Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysisEmil E. Vorsteveld, Ruben L. Smeets, Christian Gilissen et al.|Clinical Immunology|2024Cited by 18
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variantJeroen J. Smits, Suzanne E. de Bruijn, Cris Lanting et al.|Human Genetics|2021Cited by 16
Clinical exome sequencing data from patients with inborn errors of immunity: cohort level meta-analysis and the benefit of systematic reanalysisEmil E. Vorsteveld, Alexander Hoischen, Caspar I. van der Made et al.|medRxiv|2024Cited by 1
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variantJeroen J. Smits, Suzanne E. de Bruijn, Cris Lanting et al.|Human Genetics|2021Cited by 0