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

Year Number of Results
2009 3
2010 3
2011 3
2012 3
2013 3
2014 3
2015 2
2016 2
2017 3
2018 7
2019 11
2020 7
2021 6
2022 4
2023 6
2024 4

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58 results

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Page 1
Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service.
Westra D, Schouten MI, Stunnenberg BC, Kusters B, Saris CGJ, Erasmus CE, van Engelen BG, Bulk S, Verschuuren-Bemelmans CC, Gerkes EH, de Geus C, van der Zwaag PA, Chan S, Chung B, Barge-Schaapveld DQCM, Kriek M, Sznajer Y, van Spaendonck-Zwarts K, van der Kooi AJ, Krause A, Schönewolf-Greulich B, de Die-Smulders C, Sallevelt SCEH, Krapels IPC, Rasmussen M, Maystadt I, Kievit AJA, Witting N, Pennings M, Meijer R, Gillissen C, Kamsteeg EJ, Voermans NC. Westra D, et al. Among authors: van der zwaag pa. J Neuromuscul Dis. 2019;6(2):241-258. doi: 10.3233/JND-180376. J Neuromuscul Dis. 2019. PMID: 31127727
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: van der zwaag pa. 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.
Prevalence and cardiac phenotype of patients with a phospholamban mutation.
Hof IE, van der Heijden JF, Kranias EG, Sanoudou D, de Boer RA, van Tintelen JP, van der Zwaag PA, Doevendans PA. Hof IE, et al. Among authors: van der zwaag pa. Neth Heart J. 2019 Feb;27(2):64-69. doi: 10.1007/s12471-018-1211-4. Neth Heart J. 2019. PMID: 30547415 Free PMC article. Review.
Counsel the genotype, treat the phenotype.
van der Zwaag PA, van Tintelen JP. van der Zwaag PA, et al. Eur J Heart Fail. 2011 Nov;13(11):1159-60. doi: 10.1093/eurjhf/hfr131. Epub 2011 Sep 29. Eur J Heart Fail. 2011. PMID: 21965524 Free article. No abstract available.
A randomized controlled trial of eplerenone in asymptomatic phospholamban p.Arg14del carriers.
de Brouwer R, Te Rijdt WP, Hoorntje ET, Amin A, Asselbergs FW, Cox MGPJ, van der Heijden JF, Hillege H, Karper JC, Mahmoud B, van der Meer P, Oomen A, Te Riele ASJM, Silljé HHW, Tan HL, van Tintelen JP, van Veldhuisen DJ, Westenbrink BD, Wiesfeld ACP, Willems TP, van der Zwaag PA, Wilde AAM, de Boer RA, van den Berg MP. de Brouwer R, et al. Among authors: van der zwaag pa. Eur Heart J. 2023 Oct 21;44(40):4284-4287. doi: 10.1093/eurheartj/ehad292. Eur Heart J. 2023. PMID: 37210081 Free PMC article. No abstract available.
Phenotypic variability of filamin C-related cardiomyopathy: Insights from a novel Dutch founder variant.
Schoonvelde SAC, Ruijmbeek CWB, Hirsch A, van Slegtenhorst MA, Wessels MW, von der Thüsen JH, Baas AF, Stroeks SLVM, Verdonschot JAJ, van der Zwaag PA, Verhagen JMA, Michels M. Schoonvelde SAC, et al. Among authors: van der zwaag pa. Heart Rhythm. 2023 Nov;20(11):1512-1521. doi: 10.1016/j.hrthm.2023.08.003. Epub 2023 Aug 9. Heart Rhythm. 2023. PMID: 37562486
Genetic diagnosis through whole-exome sequencing.
van der Zwaag PA, Jongbloed JD, van Tintelen JP. van der Zwaag PA, et al. N Engl J Med. 2014 Mar 13;370(11):1067. doi: 10.1056/NEJMc1315908. N Engl J Med. 2014. PMID: 24620873 No abstract available.
Dyssynchronopathy Can be a Manifestation of Heritable Cardiomyopathy.
Te Rijdt WP, Hoedemaekers YM, Jongbloed JDH, Damman K, van der Zwaag PA, de Boer RA, Maass AH, van den Berg MP. Te Rijdt WP, et al. Among authors: van der zwaag pa. Circ Genom Precis Med. 2019 May;12(5):e002528. doi: 10.1161/CIRCGEN.119.002528. Circ Genom Precis Med. 2019. PMID: 31112419 No abstract available.
Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST).
Te Rijdt WP, Hoorntje ET, de Brouwer R, Oomen A, Amin A, van der Heijden JF, Karper JC, Westenbrink BD, Silljé HHW, Te Riele ASJM, Wiesfeld ACP, van Gelder IC, Willems TP, van der Zwaag PA, van Tintelen JP, Hillege JH, Tan HL, van Veldhuisen DJ, Asselbergs FW, de Boer RA, Wilde AAM, van den Berg MP. Te Rijdt WP, et al. Among authors: van der zwaag pa. Neth Heart J. 2022 Feb;30(2):84-95. doi: 10.1007/s12471-021-01584-5. Epub 2021 Jun 18. Neth Heart J. 2022. PMID: 34143416 Free PMC article.
Sex-specific aspects of phospholamban cardiomyopathy: The importance and prognostic value of low-voltage electrocardiograms.
de Brouwer R, Meems LMG, Verstraelen TE, Mahmoud B, Proost V, Wilde AAM, Bosman LP, van Drie E, van der Zwaag PA, van Tintelen JP, Houweling AC, van den Berg MP, de Boer RA. de Brouwer R, et al. Among authors: van der zwaag pa. Heart Rhythm. 2022 Mar;19(3):427-434. doi: 10.1016/j.hrthm.2021.11.009. Epub 2021 Nov 9. Heart Rhythm. 2022. PMID: 34767988 Free article.
58 results