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Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy.
Lennermann DC, Pepin ME, Grosch M, Konrad L, Kemmling E, Hartmann J, Nolte JL, Clauder-Münster S, Kayvanpour E, Sedaghat-Hamedani F, Haas J, Meder B, van den Boogaard M, Amin AS, Dewenter M, Krüger M, Steinmetz LM, Backs J, van den Hoogenhof MMG. Lennermann DC, et al. Among authors: haas j. Am J Physiol Heart Circ Physiol. 2022 Dec 1;323(6):H1296-H1310. doi: 10.1152/ajpheart.00328.2022. Epub 2022 Nov 11. Am J Physiol Heart Circ Physiol. 2022. PMID: 36367695 Free article.
Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies.
Meder B, Haas J, Keller A, Heid C, Just S, Borries A, Boisguerin V, Scharfenberger-Schmeer M, Stähler P, Beier M, Weichenhan D, Strom TM, Pfeufer A, Korn B, Katus HA, Rottbauer W. Meder B, et al. Among authors: haas j. Circ Cardiovasc Genet. 2011 Apr;4(2):110-22. doi: 10.1161/CIRCGENETICS.110.958322. Epub 2011 Jan 20. Circ Cardiovasc Genet. 2011. PMID: 21252143
Alterations in cardiac DNA methylation in human dilated cardiomyopathy.
Haas J, Frese KS, Park YJ, Keller A, Vogel B, Lindroth AM, Weichenhan D, Franke J, Fischer S, Bauer A, Marquart S, Sedaghat-Hamedani F, Kayvanpour E, Köhler D, Wolf NM, Hassel S, Nietsch R, Wieland T, Ehlermann P, Schultz JH, Dösch A, Mereles D, Hardt S, Backs J, Hoheisel JD, Plass C, Katus HA, Meder B. Haas J, et al. EMBO Mol Med. 2013 Mar;5(3):413-29. doi: 10.1002/emmm.201201553. Epub 2013 Jan 22. EMBO Mol Med. 2013. PMID: 23341106 Free PMC article.
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.
Meder B, Rühle F, Weis T, Homuth G, Keller A, Franke J, Peil B, Lorenzo Bermejo J, Frese K, Huge A, Witten A, Vogel B, Haas J, Völker U, Ernst F, Teumer A, Ehlermann P, Zugck C, Friedrichs F, Kroemer H, Dörr M, Hoffmann W, Maisch B, Pankuweit S, Ruppert V, Scheffold T, Kühl U, Schultheiss HP, Kreutz R, Ertl G, Angermann C, Charron P, Villard E, Gary F, Isnard R, Komajda M, Lutz M, Meitinger T, Sinner MF, Wichmann HE, Krawczak M, Ivandic B, Weichenhan D, Gelbrich G, El-Mokhtari NE, Schreiber S, Felix SB, Hasenfuß G, Pfeufer A, Hübner N, Kääb S, Arbustini E, Rottbauer W, Frey N, Stoll M, Katus HA. Meder B, et al. Among authors: haas j. Eur Heart J. 2014 Apr;35(16):1069-77. doi: 10.1093/eurheartj/eht251. Epub 2013 Jul 12. Eur Heart J. 2014. PMID: 23853074
Fast data-driven calibration of a cardiac electrophysiology model from images and ECG.
Zettinig O, Mansi T, Georgescu B, Kayvanpour E, Sedaghat-Hamedani F, Amr A, Haas J, Steen H, Meder B, Katus H, Navab N, Kamen A, Comaniciul D. Zettinig O, et al. Among authors: haas j. Med Image Comput Comput Assist Interv. 2013;16(Pt 1):1-8. doi: 10.1007/978-3-642-40811-3_1. Med Image Comput Comput Assist Interv. 2013. PMID: 24505642
Data-driven estimation of cardiac electrical diffusivity from 12-lead ECG signals.
Zettinig O, Mansi T, Neumann D, Georgescu B, Rapaka S, Seegerer P, Kayvanpour E, Sedaghat-Hamedani F, Amr A, Haas J, Steen H, Katus H, Meder B, Navab N, Kamen A, Comaniciu D. Zettinig O, et al. Among authors: haas j. Med Image Anal. 2014 Dec;18(8):1361-76. doi: 10.1016/j.media.2014.04.011. Epub 2014 Apr 26. Med Image Anal. 2014. PMID: 24857832
The symptom complex of familial sinus node dysfunction and myocardial noncompaction is associated with mutations in the HCN4 channel.
Schweizer PA, Schröter J, Greiner S, Haas J, Yampolsky P, Mereles D, Buss SJ, Seyler C, Bruehl C, Draguhn A, Koenen M, Meder B, Katus HA, Thomas D. Schweizer PA, et al. Among authors: haas j. J Am Coll Cardiol. 2014 Aug 26;64(8):757-67. doi: 10.1016/j.jacc.2014.06.1155. J Am Coll Cardiol. 2014. PMID: 25145518 Free article.
2,326 results