Carsten Bergmann

14.7k total citations · 1 hit paper
168 papers, 5.2k citations indexed

About

Carsten Bergmann is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Carsten Bergmann has authored 168 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Molecular Biology, 98 papers in Genetics and 24 papers in Nephrology. Recurrent topics in Carsten Bergmann's work include Genetic and Kidney Cyst Diseases (74 papers), Renal and related cancers (59 papers) and Genetic Syndromes and Imprinting (37 papers). Carsten Bergmann is often cited by papers focused on Genetic and Kidney Cyst Diseases (74 papers), Renal and related cancers (59 papers) and Genetic Syndromes and Imprinting (37 papers). Carsten Bergmann collaborates with scholars based in Germany, United States and Netherlands. Carsten Bergmann's co-authors include Klaus Zerres, Jan Senderek, Lisa M. Guay‐Woodford, Peter C. Harris, Dorien J.M. Peters, Vicente E. Torres, Shigeo Horie, Hanno J. Bolz, Sabine Rudnik‐Schöneborn and Thomas Eggermann and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Carsten Bergmann

161 papers receiving 5.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Polycystic kidney disease

2018 451 citations Carsten Bergmann et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Carsten Bergmann Germany	38	3.5k	3.4k	645	617	536	168	5.2k
Toshio Mochizuki Japan	27	2.3k 0.7×	2.2k 0.6×	278 0.4×	737 1.2×	761 1.4×	109	4.1k
Gabriele Gillessen‐Kaesbach Germany	38	2.8k 0.8×	2.8k 0.8×	949 1.5×	215 0.3×	181 0.3×	133	4.7k
Martine Le Merrer France	46	4.0k 1.2×	4.6k 1.3×	642 1.0×	219 0.4×	212 0.4×	130	7.9k
Marco Seri Italy	38	1.4k 0.4×	2.3k 0.7×	202 0.3×	279 0.5×	394 0.7×	193	5.3k
Marc Jeanpierre France	37	1.3k 0.4×	3.8k 1.1×	515 0.8×	298 0.5×	175 0.3×	120	4.7k
Oxana Ibraghimov‐Beskrovnaya United States	29	2.0k 0.6×	3.7k 1.1×	160 0.2×	624 1.0×	203 0.4×	43	4.6k
Sabine Rudnik‐Schöneborn Germany	40	1.7k 0.5×	4.0k 1.2×	628 1.0×	320 0.5×	112 0.2×	154	5.9k
Andreas Winterpacht Germany	33	1.4k 0.4×	2.5k 0.7×	275 0.4×	122 0.2×	330 0.6×	85	3.7k
M. Todd Valerius United States	30	1.1k 0.3×	5.5k 1.6×	579 0.9×	202 0.3×	867 1.6×	43	7.1k
Carol A. Wise United States	35	1.2k 0.4×	2.7k 0.8×	103 0.2×	359 0.6×	175 0.3×	85	5.7k

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-authorship network of co-authors of Carsten Bergmann

This figure shows the co-authorship network connecting the top 25 collaborators of Carsten Bergmann. A scholar is included among the top collaborators of Carsten Bergmann 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 Carsten Bergmann. Carsten Bergmann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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

20 of 20 papers shown

Schönauer, Ria, Georgia Vasileiou, Alma Kuechler, et al.. (2024). Pathogenic PHIP Variants are Variably Associated With CAKUT. Kidney International Reports. 9(8). 2484–2497. 3 indexed citations

Bachmann, Nadine, Bernd Auber, Anibh M. Das, et al.. (2023). Differenzierte Herangehensweise und Testung seltener genetischer Erkrankungen im Kindes- und Jugendalter. Monatsschrift Kinderheilkunde. 172(7). 587–594.

Kummer, Sebastian, Susanne Rinné, Gunnar Seemann, et al.. (2022). Hyperinsulinemic Hypoglycemia Associated with a CaV1.2 Variant with Mixed Gain- and Loss-of-Function Effects. International Journal of Molecular Sciences. 23(15). 8097–8097. 3 indexed citations

Schönauer, Ria, Anja Friedrich, Janett Fischer, et al.. (2022). Modelling polycystic liver disease progression using age-adjusted liver volumes and targeted mutational analysis. JHEP Reports. 4(11). 100579–100579. 3 indexed citations

Schönauer, Ria, Anette Bachmann, Julia Hentschel, et al.. (2019). Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease. Kidney International. 96(1). 222–230. 52 indexed citations

Hoff, Sylvia, Daniel Epting, Nathalie Falk, et al.. (2018). The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development. Journal of Biological Chemistry. 293(39). 15243–15255. 11 indexed citations

Schalk, Gesa, Michael Kirschfink, Cyrill Wehling, et al.. (2015). A complicated case of atypical hemolytic uremic syndrome with frequent relapses under eculizumab. Pediatric Nephrology. 30(6). 1039–1042. 13 indexed citations

Khan, Arif O., et al.. (2015). Peripherin mutations cause a distinct form of recessive Leber congenital amaurosis and dominant phenotypes in asymptomatic parents heterozygous for the mutation. British Journal of Ophthalmology. 100(2). 209–215. 17 indexed citations

Khan, Arif O., Carsten Bergmann, Christine Neuhaus, & Hanno J. Bolz. (2014). A Distinct Vitreo-retinal Dystrophy with Early-onset Cataract from RecessiveKCNJ13Mutations. Ophthalmic Genetics. 36(1). 79–84. 22 indexed citations

10.

Neuhaus, Christopher, Christian Betz, Carsten Bergmann, & Hanno J. Bolz. (2014). Genetik der kongenitalen Aniridie. Der Ophthalmologe. 111(12). 1157–1163. 9 indexed citations

11.

Bergmann, Carsten, Saeed Reza Ghaffari, Manfred Schürmann, et al.. (2012). Next-generation Sequencing Of All Known Genes For RP And Allied Diseases Identifies The Causative Mutations In The Majority Of Patients. Investigative Ophthalmology & Visual Science. 53(14). 4525–4525. 1 indexed citations

12.

Bergmann, Carsten, et al.. (2012). Une cause rare de douleurs abdominales. La Revue de Médecine Interne. 33(10). 593–594. 1 indexed citations

13.

Chaki, Moumita, Julia Hoefele, Susan J. Allen, et al.. (2011). Genotype–phenotype correlation in 440 patients with NPHP-related ciliopathies. Kidney International. 80(11). 1239–1245. 83 indexed citations

14.

Fischer, Dagmar‐C., Lars Pape, Christopher J. Ward, et al.. (2009). Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD). Nephrology Dialysis Transplantation. 24(6). 1819–1827. 64 indexed citations

15.

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

16.

Fiedler, Jörg, Carsten Bergmann, & Rolf E. Brenner. (2003). X-linked spondyloepiphyseal dysplasia tardaMolecular cause of a heritable disorder associated with early degenerative joint disease. Acta Orthopaedica Scandinavica. 74(6). 737–741. 8 indexed citations

17.

Bergmann, Carsten. (2003). Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia. Brain. 126(7). 1537–1544. 93 indexed citations

18.

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

19.

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

20.

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

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