Author

Aashish Srivastava

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Open access Jul 2026

Identification of novel variants in SSX1, CPNE1, and SPTBN5 in men with oligoasthenoteratozoospermia using whole-genome sequencing.

Rare candidate variants in SSX1, CPNE1, and SPTBN5 that may potentially be associated with the molecular basis of oligoasthenoteratozoospermia are identified and support the application of WGS in unresolved male infertility.

Sara Sadeghzadeh, A. Malcher, Razieh Ebrahimi Askari et al. · Journal of Applied Genetics · 0 citations

Open access Aug 2026

Whole-Genome Sequencing Identifies Potentially Causative Variants in SOX30, AKAP4, and RNF220 in Non-Obstructive Azoospermia

The co-occurrence of variants in AKAP4 and RNF220 may suggest an oligogenic etiology of NOA and contribute to the phenotypic variability associated with AKAP4 variants.

Razieh Ebrahimi Askari, A. Malcher, Fateme Sefid et al. · International Journal of Mol... · 0 citations