npj Genomic Medicine : Impact Factor & More
eISSN: 2056-7944pISSN: 2056-7944
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Key Metrics
CiteScore 
7.5
Eigenfactor
0.001 - 0.005
Impact Factor
5 - 10
SJR
Q1Genetics
SNIP
1.61
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Topics Covered on npj Genomic Medicine
npj Genomic Medicine Journal Specifications
Indexed in the following public directories
Web of Science 
Scopus 
DOAJ 
SJR
| Overview | |
| Publisher | NATURE PORTFOLIO |
| Language | English |
| Frequency | Continuous publication |
| Article Processing Charges | EUR 3190 | USD 3790 | GBP 2790 |
| Publication Time | 17 |
| Editorial Review Process | Anonymous peer review |
| General Details | |
| Language | English |
| Society/Institute/Sponsor | Center of Excellence in Genomic Medicine Research, King Abdulaziz University |
| Frequency | Continuous publication |
| Publication Start Year | 2016 |
| Website URL | Visit website |
| Publication Details | |
| Editorial Review Detail | |
| Information for authors | |
| Author instructions | Visit website |
| Copyright Details | Visit website |
| Deposit Policy | Sherpa/Romeo |
| License type | CC BY |
| OA statement | Visit website |
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Recently Published Papers in npj Genomic Medicine
Artificial intelligence in genomic medicine: dispelling three myths.
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Genetic variants in Rps4x cause intellectual disability with dysmorphic features, microcephaly, and autism.
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Low-penetrance TP53 variants are mainly hypomorphic: an underestimated issue with high clinical significance.
- 18 Apr 2026
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Clinical validation of a high-performance somatic exome sequencing assay: from target-enrichment strategy to variant calling.
- 10 Apr 2026
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Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.
- 10 Apr 2026
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Artificial intelligence in genomic medicine: dispelling three myths.
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Genetic variants in Rps4x cause intellectual disability with dysmorphic features, microcephaly, and autism.
- 24 Apr 2026
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Immuno-molecular features associated with exceptional recurrence-free survivorship from Ovarian Cancer in the pre-PARP era.
- 23 Apr 2026
- NPJ genomic medicine
Low-penetrance TP53 variants are mainly hypomorphic: an underestimated issue with high clinical significance.
- 18 Apr 2026
- NPJ genomic medicine
Clinical validation of a high-performance somatic exome sequencing assay: from target-enrichment strategy to variant calling.
- 10 Apr 2026
- NPJ genomic medicine
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.
- 10 Apr 2026
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