European Journal of Human Genetics

169.5k citations
5.5k papers · · active since 1950

Impact in

  • Genetics top 1%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Genetic Associations and Epidemiology
    • Epigenetics and DNA Methylation
    • Mitochondrial Function and Pathology

Papers in

    • Genomic variations and chromosomal abnormalities 657
    • Genomics and Rare Diseases 626
    • Genetic Associations and Epidemiology 512
    • BRCA gene mutations in cancer 437
    • Genetics and Neurodevelopmental Disorders 419
    • RNA modifications and cancer 283
    • Mitochondrial Function and Pathology 244

European Journal of Human Genetics

5.2k papers receiving 164.2k citations

Peers

European Journal of Human Genetics
Comparison fields: 5 of 231
  • Genetics 63.0k
  • Molecular Biology 66.1k
  • Pediatrics, Perinatology and Child Health 14.7k
  • Genetics 7.5k
  • Sensory Systems 3.4k
Replace Clinical Genetics with:
Clinical Genetics United States
American Journal of Medical Genetics Part A United States
European Journal of Endocrinology United States
Reproduction United States
Human Mutation United States
Frontiers in Physiology United States
Journal of Medical Genetics United Kingdom
The Anatomical Record United States
Genetics in Medicine United States
Experimental Biology and Medicine United States
European Journal of Human Genetics relative to Clinical Genetics United States Clinical Genetics's profile →
Citations per field
00.5×1.5×1.8×
Clinical Genetics · 1×
Citations per year

Countries where authors publish in European Journal of Human Genetics

Since Specialization
Citations

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

Fields of papers published in European Journal of Human Genetics

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers published in European Journal of Human Genetics. 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 European Journal of Human Genetics.

About European Journal of Human Genetics

The 5.5k papers published in European Journal of Human Genetics in the last decades have received a total of 169.5k indexed citations . Papers published in European Journal of Human Genetics usually cover Genetics (2.7k papers), Molecular Biology (2.5k papers), Pediatrics, Perinatology and Child Health (544 papers), Genetics (309 papers) and Clinical Biochemistry (175 papers) specifically the topics of Genomic variations and chromosomal abnormalities (657 papers), Genomics and Rare Diseases (626 papers), Genetic Associations and Epidemiology (512 papers), BRCA gene mutations in cancer (437 papers), Genetics and Neurodevelopmental Disorders (419 papers), Prenatal Screening and Diagnostics (368 papers), RNA modifications and cancer (283 papers) and Mitochondrial Function and Pathology (244 papers). The most active scholars publishing in European Journal of Human Genetics are Isabelle Touitou, Gunnar Kaati, Sören Edvinsson, Han G. Brunner, Raoul C. M. Hennekam, Zeynep Tümer, Christine Van Broeckhoven, Philip L. Beales, Elizabeth Forsythe and Gert Matthijs.

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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