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Author

Razieh Ebrahimi Askari

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3 papers indexed here

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Open access Aug 2026

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study

Abstract Background Oligoasthenoteratozoospermia (OAT) is a major cause of male infertility, characterized by low sperm count, poor motility, and abnormal morphology. While genetic factors contribute to a substantial proportion of cases, the specific variants underlying OAT remain largely unknown, especially in populat...

Sara Sadeghzadeh, A. Malcher, Razieh Ebrahimi Askari et al. · 0 citations
Open access Jul 2026

Whole-genome sequencing identifies a potentially causative homozygous splicing variant in RAD54 like in non-obstructive azoospermia

This study proposes RAD54L as a potential novel candidate gene linked to NOA and underscores the efficacy of WGS in identifying rare genetic etiologies of idiopathic male infertility.

Razieh Ebrahimi Askari, A. Malcher, Sara Sadeghzadeh et al. · 0 citations

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