Paperpal Prime Logo

Neurogenetics : Impact Factor & More

eISSN: 1364-6753pISSN: 1364-6745

Key Metrics

CiteScore
4.6
Impact Factor
< 5
SNIP
1.18
Recommended pre-submission checks
Powered by Paperpal by Editage

Topics Covered on Neurogenetics

Neurogenetics Journal Specifications

Overview
Publisher SPRINGER
Language English
Frequency Quarterly
General Details
LanguageEnglish
FrequencyQuarterly
Publication Start Year1997
Publisher URLVisit website
Website URLVisit website
View less

Planning to publish in Neurogenetics ?

Upload your Manuscript to get

  • Degree of match
  • Common matching concepts
  • Additional journal recommendations
Free Report

Recently Published Papers in Neurogenetics

Copy number variants across the developmental epilepsy-developmental and epileptic encephalopathy spectrum: an Indonesian case series.
  • 24 Oct 2026
  • Neurogenetics
MiR‑660‑5p ameliorates neuronal damage in Alzheimer's disease via targeting APP.
  • 17 Oct 2026
  • Neurogenetics
ATP1A3-related neurological disorders: updated insights into clinical heterogeneity, molecular mechanisms and precision therapeutics.
  • 14 Oct 2026
  • Neurogenetics
Contrasting clinical trajectories in two ALS patients with rare FUS variants: implications for variant interpretation, penetrance, and trial readiness.
  • 8 Oct 2026
  • Neurogenetics
Genetic findings in a Turkish clinical cohort with hereditary Parkinson's disease.
  • 6 Oct 2026
  • Neurogenetics
Short-chain enoyl-CoA hydratase deficiency: a systematic review of clinical spectrum, genotype-phenotype correlations and survival predictors.
  • 2 Oct 2026
  • Neurogenetics
Copy number variants across the developmental epilepsy-developmental and epileptic encephalopathy spectrum: an Indonesian case series.
  • 24 Oct 2026
  • Neurogenetics
MiR‑660‑5p ameliorates neuronal damage in Alzheimer's disease via targeting APP.
  • 17 Oct 2026
  • Neurogenetics
ATP1A3-related neurological disorders: updated insights into clinical heterogeneity, molecular mechanisms and precision therapeutics.
  • 14 Oct 2026
  • Neurogenetics
Contrasting clinical trajectories in two ALS patients with rare FUS variants: implications for variant interpretation, penetrance, and trial readiness.
  • 8 Oct 2026
  • Neurogenetics
Genetic findings in a Turkish clinical cohort with hereditary Parkinson's disease.
  • 6 Oct 2026
  • Neurogenetics
Short-chain enoyl-CoA hydratase deficiency: a systematic review of clinical spectrum, genotype-phenotype correlations and survival predictors.
  • 2 Oct 2026
  • Neurogenetics

FAQs on Neurogenetics