David Curtis
David Curtis
UCL Genetics Institute
Підтверджена електронна адреса в ucl.ac.uk - Домашня сторінка
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Посилання
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
BMN Brendan K. Bulik-Sullivan, Po-Ru Loh, Hilary Finucane, Stephan Ripke ...
Nat Genet 47, 291–295, 2015
16352015
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
16322013
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
13672014
Rare chromosomal deletions and duplications increase risk of schizophrenia
International Schizophrenia Consortium
Nature 455 (7210), 237, 2008
13372008
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
12012016
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
MAR Ferreira, MC O'Donovan, YA Meng, IR Jones, DM Ruderfer, L Jones, ...
Nature genetics 40 (9), 1056-1058, 2008
11772008
Monte Carlo tests for associations between disease and alleles at highly polymorphic loci
PC Sham, D Curtis
Annals of human genetics 59 (1), 97-105, 1995
10021995
An extended transmission/disequilibrium test (TDT) for multi‐allele marker loci
PC Sham, D Curtis
Annals of human genetics 59 (3), 323-336, 1995
7381995
Whole-genome association study of bipolar disorder
P Sklar, JW Smoller, J Fan, MAR Ferreira, RH Perlis, K Chambert, ...
Molecular psychiatry 13 (6), 558-569, 2008
7282008
The UK10K project identifies rare variants in health and disease
UK10K consortium
Nature 526 (7571), 82-90, 2015
6612015
Transcriptional plasticity promotes primary and acquired resistance to BET inhibition
P Rathert, M Roth, T Neumann, F Muerdter, JS Roe, M Muhar, S Deswal, ...
Nature 525 (7570), 543-547, 2015
585*2015
Model-free analysis and permutation tests for allelic associations
JH Zhao, D Curtis, PC Sham
Human heredity 50 (2), 133-139, 2000
4982000
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
4902018
Concomitant leflunomide therapy in patients with active rheumatoid arthritis despite stable doses of methotrexate: a randomized, double-blind, placebo-controlled trial
JM Kremer, MC Genovese, GW Cannon, JR Caldwell, JJ Cush, DE Furst, ...
Annals of internal medicine 137 (9), 726-733, 2002
4722002
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
WHH Vilhjálmsson BJ, Yang J, Finucane HK, Gusev A, Lindström S, Ripke S ...
Am J Hum Genet. 97, 576-592, 2015
4622015
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32. 2, 5q33. 2, and 8p21-22 and provides support for …
HMD Gurling, G Kalsi, J Brynjolfson, T Sigmundsson, R Sherrington, ...
The American Journal of Human Genetics 68 (3), 661-673, 2001
4252001
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
CNVSWG the Psychiatric Genomics Consortium
Nature Genetics 49, 27-35, 2017
354*2017
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
FV Elmslie, M Rees, MP Williamson, M Kerr, MJ Kjeldsen, K An Pang, ...
Human Molecular Genetics 6 (8), 1329-1334, 1997
3111997
A note on the calculation of empirical P values from Monte Carlo procedures
BV North, D Curtis, PC Sham
The American Journal of Human Genetics 71 (2), 439-441, 2002
3052002
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Статті 1–20