Egyptian Journal of Medical Human Genetics

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Journal Properties
  • Country
    Germany
  • Language
    English
  • Number of Articles
    491
  • Abbreviation
    Egypt J Med Hum Genet
  • ISSN
    1110-8630
  • Main Publisher
    Ain Shams University
  • Publisher
    Springer Science and Business Media LLC
  • Indian UGC
  • DOAJ (latest)
Journal Properties
  • Final Decision (day)
    126
  • Medicine
    Medicine (General)
    Science
    Biology (General)
    Genetics
  • website
Description
The Egyptian Journal of Medical Human Genetics is a peer-reviewed publication focusing on advancements in the field of medical genetics. It covers a wide range of topics related to the genetic basis of human diseases. This journal serves as a vital platform for researchers to share their findings in this rapidly evolving field. The initial goal of the first 150 characters is to highlight the genetics behind diseases. The journal's scope encompasses various aspects of human genetics, including but not limited to the molecular mechanisms of inherited disorders, genetic epidemiology, clinical genetics, and the development of new diagnostic and therapeutic approaches. It explores the impact of genetic variations on human health and disease susceptibility. The journal offers insights into gene therapy, personalized medicine, and the ethical considerations surrounding genetic testing and research. By including these factors, the Egyptian Journal of Medical Human Genetics is highly informative. The journal is indexed in prominent scientific databases, ensuring its visibility to a broad audience of researchers and clinicians. Contributing to this journal offers researchers an opportunity to disseminate their work to a global audience, thereby influencing clinical practice and contributing to improved patient care. The journal emphasizes the importance of understanding the genetic underpinnings of diseases for the development of more effective treatments. Researchers are encouraged to submit their latest findings and contribute to the ongoing progress in medical genetics. This could lead to better treatment and prevention.
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