Elliott Rees
Elliott Rees
Verified email at cf.ac.uk
Title
Cited by
Cited by
Year
De novo mutations in schizophrenia implicate synaptic networks
M Fromer, AJ Pocklington, DH Kavanagh, HJ Williams, S Dwyer, ...
Nature 506 (7487), 179-184, 2014
12642014
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
G Kirov, AJ Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, ...
Molecular psychiatry 17 (2), 142-153, 2012
7032012
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
AF Pardiņas, P Holmans, AJ Pocklington, V Escott-Price, S Ripke, ...
Nature genetics 50 (3), 381-389, 2018
5132018
Analysis of copy number variations at 15 schizophrenia-associated loci
E Rees, JTR Walters, L Georgieva, AR Isles, KD Chambert, AL Richards, ...
The British Journal of Psychiatry 204 (2), 108-114, 2014
2982014
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
T Singh, MI Kurki, D Curtis, SM Purcell, L Crooks, J McRae, J Suvisaari, ...
Nature neuroscience 19 (4), 571-577, 2016
2572016
The penetrance of copy number variations for schizophrenia and developmental delay
G Kirov, E Rees, JTR Walters, V Escott-Price, L Georgieva, AL Richards, ...
Biological psychiatry 75 (5), 378-385, 2014
2542014
Copy number variation in schizophrenia in Sweden
JP Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, JL Moran, ...
Molecular psychiatry 19 (7), 762-773, 2014
2102014
Evidence that duplications of 22q11. 2 protect against schizophrenia
E Rees, G Kirov, A Sanders, JTR Walters, KD Chambert, J Shi, ...
Molecular Psychiatry 19 (1), 37-40, 2014
1502014
Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia
AJ Pocklington, E Rees, JTR Walters, J Han, DH Kavanagh, KD Chambert, ...
Neuron 86 (5), 1203-1214, 2015
1352015
Copy number variation in bipolar disorder
EK Green, E Rees, JTR Walters, KG Smith, L Forty, D Grozeva, JL Moran, ...
Molecular psychiatry 21 (1), 89-93, 2016
1322016
Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders
S Heyes, WS Pratt, E Rees, S Dahimene, L Ferron, MJ Owen, AC Dolphin
Progress in neurobiology 134, 36-54, 2015
1192015
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
T Singh, JTR Walters, M Johnstone, D Curtis, J Suvisaari, M Torniainen, ...
Nature genetics 49 (8), 1167-1173, 2017
1072017
De novo rates and selection of schizophrenia-associated copy number variants
E Rees, V Moskvina, MJ Owen, MC O'Donovan, G Kirov
Biological psychiatry 70 (12), 1109-1114, 2011
922011
Common alleles contribute to schizophrenia in CNV carriers
KE Tansey, E Rees, DE Linden, S Ripke, KD Chambert, JL Moran, ...
Molecular psychiatry 21 (8), 1085-1089, 2016
872016
Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK Biobank subjects
KM Kendall, E Rees, V Escott-Price, M Einon, R Thomas, J Hewitt, ...
Biological psychiatry 82 (2), 103-110, 2017
852017
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
E Rees, JTR Walters, KD Chambert, C O'Dushlaine, J Szatkiewicz, ...
Human molecular genetics 23 (6), 1669-1676, 2014
842014
Analysis of intellectual disability copy number variants for association with schizophrenia
E Rees, K Kendall, AF Pardiņas, SE Legge, A Pocklington, V Escott-Price, ...
JAMA psychiatry 73 (9), 963-969, 2016
802016
Opicapone as adjunct to levodopa therapy in patients with Parkinson disease and motor fluctuations: a randomized clinical trial
AJ Lees, J Ferreira, O Rascol, W Poewe, JF Rocha, M McCrory, ...
JAMA neurology 74 (2), 197-206, 2017
712017
De novo CNVs in bipolar affective disorder and schizophrenia
L Georgieva, E Rees, JL Moran, KD Chambert, V Milanova, N Craddock, ...
Human molecular genetics 23 (24), 6677-6683, 2014
712014
Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome
AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ...
Neuron 94 (6), 1101-1111. e7, 2017
682017
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