Genetics in Medicine

214.3k citations
4.3k papers · · active since 2016

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

    • Genomics and Rare Diseases 759
    • BRCA gene mutations in cancer 665
    • Genomic variations and chromosomal abnormalities 266
    • Metabolism and Genetic Disorders 190

Genetics in Medicine

3.4k papers receiving 185.8k citations

Peers

Genetics in Medicine
Comparison fields: 5 of 234
  • Genetics 85.0k
  • Clinical Biochemistry 8.9k
  • Pediatrics, Perinatology and Child Health 21.6k
  • Cancer Research 14.1k
  • Genetics 8.7k
Replace Clinical Genetics with:
Clinical Genetics United States
European Journal of Human Genetics United States
American Journal of Medical Genetics Part A United States
Human Mutation United States
Human Genetics United States
Genomics United States
Experimental Biology and Medicine United States
Journal of Medical Genetics United Kingdom
Journal of Molecular Medicine Germany
Digestive Diseases and Sciences United States
Genetics in Medicine relative to Clinical Genetics United States Clinical Genetics's profile →
Citations per field
00.5×2×3.1×
Clinical 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 4.3k papers published in Genetics in Medicine in the last decades have received a total of 214.3k indexed citations . Papers published in Genetics in Medicine usually cover Genetics (1.8k papers), Clinical Biochemistry (192 papers), Pediatrics, Perinatology and Child Health (329 papers), Physiology (278 papers) and Genetics (115 papers) specifically the topics of Genomics and Rare Diseases (759 papers), BRCA gene mutations in cancer (665 papers), Genomic variations and chromosomal abnormalities (266 papers), Prenatal Screening and Diagnostics (245 papers), Metabolism and Genetic Disorders (190 papers), Lysosomal Storage Disorders Research (167 papers), Ethics in Clinical Research (161 papers) and Genetic factors in colorectal cancer (150 papers). The most active scholars publishing in Genetics in Medicine are Thomas William Valente, Wayne W. Grody, Heidi L. Rehm, Sherri J. Bale, Madhuri Hegde, Elaine Lyon, Soma Das, Elaine Spector, David P Bick and Sue M. Richards.

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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