About the journal
Genetics in Medicine is a journal published by Elsevier BV in United States. It is listed in MEDLINE and PUBMED according to the sources read. Declared publication charge: 4,200 USD. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Elsevier BV
- ISSN
- 1098-3600 · 1530-0366
- Country
- United States
- Access
- Not open access / not declared
- Declared publication charge
- 4,200 USD
- Declared peer-review model
- peer_review
- Official website
- https://www.sciencedirect.com/journal/genetics-in-medicine
Index listings
- MEDLINE · 1998-01-01
- PUBMED · 2011-09-26
- Indexing
- MEDLINE · PUBMED
- APC
- 4,200 USD
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 229 days received→accepted — computed from PubMed (n=100)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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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.
Works in OpenAlex
6222
Last recorded publication year
2026
h-index
206
i10-index
3212
From OpenAlex open data (CC0).
Editorial & policy4
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 79%
- ORCID iDs in current deposits
- 77%
- Deposits licence metadata at Crossref
- ✓
Identity & continuity4
- Alternate titles
- Genetics medicineGIM
- Source type
- journal
- NLM unique ID (PubMed)
- 9815831
- Society affiliations
- American College of Medical Genetics and Genomics
Classification(no data)
No data available to the platform for this group
No platform data for: Classification — absence is not a judgment about the journal.
Subject areas
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
Show all subjects (50)
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- Ethics in Clinical Research
- Ethics in Clinical Research
- Cancer Genomics and Diagnostics
- Cancer Genomics and Diagnostics
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Lysosomal Storage Disorders Research
- Lysosomal Storage Disorders Research
- Cystic Fibrosis Research Advances
- Cystic Fibrosis Research Advances
- Connective tissue disorders research
- Connective tissue disorders research
- Nutrition, Genetics, and Disease
- Nutrition, Genetics, and Disease
- Congenital heart defects research
- Congenital heart defects research
- Diverse Scientific and Economic Studies
- Diverse Scientific and Economic Studies
- Neurogenetic and Muscular Disorders Research
- Genetic Syndromes and Imprinting
- Neurogenetic and Muscular Disorders Research
- Genetic Syndromes and Imprinting
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Glycogen Storage Diseases and Myoclonus
- Glycogen Storage Diseases and Myoclonus
- Race, Genetics, and Society
- Race, Genetics, and Society
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Health Systems, Economic Evaluations, Quality of Life
- Health Systems, Economic Evaluations, Quality of Life
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Human auditory perception and evaluation
- Human auditory perception and evaluation
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