About the journal
The American Journal of Human Genetics 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: 5,150 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
- 0002-9297 · 1537-6605
- Country
- United States
- Access
- Not open access / not declared
- Declared publication charge
- 5,150 USD
- Declared peer-review model
- peer_review
Index listings
- MEDLINE · 1965-01-01
- PUBMED · 2008-05-09
- Indexing
- MEDLINE · PUBMED
- APC
- 5,150 USD
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 146 days received→accepted — computed from PubMed (n=92)
- 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
11166
Last recorded publication year
2026
h-index
388
i10-index
6514
From OpenAlex open data (CC0).
Editorial & policy4
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Norwegian register (HK-dir)— 2027
- Level 2 — top tier (~20% of the field's channels)
- Open references deposited at Crossref
- 88%
- ORCID iDs in current deposits
- 73%
- Deposits licence metadata at Crossref
- ✓
Identity & continuity3
- Alternate titles
- AJHG
- Source type
- journal
- NLM unique ID (PubMed)
- 0370475
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
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
Show all subjects (50)
- Genetic Mapping and Diversity in Plants and Animals
- Genetic Mapping and Diversity in Plants and Animals
- RNA modifications and cancer
- RNA modifications and cancer
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- RNA Research and Splicing
- RNA Research and Splicing
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Forensic and Genetic Research
- Forensic and Genetic Research
- Genetic and phenotypic traits in livestock
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Genetic and phenotypic traits in livestock
- Congenital heart defects research
- Congenital heart defects research
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- Genomics and Chromatin Dynamics
- Genomics and Chromatin Dynamics
- Nutrition, Genetics, and Disease
- Nutrition, Genetics, and Disease
- RNA and protein synthesis mechanisms
- RNA and protein synthesis mechanisms
- RNA regulation and disease
- RNA regulation and disease
- Connective tissue disorders research
- Connective tissue disorders research
- Bioinformatics and Genomic Networks
- Bioinformatics and Genomic Networks
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