Results 111 to 120 of about 342,507 (303)

Schizophrenia Genetics Modulates Clinical Depressive Features

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Schizophrenia (SCZ) genetic liability, quantified by polygenic scores (PGS), may influence clinical phenotypes in major depressive disorder (MDD). We investigated the effect of the SCZ‐PGS derived from the latest SCZ genome‐wide association study (GWAS) on MDD symptom severity, comorbidities, and treatment outcomes.
Alessandro Serretti   +13 more
wiley   +1 more source

changes in PTSD prevalence in military personnel [PDF]

open access: yes, 2018
Background: Recently, changes have been introduced to the diagnostic criteria for posttraumatic stress disorder (PTSD) according to the Diagnostic and Statistical Manual of Mental Disorders (DSM) and the International Classification of Diseases (ICD).
Ehring, Thomas   +9 more
core   +1 more source

Os transtornos alimentares nos sistemas classificatórios atuais: DSM-5 e CID-11

open access: yesDebates em Psiquiatria, 2019
Os transtornos alimentares (TA) são caracterizados por um distúrbio persistente do comportamento alimentar ou relacionado à alimentação, que resulta em consumo ou absorção alterados de alimentos e prejudica significativamente a saúde física ou o ...
João Hiluy   +3 more
doaj   +1 more source

Neurodevelopmental and Psychiatric Studies in Children and Adolescents With Neurofibromatosis Type I: A Comprehensive Scoping Review

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT A comprehensive synthesis of the broad range of neurodevelopmental and psychiatric manifestations in NF1 is needed to identify knowledge gaps and future directions for NF1 research. In the following scoping review, we identify and summarize the scope of research that examines neurodevelopmental and psychiatric manifestations, both as ...
Meera Chopra   +5 more
wiley   +1 more source

Comparison of autism spectrum disorder surveillance status based on two different diagnostic schemes: Findings from the Metropolitan Atlanta Developmental Disabilities Surveillance Program, 2012.

open access: yesPLoS ONE, 2018
For the first time, the Autism and Developmental Disabilities Monitoring Network (ADDM) at the Centers for Disease Control and Prevention (CDC) reported prevalence estimates based on two different diagnostic schemes in the 2014 surveillance period ...
Lisa Wiggins   +4 more
doaj   +1 more source

Diagnostic bingo [PDF]

open access: yes, 2016
The proposed instructional activity provides counseling instructors and supervisors an opportunity to apply diagnostic criteria utilizing the DSM-5.
Bridgmon, Krista D.
core  

DSM-5 unspecified feeding and eating disorders in adolescents: What do they look like and are they clinically significant? [PDF]

open access: yes, 2015
This is the peer reviewed version of the following article: Wade, T. D. and O'Shea, A. (2015), DSM-5 unspecified feeding and eating disorders in adolescents: What do they look like and are they clinically significant?.
O'shea, Anne, Wade, Tracey Diane
core   +1 more source

Are There Causal Associations Between Obsessive‐Compulsive Disorder and Cardiometabolic Phenotypes? A Genetic Correlation and Bi‐Directional Mendelian Randomization Study

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT In epidemiological studies, obsessive‐compulsive disorder (OCD) is robustly associated with increased risk of cardiometabolic disorders, including cardiovascular diseases, type 2 diabetes, and obesity. However, the mechanisms behind these associations are unclear. We conducted genetic correlation analyses to explore shared genetic etiology and
Robyn E. Wootton   +217 more
wiley   +1 more source

Longitudinal Behavior Phenotype Hallmarks in RNU4‐2 Syndrome: Implications for Clinical Management

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Pathogenic variants in the non‐coding spliceosomal gene RNU4‐2 underlie ReNU syndrome, one of the most prevalent monogenic causes of neurodevelopmental disorders, accounting for ~0.4% of cases. Despite increasing recognition, little is known about the longitudinal behavioral and neuropsychiatric phenotype of affected individuals. We report two
Paola Francesca Ajmone   +8 more
wiley   +1 more source

Social (pragmatic) communication disorders and autism spectrum disorder [PDF]

open access: yes, 2015
Changes have been made to the diagnostic criteria for autism spectrum disorder (ASD) in the recent revision of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5), and similar changes are likely in the WHO International Classification of ...
Baird, G, Norbury, CF
core  

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