Journal of Genomics and Precision Medicine
Clinical Genomics
Clinical genomics applies genomic technologies directly to patient care, providing insights that enhance diagnosis, treatment, and disease prevention. By sequencing a patient’s genome or analyzing specific gene panels, clinicians can uncover genetic mutations responsible for inherited disorders, cancer susceptibility, pharmacogenomic variations, and complex disease risk. The integration of genomic data into routine healthcare allows for early detection of at-risk individuals and the development of personalized treatment plans. Clinical genomics also supports reproductive planning, newborn screening, infectious disease tracking, and precision oncology. As genomic databases grow and artificial intelligence improves variant interpretation, clinicians gain access to increasingly detailed and actionable information.
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