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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

eLife, 2022-08, Vol.11

2022

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Genetic and non-genetic influences on the development of co-occurring alcohol problem use and internalizing symptomatology in adolescence: a review

Addiction (Abingdon, England), 2009-07, Vol.104 (7), p.1100-1121

2009

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Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs

Psychological medicine, 2022-02, Vol.52 (3), p.574-586

2022

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Psychopathology and cognition in children with 22q11.2 deletion syndrome

British journal of psychiatry, 2014-01, Vol.204 (1), p.46-54

2014

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Psychiatric disorders in children with 16p11.2 deletion and duplication

Translational psychiatry, 2019-01, Vol.9 (1), p.8, Article 8

2019

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Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome

British journal of psychiatry, 2018-01, Vol.212 (1), p.27-33

2018

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Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome

Journal of neurodevelopmental disorders, 2019-06, Vol.11 (1), p.8-8, Article 8

2019

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Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions

Translational psychiatry, 2023-01, Vol.13 (1), p.7-7, Article 7

2023

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Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach

Molecular autism, 2023-05, Vol.14 (1), p.19-19, Article 19

2023

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The relationship between childhood depressive symptoms and problem alcohol use in early adolescence: findings from a large longitudinal population-based study

Addiction (Abingdon, England), 2012-03, Vol.107 (3), p.567-577

2012

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Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD

Molecular autism, 2020-06, Vol.11 (1), p.42-42, Article 42

2020

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The psychiatric phenotypes of 1q21 distal deletion and duplication

Translational psychiatry, 2021-02, Vol.11 (1), p.105-10, Article 105

2021

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A systematic review of the relationships between family functioning, pubertal timing and adolescent substance use

Addiction (Abingdon, England), 2013-03, Vol.108 (3), p.487-496

2013

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Psychopathology in adults with copy number variants

Psychological medicine, 2023-05, Vol.53 (7), p.3142-3149

2023

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Associations between maternal older age, family environment and parent and child wellbeing in families using assisted reproductive techniques to conceive

Social science & medicine (1982), 2009-06, Vol.68 (11), p.1948-1955

2009

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Coordination difficulties, IQ and psychopathology in children with high-risk copy number variants

Psychological medicine, 2021-01, Vol.51 (2), p.290-299

2021

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Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort

British journal of psychiatry, 2019-11, Vol.215 (5), p.647-653

2019

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Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication

Translational psychiatry, 2021-06, Vol.11 (1), p.372-372, Article 372

2021

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The Moderating Role of Close Friends in the Relationship Between Conduct Problems and Adolescent Substance Use

Journal of adolescent health, 2010-07, Vol.47 (1), p.35-42

2010

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Psychopathology in young people experiencing homelessness: a systematic review

American journal of public health (1971), 2013-06, Vol.103 (6), p.e24-e37

2013

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In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome

Molecular psychiatry, 2023-10, Vol.28 (10), p.4342-4352

2023

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Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders

Epilepsia (Copenhagen), 2019-05, Vol.60 (5), p.818-829

2019

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Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders

Neuropsychopharmacology (New York, N.Y.), 2024-01, Vol.49 (2), p.368-376

2024

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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

Genetic and non-genetic influences on the development of co-occurring alcohol problem use and internalizing symptomatology in adolescence: a review

Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs

Psychopathology and cognition in children with 22q11.2 deletion syndrome

Psychiatric disorders in children with 16p11.2 deletion and duplication

Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome

Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome

Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions

Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach

The relationship between childhood depressive symptoms and problem alcohol use in early adolescence: findings from a large longitudinal population-based study

Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD

The psychiatric phenotypes of 1q21 distal deletion and duplication

A systematic review of the relationships between family functioning, pubertal timing and adolescent substance use

Psychopathology in adults with copy number variants

Associations between maternal older age, family environment and parent and child wellbeing in families using assisted reproductive techniques to conceive

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

Coordination difficulties, IQ and psychopathology in children with high-risk copy number variants

Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort

Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication

The Moderating Role of Close Friends in the Relationship Between Conduct Problems and Adolescent Substance Use

Psychopathology in young people experiencing homelessness: a systematic review

In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome

Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders

Author Correction: Using rare genetic mutations to revisit structural brain asymmetry

Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders

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