Pages that link to "Q47438571"
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The following pages link to Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome (Q47438571):
Displaying 50 items.
- Behavioural phenotypes and special educational needs: is aetiology important in the classroom? (Q22242621) (← links)
- Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome (Q26824150) (← links)
- Cognitive remediation for adolescents with 22q11 deletion syndrome (22q11DS): a preliminary study examining effectiveness, feasibility, and fidelity of a hybrid strategy, remote and computer-based intervention (Q27303880) (← links)
- Reduced fronto-temporal and limbic connectivity in the 22q11.2 deletion syndrome: vulnerability markers for developing schizophrenia? (Q27335014) (← links)
- Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome (Q28081645) (← links)
- Practical guidelines for managing patients with 22q11.2 deletion syndrome (Q28237543) (← links)
- Animal models of neuropsychiatric disorders (Q29619899) (← links)
- Assessing the Cognitive Translational Potential of a Mouse Model of the 22q11.2 Microdeletion Syndrome. (Q30374178) (← links)
- Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders (Q30439224) (← links)
- Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model (Q30459881) (← links)
- 22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia (Q30478713) (← links)
- Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study (Q30499844) (← links)
- The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome (Q33629249) (← links)
- Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times (Q33656756) (← links)
- Clinical and cognitive risk factors for psychotic symptoms in 22q11.2 deletion syndrome: a transversal and longitudinal approach (Q33701137) (← links)
- No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients. (Q33707657) (← links)
- Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome (Q33710925) (← links)
- A Synaptic Function Approach to Investigating Complex Psychiatric Diseases (Q33756893) (← links)
- Schizophrenia-Related Microdeletion Impairs Emotional Memory through MicroRNA-Dependent Disruption of Thalamic Inputs to the Amygdala. (Q33759010) (← links)
- Mouse Models of 22q11.2-Associated Autism Spectrum Disorder (Q33988040) (← links)
- Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome (Q33989539) (← links)
- The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI study (Q34005465) (← links)
- Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study (Q34054916) (← links)
- Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome (Q34131454) (← links)
- Subthreshold psychotic symptoms in 22q11.2 deletion syndrome (Q34156406) (← links)
- Nonverbal learning disabilities: A critical review (Q34175524) (← links)
- 22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis (Q34393037) (← links)
- Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome (Q34398230) (← links)
- Altered white matter microstructure is associated with social cognition and psychotic symptoms in 22q11.2 microdeletion syndrome (Q34488387) (← links)
- Is child intelligence associated with parent and sibling intelligence in individuals with developmental disorders? An investigation in youth with 22q11.2 deletion (velo-cardio-facial) syndrome (Q34620870) (← links)
- Intervention in the context of development: pathways toward new treatments (Q34675928) (← links)
- Educational paper: syndromic forms of primary immunodeficiency (Q34746176) (← links)
- Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes (Q34823932) (← links)
- Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome (Q34847296) (← links)
- A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders. (Q35009738) (← links)
- Role of Imaging and Cytogenetics in Evaluation of DiGeorge Syndrome - A Rare Entity in Clinical Practice (Q35065803) (← links)
- Balancing histone methylation activities in psychiatric disorders. (Q35100274) (← links)
- Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome (Q35115389) (← links)
- Neural substrates of inhibitory control deficits in 22q11.2 deletion syndrome. (Q35197415) (← links)
- New findings in the genetics of major psychoses (Q35237172) (← links)
- Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome (Q35252391) (← links)
- Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome (Q35499123) (← links)
- An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome (Q35599290) (← links)
- Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities (Q35670551) (← links)
- Psychiatric disorders in 22q11.2 deletion syndrome are prevalent but undertreated. (Q35704408) (← links)
- Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder (Q35705783) (← links)
- Structural and functional connectivity in the default mode network in 22q11.2 deletion syndrome (Q35908141) (← links)
- Elucidating X chromosome influences on Attention Deficit Hyperactivity Disorder and executive function (Q35927764) (← links)
- Neural mechanisms of response inhibition and impulsivity in 22q11.2 deletion carriers and idiopathic attention deficit hyperactivity disorder (Q36106335) (← links)
- Cortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: a longitudinal study (Q36148740) (← links)