neurodegenerative Diseases (19 papers) and Genetic and Kidney Cyst Diseases (15 papers). Jan Senderek is often cited by papers focused on Hereditary Neurological Disorders (43 papers), Genetic Neurodegenerative Diseases (19 papers) and Genetic and Kidney Cyst Diseases (15 papers). Jan Senderek collaborates with scholars based in Germany, United States and Switzerland. Jan Senderek's co-authors include Carsten Bergmann, Klaus Zerres, Sabine Rudnik‐Schöneborn, Thomas Eggermann, Lisa M. Guay‐Woodford, Gregory G. Germino, Laszlo Furu, Luiz F. Onuchic, Stefan Somlo and Reinhard Büttner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Brain.

In The Last Decade

Jan Senderek

91 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jan Senderek Germany 37 2.2k 1.5k 1.4k 670 552 92 3.9k
Elizabeth C. Engle United States 39 1.9k 0.9× 1.2k 0.8× 631 0.5× 799 1.2× 477 0.9× 112 4.4k
Elise Héon Canada 44 5.1k 2.3× 1.7k 1.1× 775 0.6× 833 1.2× 162 0.3× 144 7.3k
Tayfun Özçelık Türkiye 30 1.5k 0.7× 859 0.6× 541 0.4× 317 0.5× 218 0.4× 59 3.1k
Esther de Graaff Netherlands 35 2.4k 1.1× 2.1k 1.4× 605 0.4× 477 0.7× 668 1.2× 61 4.4k
H. David Shine United States 30 1.5k 0.7× 1.0k 0.7× 1.2k 0.9× 178 0.3× 238 0.4× 50 3.7k
James M. Killian United States 27 1.0k 0.5× 522 0.4× 1.6k 1.2× 271 0.4× 1.0k 1.8× 39 3.6k
Bernd Wollnik Germany 36 2.8k 1.3× 1.6k 1.1× 306 0.2× 304 0.5× 173 0.3× 138 4.3k
Dennis Dooijes Netherlands 38 3.2k 1.5× 619 0.4× 598 0.4× 304 0.5× 689 1.2× 110 5.7k
Alfredo Brusco Italy 32 2.2k 1.0× 799 0.5× 859 0.6× 188 0.3× 355 0.6× 141 3.3k
Anthony Antonellis United States 30 2.4k 1.1× 716 0.5× 931 0.7× 539 0.8× 179 0.3× 75 3.8k

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-authorship network of co-authors of Jan Senderek

This figure shows the co-authorship network connecting the top 25 collaborators of Jan Senderek. A scholar is included among the top collaborators of Jan Senderek 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 Jan Senderek. Jan Senderek 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.
Roos, Andreas, Martin Häusler, Laxmikanth Kollipara, et al.. (2024). HNRNPA1 de novo Variant Associated with Early Childhood Onset, Rapidly Progressive Generalized Myopathy. Journal of Neuromuscular Diseases. 11(5). 1131–1137. 2 indexed citations
2.
Laššuthová, Petra, Katharina Vill, Sevim Erdem‐Özdamar, et al.. (2018). Novel SBF2 mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2. Clinical Genetics. 94(5). 467–472. 7 indexed citations
3.
Kleffner, Ilka, Burkhard Gess, Catharina Korsukewitz, et al.. (2015). Behr syndrome with homozygous C19ORF12 mutation. Journal of the Neurological Sciences. 357(1-2). 115–118. 15 indexed citations
4.
Lupo, Vincenzo, Eduardo Calpena, Luca Bartesaghi, et al.. (2013). Sh3tc2 deficiency affects neuregulin‐1/ErbB signaling. Glia. 61(7). 1041–1051. 36 indexed citations
5.
Schneiderat, Peter, Wolfram Kreß, Bernd Rautenstrauß, et al.. (2013). Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes. BMC Medical Genetics. 14(1). 92–92. 17 indexed citations
6.
Synofzik, Matthis, Anne S. Soehn, Janina Gburek‐Augustat, et al.. (2013). Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum. Orphanet Journal of Rare Diseases. 8(1). 41–41. 125 indexed citations
7.
Wüller, Stefan, et al.. (2009). Proteasomal inhibition alters the trafficking of the neurotrophin receptor TrkA. Biochemical and Biophysical Research Communications. 387(2). 360–364. 15 indexed citations
8.
Kurth, Ingo, J. Christopher Hennings, Antje K. Huebner, et al.. (2009). Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy. Nature Genetics. 41(11). 1179–1181. 184 indexed citations
9.
Brüchle, Nadina Ortiz, Jorge Frank, Valeska Frank, et al.. (2007). RSPO4 Is the Major Gene in Autosomal-Recessive Anonychia and Mutations Cluster in the Furin-Like Cysteine-Rich Domains of the Wnt Signaling Ligand R-spondin 4. Journal of Investigative Dermatology. 128(4). 791–796. 35 indexed citations
10.
Neusch, Clemens, et al.. (2007). Mitofusin 2 gene mutation (R94Q) causing severe early‐onset axonal polyneuropathy (CMT2A). European Journal of Neurology. 14(5). 575–577. 23 indexed citations
11.
Frank, Valeska, Nadina Ortiz Brüchle, Suzanna G.M. Frints, et al.. (2007). Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome. Human Mutation. 28(6). 638–639. 17 indexed citations
12.
Roos, Andreas, Sabine Rudnik‐Schöneborn, Katja Eggermann, et al.. (2006). Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH. European Journal of Medical Genetics. 49(6). 505–510. 5 indexed citations
13.
Senderek, Jan. (2003). Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15. Human Molecular Genetics. 12(3). 349–356. 197 indexed citations
14.
Senderek, Jan. (2003). Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15. Human Molecular Genetics. 12(3). 349–356. 2 indexed citations
15.
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
16.
Onuchic, Luiz F., Laszlo Furu, Yasuyuki Nagasawa, et al.. (2002). 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. 70(5). 1305–1317. 340 indexed citations
17.
Ramaekers, V., Jan Senderek, Martin Häusler, et al.. (2001). A Novel Neurodevelopmental Syndrome Responsive to 5-Hydroxytryptophan and Carbidopa. Molecular Genetics and Metabolism. 73(2). 179–187. 13 indexed citations
18.
Senderek, Jan, et al.. (2001). Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain. Journal of the Neurological Sciences. 192(1-2). 49–51. 12 indexed citations
19.
Bergmann, Carsten, Jan Senderek, Benita Hermanns, et al.. (2000). Becker muscular dystrophy combined with x-linked Charcot-Marie-Tooth neuropathy. Muscle & Nerve. 23(5). 818–823. 16 indexed citations
20.
Senderek, Jan, Benita Hermanns, Ute Lehmann, et al.. (2000). Charcot‐Marie‐Tooth Neuropathy Type 2 and P0 Point Mutations: Two Novel Amino Acid Substitutions (Asp61Gly; Tyr119Cys) and a Possible “Hotspot” on Thr124Met. Brain Pathology. 10(2). 235–248. 55 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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