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期刊名:Psychiatric genetics

缩写:PSYCHIAT GENET

ISSN:0955-8829

e-ISSN:1473-5873

IF/分区:1.4/Q4

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Min Zhang,Yongli Wu,Yujie Qin Min Zhang
Background: Epidemiological evidence suggests a link between schizophrenia (SCZ) and increased breast cancer (BC) risk, but the genetic mechanisms remain unclear. Exploring their shared genetic susceptibility may help rev...
Aydeniz Aydin Gumus,Mustafa Dogan,Alper Gezdirici et al. Aydeniz Aydin Gumus et al.
Objectives: The catalytic subunit of NatA, the main component of the N-terminal acetyltransferase complex, which is involved in most of the acetylation of the human proteome, is encoded by the NAA10 gene. Mutations in the...
Sigrun Hope,Aihua Lin,Linn Rodevand et al. Sigrun Hope et al.
Objective: Deficits in social communication and social interaction are core features of autism spectrum disorder (ASD), and studies suggest that loneliness and social isolation are common. ASD has a strong genetic basis, ...
Tuba Tuğ Altunöz,Nazan Dolapoğlu,Özgür Baykan et al. Tuba Tuğ Altunöz et al.
Background: Glutamate, an excitatory neurotransmitter in the central nervous system, plays a role in neurodevelopment, learning, and memory. It is thought to interact with the GABAergic system in the development of panic ...
Qinghua Luo,Jiawen Wang,Mingwei An et al. Qinghua Luo et al.
Background: Mood swings and irritable bowel syndrome (IBS) are closely related. However, the reason for the clinical concurrence of this phenomenon is unknown, and maybe it is because the two share genetic underpinnings. ...
Qinghua Luo,Jiawen Wang,Mingwei An et al. Qinghua Luo et al.
Background: Mood swings and irritable bowel syndrome (IBS) are closely related. However, the reason for the clinical concurrence of this phenomenon is unknown, and maybe it is because the two share genetic underpinnings. ...
Yanzhao Chen,Yaming Xia,Lipeng Chen et al. Yanzhao Chen et al.
Objective: Developmental and epileptic encephalopathy 9 (DEE9) is an X-linked genetic disorder characterized by the onset of seizures during infancy. Mutations in protocadherin 19 (PCDH19) are the main cause of DEE9. Our ...
Kai Yao,Alexandra Burton,Samira Heinkel et al. Kai Yao et al.
Objective: Patients with severe mental illness (SMI) experience increased cardiovascular risks, leading to reduced life expectancy. Polygenic risk scores (PRS) prediction is promising for assessing cardiovascular risks. T...
Jun He,Jingjing Zhang,Shuanglin Xiang et al. Jun He et al.
Background: Newborn screening (NBS) is a public health service aimed at identifying infants with severe genetic disorders. Genetic testing is now commonly used for secondary or confirmatory testing after a positive result...
Uddip Talukdar,Abhijit Bharali,Swapna D Kakoty et al. Uddip Talukdar et al.
Background: Schizophrenia is a chronic neuropsychiatric disorder characterised by a range of positive and negative symptoms. The genetic aspect of schizophrenia is highly pleiotropic, as the complete set of neurodevelopme...