Frank Rühle

1.0k total citations
28 papers, 366 citations indexed

About

Frank Rühle is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Frank Rühle has authored 28 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 8 papers in Hematology and 6 papers in Genetics. Recurrent topics in Frank Rühle's work include Blood Coagulation and Thrombosis Mechanisms (6 papers), Cancer-related molecular mechanisms research (4 papers) and Genetic Associations and Epidemiology (4 papers). Frank Rühle is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (6 papers), Cancer-related molecular mechanisms research (4 papers) and Genetic Associations and Epidemiology (4 papers). Frank Rühle collaborates with scholars based in Germany, Netherlands and United States. Frank Rühle's co-authors include Monika Stoll, Milan Hiersche, Anika Witten, Ulrike Nowak‐Göttl, Andrei Barysenka, Roberto Quaranta, Arie O. Verkerk, Jyoti Rao, Marcos J. Araúzo‐Bravo and Ilaria Piccini and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Frank Rühle

26 papers receiving 364 citations

Peers

Frank Rühle

GENET

HEMAT

CCM

Shu Song China

Bianca Rocca Italy

Weifang Yu China

Zehra Pamuklar United States

Mariia Kumskova United States

Sean McGee United States

Kevin W. McCool United States

Sweena M. Chaudhari Germany

Ali R. Keramati United States

Shu Song China

Frank Rühle

122 ×0.6

63 ×0.9

32 ×0.5

GENET

11 ×0.2

HEMAT

11 ×0.3

CCM

Citations per year, relative to Frank Rühle Frank Rühle (= 1×) peers Shu Song

Countries citing papers authored by Frank Rühle

Since Specialization

Citations

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

Fields of papers citing papers by Frank Rühle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frank Rühle

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

All Works

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20 of 20 papers shown

Pan, Qiaowei, Frank Rühle, Peter Refsing Andersen, et al.. (2025). Convergent evolution of H4K16ac-mediated dosage compensation in the ZW species Artemia franciscana. PLoS Genetics. 21(10). e1011895–e1011895.

Marois, Éric, Magdalena Kozielska, Franz J. Weissing, et al.. (2023). The sex-specific factor SOA controls dosage compensation in Anopheles mosquitoes. Nature. 623(7985). 175–182. 15 indexed citations

Rühle, Frank, et al.. (2023). Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons. Nature Communications. 14(1). 8363–8363. 7 indexed citations

Fischer, Bernd, Matthias Meurer, Ilia Kats, et al.. (2021). Timer-based proteomic profiling of the ubiquitin-proteasome system reveals a substrate receptor of the GID ubiquitin ligase. Molecular Cell. 81(11). 2460–2476.e11. 37 indexed citations

Rühle, Frank, Lennart Martens, Virginie Kinet, et al.. (2021). LncRNA Bigheart stimulates Regulator of calcineurin 1 (Rcan1) expression in an auto-amplification loop that stimulates calcineurin-NFAT signalling in heart failure. European Heart Journal. 42(Supplement_1). 1 indexed citations

Witten, Anika, Frank Rühle, Andrei Barysenka, et al.. (2020). ADAMTS12, a new candidate gene for pediatric stroke. PLoS ONE. 15(8). e0237928–e0237928. 6 indexed citations

Majo, Federica De, Frank Rühle, Christian Bär, et al.. (2020). Dichotomy between the transcriptomic landscape of naturally versus accelerated aged murine hearts. Scientific Reports. 10(1). 8136–8136. 1 indexed citations

Schulz, Angela, Andreas Eisenreich, Andrei Barysenka, et al.. (2019). Analysis of the genomic architecture of a complex trait locus in hypertensive rat models links Tmem63c to kidney damage. eLife. 8. 23 indexed citations

Quaranta, Roberto, Frank Rühle, Jyoti Rao, et al.. (2018). Revised roles of ISL1 in a hES cell-based model of human heart chamber specification. eLife. 7. 36 indexed citations

10.

Witten, Anika, Juliane Bolbrinker, Andrei Barysenka, et al.. (2018). Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study. Journal of Molecular Medicine. 96(8). 765–775. 12 indexed citations

11.

Rühle, Frank, et al.. (2017). LncRNA secondary structure in the cardiovascular system. Non-coding RNA Research. 2(3-4). 137–142. 16 indexed citations

12.

Rühle, Frank & Monika Stoll. (2017). Genetic factors in pediatric venous thromboembolism. Thrombosis Research. 151. S97–S99. 1 indexed citations

13.

Rühle, Frank & Monika Stoll. (2017). Advances in predicting venous thromboembolism risk in children. British Journal of Haematology. 180(5). 654–665. 15 indexed citations

14.

Rühle, Frank, Anika Witten, Andrei Barysenka, et al.. (2016). Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. Blood. 129(6). 783–790. 17 indexed citations

15.

Rühle, Frank & Monika Stoll. (2016). Long Non-Coding RNA Databases in Cardiovascular Research. Genomics Proteomics & Bioinformatics. 14(4). 191–199. 34 indexed citations

16.

Backes, Christina, Benjamin Meder, Alan Lai, et al.. (2015). Pathway-based variant enrichment analysis on the example of dilated cardiomyopathy. Human Genetics. 135(1). 31–40. 8 indexed citations

17.

Neuber, Christiane, Oliver J. Müller, Alexandra Eder, et al.. (2014). Paradoxical Effects on Force Generation after Efficient β1-Adrenoceptor Knockdown in Reconstituted Heart Tissue. Journal of Pharmacology and Experimental Therapeutics. 349(1). 39–46. 4 indexed citations

18.

Backes, Christina, Frank Rühle, Monika Stoll, et al.. (2014). Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis. BMC Genomics. 15(1). 622–622. 18 indexed citations

19.

Hiersche, Milan, Frank Rühle, & Monika Stoll. (2013). Postgwas: Advanced GWAS Interpretation in R. PLoS ONE. 8(8). e71775–e71775. 21 indexed citations

20.

Luchtefeld, Maren, Christoph Preuß, Frank Rühle, et al.. (2011). Gp130-Dependent Release of Acute Phase Proteins Is Linked to the Activation of Innate Immune Signaling Pathways. PLoS ONE. 6(5). e19427–e19427. 18 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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