Clinical Genetics : Impact Factor & More
eISSN: 1399-0004pISSN: 0009-9163
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Aims and Scope of Clinical Genetics
Clinical Genetics is a monthly peer-reviewed medical journal covering medical genetics. It was established in 1970 and is published by Wiley-Blackwell. The editor-in-chief is Reiner A. Veitia (University of Paris). Less
Key Metrics
CiteScore 
7.3
Eigenfactor
0.01 - 0.05
H-Index
112
Impact Factor
< 5
SJR
Q1Genetics
SNIP
1.43
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Topics Covered on Clinical Genetics
Clinical Genetics Journal Specifications
| Overview | |
| Publisher | WILEY |
| Language | English |
| Frequency | Monthly |
| General Details | |
| Language | English |
| Frequency | Monthly |
| Publication Start Year | 1970 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Clinical Genetics
Homozygous Loss-of-Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental Abnormalities.
- 1 Jul 2026
- Clinical genetics
Whole Exome Sequencing for Romanian Patients With Neurodevelopmental Disorders Through an International Collaboration.
- 1 Jul 2026
- Clinical genetics
Clinical Analysis of SYNGAP1 Variant-Related Neurodevelopmental Disorders in Chinese Children.
- 1 Jul 2026
- Clinical genetics
Molecular Basis and Clinical Spectrum of WNT10A-Related Oligodontia.
- 1 Jul 2026
- Clinical genetics
From Pathogenicity to Mechanism: A Variant Interpretation Framework for Monogenic Epilepsy.
- 1 Jul 2026
- Clinical genetics
Optic Atrophy Associated With a Mitochondrial G8363A Mutation in a Family.
- 1 Jul 2026
- Clinical genetics
Homozygous Loss-of-Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental Abnormalities.
- 1 Jul 2026
- Clinical genetics
Whole Exome Sequencing for Romanian Patients With Neurodevelopmental Disorders Through an International Collaboration.
- 1 Jul 2026
- Clinical genetics
Clinical Analysis of SYNGAP1 Variant-Related Neurodevelopmental Disorders in Chinese Children.
- 1 Jul 2026
- Clinical genetics
Molecular Basis and Clinical Spectrum of WNT10A-Related Oligodontia.
- 1 Jul 2026
- Clinical genetics
From Pathogenicity to Mechanism: A Variant Interpretation Framework for Monogenic Epilepsy.
- 1 Jul 2026
- Clinical genetics
Optic Atrophy Associated With a Mitochondrial G8363A Mutation in a Family.
- 1 Jul 2026
- Clinical genetics
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