Rivista di Psichiatria : Impact Factor & More
eISSN: 2038-2502pISSN: 0035-6484
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Key Metrics
CiteScore 
3.1
H-Index
24
Impact Factor
< 5
SJR
Q2Psychiatry and Mental Health
SNIP
0.7
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Rivista di Psichiatria Journal Specifications
Indexed in the following public directories
Web of Science 
Scopus 
SJR
| Overview | |
| Publisher | PENSIERO SCIENTIFICO EDITORE |
| Language | Italian |
| Frequency | Bi-monthly |
| General Details | |
| Language | Italian |
| Frequency | Bi-monthly |
| Publication Start Year | 1965 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Rivista di Psichiatria
Functional evidence for SCN8A splice-donor variant c.4419+1 A > G causing loss of function.
- 29 Jun 2026
- Human genome variation
A novel truncating FBN1 variant in a family with Marfan syndrome.
- 12 Jun 2026
- Human genome variation
Post-mortem diagnosis of CACT deficiency with a novel SLC25A20 variant.
- 12 Jun 2026
- Human genome variation
Integrated targeted whole-genome and RNA-sequencing analysis of an intronic GNE variant in GNE myopathy.
- 10 Jun 2026
- Human genome variation
Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.
- 4 Jun 2026
- Human genome variation
Carney complex with PRKAR1A variant and breast/fibrolamellar carcinomas.
- 28 May 2026
- Human genome variation
Functional evidence for SCN8A splice-donor variant c.4419+1 A > G causing loss of function.
- 29 Jun 2026
- Human genome variation
A novel truncating FBN1 variant in a family with Marfan syndrome.
- 12 Jun 2026
- Human genome variation
Post-mortem diagnosis of CACT deficiency with a novel SLC25A20 variant.
- 12 Jun 2026
- Human genome variation
Integrated targeted whole-genome and RNA-sequencing analysis of an intronic GNE variant in GNE myopathy.
- 10 Jun 2026
- Human genome variation
Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.
- 4 Jun 2026
- Human genome variation
Carney complex with PRKAR1A variant and breast/fibrolamellar carcinomas.
- 28 May 2026
- Human genome variation
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