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Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
Behr ER, Savio-Galimberti E, Barc J, Holst AG, Petropoulou E, Prins BP, Jabbari J, Torchio M, Berthet M, Mizusawa Y, Yang T, Nannenberg EA, Dagradi F, Weeke P, Bastiaenan R, Ackerman MJ, Haunso S, Leenhardt A, Kääb S, Probst V, Redon R, Sharma S, Wilde A, Tfelt-Hansen J, Schwartz P, Roden DM, Bezzina CR, Olesen M, Darbar D, Guicheney P, Crotti L; UK10K Consortium; Jamshidi Y. Behr ER, et al. Among authors: haunso s. Cardiovasc Res. 2015 Jun 1;106(3):520-9. doi: 10.1093/cvr/cvv042. Epub 2015 Feb 17. Cardiovasc Res. 2015. PMID: 25691538 Free PMC article.
Common and rare variants in SCN10A modulate the risk of atrial fibrillation.
Jabbari J, Olesen MS, Yuan L, Nielsen JB, Liang B, Macri V, Christophersen IE, Nielsen N, Sajadieh A, Ellinor PT, Grunnet M, Haunsø S, Holst AG, Svendsen JH, Jespersen T. Jabbari J, et al. Among authors: haunso s. Circ Cardiovasc Genet. 2015 Feb;8(1):64-73. doi: 10.1161/HCG.0000000000000022. Circ Cardiovasc Genet. 2015. PMID: 25691686 Free PMC article. Clinical Trial.
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.
A novel nonsense variant in Nav1.5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias.
Olesen MS, Jensen NF, Holst AG, Nielsen JB, Tfelt-Hansen J, Jespersen T, Sajadieh A, Haunsø S, Lund JT, Calloe K, Schmitt N, Svendsen JH. Olesen MS, et al. Among authors: haunso s. Can J Cardiol. 2011 Jul-Aug;27(4):523.e17-23. doi: 10.1016/j.cjca.2011.01.003. Epub 2011 May 28. Can J Cardiol. 2011. PMID: 21621375 English, French.
256 results