Mutations in Genes Associated with Abnormalities of Reproductive Development: Molecular Basis and Clinical Perspectives

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About this Research Topic

Submission deadlines

  1. Manuscript Submission Deadline 20 August 2026

  2. This Research Topic is currently accepting articles

Background

Reproductive health, crucial for global human well-being, faces unique challenges. Normal individual reproductive development is a prerequisite for successful human reproduction, a process in which genes associated with ovarian development and testicular development function in coordination with each other to ensure the normal occurrence of sperm and ovum. Mutations in the genes involved in reproductive development have led to many human reproductive diseases. For instance, meiotic gene mutations in oocytes and spermatocytes lead to female and male reproductive dysfunctions. Despite recent advances in the field of reproduction, the mechanisms of reproductive developmental disorders caused by mutations in the genes involved are currently not fully understood, and the role of these mutations in reproductive disorders is not yet clear. Therefore, there is a need to further elucidate the underlying mechanisms and clinical perspectives to provide new approaches for the intervention and treatment of reproductive diseases.

This research project undertakes a comprehensive compilation of articles centered around the theme "Mutations in Genes Associated with Abnormalities of Reproductive Development: Molecular Basis and Clinical Perspectives". The overarching objective is to spotlight the most recent advancements in the domain of gene mutations related to reproductive development within the context of reproductive diseases. Moreover, it endeavors to probe into the underlying mechanisms and clinical outlooks of these gene mutations that give rise to reproductive developmental disorders.

We welcome submissions of Original Research articles, Reviews, Mini-Review and Systematic Review articles that focus on, but are not limited to, the following topics:
• Mechanism of abnormal follicular development caused by genetic mutations related to reproductive development.
• Mechanisms of abnormal spermatogenesis caused by genetic mutations related to reproductive development.
• Study the biological mechanism of gamete damage induced by genetic mutations related to reproductive development.
• Treatment of reproductive diseases caused by related gene mutations.
• Drug development and clinical application related to genetic mutations in reproductive diseases.

Article types and fees

This Research Topic accepts the following article types, unless otherwise specified in the Research Topic description:

  • Brief Research Report
  • Data Report
  • Editorial
  • FAIR² Data
  • General Commentary
  • Hypothesis and Theory
  • Methods
  • Mini Review
  • Opinion

Articles that are accepted for publication by our external editors following rigorous peer review incur a publishing fee charged to Authors, institutions, or funders.

Keywords: reproductive development, oocyte, sperm, reproductive diseases, mutation

Important note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.

Topic editors

Manuscripts can be submitted to this Research Topic via the main journal or any other participating journal.

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