Human Genetics
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Aims and Scope
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
View Chart Journal Specifications
- PublisherSPRINGER
- LanguageEnglish
- FrequencyMonthly
- LanguageEnglish
- FrequencyMonthly
- Publication Start Year1976
- Publisher URL
- Website URL
| Months | % Papers published |
|---|---|
| 0-3 | 36% |
| 4-6 | 47% |
| 7-9 | 13% |
| >9 | 4% |
Topics Covered
Year-wise Publication
- 5Y
- 10Y
FAQs
Since when has Human Genetics been publishing? 
The Human Genetics has been publishing since 1976 till date.
How frequently is the Human Genetics published?
Human Genetics is published Monthly.
What is the H-index. SNIP score, Citescore and SJR of Human Genetics?
Human Genetics has a H-index score of 148, Citescore of 7.8, SNIP score of 1.46, & SJR of Q1
Who is the publisher of Human Genetics?
The publisher of Human Genetics is SPRINGER.
Where can I find a journal's aims and scope of Human Genetics?
For the Human Genetics's Aims and Scope, please refer to the section above on the page.
How can I view the journal metrics of Human Genetics on editage?
For the Human Genetics metrics, please refer to the section above on the page.
What is the eISSN and pISSN number of Human Genetics?
The eISSN number is 1432-1203 and pISSN number is 0340-6717 for Human Genetics.
What is the focus of this journal?
The journal covers a wide range of topics inlcuding Genome, Hypopituitarism, Dark matter, Infertility, Precision medicine, Azoospermia, Genetic variants, Coloboma, Intellectual disability, Exome sequencing, Retinal atrophy, Hearing loss, Genetic predisposition, Aneuploidy, Mitochondrial DNA, Causal association, Osteoporosis, Short stature, Whole genome sequencing, Genotype imputation.
Why is it important to find the right journal for my research?
Choosing the right journal ensures that your research reaches the most relevant audience, thereby maximizing its scholarly impact and contribution to the field.
Can the choice of journal affect my academic career?
Absolutely. Publishing in reputable journals can enhance your academic profile, making you more competitive for grants, tenure, and other professional opportunities.
Is it advisable to target high-impact journals only?
While high-impact journals offer greater visibility, they are often highly competitive. It's essential to balance the journal's impact factor with the likelihood of your work being accepted.