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SCIESCOPUSQ3

European Journal of Medical Genetics

ELSEVIER, France

European Journal of Medical Genetics is an academic journal published by ELSEVIER (France). Identifiers: ISSN 1769-7212, eISSN 1878-0849. Indexed in SCIE, SCOPUS. Metrics: JIF 1.7, CiteScore 3.7, SJR 0.748, SNIP 0.86. Subject areas: GENETICS & HEREDITY. tlooto lists 2,840 papers from this journal.

CiteScore

3.70

Scopus citation metric

SJR

0.748

SCImago rank

SNIP

0.86

Source normalized impact

Percentage rank

-

JIF percentile rank

Journal profile

ISSN
1769-7212
eISSN
1878-0849
Abbreviation
EUR J MED GENET
Publisher
ELSEVIER
Country
France

Web of Science categories

SCIEGENETICS & HEREDITY

Scopus ASJC categories

1311 Genetics2716 Genetics (clinical)

Keywords

Genetics & Heredity

Papers in this journal

Recent papers

  1. Intrafamilial variability of myoclonic dystonia in a large French family carrying a novel SGCE variant.

    2026

  2. Horizontal gaze palsy with progressive scoliosis (HGPPS): expanding ROBO3 molecular spectrum and refining clinical-neuroimaging phenotypes.

    2026

  3. Novelty and idiosyncrasy: the clay feet of rare disease descriptions.

    2026

  4. Thoracic Chordoma Following Intracranial Meningioma in a Patient with a Novel Germline SMARCE1 Variant.

    2026

  5. Phenotypic discordance in monozygotic twins with a CDH2 variant.

    2026

Most cited papers

  1. Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism: epidemiology, metabolism and the associated diseases.

    2015 · 412 citations

  2. Infantile hydrocephalus: a review of epidemiology, classification and causes

    2014 · 355 citations

  3. Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries.

    2005 · 283 citations

  4. Arthrogryposis (multiple congenital contractures): diagnostic approach to etiology, classification, genetics, and general principles.

    2014 · 265 citations

  5. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

    2009 · 241 citations