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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Nat Genet. 2022 Mar;54(3):232-239. doi: 10.1038/s41588-021-01007-6. Epub 2022 Feb 24.
Nat Genet. 2022.
PMID: 35210625
Free PMC article.
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: ortuno cg.
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.
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Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, Anys S, Minois D, Arnaud M, Duchateau J, Wijeyeratne YD, Muir A, Papadakis M, Castelletti S, Torchio M, Ortuño CG, Lacunza J, Giachino DF, Cerrato N, Martins RP, Campuzano O, Van Dooren S, Thollet A, Kyndt F, Mazzanti A, Clémenty N, Bisson A, Corveleyn A, Stallmeyer B, Dittmann S, Saenen J, Noël A, Honarbakhsh S, Rudic B, Marzak H, Rowe MK, Federspiel C, Le Page S, Placide L, Milhem A, Barajas-Martinez H, Beckmann BM, Krapels IP, Steinfurt J, Winkel BG, Jabbari R, Shoemaker MB, Boukens BJ, Škorić-Milosavljević D, Bikker H, Manevy F, Lichtner P, Ribasés M, Meitinger T, Müller-Nurasyid M; KORA-Study Group; Veldink JH, van den Berg LH, Van Damme P, Cusi D, Lanzani C, Rigade S, Charpentier E, Baron E, Bonnaud S, Lecointe S, Donnart A, Le Marec H, Chatel S, Karakachoff M, Bézieau S, London B, Tfelt-Hansen J, Roden D, Odening KE, Cerrone M, Chinitz LA, Volders PG, van de Berg MP, Laurent G, Faivre L, Antzelevitch C, Kääb S, Arnaout AA, Dupuis JM, Pasquie JL, Billon O, Roberts JD, Jesel L, Borggrefe M, Lambiase PD, Mansourati…
See abstract for full author list ➔
Barc J, et al. Among authors: ortuno cg.
Nat Genet. 2022 May;54(5):735. doi: 10.1038/s41588-022-01079-y.
Nat Genet. 2022.
PMID: 35474365
No abstract available.
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Portal vein thrombosis associated to prothrombin G20210A mutation and protein C deficiency.
Mira Y, García del Castillo G, Estellés A, Villa P, Vayá A, Ortuño C, Aznar J.
Mira Y, et al.
Clin Appl Thromb Hemost. 2000 Jul;6(3):179-80. doi: 10.1177/107602960000600311.
Clin Appl Thromb Hemost. 2000.
PMID: 10898280
Free article.
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Spontaneous cervical epidural hematoma associated with oral anticoagulant therapy.
Vayá A, Resurección M, Ricart JM, Ortuño C, Ripoll F, Mira Y, Aznar J.
Vayá A, et al.
Clin Appl Thromb Hemost. 2001 Apr;7(2):166-8. doi: 10.1177/107602960100700215.
Clin Appl Thromb Hemost. 2001.
PMID: 11292196
Free article.
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Intraindividual variability in plasma viscosity in relation to their utility as a cardiovascular risk factor.
Vayá A, Martínez M, Ortuño C, López JM, Aznar J.
Vayá A, et al.
Thromb Haemost. 1999 Jul;82(1):155.
Thromb Haemost. 1999.
PMID: 10456475
No abstract available.
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Thrombomodulin levels in asymptomatic familial hypercholesterolemia.
Vayá A, Martínez M, Ballesta A, Martí R, Ortuño C, Aznar J.
Vayá A, et al.
Clin Hemorheol Microcirc. 1999;20(2):91-6.
Clin Hemorheol Microcirc. 1999.
PMID: 10416810
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