Jan Senderek

11.0k citations

92 papers · 4.3k · h-index 39

Impact in

Cellular and Molecular Neuroscience top 1%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting

Papers in

Cellular and Molecular Neuroscience 46
- Hereditary Neurological Disorders 42
- Genetic Neurodegenerative Diseases 16
Molecular Biology 38
- Renal and related cancers 8

Co-authors: Carsten Bergmann (28 shared papers)Klaus Zerres (30 shared papers)Sabine Rudnik‐Schöneborn (20 shared papers)Thomas Eggermann (12 shared papers)Gregory G. Germino (5 shared papers)Stefan Somlo (5 shared papers)Lisa M. Guay‐Woodford (5 shared papers)Laszlo Furu (5 shared papers)
Journals: Neurology (5 papers)Clinical Genetics (5 papers)Brain (5 papers)Human Mutation (5 papers)Human Molecular Genetics (4 papers)
Partner nations: Germany Switzerland United States

In The Last Decade

Jan Senderek

92 papers receiving 4.1k citations

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 92 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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, Ernie Esquivel, Raoul Zeltner, Sabine Rudnik‐Schöneborn, Michael Mrug, William E. Sweeney, Ellis D. Avner, Klaus Zerres, Lisa M. Guay‐Woodford, Stefan Somlo, Gregory G. Germino	2002	392
2	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 Schneider, Christian Dornia, Sabine Rudnik‐Schöneborn, Martin Konrad, Claus Peter Schmitt, Tomáš Seeman, Thomas J. Neuhaus, Udo Vester, Jutta Kirfel, Reinhard Büttner, Klaus Zerres	2005	229
3	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	212
4	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, Haluk Topaloğlu, Sandra A. Farrell, Gudrun Nürnberg, Peter Nürnberg, Peter De Jonghe, Andreas Gal, Christoph Kaether, Vincent Timmerman, Christian A. Hübner	2009	195
5	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, Luiz F. Onuchic, Monica de Baca, Gregory G. Germino, Lisa M. Guay‐Woodford, Stefan Somlo, Markus Moser, (unknown), Klaus Zerres	2003	165
6	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, M. Schöning, Saskia Biskup, Sabine Rudnik‐Schöneborn, Jan Senderek, Karl‐Titus Hoffmann, Patrick MacLeod, Johannes Schwarz, Benjamin Bender, Stefan Krüger, Friedmar R. Kreuz, Peter Bauer, Lüdger Schöls	2013	134
7	PKHD1mutations in autosomal recessive polycystic kidney disease (ARPKD) Human Mutation ·Carsten Bergmann, Jan Senderek, Fabian Küpper, Frank Schneider, Christian Dornia, Ellen Windelen, Thomas Eggermann, Sabine Rudnik‐Schöneborn, Jutta Kirfel, Laszlo Furu, Luiz F. Onuchic, Sandro Rossetti, Peter C. Harris, Stefan Somlo, Lisa M. Guay‐Woodford, Gregory G. Germino, Markus Moser, Reinhard Büttner, Klaus Zerres	2004	128
8	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, Susanne Roosing, Jan Senderek, Peter Nürnberg, Frans P.M. Cremers, Klaus Zerres, Carsten Bergmann	2007	112
9	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 G. Gharavi, Xiaoying Hou, Ernie Esquivel, Yasuyuki Nagasawa, Carsten Bergmann, Jan Senderek, Ellis D. Avner, Klaus Zerres, Gregory G. Germino, Lisa M. Guay‐Woodford, Stefan Somlo	2003	99
10	Identification and Characterization of Pkhd1, the Mouse Orthologue of the Human ARPKD Gene Journal of the American Society of Nephrology ·Yasuyuki Nagasawa, Sonja Matthiesen, Luiz F. Onuchic, Xiaoying Hou, Carsten Bergmann, Ernie Esquivel, Jan Senderek, Zhiyong Ren, Raoul Zeltner, Laszlo Furu, Ellis D. Avner, Markus Moser, Stefan Somlo, Lisa M. Guay‐Woodford, Reinhard Büttner, Klaus Zerres, Gregory G. Germino	2002	98
11	Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy Brain ·Jan Senderek	2003	97
12	Transient, Recurrent, White Matter Lesions in X-linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation Archives of Neurology ·C. Oliver Hanemann, Carsten Bergmann, Jan Senderek, Klaus Zerres, Ann-Dorte Sperfeld	2003	92
13	SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system Proceedings of the National Academy of Sciences ·Estelle Arnaud, Jennifer Zenker, Anne-Sophie de Preux Charles, Claudia Stendel, Andreas Roos, Jean‐Jacques Médard, Nicolas Tricaud, H. O. Kleine, Bernhard Lüscher, Joachim Weis, Ueli Suter, Jan Senderek, Roman Chrast	2009	88
14	Reduced folate transport to the CNS in female Rett patients Neurology ·V. Ramaekers, Steen Ingemann Hansen, Jan Holm, Thomas Opladen, Jan Senderek, Martin Häusler, G. Heimann, Brian Fowler, Robert Maiwald, Nenad Blau	2003	84
15	Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations Neurology ·Hamid Azzedine, N. Ravisé, Christophe Verny, A.A.W.M. Gabreëls‐Festen, Martin Lammens, D. Grid, Jean‐Michel Vallat, G. Durosier, Jan Senderek, Sonia Nouioua, Tarik Hamadouche, Ahmed Bouhouche, A. Guilbot, Claudia Stendel, Merle Ruberg, Alexis Brice, Nazha Birouk, O. Dubourg, Mériem Tazir, Éric Leguern	2006	83
16	SH3TC2, a protein mutant in Charcot–Marie–Tooth neuropathy, links peripheral nerve myelination to endosomal recycling Brain ·Claudia Stendel, Andreas Roos, H. O. Kleine, Estelle Arnaud, Murat Özçelik, Páris Sidiropoulos, Jennifer Zenker, Fanny Schüpfer, Ute Lehmann, Radoslaw M. Sobota, David W. Litchfield, Bernhard Lüscher, Roman Chrast, Ueli Suter, Jan Senderek	2010	78
17	Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia The American Journal of Human Genetics ·Carsten Bergmann, Jan Senderek, Dirk Anhuf, Christian T. Thiel, Arif B. Ekici, Pamela Poblete‐Gutiérrez, Maurice A. M. Van Steensel, Dominik Seelow, Gudrun Nürnberg, Hans H. Schild, Peter Nürnberg, André Reis, Jorge Frank, Klaus Zerres	2006	76
18	X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations Journal of the Neurological Sciences ·Jan Senderek, Benita Hermanns, Carsten Bergmann, Babak Boroojerdi, Malek Bajbouj, Marcel Hungs, Vincent T. Ramaekers, Stefan Quasthoff, Dieter Karch, J. M. Schröder	1999	73
19	A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)† Hepatology ·Markus Moser, Sonja Matthiesen, Jutta Kirfel, Hubert Schorle, Carsten Bergmann, Jan Senderek, Sabine Rudnik‐Schöneborn, Klaus Zerres, Reinhard Buettner	2005	70
20	Diagnostic algorithms in Charcot–Marie–Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients Clinical Genetics ·Sabine Rudnik‐Schöneborn, D.V. Tolle, Jan Senderek, Katja Eggermann, Miriam Elbracht, Uwe Kornak, Maja von der Hagen, Janbernd Kirschner, Barbara Leube, Wolfgang Müller‐Felber, Ulrike Schara, Katja von Au, Dagmar Wieczorek, Caroline Bußmann, Klaus Zerres	2015	66

About Jan Senderek

Jan Senderek is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology, Genetics and Neurology, having authored 92 papers that have together received 4.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (42 papers), Genetic Neurodegenerative Diseases (16 papers), Genetic and Kidney Cyst Diseases (15 papers), Cellular transport and secretion (12 papers), Cellular Mechanics and Interactions (11 papers), Neurological diseases and metabolism (10 papers), Renal and related cancers (8 papers) and Genetic Syndromes and Imprinting (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.4k citations), Genetics (1.6k citations), Neurology (428 citations), Cell Biology (632 citations) and Neurology (510 citations). Jan Senderek has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Carsten Bergmann, Klaus Zerres, Sabine Rudnik‐Schöneborn, Thomas Eggermann, Gregory G. Germino, Stefan Somlo, Lisa M. Guay‐Woodford, Laszlo Furu, Luiz F. Onuchic and Fabian Küpper. Their work appears in journals such as Neurology, Clinical Genetics, Brain, Human Mutation and Human Molecular 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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About Jan Senderek

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