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No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes.
Damgaard D, Jensen JM, Larsen ML, Soerensen VR, Jensen HK, Gregersen N, Jensen LG, Faergeman O. Damgaard D, et al. Among authors: jensen jm, jensen hk, jensen lg. Atherosclerosis. 2004 Dec;177(2):415-22. doi: 10.1016/j.atherosclerosis.2004.07.028. Atherosclerosis. 2004. PMID: 15530918
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: jensen hk. BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31. BMC Med Genet. 2014. PMID: 24606995 Free PMC article.
[The genome and cardiology].
Bundgaard H, Diness BR, Tfelt-Hansen J, Henriksen FL, Eschen O, Skovby F, Havndrup O, Jensen HK, Tybjærg-Hansen A. Bundgaard H, et al. Among authors: jensen hk. Ugeskr Laeger. 2014 Nov 10;176(46):V06140376. Ugeskr Laeger. 2014. PMID: 25394933 Free article. Review. Danish.
The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J. Winkel BG, et al. Among authors: jensen hk. J Cardiovasc Electrophysiol. 2012 Oct;23(10):1092-8. doi: 10.1111/j.1540-8167.2012.02371.x. Epub 2012 Aug 6. J Cardiovasc Electrophysiol. 2012. PMID: 22882672
324 results