James Walters
Title
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Cited by
Year
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
BK Bulik-Sullivan, PR Loh, HK Finucane, S Ripke, J Yang, N Patterson, ...
Nature genetics 47 (3), 291-295, 2015
16482015
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421-427, 2014
13742014
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
S Ripke, C O'Dushlaine, K Chambert, JL Moran, AK Kähler, S Akterin, ...
Nature genetics 45 (10), 1150, 2013
13362013
Schizophrenia risk from complex variation of complement component 4
A Sekar, AR Bialas, H de Rivera, A Davis, TR Hammond, N Kamitaki, ...
Nature 530 (7589), 177-183, 2016
12132016
Partitioning heritability by functional annotation using genome-wide association summary statistics
HK Finucane, B Bulik-Sullivan, A Gusev, G Trynka, Y Reshef, PR Loh, ...
Nature genetics 47 (11), 1228, 2015
9222015
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
4992018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
AF Pardiñas, P Holmans, AJ Pocklington, V Escott-Price, S Ripke, ...
Nature genetics 50 (3), 381, 2018
4782018
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
4762015
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ...
The American Journal of Human Genetics 95 (5), 535-552, 2014
4222014
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature Genetics, 2017
3602017
Treatment-resistant schizophrenia: treatment response and resistance in psychosis (TRRIP) working group consensus guidelines on diagnosis and terminology
OD Howes, R McCutcheon, O Agid, A De Bartolomeis, NJM Van Beveren, ...
American Journal of Psychiatry 174 (3), 216-229, 2017
2962017
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
2902014
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
PR Loh, G Bhatia, A Gusev, HK Finucane, BK Bulik-Sullivan, SJ Pollack, ...
Nature genetics 47 (12), 1385, 2015
2712015
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
2512016
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
2482014
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC
ML Hamshere, JTR Walters, R Smith, AL Richards, E Green, D Grozeva, ...
Molecular psychiatry 18 (6), 708-712, 2013
2372013
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 1-9, 2015
2172015
Wake-up call for British psychiatry
N Craddock, D Antebi, MJ Attenburrow, A Bailey, A Carson, P Cowen, ...
The British Journal of Psychiatry 193 (1), 6-9, 2008
2112008
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
2062014
Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate
OA Andreassen, WK Thompson, AJ Schork, S Ripke, M Mattingsdal, ...
PLoS Genet 9 (4), e1003455, 2013
2022013
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