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About the journal
Genetics in Medicine Open is an open-access journal published by Elsevier in United States, publishing in english. It is listed in DOAJ according to the sources read. Declared publication charge: 3,200 USD. Declared review time at DOAJ: 34 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Elsevier
- ISSN
- 2949-7744
- Country
- United States
- Languages
- english
- Access
- Open access
- Declared publication charge
- 3,200 USD
- Articles in DOAJ
- 2846
- Declared review time
- 34 weeks
- Declared peer-review model
- double_blind
- Official website
- https://www.sciencedirect.com/journal/genetics-in-medicine-open
Index listings
- DOAJ · 2023-08-31
- Indexing
- DOAJ
- APC
- 3,200 USD
- Declared review time (DOAJ)
- 34 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
2846
Most recent article
2 months ago
Average review time (journal-declared via DOAJ)
34weeks
Works in OpenAlex
3772
Last recorded publication year
2026
Reported by OpenAlex in 2 of 3 sources (CC0 flags, not verified indexing)DOAJSciELOOpenAlex Core
h-index
12
i10-index
20
From OpenAlex open data (CC0).
Editorial & policy11
- Last DOAJ review date
- 2026-04-27
- Added to DOAJ
- 2023-08-31
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Open references deposited at Crossref
- 7%
- ORCID iDs in current deposits
- 7%
- Deposits licence metadata at Crossref
- ✓
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 9918734281906676
Classification4
Subjects (DOAJ)
Science: Biology (General): GeneticsMedicine
LCC codes
QH426-470R
Subject areas
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Metabolism and Genetic Disorders
- Genomic variations and chromosomal abnormalities
- Prenatal Screening and Diagnostics
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
Show all subjects (75)
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Lysosomal Storage Disorders Research
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Genetic Associations and Epidemiology
- Cancer Genomics and Diagnostics
- Cancer Genomics and Diagnostics
- Glycogen Storage Diseases and Myoclonus
- Genetic factors in colorectal cancer
- Connective tissue disorders research
- Connective tissue disorders research
- Cancer Genomics and Diagnostics
- Genetics and Neurodevelopmental Disorders
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- Genetics and Neurodevelopmental Disorders
- Diverse Scientific and Economic Studies
- Diverse Scientific and Economic Studies
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Lysosomal Storage Disorders Research
- Genetic Associations and Epidemiology
- Lysosomal Storage Disorders Research
- Genetic Associations and Epidemiology
- Fetal and Pediatric Neurological Disorders
- Genomics and Phylogenetic Studies
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Congenital heart defects research
- Congenital heart defects research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Immunodeficiency and Autoimmune Disorders
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Genetic Neurodegenerative Diseases
- Medical and Health Sciences Research
- Genetics, Bioinformatics, and Biomedical Research
- Genetics, Bioinformatics, and Biomedical Research
- RNA modifications and cancer
- RNA modifications and cancer
- Glycogen Storage Diseases and Myoclonus
- Legal Cases and Commentary
- Legal Cases and Commentary
- Glycogen Storage Diseases and Myoclonus
- Genetic Syndromes and Imprinting
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Craniofacial Disorders and Treatments
- Genetic and rare skin diseases.
- Mitochondrial Function and Pathology
- Epilepsy research and treatment
- Ethics in Clinical Research
- Health Systems, Economic Evaluations, Quality of Life
- Health Systems, Economic Evaluations, Quality of Life
- Nutrition, Genetics, and Disease
- Nutrition, Genetics, and Disease
- RNA regulation and disease
- RNA regulation and disease
Keywords (DOAJ)
- genomic medicine
- medical genetics
- genomics
- laboratory genetics and genomics
- clinical genomics
- therapeutics
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