Variant effect predictors: a systematic review and practical guide Cristian RiccioMax L. JansenAndreas Ziegler Review Open access 04 April 2024 Pages: 625 - 634
Cross-ancestry genetic architecture and prediction for cholesterol traits Md. Moksedul MominXuan ZhouS. Hong Lee Original Investigation 27 March 2024 Pages: 635 - 648
Semiautomated approach focused on new genomic information results in time and effort-efficient reannotation of negative exome data Alejandro FerrerPatrick DuffyEric W. Klee Original Investigation 27 March 2024 Pages: 649 - 666
Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy Ahmed N. SahlyJuan Sierra-MarquezKenneth A. Myers Original Investigation 05 April 2024 Pages: 667 - 681
Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy Johannes KoppLeonard A. KochBjörn Fischer-Zirnsak Original Investigation Open access 09 April 2024 Pages: 683 - 694
VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19 Noam HadarVadim DolginOhad S. Birk Original Investigation 12 April 2024 Pages: 695 - 701
Examination of the shared genetic architecture between multiple sclerosis and systemic lupus erythematosus facilitates discovery of novel lupus risk loci Sophia KernsKatherine A. OwenPeter E. Lipsky Original Investigation 12 April 2024 Pages: 703 - 719
The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis Brett M. ColbertCris LantingXue Zhong Liu Original Investigation Open access 30 April 2024 Pages: 721 - 734