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Biological Psychiatry|March 8, 2021
Rare Copy Number Variants Are Associated With Poorer Cognition in SchizophreniaLeon Hubbard, Elliott Rees, Derek W Morris, et al.Molecular Psychiatry|October 18, 2023
Genomic findings in schizophrenia and their implicationsMichael J Owen, Sophie E Legge, Elliott Rees, et al.Genomics|September 19, 2003
Variation in the protocadherin gamma A gene clusterGeorge Kirov, Lyudmila Georgieva, Nigel Williams, et al.Investigative Ophthalmology & Visual Science|August 25, 2004
Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. familiesJane E Farbrother, George Kirov, Michael J Owen, et al.Journal of Medical Genetics|November 15, 2022
Characterising heart rhythm abnormalities associated with Xp22.31 deletionGeorgina Wren, Emily Baker, Jack Underwood, et al.Psychiatric Genetics|September 10, 2002
Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studiesAlbena Dimitrova, Lyudmila Georgieva, Ivan Nikolov, et al.Molecular Psychiatry|April 10, 2026
Analysis of rare coding variants in schizophrenia-associated genes and generalised cognition in the UK BiobankEilidh Fenner, Peter Holmans, Michael C O'Donovan, et al.Biological Psychiatry Global Open Science|October 26, 2023
Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive PerformanceXavier Caseras, Sophie E Legge, Matthew Bracher-Smith, et al.The American Journal of Psychiatry|January 5, 2019
The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK BiobankValentina Escott-Price, Antonio F Pardiñas, Enrique Santiago, et al.NPJ Genomic Medicine|September 28, 2024
Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK BiobankThomas J Dinneen, Fiana Ní Ghrálaigh, Cathal Ormond, et al.Pageof 20