Evolutionary Patterns of Non-Coding RNA in Cardiovascular Biology von Gandhi, Shrey, Ruehle, Frank, Stoll, Monika

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Advances in predicting venous thromboembolism risk in children von Rühle, Frank, Stoll, Monika

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Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons von Kong, Ka-Yiu Edwin, Shankar, Susmitha, Rühle, Frank, Khmelinskii, Anton

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Timer-based proteomic profiling of the ubiquitin-proteasome system reveals a substrate receptor of the GID ubiquitin ligase von Kong, Ka-Yiu Edwin, Fischer, Bernd, Meurer, Matthias, Kats, Ilia, Li, Zhaoyan, Rühle, Frank, Barry, Joseph D., Kirrmaier, Daniel, Chevyreva, Veronika, San Luis, Bryan-Joseph, Costanzo, Michael, Huber, Wolfgang, Andrews, Brenda J., Boone, Charles, Knop, Michael, Khmelinskii, Anton

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The sex-specific factor SOA controls dosage compensation in Anopheles mosquitoes von Kalita, Agata Izabela, Marois, Eric, Kozielska, Magdalena, Weissing, Franz J., Jaouen, Etienne, Möckel, Martin M., Rühle, Frank, Butter, Falk, Basilicata, M. Felicia, Keller Valsecchi, Claudia Isabelle

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ID2 controls differentiation of enteroendocrine cells in mouse small intestine von Zinina, Valeriya V., Ruehle, Frank, Winkler, Patricia, Rebmann, Lisa, Lukas, Hanna, Möckel, Stefanie, Diefenbach, Andreas, Mendez‐Lago, Maria, Soshnikova, Natalia

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Long non-coding RNA Databases in Cardiovascular Research von Frank Ruhle Monika Stoll

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Genetic factors in pediatric venous thromboembolism von Rühle, Frank, Stoll, Monika, PhD

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Genomic instability in the naturally and prematurely aged myocardium von De Majo, Federica, Martens, Leonie, Hegenbarth, Jana-Charlotte, Rühle, Frank, Hamczyk, Magda R., Nevado, Rosa M., Andrés, Vicente, Hilbold, Erika, Bär, Christian, Thum, Thomas, de Boer, Martine, Duncker, Dirk J., Schroen, Blanche, Armand, Anne-Sophie, Stoll, Monika, De Windt, Leon J.

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Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study von Witten, Anika, Bolbrinker, Juliane, Barysenka, Andrei, Huber, Matthias, Rühle, Frank, Nowak-Göttl, Ulrike, Garbe, Edeltraut, Kreutz, Reinhold, Stoll, Monika

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Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy von Heinig, Matthias, Adriaens, Michiel E, Schafer, Sebastian, van Deutekom, Hanneke W M, Lodder, Elisabeth M, Ware, James S, Schneider, Valentin, Felkin, Leanne E, Creemers, Esther E, Meder, Benjamin, Katus, Hugo A, Rühle, Frank, Stoll, Monika, Cambien, François, Villard, Eric, Charron, Philippe, Varro, Andras, Bishopric, Nanette H, George, Jr, Alfred L, Dos Remedios, Cristobal, Moreno-Moral, Aida, Pesce, Francesco, Bauerfeind, Anja, Rüschendorf, Franz, Rintisch, Carola, Petretto, Enrico, Barton, Paul J, Cook, Stuart A, Pinto, Yigal M, Bezzina, Connie R, Hubner, Norbert

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A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy von Martens, Leonie, Rühle, Frank, Witten, Anika, Meder, Benjamin, Katus, Hugo A., Arbustini, Eloisa, Hasenfuß, Gerd, Sinner, Moritz F., Kääb, Stefan, Pankuweit, Sabine, Angermann, Christiane, Bornberg-Bauer, Erich, Stoll, Monika

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Postgwas: advanced GWAS interpretation in R von Hiersche, Milan, Rühle, Frank, Stoll, Monika

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ADAMTS12, a new candidate gene for pediatric stroke von Witten, Anika, Ruehle, Frank, de Witt, Marlous, Barysenka, Andrei, Stach, Michael, Junker, Ralf, Nowak-Goettl, Ulrike, Stoll, Monika

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Adrenergic Repression of the Epigenetic Reader MeCP2 Facilitates Cardiac Adaptation in Chronic Heart Failure von Mayer, Sandra C, Gilsbach, Ralf, Preissl, Sebastian, Monroy Ordonez, Elsa Beatriz, Schnick, Tilman, Beetz, Nadine, Lother, Achim, Rommel, Carolin, Ihle, Hannah, Bugger, Heiko, Rühle, Frank, Schrepper, Andrea, Schwarzer, Michael, Heilmann, Claudia, Bönisch, Ulrike, Gupta, Shashi Kumar, Wilpert, Jochen, Kretz, Oliver, von Elverfeldt, Dominik, Orth, Joachim, Aktories, Klaus, Beyersdorf, Friedhelm, Bode, Christoph, Stiller, Brigitte, Krüger, Markus, Thum, Thomas, Doenst, Torsten, Stoll, Monika, Hein, Lutz

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Human atherosclerotic plaque transcriptomics reveals endothelial beta-2 spectrin as a potential regulator a leaky plaque microvasculature phenotype von Rademakers, Timo, Manca, Marco, Jin, Han, Orban, Tanguy, Perisic, Ljubica Matic, Frissen, Hubertus J. M., Rühle, Frank, Hautvast, Petra, van Rijssel, Jos, van Kuijk, Kim, Mees, Barend M. E., Peutz-Kootstra, Carine J., Heeneman, Sylvia, Daemen, Mat J. A. P., Pasterkamp, Gerard, Stoll, Monika, van Zandvoort, Marc A. M. J., Hedin, Ulf, Dequiedt, Franck, van Buul, Jaap D., Sluimer, Judith C., Biessen, Erik A. L.

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Revised roles of ISL1 in a hES cell-based model of human heart chamber specification von Quaranta, Roberto, Fell, Jakob, Rühle, Frank, Rao, Jyoti, Piccini, Ilaria, Araúzo-Bravo, Marcos J, Verkerk, Arie O, Stoll, Monika, Greber, Boris

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Pathway-based variant enrichment analysis on the example of dilated cardiomyopathy von Backes, Christina, Meder, Benjamin, Lai, Alan, Stoll, Monika, Rühle, Frank, Katus, Hugo A., Keller, Andreas

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Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study von Limperger, Verena, Kenet, Gili, Kiesau, Bettina, Köther, Max, Schmeiser, Malin, Langer, Florian, Juhl, David, Shneyder, Maria, Franke, Andre, Klostermeier, Ulrich K., Mesters, Rolf, Rühle, Frank, Stoll, Monika, Steppat, Dagmar, Kowalski, Dorothee, Rocke, Angela, Kuta, Piotr, Bajorat, Tido, Torge, Antje, Neuner, Bruno, Junker, Ralf, Nowak-Göttl, Ulrike

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Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism von Rühle, Frank, Witten, Anika, Barysenka, Andrei, Huge, Andreas, Arning, Astrid, Heller, Christine, Krümpel, Anne, Mesters, Rolf, Franke, Andre, Lieb, Wolfgang, Riemenschneider, Mona, Hiersche, Milan, Limperger, Verena, Nowak-Göttl, Ulrike, Stoll, Monika

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