Matthias Klaften

682 total citations
22 papers, 460 citations indexed

About

Matthias Klaften is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Matthias Klaften has authored 22 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Matthias Klaften's work include Ion Transport and Channel Regulation (3 papers), Metabolism and Genetic Disorders (2 papers) and Renal and related cancers (2 papers). Matthias Klaften is often cited by papers focused on Ion Transport and Channel Regulation (3 papers), Metabolism and Genetic Disorders (2 papers) and Renal and related cancers (2 papers). Matthias Klaften collaborates with scholars based in Germany, France and United States. Matthias Klaften's co-authors include Martin Hrabě de Angelis, Birgit Rathkolb, Eckhard Wolf, Bernhard Aigner, Elisabeth Kemter, Rüdiger Wanke, Helmut Fuchs, Nadja Herbach, Philippe A. Halban and Sibylle Wagner and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Diabetes.

In The Last Decade

Matthias Klaften

22 papers receiving 453 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthias Klaften Germany 13 255 136 115 93 57 22 460
Christopher Cahill United States 8 194 0.8× 135 1.0× 53 0.5× 34 0.4× 193 3.4× 8 484
Tianming Liu China 4 166 0.7× 66 0.5× 76 0.7× 30 0.3× 15 0.3× 11 363
Shalabh Srivastava United Kingdom 15 405 1.6× 50 0.4× 384 3.3× 49 0.5× 25 0.4× 25 632
Gang Cheng China 11 240 0.9× 43 0.3× 47 0.4× 57 0.6× 16 0.3× 19 374
Keisuke Ina Japan 10 88 0.3× 96 0.7× 53 0.5× 25 0.3× 36 0.6× 30 325
Jianglei Chen United States 10 157 0.6× 25 0.2× 48 0.4× 28 0.3× 13 0.2× 15 359
Velibor Tasic Germany 10 383 1.5× 74 0.5× 114 1.0× 225 2.4× 12 0.2× 14 620
Stephen W. Anderson United States 10 96 0.4× 117 0.9× 179 1.6× 14 0.2× 127 2.2× 12 405
Tashjian Ah United States 10 127 0.5× 62 0.5× 72 0.6× 15 0.2× 152 2.7× 14 495
Wai Yan Sun Australia 11 219 0.9× 59 0.4× 20 0.2× 63 0.7× 19 0.3× 16 376

Countries citing papers authored by Matthias Klaften

Since Specialization
Citations

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

Fields of papers citing papers by Matthias Klaften

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthias Klaften

This figure shows the co-authorship network connecting the top 25 collaborators of Matthias Klaften. A scholar is included among the top collaborators of Matthias Klaften 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 Matthias Klaften. Matthias Klaften 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.
Klaften, Matthias, et al.. (2024). P20 Clinical metagenomics from cell-free DNA: overview and lessons learned from 4 years as a clinical metagenomics provider. JAC-Antimicrobial Resistance. 6(Supplement_1). 1 indexed citations
2.
Yan, Xiaohe, Jenny Atorf, David Ramos‐Barbón, et al.. (2020). Mutation inBmpr1bLeads to Optic Disc Coloboma and Ventral Retinal Gliosis in Mice. Investigative Ophthalmology & Visual Science. 61(2). 44–44. 10 indexed citations
3.
Dalke, Claudia, Helmut Fuchs, Matthias Klaften, et al.. (2015). New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts. PLoS ONE. 10(5). e0125304–e0125304. 19 indexed citations
4.
Rathkolb, Birgit, Martina Klempt, Sibylle Sabrautzki, et al.. (2015). Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels. BioMetals. 28(2). 293–306. 3 indexed citations
5.
Sabrautzki, Sibylle, Isabel Rubio‐Aliaga, Wolfgang Hans, et al.. (2012). New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis. Mammalian Genome. 23(7-8). 416–430. 26 indexed citations
6.
Fuchs, Helmut, Sibylle Sabrautzki, H. Seedorf, et al.. (2012). Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin‐mutant mouse lines. European Journal Of Oral Sciences. 120(4). 269–277. 6 indexed citations
7.
Aigner, Bernhard, Birgit Rathkolb, Martina Klempt, et al.. (2011). Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters. Mammalian Genome. 22(9-10). 495–505. 17 indexed citations
8.
Kemter, Elisabeth, Birgit Rathkolb, Lise Bankir, et al.. (2010). Mutation of the Na+-K+-2Cl−cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia. American Journal of Physiology-Renal Physiology. 298(6). F1405–F1415. 30 indexed citations
9.
Soewarto, Dian, Matthias Klaften, & Isabel Rubio‐Aliaga. (2009). Features and Strategies of ENU Mouse Mutagenesis. Current Pharmaceutical Biotechnology. 10(2). 198–213. 9 indexed citations
10.
Aigner, Bernhard, Birgit Rathkolb, Matthias Klaften, et al.. (2009). Generation of N‐ethyl‐N‐nitrosourea‐induced mouse mutants with deviations in plasma enzyme activities as novel organ‐specific disease models. Experimental Physiology. 94(4). 412–421. 16 indexed citations
11.
Abe, Koichiro, Matthias Klaften, Akira Narita, et al.. (2009). Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice. Mammalian Genome. 20(3). 152–161. 4 indexed citations
12.
Blutke, Andreas, Birgit Rathkolb, Matthias Klaften, et al.. (2009). Phenotypic and pathomorphological characteristics of a novel mutant mouse model for maturity-onset diabetes of the young type 2 (MODY 2). American Journal of Physiology-Endocrinology and Metabolism. 298(3). E512–E523. 8 indexed citations
13.
Klaften, Matthias, et al.. (2009). A new design for a micro-CT scanner. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 7258. 72585D–72585D. 2 indexed citations
14.
Puk, Oliver, Claudia Dalke, Julia Calzada‐Wack, et al.. (2009). Reduced Corneal Thickness and Enlarged Anterior Chamber in a Novel ColVIIIa2G257DMutant Mouse. Investigative Ophthalmology & Visual Science. 50(12). 5653–5653. 30 indexed citations
15.
Michel, Geert, et al.. (2007). Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies. Biochemical and Biophysical Research Communications. 359(4). 947–951. 31 indexed citations
16.
Aigner, Bernhard, Birgit Rathkolb, Nadja Herbach, et al.. (2007). Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models. American Journal of Physiology-Renal Physiology. 292(5). F1560–F1567. 12 indexed citations
17.
Seedorf, H., Matthias Klaften, Felicia U. Eke, et al.. (2007). A Mutation in the Enamelin Gene in a Mouse Model. Journal of Dental Research. 86(8). 764–768. 20 indexed citations
18.
Runkel, Fabian, Matthias Klaften, Volker Böhnert, et al.. (2006). Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13. Mammalian Genome. 17(12). 1172–1182. 31 indexed citations
19.
Rubio‐Aliaga, Isabel, Dian Soewarto, Sibylle Wagner, et al.. (2006). A Genetic Screen for Modifiers of the Delta1-Dependent Notch Signaling Function in the Mouse. Genetics. 175(3). 1451–1463. 20 indexed citations
20.
Klaften, Matthias & Martin Hrabě de Angelis. (2005). ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants. Nucleic Acids Research. 33(Web Server). W496–W500. 15 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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