Genetics in Medicine

162.4k citations
3.3k papers · · active since 1950

Impact in

  • Genetics top 1%
    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • BRCA gene mutations in cancer 538
    • Genomics and Rare Diseases 518
    • Genomic variations and chromosomal abnormalities 197
    • Metabolism and Genetic Disorders 152

Genetics in Medicine

2.6k papers receiving 144.3k citations

Peers

Genetics in Medicine
Comparison fields: 5 of 234
  • Genetics 60.4k
  • Clinical Biochemistry 6.6k
  • Pediatrics, Perinatology and Child Health 17.0k
  • Cancer Research 9.6k
  • Genetics 6.6k
Replace European Journal of Human Genetics with:
European Journal of Human Genetics United States
Human Mutation United States
Science Translational Medicine United States
Trends in Genetics United States
Annals of Human Genetics United Kingdom
Journal of Internal Medicine Sweden
PLoS Medicine United States
Annual Review of Medicine United States
The International Journal of Biochemistry & Cell Biology United States
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease United States
Genetics in Medicine relative to European Journal of Human Genetics United States European Journal of Human Genetics's profile →
Citations per field
00.5×1.7×
European Journal of Human Genetics · 1×
Citations per year

Countries where authors publish in Genetics in Medicine

Since Specialization
Citations

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

Fields of papers published in Genetics in Medicine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers published in Genetics in Medicine. 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 Genetics in Medicine.

About Genetics in Medicine

The 3.3k papers published in Genetics in Medicine in the last decades have received a total of 162.4k indexed citations . Papers published in Genetics in Medicine usually cover Genetics (1.4k papers), Clinical Biochemistry (154 papers), Pediatrics, Perinatology and Child Health (251 papers), Genetics (98 papers) and Physiology (224 papers) specifically the topics of BRCA gene mutations in cancer (538 papers), Genomics and Rare Diseases (518 papers), Genomic variations and chromosomal abnormalities (197 papers), Prenatal Screening and Diagnostics (184 papers), Metabolism and Genetic Disorders (152 papers), Lysosomal Storage Disorders Research (139 papers), Ethics in Clinical Research (125 papers) and Cystic Fibrosis Research Advances (117 papers). The most active scholars publishing in Genetics in Medicine are Thomas W. Valente, Wayne W. Grody, Heidi L. Rehm, Sherri J. Bale, Madhuri Hegde, Elaine Lyon, Soma Das, Elaine Spector, Sue Richards and David Bick.

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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