Ylva Mende

412 total citations
7 papers, 326 citations indexed

About

Ylva Mende is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Ylva Mende has authored 7 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Ylva Mende's work include RNA modifications and cancer (5 papers), RNA Research and Splicing (3 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Ylva Mende is often cited by papers focused on RNA modifications and cancer (5 papers), RNA Research and Splicing (3 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Ylva Mende collaborates with scholars based in Germany, United States and Slovenia. Ylva Mende's co-authors include Brunhilde Wirth, Markus Rießland, Anja Förster, Eric Hahnen, Lutz Garbes, Ingmar Blümcke, Jan Hauke, André Kleinridders, Thorsten Buch and Christoph Köhler and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Ylva Mende

7 papers receiving 322 citations

Peers

Ylva Mende
L. Skordis United Kingdom
Leonidas Panousopoulos United Kingdom
Ying Hsiu Liu United States
Chao-Jen Wong United States
L. Skordis United Kingdom
Ylva Mende
Citations per year, relative to Ylva Mende Ylva Mende (= 1×) peers L. Skordis

Countries citing papers authored by Ylva Mende

Since Specialization
Citations

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

Fields of papers citing papers by Ylva Mende

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ylva Mende

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

All Works

7 of 7 papers shown
1.
Mende, Ylva, et al.. (2016). Manipulating the Prion Protein Gene Sequence and Expression Levels with CRISPR/Cas9. PLoS ONE. 11(4). e0154604–e0154604. 18 indexed citations
2.
Fu, Kang, Ylva Mende, Bhupal P. Bhetwal, et al.. (2012). Tra2β Protein Is Required for Tissue-specific Splicing of a Smooth Muscle Myosin Phosphatase Targeting Subunit Alternative Exon. Journal of Biological Chemistry. 287(20). 16575–16585. 16 indexed citations
3.
Grellscheid, Sushma Nagaraja, Caroline Dalgliesh, Markus Storbeck, et al.. (2011). Identification of Evolutionarily Conserved Exons as Regulated Targets for the Splicing Activator Tra2β in Development. PLoS Genetics. 7(12). e1002390–e1002390. 61 indexed citations
4.
Fisher, Steven A., Ylva Mende, Brunhilde Wirth, & Kang Fu. (2011). Transformer (Tra2β): master regulator of myosin phosphatase alternative splicing and smooth muscle responses to NO/cGMP signaling. BMC Pharmacology. 11(S1). 1 indexed citations
5.
Rießland, Markus, Anja Förster, Jan Hauke, et al.. (2010). SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy. Human Molecular Genetics. 19(8). 1492–1506. 177 indexed citations
6.
Mende, Ylva, Markus Rießland, Frank J. Schoenen, et al.. (2010). Deficiency of the splicing factor Sfrs10 results in early embryonic lethality in mice and has no impact on full-length SMN/Smn splicing. Human Molecular Genetics. 19(11). 2154–2167. 47 indexed citations
7.
Mende, Ylva, Paul M. Schneider, Stephan Baldus, & Walter Doerfler. (2004). PCR-screening of human esophageal and bronchial cancers reveals absence of adenoviral DNA sequences. Virus Research. 104(1). 81–85. 6 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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