Bärbel Klauke

560 total citations
9 papers, 267 citations indexed

About

Bärbel Klauke is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cell Biology. According to data from OpenAlex, Bärbel Klauke has authored 9 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cardiology and Cardiovascular Medicine, 4 papers in Molecular Biology and 4 papers in Cell Biology. Recurrent topics in Bärbel Klauke's work include Skin and Cellular Biology Research (4 papers), Cardiomyopathy and Myosin Studies (4 papers) and Nuclear Structure and Function (2 papers). Bärbel Klauke is often cited by papers focused on Skin and Cellular Biology Research (4 papers), Cardiomyopathy and Myosin Studies (4 papers) and Nuclear Structure and Function (2 papers). Bärbel Klauke collaborates with scholars based in Germany, Canada and Sri Lanka. Bärbel Klauke's co-authors include Hendrik Milting, Jan Gummert, Andreas Brodehl, Lech Paluszkiewicz, Dario Anselmetti, Anna Gaertner, Uwe Schulz, Volker Walhorn, Mareike Dieding and Reiner Körfer and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Molecular and Cellular Cardiology and Human Mutation.

In The Last Decade

Bärbel Klauke

9 papers receiving 266 citations

Peers

Bärbel Klauke

CCM

SURGE

TRANS

Viswajit Kandula United States

Agata Barchitta Italy

Maria Franaszczyk Poland

Sven Dittmann Germany

Bradley Nelson United States

Alexander Dutsch Germany

Julie Berthy United States

Alexander F.A. Androulakis Netherlands

Shinichiro Okata Japan

Cornelia Köhler Germany

Viswajit Kandula United States

Bärbel Klauke

22 ×0.1

CCM

104 ×1.0

44 ×0.6

62 ×2.0

SURGE

16 ×0.6

TRANS

Citations per year, relative to Bärbel Klauke Bärbel Klauke (= 1×) peers Viswajit Kandula

Countries citing papers authored by Bärbel Klauke

Since Specialization

Citations

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

Fields of papers citing papers by Bärbel Klauke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bärbel Klauke

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

All Works

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9 of 9 papers shown

Brodehl, Andreas, Anna Gaertner, Bärbel Klauke, et al.. (2021). The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3. Biomedicines. 9(10). 1400–1400. 22 indexed citations

Brodehl, Andreas, Jürgen Weiß, Caroline Stanasiuk, et al.. (2020). A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. Journal of Molecular and Cellular Cardiology. 141. 17–29. 26 indexed citations

Brodehl, Andreas, Anna Gaertner, Bärbel Klauke, et al.. (2017). The novel αB‐crystallin ( CRYAB ) mutation p.D109G causes restrictive cardiomyopathy. Human Mutation. 38(8). 947–952. 53 indexed citations

Dieding, Mareike, Bärbel Klauke, Andreas Brodehl, et al.. (2017). A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy. Molecular Genetics & Genomic Medicine. 6(2). 288–293. 20 indexed citations

Gaertner, Anna, Bärbel Klauke, Lech Paluszkiewicz, et al.. (2016). Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases. EP Europace. 19(11). euw247–euw247. 24 indexed citations

Brodehl, Andreas, Mareike Dieding, Niklas Biere, et al.. (2015). Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect. Journal of Molecular and Cellular Cardiology. 91. 207–214. 34 indexed citations

Brodehl, Andreas, Per Niklas Hedde, Mareike Dieding, et al.. (2012). Dual Color Photoactivation Localization Microscopy of Cardiomyopathy-associated Desmin Mutants. Journal of Biological Chemistry. 287(19). 16047–16057. 47 indexed citations

Klauke, Bärbel, Armin Zittermann, Birte Bohms, et al.. (2008). No Association Between Single Nucleotide Polymorphisms and the Development of Nephrotoxicity After Orthotopic Heart Transplantation. The Journal of Heart and Lung Transplantation. 27(7). 741–745. 28 indexed citations

Milting, Hendrik, Astrid Kassner, Latif Arusoglu, et al.. (2005). Influence of ACE-Inhibition and Mechanical Unloading on the Regulation of Extracellular Matrix Proteins in the Myocardium of Heart Transplantation Candidates Bridged by Ventricular Assist Devices. European Journal of Heart Failure. 8(3). 278–283. 13 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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