Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism J Ghouse, V Tragante, G Ahlberg, SA Rand, JB Jespersen, EB Leinøe, ... Nature Genetics 55 (3), 399-409, 2023 | 48 | 2023 |
Whole genome and transcriptome sequencing of post-mortem cardiac tissues from sudden cardiac death victims identifies a gene regulatory variant in NEXN JD Andersen, SB Jacobsen, LC Trudsø, ML Kampmann, J Banner, ... International Journal of Legal Medicine 133, 1699-1709, 2019 | 28 | 2019 |
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study H Yu Chen, C Dina, AM Small, CM Shaffer, RT Levinson, A Helgadóttir, ... European heart journal 44 (21), 1927-1939, 2023 | 25 | 2023 |
A comparative study of single nucleotide variant detection performance using three massively parallel sequencing methods LC Trudsø, JD Andersen, SB Jacobsen, SL Christiansen, ... PLoS One 15 (9), e0239850, 2020 | 12 | 2020 |
Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy SN Christiansen, SB Jacobsen, JD Andersen, ML Kampmann, LC Trudsø, ... International Journal of Molecular Sciences 22 (6), 2790, 2021 | 6 | 2021 |
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci J Ghouse, V Tragante, A Muhammad, G Ahlberg, MW Skov, DM Roden, ... European Heart Journal 43 (45), 4707-4718, 2022 | 5 | 2022 |
Association of PCSK9 Loss-of-Function Variants With Risk of Heart Failure LC Trudsø, J Ghouse, G Ahlberg, H Bundgaard, MS Olesen JAMA cardiology 8 (2), 159-166, 2023 | 2 | 2023 |
Loss-of-function variants in founder population highlight atrial myopathy as susceptibility to atrial fibrillation C Paludan-Muller, OB Vad, K Kahnert, G Ahlberg, LM Monfort, SA Rand, ... European Heart Journal 43 (Supplement_2), ehac544. 2875, 2022 | 1 | 2022 |