European Journal of Human Genetics

Published by Springer

United Kingdom · Genomics and Rare Diseases

Journal at a glance

ISSN

1018-4813

Publisher

Springer

Country

United Kingdom

Language

en

Also known as: Eur J Hum Genet (Abbreviation), Europ J Hum Genet (Alternate title), EJHG (Alternate title)

Indexing

• Web of Science (SCIE): Indexed
• Scopus: Indexed
• Medline: Active
• Pubmed: Active

Metrics

Subjects

• Genomics and Rare Diseases
• Genomic variations and chromosomal abnormalities
• BRCA gene mutations in cancer
• Genetic Associations and Epidemiology
• Genetics and Neurodevelopmental Disorders
• Prenatal Screening and Diagnostics
• RNA modifications and cancer

Articles on PubPorta

The most recent records PubPorta holds for this journal.

• Patients’ and parents’ views on how digital tools enable personalized and partnered care in genetics: a qualitative study (2026)
• The co-design, development, and preliminary evaluation of a comprehensive breast cancer risk report incorporating polygenic risk information (2026)
• Clinical implementation of polygenic risk scores—updates on ancestry-adjusted PRS and their use in practice (2026)
• To screen or not to screen G6PD deficiency in gNBS: insights from the BabyDetect pilot and current evidence (2026)
• Beyond the sequence (2026)

Similar journals

• Journal of Medical Genetics — United Kingdom · — · Same subject: BRCA gene mutations in cancer, Same subject: Genetics and Neurodevelopmental Disorders, 5 shared subjects in total, Same country
• npj Genomic Medicine — United Kingdom · Open access · Same subject: Genetic Associations and Epidemiology, Same subject: Genetics and Neurodevelopmental Disorders, 5 shared subjects in total, Same country
• Journal of Human Genetics — Japan · — · Same subject: Genetic Associations and Epidemiology, Same subject: Genetics and Neurodevelopmental Disorders, 5 shared subjects in total
• European Journal of Medical Genetics — France · — · Same subject: Genetics and Neurodevelopmental Disorders, Same subject: Genomic variations and chromosomal abnormalities, 5 shared subjects in total
• Molecular Genetics and Genomic Medicine — United States · Open access · Same subject: BRCA gene mutations in cancer, Same subject: Genetics and Neurodevelopmental Disorders, 5 shared subjects in total
• Application of Clinical Genetics — New Zealand · Open access · Same subject: BRCA gene mutations in cancer, Same subject: Genetics and Neurodevelopmental Disorders, 5 shared subjects in total

Sources: OpenAlex, NLM Catalog, Crossref, Web of Science (Clarivate), Scopus · Last verified 2026-09-05

Journal homepage