Human Mutation (HM)

Human Mutation is a peer-reviewed international scientific journal that focuses on all aspects of human genetic variation and mutation research. Established in 1992, the journal publishes high-quality original research articles, reviews, mutation updates, rapid communications, database reports, and methodological advances in molecular genetics. It serves as a key platform for researchers studying genetic mutations and their role in human disease, population genetics, and genomic variation. The journal emphasizes novel findings related to DNA sequence changes, genotype–phenotype relationships, and clinical implications of genetic variation. It also publishes studies on new molecular diagnostic tools, genomic technologies, and bioinformatic approaches used to identify and interpret mutations. Human Mutation is widely used by clinical geneticists, molecular biologists, and biomedical researchers working in translational genomics. The journal plays an important role in bridging basic genetic research and clinical applications, particularly in the diagnosis and understanding of inherited disorders. It is indexed in major scientific databases and maintains a strong reputation in the field of genetics and medical genomics. Published monthly by Wiley on behalf of the Human Genome Variation Society, it continues to contribute significantly to advancements in human genetics and precision medicine.

Human Mutation (HM) is :-

• International, Peer-Reviewed, Open Access, Refereed, Human Genetics, Medical Genetics, Molecular Genetics, Clinical Genetics, Mutation Research, Biochemistry, Genetics and Molecular Biology, Genetic basis of human diseases, Clinical impact of gene mutations, Genotype–phenotype relationships, Genomic variation and SNP analysis, Molecular diagnostic methods in genetics, Functional and computational genomics , Online or Print , Monthly Journal

• UGC Approved, ISSN Approved: P-ISSN P-ISSN: 1059-7794, E-ISSN: 1098-1004, Established: 1992,
• Provides Crossref DOI

• Not indexed in Scopus, WoS, DOAJ, PubMed, UGC CARE