Stoll M - Search Results

1

Long non-coding RNA Databases in Cardiovascular Research.

Rühle F, Stoll M. Rühle F, et al. Among authors: stoll m. Genomics Proteomics Bioinformatics. 2016 Aug;14(4):191-9. doi: 10.1016/j.gpb.2016.03.001. Epub 2016 Apr 2. Genomics Proteomics Bioinformatics. 2016. PMID: 27049585 Free PMC article. Review.

2

Gp130-dependent release of acute phase proteins is linked to the activation of innate immune signaling pathways.

Luchtefeld M, Preuss C, Rühle F, Bogalle EP, Sietmann A, Figura S, Müller W, Grote K, Schieffer B, Stoll M. Luchtefeld M, et al. Among authors: stoll m. PLoS One. 2011 May 4;6(5):e19427. doi: 10.1371/journal.pone.0019427. PLoS One. 2011. PMID: 21573245 Free PMC article.

3

Postgwas: advanced GWAS interpretation in R.

Hiersche M, Rühle F, Stoll M. Hiersche M, et al. Among authors: stoll m. PLoS One. 2013 Aug 19;8(8):e71775. doi: 10.1371/journal.pone.0071775. eCollection 2013. PLoS One. 2013. PMID: 23977141 Free PMC article.

4

Advances in understanding stroke risk in children--a geneticist's view.

Stoll M, Rühle F, Nowak-Göttl U. Stoll M, et al. Br J Haematol. 2014 Mar;164(5):636-45. doi: 10.1111/bjh.12706. Epub 2013 Dec 19. Br J Haematol. 2014. PMID: 24354735 Free article. Review.

5

Paradoxical effects on force generation after efficient β1-adrenoceptor knockdown in reconstituted heart tissue.

Neuber C, Müller OJ, Hansen FC, Eder A, Witten A, Rühle F, Stoll M, Katus HA, Eschenhagen T, El-Armouche A. Neuber C, et al. Among authors: stoll m. J Pharmacol Exp Ther. 2014 Apr;349(1):39-46. doi: 10.1124/jpet.113.210898. Epub 2014 Jan 15. J Pharmacol Exp Ther. 2014. PMID: 24431469

6

Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis.

Backes C, Rühle F, Stoll M, Haas J, Frese K, Franke A, Lieb W, Wichmann HE, Weis T, Kloos W, Lenhof HP, Meese E, Katus H, Meder B, Keller A. Backes C, et al. Among authors: stoll m. BMC Genomics. 2014 Jul 22;15:622. doi: 10.1186/1471-2164-15-622. BMC Genomics. 2014. PMID: 25052024 Free PMC article.

7

Adrenergic Repression of the Epigenetic Reader MeCP2 Facilitates Cardiac Adaptation in Chronic Heart Failure.

Mayer SC, Gilsbach R, Preissl S, Monroy Ordonez EB, Schnick T, Beetz N, Lother A, Rommel C, Ihle H, Bugger H, Rühle F, Schrepper A, Schwarzer M, Heilmann C, Bönisch U, Gupta SK, Wilpert J, Kretz O, von Elverfeldt D, Orth J, Aktories K, Beyersdorf F, Bode C, Stiller B, Krüger M, Thum T, Doenst T, Stoll M, Hein L. Mayer SC, et al. Among authors: stoll m. Circ Res. 2015 Sep 11;117(7):622-33. doi: 10.1161/CIRCRESAHA.115.306721. Epub 2015 Jul 20. Circ Res. 2015. PMID: 26195221 Free PMC article.

8

Pathway-based variant enrichment analysis on the example of dilated cardiomyopathy.

Backes C, Meder B, Lai A, Stoll M, Rühle F, Katus HA, Keller A. Backes C, et al. Among authors: stoll m. Hum Genet. 2016 Jan;135(1):31-40. doi: 10.1007/s00439-015-1609-7. Epub 2015 Nov 7. Hum Genet. 2016. PMID: 26547721

9

Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric Stroke.

Stoll M, Rühle F, Witten A, Barysenka A, Arning A, Strauss C, Nowak-Göttl U. Stoll M, et al. Circ Cardiovasc Genet. 2016 Aug;9(4):357-67. doi: 10.1161/CIRCGENETICS.115.001184. Epub 2016 Jul 13. Circ Cardiovasc Genet. 2016. PMID: 27412500

10

Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.

Rühle F, Witten A, Barysenka A, Huge A, Arning A, Heller C, Krümpel A, Mesters R, Franke A, Lieb W, Riemenschneider M, Hiersche M, Limperger V, Nowak-Göttl U, Stoll M. Rühle F, et al. Among authors: stoll m. Blood. 2017 Feb 9;129(6):783-790. doi: 10.1182/blood-2016-07-728840. Epub 2016 Dec 23. Blood. 2017. PMID: 28011674 Free article.

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