Impact Factor
3.30
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
2.56
555 total citations
h5-index
26
h5 depth signal
Cited share
71.7%
162 of 226
Total citations
555
Citation footprint
Metric signal
2.27
External metric anchor
Self-citation
1.8%
10 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
France
241
United States
213
Italy
185
United Kingdom
159
Germany
147
Citing Fields of Research
Cytogenetics
692
Genetics & Genomics
672
Congenital Disorders
389
Neurodevelopmental Disorders
132
Cell Differentiation & Development
118
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
2,899
Articles tracked across the journal lifetime
Indexed publication set
226
162 cited publications
Last 12 months
54
4.5 publications/month
Open access share
98.1%
53 OA publications in the last year
Leading citing country
France
241 citing publications
Leading citing field
Cytogenetics
692 citing publications
Latest tracked publication
12 October 2026
10 recent records available
Coverage & Indexing History
v48n1, Jan./Mar. 2005-
v48n1, Jan./Mar. 2005-
Research Focus & Classification
Indexed Subjects
Cytogenetics
Genetics & Genomics
Congenital Disorders
Neurodevelopmental Disorders
Broad Categories
Genetics, Medical
Cytogenetics
Genetics & Genomics
Cell Differentiation & Development
Osteopathies
Hematology
MeSH Descriptors
Chromosome Aberrations
Genetic Diseases, Inborn
Genetics, Medical
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1016/j.ejmg.2026.105108
Open DOI
Genetic susceptibility in Takotsubo syndrome: a candidate gene association analysis in the French TAKOGENE cohort
02
DOI 10.1016/j.ejmg.2026.105109
Open DOI
Rare SERPINH1 and SERPINF1 variants in autosomal recessive osteogenesis imperfecta type X and type VI
03
04
DOI 10.1016/j.ejmg.2026.105106
Open DOI
A de novo gain-of-function variant of DNM1L causes developmental encephalopathy
05
06
DOI 10.1016/j.ejmg.2026.105103
Open DOI
Long-term impact of FN1-related spondylometaphyseal dysplasia, corner fracture type (SMD-CF)
07
DOI 10.1016/j.ejmg.2026.105102
Open DOI
Spontaneous splenic rupture and uterine serosal bleeding at 26 Weeks in COL3A1-related vascular Ehlers–Danlos syndrome
08
DOI 10.1016/j.ejmg.2026.105101
Open DOI
WLS-related Zaki syndrome: New clinical features and evidence for p.(Tyr478Cys) variant as a possible mutational hotspot
09
DOI 10.1016/j.ejmg.2026.105099
Open DOI
Exploring national support mechanisms for European reference network centres
10
Bibliographical & Catalog Notes
Print issues ceased with Vol. 52 (2009).
Also issued online.