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Scientific Reports|May 18, 2016
Gender differences in CNV burden do not confound schizophrenia CNV associationsJun Han, James T R Walters, George Kirov, et al.JAMA Psychiatry|August 17, 2022
Ultrarare Coding Variants and Cognitive Function in SchizophreniaHugo D J Creeth, Elliott Rees, Sophie E Legge, et al.Human Molecular Genetics|May 9, 2022
Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-functionNicholas E Clifton, Matthew L Bosworth, Niels Haan, et al.Bone|June 10, 2006
Correction of the mineralization defect in hyp mice treated with protease inhibitors CA074 and pepstatinPeter S N Rowe, Naoko Matsumoto, Oak D Jo, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|February 4, 2024
Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophreniaDjenifer B Kappel, Elliott Rees, Eilidh Fenner, et al.Biological Psychiatry|October 25, 2016
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank SubjectsKimberley M Kendall, Elliott Rees, Valentina Escott-Price, et al.The British Journal of Psychiatry : the Journal of Mental Science|February 16, 2019
Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK BiobankKimberley M Kendall, Matthew Bracher-Smith, Harry Fitzpatrick, et al.Nature Communications|August 2, 2025
Whole-exome sequencing analysis identifies risk genes for schizophreniaSophie L Chick, Peter Holmans, Darren Cameron, et al.JAMA Psychiatry|April 18, 2019
Association of Rare Copy Number Variants With Risk of DepressionKimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, et al.Human Molecular Genetics|November 14, 2012
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease riskJade Chapman, Elliott Rees, Denise Harold, et al.Pageof 9