Human Genomics

26.0k citations
1.1k papers · · active since 2016

Impact in

    • Cancer Genomics and Diagnostics
    • Cancer-related molecular mechanisms research
  • Genetics top 10%
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases

Papers in

    • Genetic Associations and Epidemiology 87
    • Genomics and Rare Diseases 82
    • Genomic variations and chromosomal abnormalities 36
    • Cancer Genomics and Diagnostics 34

Human Genomics

784 papers receiving 23.1k citations

Peers

Human Genomics
Comparison fields: 5 of 209
  • Cancer Research 3.0k
  • Genetics 5.0k
  • Pharmacology 1.4k
  • Molecular Biology 10.4k
  • Developmental Biology 219
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Human Genomics relative to Expert Reviews in Molecular Medicine United States Expert Reviews in Molecular Medicine's profile →
Citations per field
00.5×2×3.1×
Expert Reviews in Molecular Medicine · 1×
Citations per year

Countries where authors publish in Human Genomics

Since Specialization
Citations

This map shows the geographic impact of research published in Human Genomics. 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 Genomics with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Human Genomics more than expected).

Fields of papers published in Human Genomics

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers published in Human Genomics. 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 Genomics.

About Human Genomics

The 1.1k papers published in Human Genomics in the last decades have received a total of 26.0k indexed citations . Papers published in Human Genomics usually cover Genetics (276 papers), Cancer Research (74 papers), Molecular Biology (349 papers), Pharmacology (37 papers) and Sensory Systems (15 papers) specifically the topics of Genetic Associations and Epidemiology (87 papers), Genomics and Rare Diseases (82 papers), Bioinformatics and Genomic Networks (51 papers), Gene expression and cancer classification (47 papers), Pharmacogenetics and Drug Metabolism (36 papers), Genomic variations and chromosomal abnormalities (36 papers), Cancer Genomics and Diagnostics (34 papers) and Genomics and Phylogenetic Studies (33 papers). The most active scholars publishing in Human Genomics are Daniel W. Nebert, Vasilis Vasiliou, David R. Nelson, Dennis R. Petersen, D.N. Cooper, Michael P. H. Stumpf, Hongyu Zhao, Matt W. Wright, Elspeth A. Bruford and Ming Chen.

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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