Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved cases. - Velde HM; Vaseghi-Shanjani M; Smits JJ; Ramakrishnan G; Oostrik J; Wesdorp M; Astuti G; Yntema HG; Hoefsloot L; Lanting CP; Huynen MA; Lehman A; et al. (Human genetics, 2024)