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Technological advancements have increased human exposure to electromagnetic fields (EMFs). This study analyzed over 30,000 publications, identifying thousands of associated genes and diseases to understand EMFs molecular impact.

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Area of Science:

  • Environmental Health Sciences
  • Molecular Biology
  • Toxicology

Background:

  • Technological progress over the last century has led to a significant rise in anthropogenic electromagnetic fields (EMFs).
  • Increased human exposure to diverse EMF subsets necessitates a deeper understanding of their biological and molecular consequences.
  • Existing literature on EMFs is vast, requiring systematic analysis to extract key biological information.

Purpose of the Study:

  • To systematically mine and analyze a large corpus of EMF-related scientific literature.
  • To identify genes, diseases, and molecular mechanisms linked to exposure to six distinct subsets of EMFs.
  • To highlight the molecular underpinnings of increasing human exposure to electromagnetic fields.

Main Methods:

  • Conducted a comprehensive literature mining process on over 30,000 EMF-related publications.
  • Extracted and cataloged disease terms (MeSH terms) and gene information associated with EMF exposure.
  • Focused analysis on six different subsets of electromagnetic fields.

Main Results:

  • Identified 3653 unique disease MeSH terms associated with EMF exposure.
  • Identified 9966 unique genes, with 4340 confirmed as human genes, linked to EMFs.
  • The data reveals a broad spectrum of molecular and disease-related impacts from EMF exposure.

Conclusions:

  • The study provides a comprehensive overview of the molecular landscape associated with EMF exposure.
  • Findings underscore the importance of understanding the genetic and disease-related consequences of rising EMF levels.
  • This work serves as a foundation for future research into the biological effects of electromagnetic fields.