Karin Mayer

2.9k total citations
52 papers, 1.0k citations indexed

About

Karin Mayer is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Karin Mayer has authored 52 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 15 papers in Molecular Biology and 13 papers in Genetics. Recurrent topics in Karin Mayer's work include Tuberous Sclerosis Complex Research (15 papers), Connective tissue disorders research (8 papers) and Polyomavirus and related diseases (6 papers). Karin Mayer is often cited by papers focused on Tuberous Sclerosis Complex Research (15 papers), Connective tissue disorders research (8 papers) and Polyomavirus and related diseases (6 papers). Karin Mayer collaborates with scholars based in Germany, United States and Netherlands. Karin Mayer's co-authors include Wolfgang G. Ballhausen, Hans‐Dieter Rott, Mark Nellist, Ulrich Linsenmaier, Brian D. Guth, Thomas Trautmann, Michael Markert, Ralf Wienecke, Dicky Halley and Thomas Licht and has published in prestigious journals such as Oncogene, International Journal of Cancer and American Journal of Kidney Diseases.

In The Last Decade

Karin Mayer

49 papers receiving 981 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karin Mayer Germany 21 390 355 218 185 152 52 1.0k
Hiroaki Mitsuhashi Japan 21 614 1.6× 129 0.4× 103 0.5× 72 0.4× 147 1.0× 55 1.1k
Pierre Chailler Canada 14 462 1.2× 235 0.7× 149 0.7× 132 0.7× 99 0.7× 30 950
Kyuyoung Song South Korea 18 666 1.7× 115 0.3× 103 0.5× 174 0.9× 49 0.3× 33 1.1k
Shaomin Yang China 18 316 0.8× 139 0.4× 54 0.2× 81 0.4× 84 0.6× 56 816
Shoshana Merchav Israel 20 337 0.9× 106 0.3× 150 0.7× 221 1.2× 32 0.2× 37 1.1k
Jason M. Tonne United States 18 397 1.0× 200 0.6× 305 1.4× 207 1.1× 172 1.1× 35 1.0k
Zinger Yang United States 15 1.0k 2.6× 218 0.6× 254 1.2× 178 1.0× 83 0.5× 20 1.4k
Meixiang Yang China 20 495 1.3× 152 0.4× 91 0.4× 204 1.1× 23 0.2× 38 1.2k
Ja‐Hyun Jang South Korea 17 382 1.0× 74 0.2× 300 1.4× 90 0.5× 27 0.2× 121 990
Matthew J. Kan United States 13 312 0.8× 140 0.4× 97 0.4× 103 0.6× 32 0.2× 16 1.1k

Countries citing papers authored by Karin Mayer

Since Specialization
Citations

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

Fields of papers citing papers by Karin Mayer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Mayer

This figure shows the co-authorship network connecting the top 25 collaborators of Karin Mayer. A scholar is included among the top collaborators of Karin Mayer 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 Karin Mayer. Karin Mayer 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.
Mayer, Karin, Saskia Biskup, Angela Abicht, et al.. (2020). Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters. Neuropediatrics. 52(2). 92–97. 8 indexed citations
2.
Hoefele, Julia, et al.. (2016). Rare co-occurrence of osteogenesis imperfecta type I and autosomal dominant polycystic kidney disease. World Journal of Pediatrics. 12(4). 501–503. 2 indexed citations
3.
Arslan‐Kirchner, Mine, Eloisa Arbustini, Cathérine Boileau, et al.. (2015). Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches. European Journal of Human Genetics. 24(1). 146–150. 17 indexed citations
4.
Mayer, Karin, Christa Fonatsch, Katharina Wimmer, Ans MW van den Ouweland, & Anneke Maat‐Kievit. (2013). Clinical utility gene card for: Tuberous sclerosis complex (TSC1, TSC2). European Journal of Human Genetics. 22(2). 293–293. 3 indexed citations
5.
Wendorff, Heiko, Jaroslav Pelisek, Alexander Zimmermann, et al.. (2013). Early venous manifestation of Ehlers–Danlos syndrome Type IV through a novel mutation in COL3A1. Cardiovascular Pathology. 22(6). 488–492. 4 indexed citations
6.
Staehler, Michael, Matthias Sauter, Andreas Helck, et al.. (2012). Nephron-sparing resection of angiomyolipoma after sirolimus pretreatment in patients with tuberous sclerosis. International Urology and Nephrology. 44(6). 1657–1661. 22 indexed citations
7.
Markert, Michael, et al.. (2012). Evaluation of a method to correct the contractility index LVdP/dtmax for changes in heart rate. Journal of Pharmacological and Toxicological Methods. 66(2). 98–105. 17 indexed citations
8.
Mayer, Karin, et al.. (2012). Empfehlung für die Haltung von Schafen und Ziegen der Deutschen Gesellschaft für die Krankheiten der kleinen Wiederkäuer, Fachgruppe der DVG. Tierärztliche Praxis Ausgabe G Großtiere / Nutztiere. 40(5). 314–325. 9 indexed citations
9.
Hoogeveen‐Westerveld, Marianne, Rosemary Ekong, Sue Povey, et al.. (2011). Functional assessment of TSC1 missense variants identified in individuals with tuberous sclerosis complex. Human Mutation. 33(3). 476–479. 34 indexed citations
10.
Wagner, Carola, Christoph Marschall, Karin Mayer, et al.. (2010). Translation of next-generation sequencing (NGS) into molecular diagnostics / Umsetzung von Next Generation Sequencing in der molekularen Diagnostik. LaboratoriumsMedizin. 34(6). 311–318. 2 indexed citations
11.
Mayer, Karin, Ingo Kennerknecht, & Beat Steinmann. (2010). Clinical utility gene card for: Ehlers–Danlos syndrome types I–VII. European Journal of Human Genetics. 18(9). 1071–1071.
12.
Markert, Michael, et al.. (2009). Validation of the normal, freely moving Göttingen minipig for pharmacological safety testing. Journal of Pharmacological and Toxicological Methods. 60(1). 79–87. 28 indexed citations
13.
14.
Wienecke, Ralf, et al.. (2006). Antitumoral Activity of Rapamycin in Renal Angiomyolipoma Associated With Tuberous Sclerosis Complex. American Journal of Kidney Diseases. 48(3). e27–e29. 97 indexed citations
15.
Nellist, Mark, Őzgür Sancak, Miriam Goedbloed, et al.. (2004). Distinct effects of single amino-acid changes to tuberin on the function of the tuberin–hamartin complex. European Journal of Human Genetics. 13(1). 59–68. 65 indexed citations
16.
Harth, W., Karin Mayer, & R Linse. (2004). The borderline syndrome in psychosomatic dermatology Overview and case report. Journal of the European Academy of Dermatology and Venereology. 18(4). 503–507. 18 indexed citations
17.
Rott, Hans‐Dieter, Beate Lemcke, Martin Zenker, et al.. (2002). Cyst‐like cerebral lesions in tuberous sclerosis. American Journal of Medical Genetics. 111(4). 435–439. 20 indexed citations
18.
Mayer, Karin, Wolfgang G. Ballhausen, & Hans‐Dieter Rott. (1999). Mutation screening of the entire coding regions of theTSC1 and theTSC2 gene with the protein truncation test (PTT) identifies frequent splicing defects. Human Mutation. 14(5). 401–411. 32 indexed citations
19.
Mayer, Karin, Thomas Hieronymus, Jan Castrop, Hans Clevers, & Wolfgang G. Ballhausen. (1997). Ectopic activation of lymphoid high mobility group-box transcription factor TCF-1 and overexpression in colorectal cancer cells. International Journal of Cancer. 72(4). 625–630. 30 indexed citations
20.
Mayer, Karin, et al.. (1995). The human high mobility group (HMG)-box transcription factor TCF-1: novel isoforms due to alternative splicing and usage of a new exon IXA. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1263(2). 169–172. 11 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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