Journal Report

Neurogenetics

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Journal Information
Journal Title
Neurogenetics
Publisher
ISSN
1364-6745
E-ISSN
Database
AERES
Domain
Health Sciences, Life Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Findings of limb-girdle muscular dystrophy R7 telethonin-related patients from a Chinese neuromuscular center
Kun Huang, Qiu-Xiang Li, Hui-Qian Duan et al.
2022-1 Vol. 23 Issue 1 Pages 37-44
DOI: 10.1007/s10048-021-00681-2
Correction to: Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant
Ivana Dzinovic, Tereza Serranová, Clement Prouteau et al.
2021-12-3 Vol. 23 Issue 1 Pages 77-77
DOI: 10.1007/s10048-021-00641-w
NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype
Maria Rosário Almeida, Inês Elias, Carolina Fernandes et al.
2021-12-1 Vol. 23 Issue 1 Pages 1-9
DOI: 10.1007/s10048-021-00679-w
Correction to: Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 gene
Berardo Rinaldi, Yu‑Han Ge, Elena Freri et al.
2021-11-27 Vol. 23 Issue 1 Pages 81-81
DOI: 10.1007/s10048-021-00678-x
In response to: Fatal status epilepticus—the broad phenotypic heterogeneity of NARS2 variants. Author: Prof. Josef Finsterer
K. Štěrbová, M. Vlčková, H. Hansíková et al.
2021-11-27 Vol. 23 Issue 1 Pages 67-68
DOI: 10.1007/s10048-021-00677-y
Fatal status epilepticus: the broad phenotypic heterogeneity of NARS2 variants
J. Finsterer
2021-11-15 Vol. 23 Issue 1 Pages 73-74
DOI: 10.1007/s10048-021-00676-z
Correction to: Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia
Eva López, Carlos Casasnovas, Javier Giménez et al.
2021-11-10 Vol. 23 Issue 1 Pages 79-79
DOI: 10.1007/s10048-021-00654-5
Mutation spectrum and genotype–phenotype correlations in 157 Korean CADASIL patients: a multicenter study
Ji-You Min, Seo-Jin Park, Eun-Joo Kang et al.
2021-11-6 Vol. 23 Issue 1 Pages 45-58
DOI: 10.1007/s10048-021-00674-1
Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 gene
Berardo Rinaldi, Yu-Han Ge, Elena Freri et al.
2021-11-3 Vol. 23 Issue 1 Pages 27-35
DOI: 10.1007/s10048-021-00666-1
Novel compound heterozygous variant of TOE1 results in a mild type of pontocerebellar hypoplasia type 7: an expansion of the clinical phenotype
Hongzhu Chen, Niu Li, Yufei Xu et al.
2021-10-30 Vol. 23 Issue 1 Pages 11-17
DOI: 10.1007/s10048-021-00675-0
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Printed: November 5, 2026 15:48