About the journal
Human Genetics is a journal published by Springer Science+Business Media in Germany. It is listed in MEDLINE and PUBMED according to the sources read. Declared publication charge: 4,690 EUR. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Springer Science+Business Media
- ISSN
- 0340-6717 · 1432-1203
- Country
- Germany
- Access
- Not open access / not declared
- Declared publication charge
- 4,690 EUR
- Declared peer-review model
- peer_review
- Official website
- http://www.springer.com/biomed/human+genetics/journal/439
Index listings
- MEDLINE · 1976-01-01
- PUBMED · 1976-01-28
- Indexing
- MEDLINE · PUBMED
- APC
- 4,690 EUR
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 189 days received→accepted — computed from PubMed (n=97)
- 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.
Works in OpenAlex
12887
Last recorded publication year
2026
h-index
208
i10-index
8880
From OpenAlex open data (CC0).
Editorial & policy6
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 98%
- ORCID iDs in current deposits
- 37%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity3
- Alternate titles
- Human genetics (Berlin. Print
- Source type
- journal
- NLM unique ID (PubMed)
- 7613873
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
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Show all subjects (50)
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Genomics and Chromatin Dynamics
- Genomics and Chromatin Dynamics
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- DNA Repair Mechanisms
- DNA Repair Mechanisms
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- RNA modifications and cancer
- RNA modifications and cancer
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Sexual Differentiation and Disorders
- Sexual Differentiation and Disorders
- RNA and protein synthesis mechanisms
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- RNA Research and Splicing
- RNA Research and Splicing
- DNA and Nucleic Acid Chemistry
- DNA and Nucleic Acid Chemistry
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Erythrocyte Function and Pathophysiology
- Erythrocyte Function and Pathophysiology
- Hemoglobinopathies and Related Disorders
- Hemoglobinopathies and Related Disorders
- Biochemical and Molecular Research
- Biochemical and Molecular Research
- Blood groups and transfusion
- Blood groups and transfusion
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Carcinogens and Genotoxicity Assessment
- Carcinogens and Genotoxicity Assessment
- Cystic Fibrosis Research Advances
- Cystic Fibrosis Research Advances
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