Olesen MS - Search Results

1

Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis.

Helgadottir A, Thorleifsson G, Snaebjarnarson A, Stefansdottir L, Sveinbjornsson G, Tragante V, Björnsson E, Steinthorsdottir V, Gretarsdottir S, Helgason H, Saemundsdottir J, Olafsson I, Thune JJ, Raja AA, Ghouse J, Olesen MS, Christensen A, Jacobsen RL, Dowsett J, Bruun MT, Nielsen K, Knowlton K, Nadauld L, Benediktsson R, Erikstrup C, Pedersen OB, Banasik K, Brunak S; DBDS Genomic Consortium; Bundgaard H, Ostrowski SR, Sulem P, Arnar DO, Thorgeirsson G, Thorsteinsdottir U, Gudbjartsson DF, Stefansson K, Holm H. Helgadottir A, et al. Among authors: olesen ms. Eur J Prev Cardiol. 2022 Dec 21;29(18):2374-2385. doi: 10.1093/eurjpc/zwac219. Eur J Prev Cardiol. 2022. PMID: 36125206

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

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.

5

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.

6

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.

7

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

8

Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Na_v1.5 gain-of-function mutation (G213D).

Calloe K, Broendberg AK, Christensen AH, Pedersen LN, Olesen MS, de Los Angeles Tejada M, Friis S, Thomsen MB, Bundgaard H, Jensen HK. Calloe K, et al. Among authors: olesen ms. Int J Cardiol. 2018 Apr 15;257:160-167. doi: 10.1016/j.ijcard.2017.11.095. Int J Cardiol. 2018. PMID: 29506689

9

Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest.

Andreasen L, Ghouse J, Skov MW, Have CT, Ahlberg G, Rasmussen PV, Linneberg A, Pedersen O, Platonov PG, Haunsø S, Svendsen JH, Hansen T, Kanters JK, Olesen MS. Andreasen L, et al. Among authors: olesen ms. Front Physiol. 2018 Jul 10;9:894. doi: 10.3389/fphys.2018.00894. eCollection 2018. Front Physiol. 2018. PMID: 30042696 Free PMC article.

10

Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts.

Paludan-Müller C, Ghouse J, Vad OB, Herfelt CB, Lundegaard P, Ahlberg G, Schmitt N, Svendsen JH, Haunsø S, Bundgaard H, Hansen T, Kanters JK, Olesen MS. Paludan-Müller C, et al. Among authors: olesen ms. Eur J Hum Genet. 2019 Sep;27(9):1427-1435. doi: 10.1038/s41431-019-0416-3. Epub 2019 May 1. Eur J Hum Genet. 2019. PMID: 31043699 Free PMC article.

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