Aims and Scope of European Journal of Human Genetics
The European Journal of Human Genetics is a monthly peer-reviewed scientific journal published by the Nature Publishing Group on behalf of the European Society of Human Genetics. It covers all aspects of human genetics. Less
Key Metrics
CiteScore 

7.6
Eigenfactor 

0.01 - 0.05
H-Index 

136
Impact Factor 

5 - 10
SJR 

Q1Genetics

SNIP 

1.64
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Topics Covered on European Journal of Human Genetics
European Journal of Human Genetics Journal Specifications
| Overview | |
| Publisher | SPRINGERNATURE |
| Language | English |
| Frequency | Monthly |
| General Details | |
| Language | English |
| Frequency | Monthly |
| Publication Start Year | 1993 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in European Journal of Human Genetics
Parent and professional experiences of a clinical trial of prenatal and postnatal stem cell therapy for severe osteogenesis imperfecta.
- 30 Jun 2026
- European journal of human genetics : EJHG
Scoping review and recommendations for development and delivery of education resources for reproductive genetic carrier screening.
- 30 Jun 2026
- European journal of human genetics : EJHG
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders.
- 27 Jun 2026
- European journal of human genetics : EJHG
Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.
- 24 Jun 2026
- European journal of human genetics : EJHG
Identifying genetic causes and establishing a diagnostic approach for WES-negative pediatric population with neurodevelopmental disorder.
- 23 Jun 2026
- European journal of human genetics : EJHG
BRCA1 c.68_69del as a founder variant in the Spanish Roma: prevalence and screening implications.
- 23 Jun 2026
- European journal of human genetics : EJHG
Parent and professional experiences of a clinical trial of prenatal and postnatal stem cell therapy for severe osteogenesis imperfecta.
- 30 Jun 2026
- European journal of human genetics : EJHG
Scoping review and recommendations for development and delivery of education resources for reproductive genetic carrier screening.
- 30 Jun 2026
- European journal of human genetics : EJHG
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders.
- 27 Jun 2026
- European journal of human genetics : EJHG
Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.
- 24 Jun 2026
- European journal of human genetics : EJHG
Identifying genetic causes and establishing a diagnostic approach for WES-negative pediatric population with neurodevelopmental disorder.
- 23 Jun 2026
- European journal of human genetics : EJHG
BRCA1 c.68_69del as a founder variant in the Spanish Roma: prevalence and screening implications.
- 23 Jun 2026
- European journal of human genetics : EJHG
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