Erratum: Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals (The American Journal of Human Genetics (2021) 108(6) (965–982), (S0002929721001403), (10.1016/j.ajhg.2021.04.009))

(The American Journal of Human Genetics 108, 965–982; June 3, 2021) In the original version of this paper, the following authors were omitted from the list of Epi25 Collaborative consortium members: Sibel Uğur-İşeri, Betül Baykan, Barış Salman, Garen Haryanyan, Emrah Yücesan, Yeşim Kesim, and Çiğdem Özkara. The consortium member list has been corrected online, and the supplemental information has been corrected to include these individuals’ affiliations. The authors apologize for this omission. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individualsMotelow et al.The American Journal of Human GeneticsApril 30, 2021In BriefBoth mild and severe epilepsies are influenced by variants in the same genes, yet an explanation for the resulting phenotypic variation is unknown. As part of the ongoing Epi25 Collaboration, we performed a whole-exome sequencing analysis of 13,487 epilepsy-affected individuals and 15,678 control individuals. While prior Epi25 studies focused on gene-based collapsing analyses, we asked how the pattern of variation within genes differs by epilepsy type. Specifically, we compared the genetic architectures of severe developmental and epileptic encephalopathies (DEEs) and two generally less severe epilepsies, genetic generalized epilepsy and non-acquired focal epilepsy (NAFE). Full-Text PDF Open Archive