Olesen MS - Search Results

1

Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.

Ghouse J, Tragante V, Ahlberg G, Rand SA, Jespersen JB, Leinøe EB, Vissing CR, Trudsø L, Jonsdottir I, Banasik K, Brunak S, Ostrowski SR, Pedersen OB, Sørensen E, Erikstrup C, Bruun MT, Nielsen KR, Køber L, Christensen AH, Iversen K, Jones D, Knowlton KU, Nadauld L, Halldorsson GH, Ferkingstad E, Olafsson I, Gretarsdottir S, Onundarson PT, Sulem P, Thorsteinsdottir U, Thorgeirsson G, Gudbjartsson DF, Stefansson K, Holm H, Olesen MS, Bundgaard H. Ghouse J, et al. Among authors: olesen ms. Nat Genet. 2023 Mar;55(3):399-409. doi: 10.1038/s41588-022-01286-7. Epub 2023 Jan 19. Nat Genet. 2023. PMID: 36658437

2

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.

Andreasen C, Nielsen JB, Refsgaard L, Holst AG, Christensen AH, Andreasen L, Sajadieh A, Haunsø S, Svendsen JH, Olesen MS. Andreasen C, et al. Among authors: olesen ms. Eur J Hum Genet. 2013 Sep;21(9):918-28. doi: 10.1038/ejhg.2012.283. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299917 Free PMC article.

3

Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants.

Paludan-Müller C, Ahlberg G, Ghouse J, Herfelt C, Svendsen JH, Haunsø S, Kanters JK, Olesen MS. Paludan-Müller C, et al. Among authors: olesen ms. Clin Genet. 2017 Jan;91(1):63-72. doi: 10.1111/cge.12847. Epub 2016 Sep 26. Clin Genet. 2017. PMID: 27538377

4

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: olesen sp, olesen ms. 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.

5

Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy.

Refsgaard L, Olesen MS, Møller DV, Christiansen M, Haunsø S, Svendsen JH, Christensen AH. Refsgaard L, et al. Among authors: olesen ms. Appl Transl Genom. 2012 Oct 1;1:44-46. doi: 10.1016/j.atg.2012.06.001. eCollection 2012 Dec 1. Appl Transl Genom. 2012. PMID: 27896052 Free PMC article.

6

Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy.

Nouhravesh N, Ahlberg G, Ghouse J, Andreasen C, Svendsen JH, Haunsø S, Bundgaard H, Weeke PE, Olesen MS. Nouhravesh N, et al. Among authors: olesen ms. Mol Genet Genomic Med. 2016 Sep 17;4(6):617-623. doi: 10.1002/mgg3.245. eCollection 2016 Nov. Mol Genet Genomic Med. 2016. PMID: 27896284 Free PMC article.

7

Electrocardiographic Preexcitation and Risk of Cardiovascular Morbidity and Mortality: Results From the Copenhagen ECG Study.

Skov MW, Rasmussen PV, Ghouse J, Hansen SM, Graff C, Olesen MS, Pietersen A, Torp-Pedersen C, Haunsø S, Køber L, Svendsen JH, Holst AG, Nielsen JB. Skov MW, et al. Among authors: olesen ms. Circ Arrhythm Electrophysiol. 2017 Jun;10(6):e004778. doi: 10.1161/CIRCEP.116.004778. Circ Arrhythm Electrophysiol. 2017. PMID: 28576781

8

Distinguishing pathogenic mutations from background genetic noise in cardiology: The use of large genome databases for genetic interpretation.

Ghouse J, Skov MW, Bigseth RS, Ahlberg G, Kanters JK, Olesen MS. Ghouse J, et al. Among authors: olesen ms. Clin Genet. 2018 Mar;93(3):459-466. doi: 10.1111/cge.13066. Epub 2017 Sep 18. Clin Genet. 2018. PMID: 28589536 Review.

9

Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease.

Paludan-Müller C, Ahlberg G, Ghouse J, Svendsen JH, Haunsø S, Olesen MS. Paludan-Müller C, et al. Among authors: olesen ms. Circ Cardiovasc Genet. 2017 Dec;10(6):e001878. doi: 10.1161/CIRCGENETICS.117.001878. Circ Cardiovasc Genet. 2017. PMID: 29237690

10

Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes.

Andreasen L, Ahlberg G, Tang C, Andreasen C, Hartmann JP, Tfelt-Hansen J, Behr ER, Pehrson S, Haunsø S, LuCamp, Weeke PE, Jespersen T, Olesen MS, Svendsen JH. Andreasen L, et al. Among authors: olesen ms. Eur J Hum Genet. 2018 May;26(5):660-668. doi: 10.1038/s41431-017-0092-0. Epub 2018 Feb 2. Eur J Hum Genet. 2018. PMID: 29396561 Free PMC article.

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