Associated Papers
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.
Marianski K et al.
Human Genetics, 2025
41442065 (PubMed )
Supplement: 439_2025_2796_MOESM4_ESM.xlsx › ST2
Genome sequencing of Pakistani families with male infertility identifies deleterious genotypes in SPAG6, CCDC9, TKTL1, TUBA3C, and M1AP.
Khan MR et al.
Andrology, 2025
Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes.
Rotte N et al.
Embo Molecular Medicine, 2025
40374915 (PubMed )
Supplement: 44321_2025_244_MOESM3_ESM.pdf
Toward clinical exomes in diagnostics and management of male infertility.
Lillepea K et al.
American Journal of Human Genetics, 2024
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