Journal Report

PSYCHIATRIC GENETICS

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Journal Information
Journal Title
PSYCHIATRIC GENETICS
Publisher
LIPPINCOTT WILLIAMS & WILKINS
ISSN
0955-8829
E-ISSN
1473-5873
Database
Clarivate
Domain
Health Sciences, Life Sciences, Social Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
In memoriam for Jules Angst
John I. Nurnberger
2026-10-28 Vol. 36 Issue 4 Pages 208-210
DOI: 10.1097/ypg.0000000000000434
Can neurodevelopmental disorders be part of brain-lung-thyroid syndrome? A case report
Selman Yildirim, Cagil Ozyilmaz, Esra Hosoglu et al.
2026-10-28 Vol. 36 Issue 4 Pages 199-200
DOI: 10.1097/ypg.0000000000000428
Female-specific associations of glyoxalase 1 polymorphisms with schizophrenia in a Han Chinese case–control study
Amy Jing-Wen Yin, Wei-Wei Wang, Wenge Zhang et al.
2026-10-28 Vol. 36 Issue 4 Pages 165-171
DOI: 10.1097/ypg.0000000000000425
UK-based mental health professionals’ perceptions of genetic and environmental risk for psychiatric conditions
Helena L. Davies, Jessica Mundy, Karla Mohoric et al.
2026-10-28 Vol. 36 Issue 4 Pages 183-192
DOI: 10.1097/ypg.0000000000000426
Causal associations between chronic hepatitis B and major depressive disorder in East Asian populations: a bidirectional two-sample Mendelian randomization study
Ya-juan Le, Hai-Ying Jin, Li-Li Cai et al.
2026-10-28 Vol. 36 Issue 4 Pages 172-182
DOI: 10.1097/ypg.0000000000000424
The role of PRKRA mutation in antipsychotic-induced extrapyramidal symptoms: a case report and implications for precision psychiatry
Mude Jeevan Naik, Simran Arora, Likhita Thippeswamy et al.
2026-10-5 Vol. 36 Issue 4 Pages 204-207
DOI: 10.1097/ypg.0000000000000430
CLCN6 mutation in an Indian patient with rapidly progressive dementia
Manik Inder Singh Sethi, Mude Jeevan Naik, Guru S. Gowda et al.
2026-10-5
DOI: 10.1097/ypg.0000000000000433
Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability
Eesha Sajjad, Shagufta Naz, Haiba Kaul et al.
2026-9-15 Vol. 36 Issue 4 Pages 193-198
DOI: 10.1097/ypg.0000000000000427
Prenatal diagnosis and genetic counseling of a de novo 10q11.22q11.23 duplication associated with a normal development at 12 months of age
Xingxing Wang, Lijun Liu, Kai Jin
2026-9-1
DOI: 10.1097/ypg.0000000000000432
A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months
Qiu Guo, Xinfang He, Xu Liu et al.
2026-9-1
DOI: 10.1097/ypg.0000000000000431
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Printed: November 7, 2026 21:53