About the journal
Case Reports in Genetics is an open-access journal published by Wiley in United Kingdom, publishing in english. It is listed in DOAJ according to the sources read. Declared publication charge: 870 USD. Declared review time at DOAJ: 13 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Wiley
- ISSN
- 2090-6544 · 2090-6552
- Country
- United Kingdom
- Languages
- english
- Access
- Open access
- Declared publication charge
- 870 USD
- Articles in DOAJ
- 341
- Declared review time
- 13 weeks
- Declared peer-review model
- peer_review
- Official website
- https://onlinelibrary.wiley.com/journal/4918
Index listings
- DOAJ · 2011-08-23
- Indexing
- DOAJ
- APC
- 870 USD
- Declared review time (DOAJ)
- 13 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
341
Most recent article
last month
Average review time (journal-declared via DOAJ)
13weeks
Works in OpenAlex
351
Last recorded publication year
2026
h-index
18
i10-index
60
From OpenAlex open data (CC0).
Editorial & policy12
- Last DOAJ review date
- 2026-03-12
- Added to DOAJ
- 2011-08-23
- 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 ↗
- Open references deposited at Crossref
- 93%
- ORCID iDs in current deposits
- 93%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 101583302
Classification2
Subjects (DOAJ)
LCC codes
Subject areas
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Congenital heart defects research
Show all subjects (50)
- Congenital heart defects research
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- Connective tissue disorders research
- Mitochondrial Function and Pathology
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- Metabolism and Genetic Disorders
- Mitochondrial Function and Pathology
- Metabolism and Genetic Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Neurogenetic and Muscular Disorders Research
- Congenital Ear and Nasal Anomalies
- Neurogenetic and Muscular Disorders Research
- Hereditary Neurological Disorders
- RNA regulation and disease
- RNA regulation and disease
- Congenital Ear and Nasal Anomalies
- RNA modifications and cancer
- Hereditary Neurological Disorders
- RNA modifications and cancer
- Hedgehog Signaling Pathway Studies
- Hedgehog Signaling Pathway Studies
- Neurological diseases and metabolism
- Neurological diseases and metabolism
- Genomics and Chromatin Dynamics
- Craniofacial Disorders and Treatments
- Genetic factors in colorectal cancer
- Genetic Neurodegenerative Diseases
- RNA Research and Splicing
- Genetic Neurodegenerative Diseases
- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- Craniofacial Disorders and Treatments
- Genetic and Kidney Cyst Diseases
- Renal and related cancers
- Renal and related cancers
- Genetic and Kidney Cyst Diseases
- Genetic factors in colorectal cancer
Keywords (DOAJ)
- genetics
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