Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Ziaeian, B. & Fonarow, G. C. Epidemiology and aetiology of heart failure. Nat. Rev. Cardiol. 13, 368–378 (2016).…
A redefined InDel taxonomy provides insights into mutational signatures
Diversity of InDel patterns in PRRd We generated a ‘ground truth’ set of isogenic cellular models by introducing…
Quantitative characterization of cell niches in spatially resolved omics data
This study relies on the analysis of previously published data, adhering to ethical guidelines for human and mouse…
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder
To expand the search for genes implicated in bipolar disorder, we performed a genome-wide LOF burden scan of…
Author Correction: Identification of genetic elements that autonomously determine DNA methylation states
Cite this article Lienert, F., Wirbelauer, C., Som, I. et al. Author Correction: Identification of genetic elements that…