Carsten Bergmann

14.7k citations

168 papers · 5.2k indexed · 1 hit paper · h-index 38

Impact in

Genetics top 0.2%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
Nephrology top 1%
- Renal Diseases and Glomerulopathies

Papers in ⓘ

Genetics 98
- Genetic and Kidney Cyst Diseases 74
- Genetic Syndromes and Imprinting 37
Nephrology 24
- Renal Diseases and Glomerulopathies 22

Co-authors: Klaus Zerres (36 shared papers)Jan Senderek (28 shared papers)Lisa M. Guay‐Woodford (7 shared papers)Peter C. Harris (2 shared papers)Dorien J.M. Peters (3 shared papers)Shigeo Horie (1 shared paper)Vicente E. Torres (1 shared paper)Hanno J. Bolz (18 shared papers)
Journals: Pediatric Nephrology (7 papers)Human Mutation (6 papers)Nephrology Dialysis Transplantation (6 papers)European Journal of Human Genetics (5 papers)The American Journal of Human Genetics (5 papers)
Partner nations: Germany United States Netherlands

In The Last Decade

Carsten Bergmann

161 papers receiving 5.1k citations

Hit Papers

align trajectories log scale

Polycystic kidney disease 2018 · 451 citations

Peers

Countries citing papers authored by Carsten Bergmann

Since Specialization

Citations

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

Fields of papers citing papers by Carsten Bergmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Carsten Bergmann, 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 Carsten Bergmann Line = papers co-authored together Carsten Bergmann links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 168 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Polycystic kidney disease Nature Reviews Disease Primers ·Carsten Bergmann, Lisa M. Guay‐Woodford, Peter C. Harris, Shigeo Horie, Dorien J.M. Peters, Vicente E. Torres Hit paper breakdown →	2018	451
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, 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	340
3	Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta The American Journal of Human Genetics ·Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno J. Bolz, Cecilia Giunta, Carsten Bergmann, Marianne Rohrbach, Friederike Koerber, Katharina Zimmermann, Petra de Vries, Brunhilde Wirth, Eckhard Schöenau, Bernd Wollnik, Joris A. Veltman, Alexander Hoischen, Christian Netzer	2011	250
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 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	186
5	Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease Journal of the American Society of Nephrology ·Carsten Bergmann, Jennifer von Bothmer, Nadina Ortiz Brüchle, Andreas Venghaus, Valeska Frank, Henry Fehrenbach, Tobias Hampel, Lars Pape, Annegret Buske, Jón J. Jónsson, Nanette Sarioglu, Antónia Santos, José Carlos Ferreira, Jan U. Becker, Reinhold Cremer, Julia Hoefele, Marcus R. Benz, Lutz T. Weber, Reinhard Buettner, Klaus Zerres	2011	161
6	Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment Journal of Medical Genetics ·Katrien Janssens, Filip Vanhoenacker, M Bonduelle, Leon Verbruggen, Lionel Van Maldergem, Stuart H. Ralston, Núria Guañabens, Nicola Migone, Shlomo Wientroub, Maria Teresa Divizia, Carsten Bergmann, Craig R. Bennett, Suat Şimşek, S. Melançon, Tim Cundy, Wim Van Hul	2005	151
7	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, Reinhard BuCombining Diaeresisttner, Klaus Zerres	2003	146
8	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	115
9	ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies Pediatric Nephrology ·Carsten Bergmann	2014	112
10	Disruption of a Ciliary B9 Protein Complex Causes Meckel Syndrome The American Journal of Human Genetics ·William E. Dowdle, Jon F. Robinson, Andreas Kneist, Ma Salomé Sirerol-Piquer, Suzanna G.M. Frints, Kevin C. Corbit, Norran A. Zaghloul, Gesina van Lijnschoten, Léon G.M. Mulders, Dideke E. Verver, Klaus Zerres, Randall R. Reed, Tania Attié‐Bitach, Colin A. Johnson, José Manuel García‐Verdugo, Nicholas Katsanis, Carsten Bergmann, Jeremy F. Reiter	2011	109
11	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	108
12	Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia Brain ·Carsten Bergmann	2003	93
13	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	90
14	Transforming Growth Factor-β1 Mutations in Camurati-Engelmann Disease Lead to Increased Signaling by Altering either Activation or Secretion of the Mutant Protein Journal of Biological Chemistry ·Katrien Janssens, Peter ten Dijke, Stuart H. Ralston, Carsten Bergmann, Wim Van Hul	2003	87
15	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	87
16	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	86
17	Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practice Nephrology Dialysis Transplantation ·Nine V.A.M. Knoers, Corinne Antignac, Carsten Bergmann, Karin Dahan, Sabrina Giglio, Laurence Heidet, Beata S. Lipska‐Ziętkiewicz, Marina Noris, Giuseppe Remuzzi, Rosa Vargas‐Poussou, Franz Schaefer	2021	86
18	Genotype–phenotype correlation in 440 patients with NPHP-related ciliopathies Kidney International ·Moumita Chaki, Julia Hoefele, Susan J. Allen, Gokul Ramaswami, Sabine Janssen, Carsten Bergmann, John R. Heckenlively, Edgar A. Otto, Friedhelm Hildebrandt	2011	83
19	Genetics of Autosomal Recessive Polycystic Kidney Disease and Its Differential Diagnoses Frontiers in Pediatrics ·Carsten Bergmann	2018	78
20	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	71

About Carsten Bergmann

Carsten Bergmann is a scholar working on Genetics, Nephrology, Transplantation, Molecular Biology and Immunology and Allergy, having authored 168 papers that have together received 5.2k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (74 papers), Renal and related cancers (59 papers), Genetic Syndromes and Imprinting (37 papers), Renal Diseases and Glomerulopathies (22 papers), Hedgehog Signaling Pathway Studies (14 papers), Complement system in diseases (12 papers), Biomedical Research and Pathophysiology (12 papers) and Hereditary Neurological Disorders (10 papers). The work is most often cited by research in Genetics (3.5k citations), Nephrology (536 citations), Molecular Biology (3.4k citations), Pathology and Forensic Medicine (617 citations) and Pediatrics, Perinatology and Child Health (645 citations). Carsten Bergmann has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Klaus Zerres, Jan Senderek, Lisa M. Guay‐Woodford, Peter C. Harris, Dorien J.M. Peters, Shigeo Horie, Vicente E. Torres, Hanno J. Bolz, Sabine Rudnik‐Schöneborn and Thomas Eggermann. Their work appears in journals such as Pediatric Nephrology, Human Mutation, Nephrology Dialysis Transplantation, European Journal of Human Genetics and The American Journal of Human 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.

Explore authors with similar magnitude of impact