About the journal
Neurology: Genetics is an open-access journal published by Wolters Kluwer in United States, publishing in english. It is listed in DOAJ according to the sources read. Declared publication charge: 3,300 USD. Declared review time at DOAJ: 15 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Wolters Kluwer
- ISSN
- 2376-7839
- Country
- United States
- Languages
- english
- Access
- Open access
- Declared publication charge
- 3,300 USD
- Articles in DOAJ
- 0
- Declared review time
- 15 weeks
- Declared peer-review model
- peer_review
- Official website
- https://ng.neurology.org
Index listings
- DOAJ · 2016-02-12
- Indexing
- DOAJ
- APC
- 3,300 USD
- Declared review time (DOAJ)
- 15 weeks — journal-declared only (not measured)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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- Choose your university and rank below ↓
Methodology signals (dated facts from their sources)
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Articles in DOAJ
0
Average review time (journal-declared via DOAJ)
15weeks
Works in OpenAlex
1035
Last recorded publication year
2026
h-index
54
i10-index
470
From OpenAlex open data (CC0).
Editorial & policy12
- Last DOAJ review date
- 2021-02-13
- Added to DOAJ
- 2016-02-12
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPMCPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 98%
- ORCID iDs in current deposits
- 94%
- Enrolled in Crossref Similarity Check
- ✓
- Peer-review policy
- View policy
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 101671068
Classification4
Subjects (DOAJ)
LCC codes
Subject areas
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
Show all subjects (50)
- Hereditary Neurological Disorders
- Amyotrophic Lateral Sclerosis Research
- Hereditary Neurological Disorders
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism
- Neurological diseases and metabolism
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Muscle Physiology and Disorders
- Muscle Physiology and Disorders
- Parkinson's Disease Mechanisms and Treatments
- Parkinson's Disease Mechanisms and Treatments
- RNA regulation and disease
- RNA regulation and disease
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Alzheimer's disease research and treatments
- Cerebrovascular and genetic disorders
- Alzheimer's disease research and treatments
- Cerebrovascular and genetic disorders
- Cardiomyopathy and Myosin Studies
- Cardiomyopathy and Myosin Studies
- Glycogen Storage Diseases and Myoclonus
- Epilepsy research and treatment
- Glycogen Storage Diseases and Myoclonus
- Epilepsy research and treatment
- Lysosomal Storage Disorders Research
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Lysosomal Storage Disorders Research
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Neurological disorders and treatments
- Neurological disorders and treatments
- RNA modifications and cancer
- RNA modifications and cancer
- RNA Research and Splicing
- RNA Research and Splicing
- Cellular transport and secretion
- Cellular transport and secretion
- Fetal and Pediatric Neurological Disorders
- Fetal and Pediatric Neurological Disorders
Keywords (DOAJ)
- neurology
- neurogenetics
- genetic disease risk
- pharmacogenomics
Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.
The journal's record in other sources:Web of Science MJLDOAJ