Vad OB - Search Results

1

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: vad ob. 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.

2

A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation.

Hansen TH, Yan Y, Ahlberg G, Vad OB, Refsgaard L, Dos Santos JL, Mutsaers N, Svendsen JH, Olesen MS, Bentzen BH, Schmitt N. Hansen TH, et al. Among authors: vad ob. Sci Rep. 2020 Jan 29;10(1):1453. doi: 10.1038/s41598-020-58475-9. Sci Rep. 2020. PMID: 31996765 Free PMC article.

3

Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation.

Vad OB, Paludan-Müller C, Ahlberg G, Kalstø SM, Ghouse J, Andreasen L, Haunsø S, Tveit A, Sajadieh A, Christophersen IE, Svendsen JH, Olesen MS. Vad OB, et al. J Clin Med. 2020 Jan 29;9(2):372. doi: 10.3390/jcm9020372. J Clin Med. 2020. PMID: 32013268 Free PMC article.

4

[Evident decline in mortality from ischaemic heart disease in Denmark from 1970 to 2015].

Haunsø S, Vad OB, Amtorp O. Haunsø S, et al. Among authors: vad ob. Ugeskr Laeger. 2020 Sep 7;182(37):V02200113. Ugeskr Laeger. 2020. PMID: 33000719 Free article. Danish.

5

Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation.

Clausen AG, Vad OB, Andersen JH, Olesen MS. Clausen AG, et al. Among authors: vad ob. Front Cardiovasc Med. 2021 Mar 9;8:650667. doi: 10.3389/fcvm.2021.650667. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 33768119 Free PMC article.

6

Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.

Vad OB, Yan Y, Denti F, Ahlberg G, Refsgaard L, Bomholtz SH, Santos JL, Rasmussen S, Haunsø S, Svendsen JH, Christophersen IE, Schmitt N, Olesen MS, Bentzen BH. Vad OB, et al. Front Genet. 2022 Jan 28;13:806429. doi: 10.3389/fgene.2022.806429. eCollection 2022. Front Genet. 2022. PMID: 35154276 Free PMC article.

7

Genetically predicted adipose tissue distribution influences the risk of atherosclerosis.

Vad OB, Paludan-Müller C, Monfort LM, Ahlberg G, Svendsen JH, Olesen MS. Vad OB, et al. Eur J Prev Cardiol. 2023 May 9;30(7):e41-e45. doi: 10.1093/eurjpc/zwad041. Eur J Prev Cardiol. 2023. PMID: 36753387 No abstract available.

8

CineECG analysis provides new insights into Familial ST-segment Depression Syndrome.

Frosted R, Paludan-Müller C, Vad OB, Olesen MS, Bundgaard H, van Dam P, Christensen AH. Frosted R, et al. Among authors: vad ob. Europace. 2023 May 19;25(5):euad116. doi: 10.1093/europace/euad116. Europace. 2023. PMID: 37140072 Free PMC article.

9

Unlocking the Genetic Code: Novel Insights Into Familial Atrial Fibrillation and Gene-Variant Interactions.

Vad OB, Olesen MS. Vad OB, et al. Can J Cardiol. 2023 Nov 30:S0828-282X(23)01963-3. doi: 10.1016/j.cjca.2023.11.036. Online ahead of print. Can J Cardiol. 2023. PMID: 38042338 No abstract available.

10

Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death.

Paludan-Müller C, Stampe NK, Monfort LM, Andreasen L, Vad OB, Ahlberg G, Johansen JB, Winkel BG, Torp-Pedersen C, Køber L, Fosbøl EL, Svendsen JH, Olesen MS. Paludan-Müller C, et al. Among authors: vad ob. J Am Heart Assoc. 2024 Apr 30:e034439. doi: 10.1161/JAHA.123.034439. Online ahead of print. J Am Heart Assoc. 2024. PMID: 38686897 Free article. No abstract available.

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