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JCPP Advances|July 8, 2026
The role of rare copy number variants in early-onset depressionCharlotte A Dennison, Ida Sønderby, Miguel Garcia-Argibay, et al.
The British Journal of Psychiatry : the Journal of Mental Science|June 4, 2019
Clinical indicators of treatment-resistant psychosisSophie E Legge, Charlotte A Dennison, Antonio F Pardiñas, et al.
JAMA Psychiatry|March 27, 2024
Genetic and Phenotypic Features of Schizophrenia in the UK BiobankSophie E Legge, Antonio F Pardiñas, Grace Woolway, et al.
Translational Psychiatry|February 27, 2019
Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structuresMark Drakesmith, Greg D Parker, Jacqueline Smith, et al.
Human Molecular Genetics|July 25, 2014
De novo CNVs in bipolar affective disorder and schizophreniaLyudmila Georgieva, Elliott Rees, Jennifer L Moran, et al.
Journal of Medical Genetics|October 22, 2018
Medical consequences of pathogenic CNVs in adults: analysis of the UK BiobankKaren Crawford, Matthew Bracher-Smith, David Owen, et al.
Neuron|June 8, 2015
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaAndrew J Pocklington, Elliott Rees, James T R Walters, et al.
Nature Communications|September 10, 2021
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutationsElliott Rees, Hugo D J Creeth, Hai-Gwo Hwu, et al.
Molecular Psychiatry|October 20, 2020
Genetic association of FMRP targets with psychiatric disordersNicholas E Clifton, Elliott Rees, Peter A Holmans, et al.
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