Journal Report

EUROPEAN JOURNAL OF MEDICAL GENETICS

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Journal Information
Journal Title
EUROPEAN JOURNAL OF MEDICAL GENETICS
Publisher
ELSEVIER
ISSN
1769-7212
E-ISSN
1878-0849
Database
Clarivate
Domain
Health Sciences, Life Sciences, Physical Sciences, Social Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
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Recent Articles
Rare SERPINH1 and SERPINF1 variants in autosomal recessive osteogenesis imperfecta type X and type VI
Fan Wang, Alice Costantini, Sare Betul Kaygusuz et al.
2026-12 Vol. 84 Pages 105109
DOI: 10.1016/j.ejmg.2026.105109
Heterogeneous biochemical responses to migalastat in real-world cases of Fabry disease
Takuya Hase, Hayaki Okamoto, Shunsuke Goto et al.
2026-12 Vol. 84 Pages 105111
DOI: 10.1016/j.ejmg.2026.105111
Neurofibromatosis 1 (NF1) gene testing reveals rising variant allele fraction as an early warning sign of juvenile myelomonocytic leukemia
Sirkku Peltonen, Christian Johansson, Marika Grönroos et al.
2026-12 Vol. 84 Pages 105104
DOI: 10.1016/j.ejmg.2026.105104
Sex chromosome dosage effects on human brain structure and function: a systematic review of neuroimaging findings in sex chromosome aneuploidies
Chaira Serrarens, Amy L. Sylvester, Davide Passaro et al.
2026-12 Vol. 84 Pages 105107
DOI: 10.1016/j.ejmg.2026.105107
Long-term impact of FN1-related spondylometaphyseal dysplasia, corner fracture type (SMD-CF)
Elis Riin Tars-Hurt, Mare Lintrop, Riina Zordania et al.
2026-12 Vol. 84 Pages 105103
DOI: 10.1016/j.ejmg.2026.105103
A de novo gain-of-function variant of DNM1L causes developmental encephalopathy
Shangsheng Dong, Yanjuan Chen, Mengfang Yan et al.
2026-12 Vol. 84 Pages 105106
DOI: 10.1016/j.ejmg.2026.105106
Efficacy and safety of exon skipping therapies for Duchenne Muscular Dystrophy: A Systematic Review
Sofía Ramírez-Guerrero, Omar H. Rojas-Tabares, Alberto Vélez-Van-Meerbeke et al.
2026-11 Pages 105112
DOI: 10.1016/j.ejmg.2026.105112
Genetic susceptibility in Takotsubo syndrome: a candidate gene association analysis in the French TAKOGENE cohort
Laury Nicolas, Sophie Garnier, Edouard Gerbaud et al.
2026-10 Pages 105108
DOI: 10.1016/j.ejmg.2026.105108
Hidden complexity of interchromosomal insertions revealed by optical genome mapping: report of two cases and literature review
Fatma MAAZOUN, Aziza LEBBAR, Aurélie COUSSEMENT et al.
2026-10 Pages 105110
DOI: 10.1016/j.ejmg.2026.105110
Identification of novel HUWE1 variants in Turner-type X-linked intellectual disability
Jingjing Zhang, Jing He, Hairui Pan et al.
2026-9 Vol. 83 Pages 105097
DOI: 10.1016/j.ejmg.2026.105097
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Printed: November 3, 2026 01:46