Human Mutation

294.8k citations
6.4k papers · · active since 1992

Impact in

    • Metabolism and Genetic Disorders
  • Genetics top 1%
    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Connective tissue disorders research

Papers in

    • Metabolism and Genetic Disorders 473
    • Genomics and Rare Diseases 1.3k
    • Genetic Associations and Epidemiology 307
    • Genomic variations and chromosomal abnormalities 241
    • Connective tissue disorders research 225
    • BRCA gene mutations in cancer 223

Human Mutation

6.3k papers receiving 285.4k citations

Peers

Human Mutation
Comparison fields: 5 of 224
  • Clinical Biochemistry 15.3k
  • Genetics 84.7k
  • Sensory Systems 6.8k
  • Molecular Biology 77.6k
  • Genetics 8.3k
Replace Human Genetics with:
Human Genetics United States
Genomics United States
Journal of Medical Genetics United Kingdom
Genetics in Medicine United States
European Journal of Human Genetics United States
Clinical Genetics United States
Advances in experimental medicine and biology United States
American Journal of Medical Genetics Part A United States
Pediatric Research United States
Gene United States
Human Mutation relative to Human Genetics United States Human Genetics's profile →
Citations per field
00.5×1.6×
Human Genetics · 1×
Citations per year

Countries where authors publish in Human Mutation

Since Specialization
Citations

This map shows the geographic impact of research published in Human Mutation. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by papers published in Human Mutation with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Human Mutation more than expected).

Fields of papers published in Human Mutation

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers published in Human Mutation. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers published in Human Mutation.

About Human Mutation

The 6.4k papers published in Human Mutation in the last decades have received a total of 294.8k indexed citations . Papers published in Human Mutation usually cover Clinical Biochemistry (475 papers), Genetics (2.5k papers), Developmental Biology (57 papers), Molecular Biology (1.5k papers) and Sensory Systems (120 papers) specifically the topics of Genomics and Rare Diseases (1.3k papers), Metabolism and Genetic Disorders (473 papers), Lysosomal Storage Disorders Research (345 papers), Genetic Associations and Epidemiology (307 papers), Genetic factors in colorectal cancer (284 papers), Genomic variations and chromosomal abnormalities (241 papers), Connective tissue disorders research (225 papers) and BRCA gene mutations in cancer (223 papers). The most active scholars publishing in Human Mutation are Johan T. den Dunnen, Stylianos E. Antonarakis, D.N. Cooper, Mauno Vihinen, Mannis van Oven, Manfred Kayser, Charis Eng, Christine Van Broeckhoven, Ada Hamosh and Eric Boerwinkle.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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