Open access
Jul 2026
Genome-wide assessment of rare protein-coding variants identifies associations with non-syndromic cleft lip/palate.
Gene-based association testing, meta-analysis, functional prioritization, and effect-size estimation revealed several novel NSCLP candidate genes and confirmed associations with previously reported genes, providing strong support for a polygenic inheritance model in NSCLP.
Yao Yu, G. Kowalczyk, Chad D. Huff et al.
· European Journal of Human Ge... · 0 citations