Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

196 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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: kanters jk. 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.
[Short QT syndrome as an inherited condition].
Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. Møller DV, et al. Ugeskr Laeger. 2011 Feb 7;173(6):420-4. Ugeskr Laeger. 2011. PMID: 21299935 Review. Danish.
MT-CYB mutations in hypertrophic cardiomyopathy.
Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jespersgaard C, Jensen M, Kanters JK, Moolman-Smook JC, Møller DV, Bundgaard H, Christiansen M. Hagen CM, et al. Among authors: kanters jk. Mol Genet Genomic Med. 2013 May;1(1):54-65. doi: 10.1002/mgg3.5. Epub 2013 Apr 12. Mol Genet Genomic Med. 2013. PMID: 24498601 Free PMC article.
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: kanters jk. BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31. BMC Med Genet. 2014. PMID: 24606995 Free PMC article.
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
Ghouse J, Have CT, Weeke P, Bille Nielsen J, Ahlberg G, Balslev-Harder M, Appel EV, Skaaby T, Olesen SP, Grarup N, Linneberg A, Pedersen O, Haunsø S, Hastrup Svendsen J, Hansen T, Kanters JK, Salling Olesen M. Ghouse J, et al. Among authors: kanters jk. Eur Heart J. 2015 Oct 1;36(37):2523-9. doi: 10.1093/eurheartj/ehv297. Epub 2015 Jul 9. Eur Heart J. 2015. PMID: 26159999
KCNE1 G38S polymorphism is not the cause of long QT syndrome.
Kanters JK, Olesen MS, Christiansen M. Kanters JK, et al. J Electrocardiol. 2016 Mar-Apr;49(2):249-50. doi: 10.1016/j.jelectrocard.2015.12.005. Epub 2015 Dec 12. J Electrocardiol. 2016. PMID: 26781364 No abstract available.
196 results