Vad OB - Search Results

1

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.

2

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.

3

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.

4

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.

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

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. 2024 Jul;40(7):1281-1282. doi: 10.1016/j.cjca.2023.11.036. Epub 2023 Nov 30. Can J Cardiol. 2024. PMID: 38042338 No abstract available.

9

Genetic Determinants of Left Atrial Function Are Associated With Stroke.

Vad OB, Paludan-Müller C, Diederichsen SZ, McKaige EA, Monfort LM, Lundegaard PR, Bertelsen L, Andreasen L, Svendsen JH, Olesen MS. Vad OB, et al. J Am Heart Assoc. 2024 Dec 3;13(23):e037490. doi: 10.1161/JAHA.124.037490. Epub 2024 Nov 22. J Am Heart Assoc. 2024. PMID: 39575717 Free article.

10

Screening for atrial fibrillation: the role of CHA₂DS₂-VASc and atrial fibrillation burden.

Xing LY, Vad OB, Engler D, Svendsen JH, Diederichsen SZ. Xing LY, et al. Among authors: vad ob. Eur Heart J Suppl. 2024 Jul 31;26(Suppl 4):iv41-iv49. doi: 10.1093/eurheartjsupp/suae078. eCollection 2024 Jul. Eur Heart J Suppl. 2024. PMID: 39099574 Free PMC article.

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