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Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT.
Andreasen L, Ahlberg G, Ægisdottir HM, Sveinbjörnsson G, Lundegaard PR, Hartmann JP, Paludan-Müller C, Hadji-Turdeghal K, Ghouse J, Pehrson S, Jensen HK, Riahi S, Hansen J, Sandgaard N, Sørensen E, Banasik K, Sækmose SG, Bruun MT, Hjalgrim H, Erikstrup C, Pedersen OB, Wittig M, Haunsø S, Ostrowski SR; DBDS Genomic Consortium; Franke A, Brunak S, Kanters JK, Ellervik C, Bundgaard H, Ullum H, Gudbjartsson DF, Thorsteinsdottir U, Holm H, Arnar DO, Stefansson K, Svendsen JH, Olesen MS. Andreasen L, et al. Among authors: haunso s. Circ Res. 2022 Oct 28;131(10):862-865. doi: 10.1161/CIRCRESAHA.122.321556. Epub 2022 Oct 7. Circ Res. 2022. PMID: 36205134 No abstract available.
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.
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.
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.
256 results