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Are obsessive-compulsive symptom dimensions familial in nonclinical individuals?
- Published in:
- 2009
- By:
- Publication type:
- Journal Article
Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 4, p. 1686, doi. 10.1093/brain/awac315
- By:
- Publication type:
- Article
Alcohol misuse in bipolar disorder. A systematic review and meta-analysis of comorbidity rates.
- Published in:
- European Psychiatry, 2014, v. 29, n. 3, p. 117, doi. 10.1016/j.eurpsy.2013.07.004
- By:
- Publication type:
- Article
The psychiatric phenotypes of 1q21 distal deletion and duplication.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01226-9
- By:
- Publication type:
- Article
The psychiatric phenotypes of 1q21 distal deletion and duplication.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01226-9
- By:
- Publication type:
- Article
Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-00998-w
- By:
- Publication type:
- Article
The Cardiff Study of all Wales and North West of England Twins (CaStANET): a longitudinal research program of child and adolescent development.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach.
- Published in:
- Molecular Autism, 2023, v. 14, n. 1, p. 1, doi. 10.1186/s13229-023-00549-2
- By:
- Publication type:
- Article
The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 8, p. 730, doi. 10.1002/ajmg.b.32378
- By:
- Publication type:
- Article
Exploring the indirect effects of catechol-O-methyltransferase ( COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 5, p. 410, doi. 10.1002/ajmg.b.32245
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- Publication type:
- Article
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions.
- Published in:
- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-022-02296-z
- By:
- Publication type:
- Article
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Using rare genetic mutations to revisit structural brain asymmetry.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46784-w
- By:
- Publication type:
- Article
Genetic and environmental influences on the relationship between peer alcohol use and own alcohol use in adolescents.
- Published in:
- Addiction, 2007, v. 102, n. 6, p. 894, doi. 10.1111/j.1360-0443.2007.01824.x
- By:
- Publication type:
- Article
Exploring the relationship between genetic and environmental influences on initiation and progression of substance use.
- Published in:
- Addiction, 2007, v. 102, n. 3, p. 413, doi. 10.1111/j.1360-0443.2006.01694.x
- By:
- Publication type:
- Article
Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome.
- Published in:
- Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9271-3
- By:
- Publication type:
- Article
Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0736-7
- By:
- Publication type:
- Article
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0441-6
- By:
- Publication type:
- Article
Psychiatric disorders in children with 16p11.2 deletion and duplication.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-018-0339-8
- By:
- Publication type:
- Article
Psychopathology in Young People Experiencing Homelessness: A Systematic Review.
- Published in:
- American Journal of Public Health, 2013, v. 103, n. 6, p. e24, doi. 10.2105/AJPH.2013.301318
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- Publication type:
- Article
ABSTRACTS.
- Published in:
- 2005
- By:
- Publication type:
- Abstract
Effects of low birth weight, maternal smoking in pregnancy and social class on the phenotypic manifestation of Attention Deficit Hyperactivity Disorder and associated antisocial behaviour: investigation in a clinical sample.
- Published in:
- BMC Psychiatry, 2007, v. 7, p. 26, doi. 10.1186/1471-244X-7-26
- By:
- Publication type:
- Article
A population-based study of anxiety as a precursor for depression in childhood and adolescence.
- Published in:
- BMC Psychiatry, 2004, v. 4, p. 43, doi. 10.1186/1471-244X-4-43
- By:
- Publication type:
- Article
Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions.
- Published in:
- JCPP Advances, 2023, v. 3, n. 2, p. 1, doi. 10.1002/jcv2.12162
- By:
- Publication type:
- Article
Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.75482
- By:
- Publication type:
- Article
Childhood risk factors for offending before first psychiatric admission for people with schizophrenia: a case-control study of high security hospital admissions.
- Published in:
- 2010
- By:
- Publication type:
- journal article
The relationship between childhood depressive symptoms and problem alcohol use in early adolescence: findings from a large longitudinal population-based study.
- Published in:
- Addiction, 2012, v. 107, n. 3, p. 567, doi. 10.1111/j.1360-0443.2011.03662.x
- By:
- Publication type:
- Article
Genetic and non-genetic influences on the development of co-occurring alcohol problem use and internalizing symptomatology in adolescence: a review.
- Published in:
- Addiction, 2009, v. 104, n. 7, p. 1100, doi. 10.1111/j.1360-0443.2009.02571.x
- By:
- Publication type:
- Article
Movement Disorder Phenotypes in Children With 22q11.2 Deletion Syndrome.
- Published in:
- 2020
- By:
- Publication type:
- Letter
The Moderating Effects of Pubertal Timing on the Longitudinal Associations Between Parent-Child Relationship Quality and Adolescent Substance Use SHELTON AND VAN DEN BREE -.
- Published in:
- Journal of Research on Adolescence (Wiley-Blackwell), 2010, v. 20, n. 4, p. 1044, doi. 10.1111/j.1532-7795.2010.00643.x
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- Publication type:
- Article
Development of a short instrument for the measurement of self-aggression. Preliminary results in female migraine patients.
- Published in:
- 1989
- By:
- Publication type:
- journal article
No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.
- Published in:
- Molecular Psychiatry, 2004, v. 9, n. 2, p. 169, doi. 10.1038/sj.mp.4001387
- By:
- Publication type:
- Article
Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa<sup />.
- Published in:
- Molecular Psychiatry, 2003, v. 8, n. 4, p. 397, doi. 10.1038/sj.mp.4001318
- By:
- Publication type:
- Article
Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.
- Published in:
- Molecular Psychiatry, 2003, v. 8, n. 2, p. 176, doi. 10.1038/sj.mp.4001216
- By:
- Publication type:
- Article
Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD.
- Published in:
- Molecular Autism, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13229-020-00343-4
- By:
- Publication type:
- Article
The COVID‐19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregivers.
- Published in:
- Journal of Intellectual Disability Research, 2022, v. 66, n. 4, p. 313, doi. 10.1111/jir.12918
- By:
- Publication type:
- Article
Association of the CHRNA5-A3-B4 Gene Cluster With Heaviness of Smoking: A Meta-Analysis.
- Published in:
- Nicotine & Tobacco Research, 2011, v. 13, n. 12, p. 1167, doi. 10.1093/ntr/ntr118
- By:
- Publication type:
- Article