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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 2
1991 1
1992 3
1993 2
1994 4
2000 1
2002 1
2003 1
2005 5
2006 1
2007 4
2008 7
2009 4
2010 5
2011 4
2012 6
2013 5
2014 2
2015 6
2016 6
2017 3
2018 1
2019 5
2020 6
2021 4
2022 2
2024 0

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71 results

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Page 1
Atlas of the clinical genetics of human dilated cardiomyopathy.
Haas J, Frese KS, Peil B, Kloos W, Keller A, Nietsch R, Feng Z, Müller S, Kayvanpour E, Vogel B, Sedaghat-Hamedani F, Lim WK, Zhao X, Fradkin D, Köhler D, Fischer S, Franke J, Marquart S, Barb I, Li DT, Amr A, Ehlermann P, Mereles D, Weis T, Hassel S, Kremer A, King V, Wirsz E, Isnard R, Komajda M, Serio A, Grasso M, Syrris P, Wicks E, Plagnol V, Lopes L, Gadgaard T, Eiskjær H, Jørgensen M, Garcia-Giustiniani D, Ortiz-Genga M, Crespo-Leiro MG, Deprez RH, Christiaans I, van Rijsingen IA, Wilde AA, Waldenstrom A, Bolognesi M, Bellazzi R, Mörner S, Bermejo JL, Monserrat L, Villard E, Mogensen J, Pinto YM, Charron P, Elliott P, Arbustini E, Katus HA, Meder B. Haas J, et al. Among authors: morner s. Eur Heart J. 2015 May 7;36(18):1123-35a. doi: 10.1093/eurheartj/ehu301. Epub 2014 Aug 27. Eur Heart J. 2015. PMID: 25163546
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, Amin AS, Nannenberg EA, Ware JS, Whiffin N, Mazzarotto F, Škorić-Milosavljević D, Krijger C, Arbelo E, Babuty D, Barajas-Martinez H, Beckmann BM, Bézieau S, Bos JM, Breckpot J, Campuzano O, Castelletti S, Celen C, Clauss S, Corveleyn A, Crotti L, Dagradi F, de Asmundis C, Denjoy I, Dittmann S, Ellinor PT, Ortuño CG, Giustetto C, Gourraud JB, Hazeki D, Horie M, Ishikawa T, Itoh H, Kaneko Y, Kanters JK, Kimoto H, Kotta MC, Krapels IPC, Kurabayashi M, Lazarte J, Leenhardt A, Loeys BL, Lundin C, Makiyama T, Mansourati J, Martins RP, Mazzanti A, Mörner S, Napolitano C, Ohkubo K, Papadakis M, Rudic B, Molina MS, Sacher F, Sahin H, Sarquella-Brugada G, Sebastiano R, Sharma S, Sheppard MN, Shimamoto K, Shoemaker MB, Stallmeyer B, Steinfurt J, Tanaka Y, Tester DJ, Usuda K, van der Zwaag PA, Van Dooren S, Van Laer L, Winbo A, Winkel BG, Yamagata K, Zumhagen S, Volders PGA, Lubitz SA, Antzelevitch C, Platonov PG, Odening KE, Roden DM, Roberts JD, Skinner JR, Tfelt-Hansen J, van den Berg MP, Olesen MS, Lambiase PD, Borggrefe M, Hayashi K, Rydberg A, Nakajima T, Yoshinaga M, Saenen JB, Kääb S, Brugada P, Robyns T, Giachino D… See abstract for full author list ➔ Walsh R, et al. Among authors: morner s. Genet Med. 2021 Jan;23(1):47-58. doi: 10.1038/s41436-020-00946-5. Epub 2020 Sep 7. Genet Med. 2021. PMID: 32893267 Free PMC article.
[Experiences from a multidisciplinary cardiogenetic clinic].
Mörner S, Carlberg B, Rydberg A, Jensen S, Lundström A, Nyberg P, Diamant UB, Hellman U, Johnson O, Näslund U. Mörner S, et al. Lakartidningen. 2021 Oct 6;118:21083. Lakartidningen. 2021. PMID: 35043387 Free article. Swedish.
Diagnosis of left ventricular hypertrophy using non-ECG-gated 15O-water PET.
Sörensen J, Nordström J, Baron T, Mörner S, Granstam SO, Lubberink M, Tolbod L, van den Berg J, Flachskampf FA, Kero T, Magnusson P, Harms HJ. Sörensen J, et al. Among authors: morner s. J Nucl Cardiol. 2022 Oct;29(5):2361-2373. doi: 10.1007/s12350-021-02734-3. Epub 2021 Jul 20. J Nucl Cardiol. 2022. PMID: 34286452 Free PMC article.
Genetic variants in cardiac calcification in Northern Sweden.
Hellman U, Mörner S, Henein M. Hellman U, et al. Among authors: morner s. Medicine (Baltimore). 2019 Apr;98(15):e15065. doi: 10.1097/MD.0000000000015065. Medicine (Baltimore). 2019. PMID: 30985656 Free PMC article.
71 results