About the journal
Human Heredity is an open-access journal published by Karger Publishers in Switzerland, publishing in english. It is listed in DOAJ and MEDLINE and PUBMED according to the sources read. Declared publication charge: 1,380 CHF. Declared review time at DOAJ: 26 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Karger Publishers
- ISSN
- 0001-5652 · 1423-0062
- Country
- Switzerland
- Languages
- english
- Access
- Open access
- Declared publication charge
- 1,380 CHF
- Articles in DOAJ
- 11
- Declared review time
- 26 weeks
- Declared peer-review model
- peer_review
- Official website
- https://karger.com/hhe
Index listings
- DOAJ · 2025-11-08
- MEDLINE · 1969-01-01
- PUBMED · 2015-03-11
- Indexing
- DOAJ · MEDLINE · PUBMED
- APC
- 1,380 CHF
- Declared review time (DOAJ)
- 26 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
11
Most recent article
3 months ago
Average review time (journal-declared via DOAJ)
26weeks
Works in OpenAlex
4316
Last recorded publication year
2025
h-index
94
i10-index
1729
From OpenAlex open data (CC0).
Editorial & policy13
- Last DOAJ review date
- 2025-11-10
- Added to DOAJ
- 2025-11-08
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- PMCPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- Portico
- Editorial board
- Official page ↗
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 63%
- ORCID iDs in current deposits
- 29%
- 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)
- 0200525
Classification2
Subjects (DOAJ)
LCC codes
Subject areas
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic Mapping and Diversity in Plants and Animals
- Diverse Scientific and Economic Studies
- Diverse Scientific and Economic Studies
- Blood groups and transfusion
- Blood groups and transfusion
Show all subjects (50)
- Human auditory perception and evaluation
- Human auditory perception and evaluation
- Hemoglobinopathies and Related Disorders
- Hemoglobinopathies and Related Disorders
- Erythrocyte Function and Pathophysiology
- Erythrocyte Function and Pathophysiology
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Genetic and phenotypic traits in livestock
- Genetic and phenotypic traits in livestock
- Neonatal Health and Biochemistry
- Neonatal Health and Biochemistry
- Forensic and Genetic Research
- Forensic and Genetic Research
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Legal Cases and Commentary
- Legal Cases and Commentary
- Gene expression and cancer classification
- Gene expression and cancer classification
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Bioinformatics and Genomic Networks
- Bioinformatics and Genomic Networks
- Iron Metabolism and Disorders
- Iron Metabolism and Disorders
- Diabetes and associated disorders
- Diabetes and associated disorders
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Hemoglobin structure and function
- Hemoglobin structure and function
- Pancreatic function and diabetes
- Pancreatic function and diabetes
- Dermatoglyphics and Human Traits
- Dermatoglyphics and Human Traits
- Educational Robotics and Engineering
- Educational Robotics and Engineering
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Nutrition, Genetics, and Disease
- Nutrition, Genetics, and Disease
Keywords (DOAJ)
- genetics
- genetic mechanisms of disease
- statistical genetics
- next-generation sequencing
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