European Journal of Medical Genetics

Published by Elsevier

France · Genomic variations and chromosomal abnormalities

Journal at a glance

ISSN

17697212

Publisher

Elsevier

Country

France

Language

en

Also known as: Eur J Med Genet (Abbreviation)

Indexing

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

Metrics

Subjects

• Genomic variations and chromosomal abnormalities
• Genetics and Neurodevelopmental Disorders
• Genomics and Rare Diseases
• Congenital heart defects research
• Prenatal Screening and Diagnostics
• Connective tissue disorders research
• RNA modifications and cancer

Articles on PubPorta

The most recent records PubPorta holds for this journal.

• Neurofibromatosis Type 1 in Brazil: Pediatric Care in the Unified Health System (2026)
• Rapidly progressive vasculopathy in an infantile-onset fibromuscular dysplasia (2026)
• Identification of novel HUWE1 variants in Turner-type X-linked intellectual disability (2026)
• Smith-Kingsmore syndrome associated neurovascular complications and stroke: report of two cases (2026)
• Two new cases of fragile X syndrome without CGG triplet expansion. Clinical-molecular characterization and review of the literature (2026)

Similar journals

• Molecular Genetics and Genomic Medicine — United States · Open access · Same subject: Congenital heart defects research, Same subject: Connective tissue disorders research, 6 shared subjects in total
• Journal of Medical Genetics — United Kingdom · — · Same subject: Connective tissue disorders research, Same subject: Genetics and Neurodevelopmental Disorders, 5 shared subjects in total
• European Journal of Human Genetics — United Kingdom · — · Same subject: Genetics and Neurodevelopmental Disorders, Same subject: Genomic variations and chromosomal abnormalities, 5 shared subjects in total
• Application of Clinical Genetics — New Zealand · Open access · Same subject: Congenital heart defects research, Same subject: Genetics and Neurodevelopmental Disorders, 5 shared subjects in total
• Clinical Genetics — United Kingdom · — · Same subject: Genetics and Neurodevelopmental Disorders, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total
• Journal of Human Genetics — Japan · — · Same subject: Genetics and Neurodevelopmental Disorders, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total

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

Journal homepage