Chromosomal microarray analysis—a routine clinical genetic test for patients with schizophrenia
Authors:
- 1 October 2014
- journal article
- Published by Elsevier in The Lancet Psychiatry
- Vol. 1 (5) , 329-331
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion SyndromeAmerican Journal of Psychiatry, 2014
- Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarraysHuman Molecular Genetics, 2013
- 1q21.1 Microduplication expression in adultsGenetics in Medicine, 2013
- A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersJournal of Medical Genetics, 2012
- Genetic investigation for adults with intellectual disabilityCurrent Opinion in Neurology, 2012
- Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophreniaSchizophrenia Research, 2012
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophreniaMolecular Psychiatry, 2011
- Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and ResearchCytogenetic and Genome Research, 2011
- Practical Guidelines for Managing Patients with 22q11.2 Deletion SyndromeThe Journal of Pediatrics, 2011
- Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital AnomaliesThe American Journal of Human Genetics, 2010