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

Although many genetic risk factors for psychiatric and neurodevelopmental disorders have been identified, the neurobiological route from genetic risk to neuropsychiatric outcome remains unclear. 22q11.2 deletion syndrome (22q11.2DS) is a copy number variant (CNV) syndrome associated with high rates...

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Veröffentlicht in:	Neuropsychopharmacology (New York, N.Y.) N.Y.), 2024-01, Vol.49 (2), p.368-376
Hauptverfasser:	Doherty, Joanne L, Cunningham, Adam C, Chawner, Samuel J R A, Moss, Hayley M, Dima, Diana C, Linden, David E J, Owen, Michael J, van den Bree, Marianne B M, Singh, Krish D
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Attention Deficit Disorder with Hyperactivity - genetics Attention deficit hyperactivity disorder Autism Autism Spectrum Disorder - complications Autism Spectrum Disorder - genetics Child Children Chromosome 22 Cognition Cognitive ability Copy number DiGeorge Syndrome - complications DiGeorge Syndrome - diagnosis DiGeorge Syndrome - genetics Haploinsufficiency Humans Magnetoencephalography Mental disorders Neural networks Neurodevelopmental disorders Risk Factors Risk groups Schizophrenia
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