Associated Papers
Trans-ancestry GWAS identifies 59 loci and improves risk prediction and fine-mapping for kidney stone disease.
Cao X et al.
Nature Communications, 2025
40216741 (PubMed )
Supplement: 41467_2025_58782_MOESM7_ESM.xls › Supplementary_Data_5
A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.
Zhang D et al.
Annals of Human Genetics, 2022
35292975 (PubMed )
Supplement: AHG-86-207-s002.xlsx › RawData
Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene.
Zhu YM et al.
Frontiers in Cell and Developmental Biology, 2021
34692690 (PubMed )
Supplement: Table_2.xlsx › Supplementary_Table_5
Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss.
Sagong B et al.
International Journal of Pediatric Otorhinolaryngology, 2016
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