Cargando…

Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions

BACKGROUND: Individuals with 22q11.2 deletion are at considerably increased risk of neurodevelopmental and psychiatric conditions. There have been very few studies investigating how this risk manifests in early childhood and what factors may underlie developmental variability. Insights into this can...

Descripción completa

Detalles Bibliográficos
Autores principales:	Chawner, Samuel J. R. A., Paine, Amy L., Dunn, Matt J., Walsh, Alice, Sloane, Poppy, Thomas, Megan, Evans, Alexandra, Hopkins‐Jones, Lucinda, Struik, Siske, Hall, Jeremy, Erichsen, Jonathan T., Leekam, Susan R., Owen, Michael J., Hay, Dale, van den Bree, Marianne B. M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2023
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519742/ https://www.ncbi.nlm.nih.gov/pubmed/37753151 http://dx.doi.org/10.1002/jcv2.12162

Ejemplares similares

Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions
por: Chawner, Samuel J. R. A., et al.
Publicado: (2023)

Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders
por: Eaton, Christopher B., et al.
Publicado: (2019)

Autism: A model of neurodevelopmental diversity informed by genomics
por: Chawner, Samuel J. R. A., et al.
Publicado: (2022)

Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study
por: Wolstencroft, Jeanne, et al.
Publicado: (2022)

Clinical evaluation of patients with a neuropsychiatric risk copy number variant
por: Chawner, Samuel JRA, et al.
Publicado: (2021)

The contribution of imprinted genes to neurodevelopmental and neuropsychiatric disorders
por: Isles, Anthony R.
Publicado: (2022)

Neurological, neuropsychiatric and neurodevelopmental complications of COVID-19
por: Pantelis, Christos, et al.
Publicado: (2020)

ULK4 in Neurodevelopmental and Neuropsychiatric Disorders
por: Luo, Shilin, et al.
Publicado: (2022)

Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs
por: Cunningham, Adam C., et al.
Publicado: (2022)

The tRNA regulome in neurodevelopmental and neuropsychiatric disease
por: Blaze, Jennifer, et al.
Publicado: (2022)

Editorial: Metabolic traits associated with neurodevelopmental and neuropsychiatric disorders
por: Jagadapillai, Rekha, et al.
Publicado: (2023)

Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
por: Donnelly, Nicholas, et al.
Publicado: (2023)

First evidence of the feasibility of gaze-contingent attention training for school children with autism
por: Powell, Georgina, et al.
Publicado: (2016)

KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders
por: Teng, Xinchen, et al.
Publicado: (2019)

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
por: Donnelly, Nicholas A, et al.
Publicado: (2022)

Psychopathology in mothers of children with pathogenic Copy Number Variants
por: Niarchou, Maria, et al.
Publicado: (2023)

A review of the cognitive impact of neurodevelopmental and neuropsychiatric associated copy number variants
por: Molloy, Ciara J., et al.
Publicado: (2023)

Restricted and repetitive behaviors and their developmental and demographic correlates in 4–8-year-old children: A transdiagnostic approach
por: Keating, Jennifer, et al.
Publicado: (2023)

The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome
por: Chawner, Samuel J.R.A., et al.
Publicado: (2019)

Editorial: Neurodevelopmental, neuropsychiatric and psychosocial correlates of joint hypermobility and related disorders
por: Guinchat, Vincent, et al.
Publicado: (2022)

Involvement of an Aberrant Vascular System in Neurodevelopmental, Neuropsychiatric, and Neuro-Degenerative Diseases
por: Ishihara, Keiichi, et al.
Publicado: (2023)

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome
por: Fiksinski, Ania M., et al.
Publicado: (2021)

Childhood cognitive development in 22q11.2 deletion syndrome: case–control study
por: Chawner, Samuel J. R. A., et al.
Publicado: (2017)

O4.8. VULNERABLE PERIODS FOR COGNITIVE DEVELOPMENT IN INDIVIDUALS AT HIGH GENOMIC RISK OF SCHIZOPHRENIA
por: Morrison, Sinead, et al.
Publicado: (2018)

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
por: Cukier, Holly N, et al.
Publicado: (2014)

Neurodevelopmental and neuropsychiatric disorders in cobalamin C disease: a case report and review of the literature
por: Nguyen, Minh G., et al.
Publicado: (2022)

Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders
por: Poppi, Lauren A., et al.
Publicado: (2021)

Deconstructing the functional neuroanatomy of the choroid plexus: an ontogenetic perspective for studying neurodevelopmental and neuropsychiatric disorders
por: Bitanihirwe, Byron K. Y., et al.
Publicado: (2022)

Haematopoietic Stem Cell Transplant for Norovirus-Induced Intestinal Failure in X-linked Agammaglobulinemia
por: Shillitoe, Ben M. J., et al.
Publicado: (2021)

NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia
por: Alsaqati, Mouhamed, et al.
Publicado: (2022)

Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk
por: Dima, Diana C., et al.
Publicado: (2020)

Pilot study to establish a prospective neonatal cohort: Study of Preterm Infants and Neurodevelopmental Genes (SPRING)
por: Wong, Hilary S, et al.
Publicado: (2020)

Intragenic deletion of RBFOX1 associated with neurodevelopmental/neuropsychiatric disorders and possibly other clinical presentations
por: Zhao, Wei-Wei
Publicado: (2013)

Modeling Neurodevelopmental and Neuropsychiatric Diseases with Astrocytes Derived from Human-Induced Pluripotent Stem Cells
por: Ren, Baiyan, et al.
Publicado: (2021)

Neurodevelopmental signatures of narcotic and neuropsychiatric risk factors in 3D human-derived forebrain organoids
por: Notaras, Michael, et al.
Publicado: (2021)

Neuropsychiatric disorders and COVID-19
por: Burchill, Ella, et al.
Publicado: (2021)

Neurodevelopmental hypothesis of schizophrenia
por: Owen, Michael J., et al.
Publicado: (2011)

Infantile nystagmus: an optometrist’s perspective
por: Zahidi, Asma AA, et al.
Publicado: (2017)

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders
por: Hu, Jie, et al.
Publicado: (2015)

SETD1A Mediated H3K4 Methylation and Its Role in Neurodevelopmental and Neuropsychiatric Disorders
por: Wang, Shan, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_ps3j9hl5au9ipmc3i02v5596sj