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Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, Toft E, Henriksen FL, Bundgaard H, Jensen HK, Kanters JK. Christiansen M, et al. Among authors: pedersen ln. BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31. BMC Med Genet. 2014. PMID: 24606995 Free PMC article.
Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.
Trolle C, Mortensen KH, Pedersen LN, Berglund A, Jensen HK, Andersen NH, Gravholt CH. Trolle C, et al. Among authors: pedersen ln. PLoS One. 2013 Jul 25;8(7):e69614. doi: 10.1371/journal.pone.0069614. Print 2013. PLoS One. 2013. PMID: 23936059 Free PMC article. Clinical Trial.
Diagnostic Yield of Genetic Testing in Young Patients With Atrioventricular Block of Unknown Cause.
Resdal Dyssekilde J, Frederiksen TC, Christiansen MK, Hasle Sørensen R, Pedersen LN, Loof Møller P, Christensen LS, Larsen JM, Thomsen KK, Lindhardt TB, Böttcher M, Molsted S, Havndrup O, Fischer T, Møller DS, Henriksen FL, Johansen JB, Nielsen JC, Bundgaard H, Nygaard M, Jensen HK. Resdal Dyssekilde J, et al. Among authors: pedersen ln. J Am Heart Assoc. 2022 May 3;11(9):e025643. doi: 10.1161/JAHA.121.025643. Epub 2022 Apr 26. J Am Heart Assoc. 2022. PMID: 35470684 Free PMC article.
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome.
Christiansen MK, Kjær-Sørensen K, Clavsen NC, Dittmann S, Jensen MF, Guldbrandsen HØ, Pedersen LN, Sørensen RH, Lildballe DL, Müller K, Müller P, Vogel K, Rudic B, Borggrefe M, Oxvig C, Aalkjær C, Schulze-Bahr E, Matchkov V, Bundgaard H, Jensen HK. Christiansen MK, et al. Among authors: pedersen ln. Heart Rhythm. 2023 Aug;20(8):1136-1143. doi: 10.1016/j.hrthm.2023.02.010. Epub 2023 Feb 15. Heart Rhythm. 2023. PMID: 36806574 Free article.
49 results