ArticleThe British journal of psychiatry : the journal of mental science2017
Childhood cognitive development in 22q11.2 deletion syndrome: case-control study.
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Article in The British journal of psychiatry : the journal of mental science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.
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27citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
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Who cites it
27 citing papers in PubMed, 49 citations in OpenAlex.
- Dimensional phenotype measurement in children with rare genetic conditions: new insights into the aetiology of neurodevelopmental and psychiatric disorders.Frontiers in psychiatry · 2026Article
- Parental Education Predicts Longitudinal IQ Trajectories in 22q11.2 Deletion Syndrome: A Three-Cohort European Study.Journal of intellectual disability research : JIDR · 2025Article
- Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate.Human molecular genetics · 2025Article
- Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletion.Journal of neurodevelopmental disorders · 2025Article
- Eating behaviour and eating disorders in individuals with rare neurodevelopmental variants: current knowledge and future research directions.Frontiers in psychiatry · 2025Article
- Review
- Prenatal alcohol exposure and cognition at midlife: Evidence of fluid cognition deficits in two cohorts.Alcohol, clinical & experimental research · 2023Article
- Altered developmental trajectories of verbal learning skills in 22q11.2DS: associations with hippocampal development and psychosis.Psychological medicine · 2023Article
- Article
- Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions.JCPP advances · 2023Article
- Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects.Journal of neurodevelopmental disorders · 2023Article
- DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts.BJPsych open · 2023Article
- A normative chart for cognitive development in a genetically selected population.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022Article
- ENIGMA-DTI: Translating reproducible white matter deficits into personalized vulnerability metrics in cross-diagnostic psychiatric research.Human brain mapping · 2022Article
- A cross-comparison of cognitive ability across 8 genomic disorders.Current opinion in genetics & development · 2021Review
- Annual Research Review: Anterior Modifiers in the Emergence of Neurodevelopmental Disorders (AMEND)-a systems neuroscience approach to common developmental disorders.Journal of child psychology and psychiatry, and allied disciplines · 2021Review
- Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders.Journal of neurodevelopmental disorders · 2021Article
- Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome.Current psychiatry reports · 2021Review
- Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.Nature medicine · 2020Article
- Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology.Translational psychiatry · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors at 2 institutions in 1 country.
Samuel J R A ChawnerSamuel J.R.A. Chawner, PhD, Joanne L. Doherty, MRCPsych, Hayley Moss, BSc, Maria Niarchou, PhD, James T.R. Walters, PhD, MRCPsych, Michael J. Owen, PhD, FRCPsych, Marianne B.M. van den Bree, PhD, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Joanne L DohertySamuel J.R.A. Chawner, PhD, Joanne L. Doherty, MRCPsych, Hayley Moss, BSc, Maria Niarchou, PhD, James T.R. Walters, PhD, MRCPsych, Michael J. Owen, PhD, FRCPsych, Marianne B.M. van den Bree, PhD, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Hayley MossSamuel J.R.A. Chawner, PhD, Joanne L. Doherty, MRCPsych, Hayley Moss, BSc, Maria Niarchou, PhD, James T.R. Walters, PhD, MRCPsych, Michael J. Owen, PhD, FRCPsych, Marianne B.M. van den Bree, PhD, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Maria NiarchouSamuel J.R.A. Chawner, PhD, Joanne L. Doherty, MRCPsych, Hayley Moss, BSc, Maria Niarchou, PhD, James T.R. Walters, PhD, MRCPsych, Michael J. Owen, PhD, FRCPsych, Marianne B.M. van den Bree, PhD, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
James T R WaltersSamuel J.R.A. Chawner, PhD, Joanne L. Doherty, MRCPsych, Hayley Moss, BSc, Maria Niarchou, PhD, James T.R. Walters, PhD, MRCPsych, Michael J. Owen, PhD, FRCPsych, Marianne B.M. van den Bree, PhD, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Michael J OwenSamuel J.R.A. Chawner, PhD, Joanne L. Doherty, MRCPsych, Hayley Moss, BSc, Maria Niarchou, PhD, James T.R. Walters, PhD, MRCPsych, Michael J. Owen, PhD, FRCPsych, Marianne B.M. van den Bree, PhD, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Marianne B M van den BreeSamuel J.R.A. Chawner, PhD, Joanne L. Doherty, MRCPsych, Hayley Moss, BSc, Maria Niarchou, PhD, James T.R. Walters, PhD, MRCPsych, Michael J. Owen, PhD, FRCPsych, Marianne B.M. van den Bree, PhD, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK vandenbreemb@cardiff.ac.uk.
Cardiff University · GBMedical Research Council · GB
Funding
5/5 International Consortium on Brain and Behavior in 22q11.2 Deletion SyndromeU01MH101724 · NIMH · CARDIFF UNIVERSITY · PI ARANGO, CELSO, MURPHY, DECLAN · 2013 to 2016
$744kMedical Research Council G0800509Medical Research Council G0801418Medical Research Council MR/L010305/1Medical Research Council MR/N022572/1MRF_ MRF-154-0001-RG-SKUSENIMH NIH HHS U01 MH101724Wellcome Trust
Abstract
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Indexed as
Child DevelopmentAdolescentCase-Control StudiesChildCognition DisordersDiGeorge SyndromeFemaleHumansLongitudinal StudiesMaleNeuropsychological Tests
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.