European Journal of Human Genetics

212.7k citations
6.2k papers · · active since 2016

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
    • Genetic Syndromes and Imprinting
    • Epigenetics and DNA Methylation

Papers in

    • Genomics and Rare Diseases 802
    • Genomic variations and chromosomal abnormalities 782
    • Genetic Associations and Epidemiology 555
    • Genetics and Neurodevelopmental Disorders 527
    • BRCA gene mutations in cancer 486
    • RNA modifications and cancer 319
    • Mitochondrial Function and Pathology 266

European Journal of Human Genetics

5.9k papers receiving 202.5k citations

Peers

European Journal of Human Genetics
Comparison fields: 5 of 232
  • Genetics 80.9k
  • Molecular Biology 81.3k
  • Pediatrics, Perinatology and Child Health 18.9k
  • Genetics 9.4k
  • Sensory Systems 4.2k
Replace Clinical Genetics with:
Clinical Genetics United States
American Journal of Medical Genetics Part A United States
Human Mutation United States
European Journal of Endocrinology United States
Genetics in Medicine United States
Genomics United States
Frontiers in Physiology United States
Human Genetics United States
Experimental Biology and Medicine United States
The Anatomical Record United States
European Journal of Human Genetics relative to Clinical Genetics United States Clinical Genetics's profile →
Citations per field
00.5×1.5×1.9×
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 6.2k papers published in European Journal of Human Genetics in the last decades have received a total of 212.7k indexed citations . Papers published in European Journal of Human Genetics usually cover Genetics (3.2k papers), Molecular Biology (2.7k papers), Genetics (353 papers), Pediatrics, Perinatology and Child Health (610 papers) and Clinical Biochemistry (189 papers) specifically the topics of Genomics and Rare Diseases (802 papers), Genomic variations and chromosomal abnormalities (782 papers), Genetic Associations and Epidemiology (555 papers), Genetics and Neurodevelopmental Disorders (527 papers), BRCA gene mutations in cancer (486 papers), Prenatal Screening and Diagnostics (409 papers), RNA modifications and cancer (319 papers) and Mitochondrial Function and Pathology (266 papers). The most active scholars publishing in European Journal of Human Genetics are Isabelle Touitou, Gunnar Kaati, Marcus E Pembrey, Sören Edvinsson, Raoul C. M. Hennekam, Han G. Brunner, Christine Van Broeckhoven, GERT L. MATTHIJS, Zeynep Tümer and Bartha Maria Knoppers.

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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