Associated Papers
Mendelian non-syndromic and syndromic hearing loss genes contribute to presbycusis.
Cornejo-Sanchez DM et al.
European Journal of Human Genetics : Ejhg, 2025
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc4.xlsx › Supplementary_Table_4
Elevator-like movements of prestin mediate outer hair cell electromotility.
Kuwabara MF et al.
Nature Communications, 2023
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Praveen K et al.
Communications Biology, 2022
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.
Ivarsdottir EV et al.
Communications Biology, 2021
34108613 (PubMed )
Supplement: 42003_2021_2224_MOESM2_ESM.pdf
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