Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders

Overview of attention for article published in European Journal of Human Genetics, September 2016

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In the top 25% of all research outputs scored by Altmetric
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@SIGPeP @DrLauraGallagh @AsIAmIreland @autismire Genetic testing for individually rare collectively common #CNVs https://t.co/QRPTuRNkpE

"CNVs were also identified in genes known to effect neurodevelopment, namely NRXN1 and GRIN2B. Furthermore deletions at 2q13, 12q21.2-21.31 and 19q13.32, and duplications at 4p16.3, 13q32.3-33.3 and Xq24-25 were observed" #ThinkGenetics https://t.co/bIM…

"Routine CMA in ID psychiatry could uncover ~11% new genetic diagnoses with potential implications for patient management. We advocate greater consideration of CMA in the assessment of adults with idiopathic ID presenting to psychiatry services" https:…

@PaulWhiteleyPhD #CNVs ? https://t.co/bIMNbmM5Tv

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