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Page 1
Atrial fibrillation: the role of common and rare genetic variants.
Olesen MS, Nielsen MW, Haunsø S, Svendsen JH. Olesen MS, et al. Among authors: haunso s. Eur J Hum Genet. 2014 Mar;22(3):297-306. doi: 10.1038/ejhg.2013.139. Epub 2013 Jul 10. Eur J Hum Genet. 2014. PMID: 23838598 Free PMC article. Review.
Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.
Gregers E, Ahlberg G, Christensen T, Jabbari J, Larsen KO, Herfelt CB, Henningsen KM, Andreasen L, Thiis JJ, Lund J, Holme S, Haunsø S, Bentzen BH, Schmitt N, Svendsen JH, Olesen MS. Gregers E, et al. Among authors: haunso s. Heart Rhythm. 2017 Oct;14(10):1531-1538. doi: 10.1016/j.hrthm.2017.05.027. Epub 2017 May 24. Heart Rhythm. 2017. PMID: 28549997
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes.
Andreasen L, Ahlberg G, Tang C, Andreasen C, Hartmann JP, Tfelt-Hansen J, Behr ER, Pehrson S, Haunsø S, LuCamp, Weeke PE, Jespersen T, Olesen MS, Svendsen JH. Andreasen L, et al. Among authors: haunso s. Eur J Hum Genet. 2018 May;26(5):660-668. doi: 10.1038/s41431-017-0092-0. Epub 2018 Feb 2. Eur J Hum Genet. 2018. PMID: 29396561 Free PMC article.
Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation.
Ahlberg G, Refsgaard L, Lundegaard PR, Andreasen L, Ranthe MF, Linscheid N, Nielsen JB, Melbye M, Haunsø S, Sajadieh A, Camp L, Olesen SP, Rasmussen S, Lundby A, Ellinor PT, Holst AG, Svendsen JH, Olesen MS. Ahlberg G, et al. Among authors: haunso s. Nat Commun. 2018 Oct 17;9(1):4316. doi: 10.1038/s41467-018-06618-y. Nat Commun. 2018. PMID: 30333491 Free PMC article.
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts.
Paludan-Müller C, Ghouse J, Vad OB, Herfelt CB, Lundegaard P, Ahlberg G, Schmitt N, Svendsen JH, Haunsø S, Bundgaard H, Hansen T, Kanters JK, Olesen MS. Paludan-Müller C, et al. Among authors: haunso s. Eur J Hum Genet. 2019 Sep;27(9):1427-1435. doi: 10.1038/s41431-019-0416-3. Epub 2019 May 1. Eur J Hum Genet. 2019. PMID: 31043699 Free PMC article.
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse.
Hadji-Turdeghal K, Andreasen L, Hagen CM, Ahlberg G, Ghouse J, Bækvad-Hansen M, Bybjerg-Grauholm J, Hougaard DM, Hedley P, Haunsø S, Svendsen JH, Kanters JK, Jepps TA, Skov MW, Christiansen M, Olesen MS. Hadji-Turdeghal K, et al. Among authors: haunso s. Cardiovasc Res. 2020 Jan 1;116(1):138-148. doi: 10.1093/cvr/cvz106. Cardiovasc Res. 2020. PMID: 31049583 Free PMC article.
Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation.
Seifert MB, Olesen MS, Christophersen IE, Nielsen JB, Carlson J, Holmqvist F, Tveit A, Haunsø S, Svendsen JH, Platonov PG. Seifert MB, et al. Among authors: haunso s. Ann Noninvasive Electrocardiol. 2019 Nov;24(6):e12661. doi: 10.1111/anec.12661. Epub 2019 Jun 1. Ann Noninvasive Electrocardiol. 2019. PMID: 31152482 Free PMC article.
256 results