Academic Journal
Q3Psychiatric Genetics
About Psychiatric Genetics
Psychiatric Genetics is a scholarly journal published by Lippincott Williams and Wilkins. SCImago 2025 lists it in Q3, with an SJR of 0.401 and H-index of 67.
Coverage: 1990-2026. Research categories: Genetics (clinical) (Q3); Psychiatry and Mental Health (Q3); Biological Psychiatry (Q4); Genetics (Q4).
Source-backed journal facts
Topics in published research
Genetic Associations and Epidemiology; Neurotransmitter Receptor Influence on Behavior; Genetics and Neurodevelopmental Disorders; Bipolar Disorder and Treatment; Schizophrenia research and treatment; Autism Spectrum Disorder Research.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
Can neurodevelopmental disorders be part of brain-lung-thyroid syndrome? A case report
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2026-10-05 · DOI: 10.1097/ypg.0000000000000428The role of PRKRA mutation in antipsychotic-induced extrapyramidal symptoms: a case report and implications for precision psychiatry
Mude Jeevan Naik, Simran Arora, Likhita Thippeswamy, Deepak S. Ghadigaonkar et al.
2026-10-05 · DOI: 10.1097/ypg.0000000000000430CLCN6 mutation in an Indian patient with rapidly progressive dementia
Manik Inder Singh Sethi, Mude Jeevan Naik, Guru S. Gowda, Satish Suhas et al.
2026-10-05 · DOI: 10.1097/ypg.0000000000000433Female-specific associations of glyoxalase 1 polymorphisms with schizophrenia in a Han Chinese case–control study
Amy Jing-Wen Yin, Wei-Wei Wang, Wenge Zhang, Xudong Luo et al.
2026-09-24 · DOI: 10.1097/ypg.0000000000000425Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability
Eesha Sajjad, Shagufta Naz, Haiba Kaul, Saima Sharif et al.
2026-09-15 · DOI: 10.1097/ypg.0000000000000427Prenatal 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
2026-09-01 · DOI: 10.1097/ypg.0000000000000432A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months
Qiu Guo, Xinfang He, Xu Liu, Hongjun Li et al.
2026-09-01 · DOI: 10.1097/ypg.0000000000000431Contrasting outcomes of 16p11.2 microdeletion and microduplication in prenatal diagnosis: phenotypic variability and genetic counseling strategies
Qiu Guo, Li Zhang, Yi Zuo, Jiale Mei et al.
2026-09 · DOI: 10.1097/ypg.0000000000000421Dissecting causal and putative mechanistic pathways from lifestyle factors to neurological diseases via the glymphatic system: a Mendelian randomization study
Weiyu Hou, Weiming Hou
2026-09 · DOI: 10.1097/ypg.0000000000000420A rare missense variant in Bruton’s tyrosine kinase is associated with bipolar disorder accompanied by psychosis
Ambreen Kanwal, Husnain Arshad Cheema, Nauman Jabbar, Amina Iftikhar et al.
2026-09 · DOI: 10.1097/ypg.0000000000000422Identification of rare missense variants of ionotropic glutamate receptor N-methyl-D-aspartate 2 genes in patients with schizophrenia
Chia-Liang Wu, Tsung-Ming Hu, Shih-Hsin Hsu, Hsin-Yao Tsai et al.
2026-09 · DOI: 10.1097/ypg.0000000000000423Expression and function of miR-218-5p in the pathogenesis of postpartum depression
Liyan Yu, Qian Liu
2026-09 · DOI: 10.1097/ypg.0000000000000417Familial co-occurrence of autism spectrum disorder and 47 XYY syndrome: revisiting the role of Y chromosome dosage in neurodevelopment
Mehri Durak, Halenur Teke
2026-06 · DOI: 10.1097/ypg.0000000000000418Prenatal diagnosis and genetic counseling for three cases of fetuses with low-level mosaic Turner syndrome
Hongbo Dai, Quanlun Li, Yan Quan
2026-06 · DOI: 10.1097/ypg.0000000000000414Case report of a boy with autism spectrum disorder and lysinuric protein intolerance
Vildan Ak, Husna Kaan, Ali Karayagmurlu
2026-09 · DOI: 10.1097/ypg.0000000000000419Are polygenic scores for psychiatric and substance use outcomes “ready” for clinical application? Current state and next steps
Danielle M. Dick, Genevieve F. Dash, I-Tzu Hung, Arianna Horgan et al.
2026-04-07 · DOI: 10.1097/ypg.0000000000000415Genetic correlation between inflammatory bowel disease and educational attainment: unveiling shared genetic mechanisms
Zhonghua Hong, Hezhai Yin
2026-06 · DOI: 10.1097/ypg.0000000000000416Prenatal diagnosis and genetic counselling of a rare de-novo 12p13.33p13.32 deletion and 15q26.2q26.3 duplication in a Chinese family
Zhenzhen Zhang, Wei Wang, Jin Xiong, Qi Xia et al.
2026-06 · DOI: 10.1097/ypg.0000000000000412The clinical significance of miR-484 in depression of older people with Alzheimer’s disease and its potential role on depressive behavior
Shuai Teng, Ying Li, Xichun Wang, Pingjing Jiang et al.
2026-06 · DOI: 10.1097/ypg.0000000000000411Elucidation of crucial metabolic pathways in the etiology of autism spectrum disorder through whole exome sequencing and chromosomal microarray
Shaik Mohammad Naushad, Shaik Esdhan Basha, Yadam Reddy Kanaka Durga Devi, Palanichamy Palanikumar et al.
2026-06 · DOI: 10.1097/ypg.0000000000000413Reviews
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October 4, 2026 at 9:23 pm
October 2, 2026