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Genetic testing in early-onset atrial fibrillation.

Kany S, Jurgens SJ, Rämö JT, et al. Genetic testing in early-onset atrial fibrillation. European heart journal. 2024. doi:10.1093/eurheartj/ehae298

[Genetic basis of atrial fibrillation-on the road to precision medicine].

Kany S, Schnabel RB. [Genetic basis of atrial fibrillation-on the road to precision medicine]. Herzschrittmachertherapie & Elektrophysiologie. 2023. doi:10.1007/s00399-023-00974-z

The functional impact of rare variation across the regulatory cascade.

Li T, Ferraro N, Strober BJ, et al. The functional impact of rare variation across the regulatory cascade. Cell genomics. 2023;3(10):100401. doi:10.1016/j.xgen.2023.100401

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.

Wang Y, Selvaraj MS, Li X, et al. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. American journal of human genetics. 2023;110(10):1704-1717. doi:10.1016/j.ajhg.2023.09.003

Rare variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome.

Ross JP, Akçimen F, Liao C, et al. Rare variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome. Genetics in medicine : official journal of the American College of Medical Genetics. 2023:100967. doi:10.1016/j.gim.2023.100967

Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes.

Karczewski KJ, Solomonson M, Chao KR, et al. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell genomics. 2022;2(9):100168. doi:10.1016/j.xgen.2022.100168