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Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.
Ghouse J, Have CT, Skov MW, Andreasen L, Ahlberg G, Nielsen JB, Skaaby T, Olesen SP, Grarup N, Linneberg A, Pedersen O, Vestergaard H, Haunsø S, Svendsen JH, Hansen T, Kanters JK, Olesen MS. Ghouse J, et al. Among authors: haunso s. Genet Med. 2017 May;19(5):521-528. doi: 10.1038/gim.2016.151. Epub 2016 Oct 6. Genet Med. 2017. PMID: 27711072 Free article.
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.
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.
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
Vad OB, Yan Y, Denti F, Ahlberg G, Refsgaard L, Bomholtz SH, Santos JL, Rasmussen S, Haunsø S, Svendsen JH, Christophersen IE, Schmitt N, Olesen MS, Bentzen BH. Vad OB, et al. Among authors: haunso s. Front Genet. 2022 Jan 28;13:806429. doi: 10.3389/fgene.2022.806429. eCollection 2022. Front Genet. 2022. PMID: 35154276 Free PMC article.
256 results