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Morteza Vaez

As seen in: JAMA Psychiatry, medRxiv
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Articles

Recurrent Copy Number Variants and Psychiatric Outcomes in the Context of Polygenic Scores

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By Morteza Vaez, Simone Montalbano, Ryan K. Waples, Morten Krebs, Kajsa-Lotta Georgii Hellberg, Jesper R. Gådin, Daniel Stow, Peter A Holmans, Anders D. Børglum, Dorte Helenius, Thomas Werge, Andrew J. Schork, Andrés Ingason, LINC Consortium, George G. Kirov, Michael Owen, James Walters, Jane Lynch, David van Heel, Sarah Finer, Nicholas J Timpson, John MacLeod Verified, Julie Clayton, Ruby Tsang, Jane Sprackman, Shahid Khan, Inês Barroso, Rupert A Payne, Mark A. Mon-Williams, Megan Wood, Nabila Ali, Hilary C. Martin, Lam O. Huang, Marianne van den Bree, Ioanna K. Katzourou, Golam M. Khandakar
| JAMA Psychiatry Verified
Recurrent Copy Number Variants and Psychiatric Outcomes in the Context of Polygenic Scores Supplement 1. eFigure 1. Associated Odds Ratios and Confidence Intervals Resulted From the Sensitivity Analysis for Grouping rCNVs Across 6 Different Approaches eFigure 2. Comparison of rCNV Group-Associated Absolute Risk Between SSD and SSD Without Comorbid Childhood-Onset Disorders in iPSYCH2015 eFigure 3.
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Evaluating the Joint Effects of Recurrent Copy Number Variants and Polygenic Scores on the Risk of Psychiatric Disorders in the iPSYCH2015 Case-Cohort Sample

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By Jonas Bybjerg-Grauholm, Morteza Vaez, Simone Montalbano, Ryan D Waples
| medRxiv
Anders D. Borglum has received a speaker fee from Lundbeck. This study was funded by the National Institute of Mental Health (NIMH), Lundbeck Foundation and EU Horizon Europe program. I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
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Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants

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By Morteza Vaez, Simone Montalbano, Kajsa-Lotta Georgii Hellberg, Joeri J. Meijsen
| jamanetwork.com
Key Points Question What is the population-based prevalence and psychiatric risk associated with recurrent copy number variants (rCNVs) and how do they differ across outcomes and rCNVs? Findings In a genetic association study of the Danish population born in 1981-2008 and followed up until 2015, most rCNV risk profiles were similar across autism, attention-deficit/hyperactivity disorder, and schizophrenia.
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