mania phenotype

Aliases

first hospitalization of mania, mania, manic episode

Related entities (16)

Mentioned in (31)

Papers in which this entity is mentioned.

• Atypical developmental trajectories of white matter microstructure in prenatal alcohol exposure: Preliminary evidence from neurite orientation dispersion and density imaging. (2023)
• Delayed cortical thinning in children and adolescents with prenatal alcohol exposure. (2023)
• Hippocampal subfield abnormalities and memory functioning in children with fetal alcohol Spectrum disorders. (2021)
• A Prospective Comparison of Bipolar I and II Subjects With and Without Comorbid Alcohol Dependence From the COGA Dataset. (2020)
• Para-limbic Structural Abnormalities Are Associated With Internalizing Symptoms in Children With Prenatal Alcohol Exposure. (2020)
• Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
• Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. (2019)
• Reliability and validity of an internalizing symptom scale based on the adolescent and adult Semi-Structured Assessment for the Genetics of Alcoholism (SSAGA). (2019)
• Executive Functioning Correlates With Communication Ability in Youth With Histories of Heavy Prenatal Alcohol Exposure. (2018)
• Two-year cortical trajectories are abnormal in children and adolescents with prenatal alcohol exposure. (2018)
• Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. (2018)
• Cortical gyrification is abnormal in children with prenatal alcohol exposure. (2017)
• Functional connectivity abnormalities and associated cognitive deficits in fetal alcohol Spectrum disorders (FASD). (2017)
• Hypomania after augmenting venlafaxine and olanzapine with sarcosine in a patient with schizophrenia: a case study. (2015)
• The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. (2014)
• In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (2014)
• CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
• The neural effects of psychotropic medications in children and adolescents. (2012)
• High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
• DSM-IV to DSM-5: the impact of proposed revisions on diagnosis of alcohol use disorders. (2011)
• Psychiatric 'diseases' versus behavioral disorders and degree of genetic influence. (2011)
• Recent research on impulsivity in individuals with drug use and mental health disorders: implications for alcoholism. (2010)
• Obesity, smoking, and frontal brain dysfunction. (2010)
• Gender-related influences of parental alcoholism on the prevalence of psychiatric illnesses: analysis of the National Epidemiologic Survey on Alcohol and Related Conditions. (2010)
• The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. (2010)
• Is there an inhibitory-response-control system in the rat? Evidence from anatomical and pharmacological studies of behavioral inhibition. (2010)
• Genome-wide association study of bipolar disorder in European American and African American individuals. (2009)
• An exploration of attitudes among black Americans towards psychiatric genetic research. (2009)
• The subgenual anterior cingulate cortex in mood disorders. (2008)
• Perinatal choline deficiency produces abnormal sensory inhibition in Sprague-Dawley rats. (2008)
• Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with 'pleasurable buzz' during early experimentation with smoking. (2008)

Merged raw entities (2)

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