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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: amin as. 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.
RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling.
van den Hoogenhof MMG, Beqqali A, Amin AS, van der Made I, Aufiero S, Khan MAF, Schumacher CA, Jansweijer JA, van Spaendonck-Zwarts KY, Remme CA, Backs J, Verkerk AO, Baartscheer A, Pinto YM, Creemers EE. van den Hoogenhof MMG, et al. Among authors: amin as. Circulation. 2018 Sep 25;138(13):1330-1342. doi: 10.1161/CIRCULATIONAHA.117.031947. Circulation. 2018. PMID: 29650543
Tropomyosin-troponin complex in inherited cardiomyopathies.
Juárez CK, Sequeira V, van den Boogaard M, Veerman CC, Hoetjes NJ, Poel E, Tanck MWT, Lekanne Deprez RH, Vermeer AMC, van der Velden J, Amin AS. Juárez CK, et al. Among authors: amin as. Heart Rhythm. 2024 Jul;21(7):1173-1175. doi: 10.1016/j.hrthm.2024.02.034. Epub 2024 Feb 19. Heart Rhythm. 2024. PMID: 38382684 Free article. Review. No abstract available.
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience.
Jurgens SJ, Rämö JT, Kramarenko DR, Wijdeveld LFJM, Haas J, Chaffin MD, Garnier S, Gaziano L, Weng LC, Lipov A, Zheng SL, Henry A, Huffman JE, Challa S, Rühle F, Verdugo CD, Krijger Juárez C, Kany S, van Orsouw CA, Biddinger K, Poel E, Elliott AL, Wang X, Francis C, Ruan R, Koyama S, Beekman L, Zimmerman DS, Deleuze JF, Villard E, Trégouët DA, Isnard R; FinnGen; VA Million Veteran Program; HERMES Consortium; Boomsma DI, de Geus EJC, Tadros R, Pinto YM, Wilde AAM, Hottenga JJ, Sinisalo J, Niiranen T, Walsh R, Schmidt AF, Choi SH, Chang KM, Tsao PS, Matthews PM, Ware JS, Lumbers RT, van der Crabben S, Laukkanen J, Palotie A, Amin AS, Charron P, Meder B, Ellinor PT, Daly M, Aragam KG, Bezzina CR. Jurgens SJ, et al. Among authors: amin as. Nat Genet. 2024 Dec;56(12):2636-2645. doi: 10.1038/s41588-024-01975-5. Epub 2024 Nov 21. Nat Genet. 2024. PMID: 39572784 Free PMC article.
Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience.
Jurgens SJ, Rämö JT, Kramarenko DR, Wijdeveld LFJM, Haas J, Chaffin MD, Garnier S, Gaziano L, Weng LC, Lipov A, Zheng SL, Henry A, Huffman JE, Challa S, Rühle F, Verdugo CD, Krijger Juárez C, Kany S, van Orsouw CA, Biddinger K, Poel E, Elliott AL, Wang X, Francis C, Ruan R, Koyama S, Beekman L, Zimmerman DS, Deleuze JF, Villard E, Trégouët DA, Isnard R; FinnGen; VA Million Veteran Program; HERMES Consortium; Boomsma DI, de Geus EJC, Tadros R, Pinto YM, Wilde AAM, Hottenga JJ, Sinisalo J, Niiranen T, Walsh R, Schmidt AF, Choi SH, Chang KM, Tsao PS, Matthews PM, Ware JS, Lumbers RT, van der Crabben S, Laukkanen J, Palotie A, Amin AS, Charron P, Meder B, Ellinor PT, Daly M, Aragam KG, Bezzina CR. Jurgens SJ, et al. Among authors: amin as. Nat Genet. 2024 Dec;56(12):2843. doi: 10.1038/s41588-024-02047-4. Nat Genet. 2024. PMID: 39633063 Free PMC article. No abstract available.
Cardiac Repolarization in Health and Disease.
Krijger Juárez C, Amin AS, Offerhaus JA, Bezzina CR, Boukens BJ. Krijger Juárez C, et al. Among authors: amin as. JACC Clin Electrophysiol. 2023 Jan;9(1):124-138. doi: 10.1016/j.jacep.2022.09.017. Epub 2022 Nov 30. JACC Clin Electrophysiol. 2023. PMID: 36697193 Free article. Review.
Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner.
Amin AS, Giudicessi JR, Tijsen AJ, Spanjaart AM, Reckman YJ, Klemens CA, Tanck MW, Kapplinger JD, Hofman N, Sinner MF, Müller M, Wijnen WJ, Tan HL, Bezzina CR, Creemers EE, Wilde AA, Ackerman MJ, Pinto YM. Amin AS, et al. Eur Heart J. 2012 Mar;33(6):714-23. doi: 10.1093/eurheartj/ehr473. Epub 2011 Dec 23. Eur Heart J. 2012. PMID: 22199116 Free PMC article.
Long QT syndrome: beyond the causal mutation.
Amin AS, Pinto YM, Wilde AA. Amin AS, et al. J Physiol. 2013 Sep 1;591(17):4125-39. doi: 10.1113/jphysiol.2013.254920. Epub 2013 Jun 10. J Physiol. 2013. PMID: 23753525 Free PMC article. Review.
Disease Modifiers of Inherited SCN5A Channelopathy.
Verkerk AO, Amin AS, Remme CA. Verkerk AO, et al. Among authors: amin as. Front Cardiovasc Med. 2018 Oct 1;5:137. doi: 10.3389/fcvm.2018.00137. eCollection 2018. Front Cardiovasc Med. 2018. PMID: 30327767 Free PMC article. Review.
Improving electrocardiogram-based detection of rare genetic heart disease using transfer learning: An application to phospholamban p.Arg14del mutation carriers.
Lopes RR, Bleijendaal H, Ramos LA, Verstraelen TE, Amin AS, Wilde AAM, Pinto YM, de Mol BAJM, Marquering HA. Lopes RR, et al. Among authors: amin as. Comput Biol Med. 2021 Apr;131:104262. doi: 10.1016/j.compbiomed.2021.104262. Epub 2021 Feb 11. Comput Biol Med. 2021. PMID: 33607378 Free article.
200 results