Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLMS08_het
A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure.
Guzmán-Jiménez A et al.
Human Reproduction Open, 2024
39678461 (PubMed )
Supplement: hoae069_supplementary_data.zip › supplementary_tables.xlsx › _S13
Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans.
Liu C et al.
The Embo Journal, 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.
Arafat M et al.
Molecular Genetics & Genomic Medicine, 2020
Single nucleotide polymorphisms of USP26 in azoospermic men.
Luddi A et al.
Systems Biology in Reproductive Medicine, 2016
Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men.
Shi YC et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2011
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