Human Genetics : Impact Factor & More
eISSN: 1432-1203pISSN: 0340-6717
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Aims and Scope of Human Genetics
Human Genetics is a peer-reviewed medical journal covering all aspects of human genetics, including legal and social issues. It was established in 1964 by Arno Motulsky and Friedrich Vogel as the German-language Humangenetik, obtaining its current title in 1976. It is published by Springer Science+Business Media. Its editors-in-chief are David N. Cooper (Cardiff University) and Thomas J. Hudson (Ontario Institute for Cancer Research). According to the Journal Citation Reports, the journal has a 2018 impact factor of 5.20. Less
Key Metrics
CiteScore 
7.8
Eigenfactor
0.005 - 0.01
H-Index
148
Impact Factor
5 - 10
SJR
Q1Genetics
SNIP
1.46
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Topics Covered on Human Genetics
Human Genetics Journal Specifications
Indexed in the following public directories
Web of Science 
Scopus 
SJR
| Overview | |
| Publisher | SPRINGER |
| Language | English |
| Frequency | Monthly |
| General Details | |
| Language | English |
| Frequency | Monthly |
| Publication Start Year | 1976 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Human Genetics
Epigenetic silencing of DLEC1 correlates with tumor immune microenvironment and predicts immunotherapy prognosis in multiple cancers.
- 20 Apr 2026
- Human genetics
Improved functional JAG1 and NOTCH2 variant testing in patients with clinical or suspected Alagille syndrome using new low-Notch activity cells.
- 18 Apr 2026
- Human genetics
Correction: Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies.
- 13 Apr 2026
- Human genetics
Integrating machine learning and spatial transcriptomics uncovers shared immunomodulatory deubiquitinases in MAFLD and HCC.
- 10 Apr 2026
- Human genetics
The genetic associations of DNAJC family members with Parkinson's disease: comprehensive evidence from burden analysis and Mendelian randomization.
- 9 Apr 2026
- Human genetics
DNA methylation signatures from peripheral blood revealed epigenetic alterations in Fanconi anemia.
- 27 Mar 2026
- Human genetics
Epigenetic silencing of DLEC1 correlates with tumor immune microenvironment and predicts immunotherapy prognosis in multiple cancers.
- 20 Apr 2026
- Human genetics
Improved functional JAG1 and NOTCH2 variant testing in patients with clinical or suspected Alagille syndrome using new low-Notch activity cells.
- 18 Apr 2026
- Human genetics
Correction: Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies.
- 13 Apr 2026
- Human genetics
Integrating machine learning and spatial transcriptomics uncovers shared immunomodulatory deubiquitinases in MAFLD and HCC.
- 10 Apr 2026
- Human genetics
The genetic associations of DNAJC family members with Parkinson's disease: comprehensive evidence from burden analysis and Mendelian randomization.
- 9 Apr 2026
- Human genetics
DNA methylation signatures from peripheral blood revealed epigenetic alterations in Fanconi anemia.
- 27 Mar 2026
- Human genetics
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