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Ugeskrift for Laeger|November 19, 2008
[Submicroscopic chromosomal anomalies as a cause of schizophrenia]Thomas Hansen, Andrés Ingason, Thomas Werge
Biological Psychiatry|June 22, 2025
The Use of Single-Cell and Spatial Omics to Study Copy Number VariantsSusmita Malwade, Andrés Ingason, Konstantin Khodosevich
Current Protocols|December 5, 2022
Accurate and Effective Detection of Recurrent Copy Number Variants in Large SNP Genotype DatasetsSimone Montalbano, Xabier Calle Sánchez, Morteza Vaez, et al.
Antioxidants & Redox Signaling|September 4, 2012
Redox dysregulation in the pathophysiology of schizophrenia and bipolar disorder: insights from animal modelsAnita Kulak, Pascal Steullet, Jan-Harry Cabungcal, et al.
BMC Bioinformatics|January 23, 2026
CNValidatron: accurate and efficient validation of PennCNV calls using computer visionSimone Montalbano, G Bragi Walters, Gudbjorn F Jonsson, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
CNValidatron: Accurate And Efficient Validation of PennCNV Calls Using Computer VisionSimone Montalbano, G Bragi Walters, Gudbjorn F Jonsson, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2022
A comprehensive map of genetic relationships among diagnostic categories based on 48.6 million relative pairs from the Danish genealogyGeorgios Athanasiadis, Joeri J Meijsen, Dorte Helenius, et al.
Schizophrenia Research|February 18, 2006
No significant association of the 5' end of neuregulin 1 and schizophrenia in a large Danish sampleAndrés Ingason, Karen Søeby, Sally Timm, et al.
Translational Psychiatry|December 14, 2023
Metabolic signature of the pathogenic 22q11.2 deletion identifies carriers and provides insight into systemic dysregulationJulie Courraud, Francesco Russo, Gonçalo Espregueira Themudo, et al.
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