Results 11 to 20 of about 2,618,764 (254)

Dopamine Transporter Knockout Rats Show Impaired Wellbeing in a Multimodal Severity Assessment Approach

open access: yesFrontiers in Behavioral Neuroscience, 2022
In preclinical psychiatry research, animals are central to modeling and understanding biological mechanisms of behavior and psychiatric disorders. We here present the first multimodal severity assessment of a genetically modified rat strain used in ...
Anne Stephanie Mallien   +15 more
doaj   +1 more source

Genome wide association study identifies four loci for early onset schizophrenia

open access: yesTranslational Psychiatry, 2021
Early onset schizophrenia (EOS, defined as first onset of schizophrenia before age 18) is a rare form of schizophrenia (SCZ). Though genome-wide association studies (GWASs) have identified multiple risk variants for SCZ, most of the cases included in ...
Suqin Guo   +8 more
doaj   +1 more source

Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia

open access: yesBMC Medicine, 2021
Background Over 200 schizophrenia risk loci have been identified by genome-wide association studies (GWASs). However, the majority of risk loci were identified in populations of European ancestry (EUR), potentially missing important biological insights ...
Jiewei Liu   +11 more
doaj   +1 more source

Bidirectional genetic overlap between bipolar disorder and intelligence

open access: yesBMC Medicine, 2022
Background Bipolar disorder (BD) is a highly heritable psychiatric illness exhibiting substantial correlation with intelligence. Methods To investigate the shared genetic signatures between BD and intelligence, we utilized the summary statistics from ...
Meng-Yuan Shang   +8 more
doaj   +1 more source

Transcriptome-wide association study identifies new susceptibility genes and pathways for depression

open access: yesTranslational Psychiatry, 2021
Depression is the most prevalent mental disorder with substantial morbidity and mortality. Although genome-wide association studies (GWASs) have identified multiple risk variants for depression, due to the complicated gene regulatory mechanisms and ...
Xiaoyan Li   +7 more
doaj   +1 more source

The schizophrenia-associated missense variant rs13107325 regulates dendritic spine density

open access: yesTranslational Psychiatry, 2022
The missense variant rs13107325 (C/T, p.Ala391Thr) in SLC39A8 consistently showed robust association with schizophrenia in recent genome-wide association studies (GWASs), suggesting the potential pathogenicity of this non-synonymous risk variant ...
Shiwu Li   +15 more
doaj   +1 more source

Robot Models of Mental Disorders [PDF]

open access: yes, 2017
Alongside technological tools to support wellbeing and treatment of mental disorders, models of these disorders can also be invaluable tools to understand, support and improve these conditions.
Cañamero, Lola, Lewis, Matthew
core   +2 more sources

Understanding inter-organizational decision coordination [PDF]

open access: yes, 2010
This article develops a theoretical framework to investigate the interaction and coordination of decision-making processes in a supply chain with multiple and inter-dependent suppliers and customers.
Acur, Nuran   +2 more
core   +1 more source

Consensus Emerging from the Bottom-up: the Role of Cognitive Variables in Opinion Dynamics [PDF]

open access: yes, 2015
The study of opinions $-$ e.g., their formation and change, and their effects on our society $-$ by means of theoretical and numerical models has been one of the main goals of sociophysics until now, but it is one of the defining topics addressed by ...
Conte, Rosaria   +2 more
core   +3 more sources

Perinatal Hypoxia and Ischemia in Animal Models of Schizophrenia

open access: yesFrontiers in Psychiatry, 2018
Intrauterine or perinatal complications constitute a major risk for psychiatric diseases. Infants who suffered from hypoxia–ischemia (HI) are at twofold risk to develop schizophrenia in later life.
Dimitri Hefter   +5 more
doaj   +1 more source

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