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Olly Burren
Olly Burren
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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
JA Todd, NM Walker, JD Cooper, DJ Smyth, K Downes, V Plagnol, ...
Nature genetics 39 (7), 857-864, 2007
16422007
Lineage-specific genome architecture links enhancers and non-coding disease variants to target gene promoters
BM Javierre, OS Burren, SP Wilder, R Kreuzhuber, SM Hill, S Sewitz, ...
Cell 167 (5), 1369-1384. e19, 2016
9552016
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nature 464 (7289), 713-720, 2010
9272010
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region
DJ Smyth, JD Cooper, R Bailey, S Field, O Burren, LJ Smink, C Guja, ...
Nature genetics 38 (6), 617-619, 2006
7892006
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
S Onengut-Gumuscu, WM Chen, O Burren, NJ Cooper, AR Quinlan, ...
Nature genetics 47 (4), 381-386, 2015
6662015
The International Human Epigenome Consortium: a blueprint for scientific collaboration and discovery
HG Stunnenberg, S Abrignani, D Adams, M de Almeida, L Altucci, V Amin, ...
Cell 167 (5), 1145-1149, 2016
5052016
Widespread seasonal gene expression reveals annual differences in human immunity and physiology
XC Dopico, M Evangelou, RC Ferreira, H Guo, ML Pekalski, DJ Smyth, ...
Nature communications 6 (1), 7000, 2015
4812015
Whole-genome sequencing of patients with rare diseases in a national health system
E Turro, WJ Astle, K Megy, S Gräf, D Greene, O Shamardina, HL Allen, ...
Nature 583 (7814), 96-102, 2020
3862020
Inherited variation in vitamin D genes is associated with predisposition to autoimmune disease type 1 diabetes
JD Cooper, DJ Smyth, NM Walker, H Stevens, OS Burren, C Wallace, ...
Diabetes 60 (5), 1624-1631, 2011
3802011
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
CA Dendrou, V Plagnol, E Fung, JHM Yang, K Downes, JD Cooper, ...
Nature genetics 41 (9), 1011-1015, 2009
3032009
A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetes
RC Ferreira, H Guo, RMR Coulson, DJ Smyth, ML Pekalski, OS Burren, ...
Diabetes 63 (7), 2538-2550, 2014
3022014
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
KA Hunt, V Mistry, NA Bockett, T Ahmad, M Ban, JN Barker, JC Barrett, ...
Nature 498 (7453), 232-235, 2013
2402013
Seven newly identified loci for autoimmune thyroid disease
JD Cooper, MJ Simmonds, NM Walker, O Burren, OJ Brand, H Guo, ...
Human molecular genetics 21 (23), 5202-5208, 2012
1792012
Whole-genome sequencing of a sporadic primary immunodeficiency cohort
JED Thaventhiran, H Lango Allen, OS Burren, W Rae, D Greene, ...
Nature 583 (7814), 90-95, 2020
1612020
Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls
MD Fortune, H Guo, O Burren, E Schofield, NM Walker, M Ban, SJ Sawcer, ...
Nature genetics 47 (7), 839-846, 2015
1582015
Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases
H Guo, MD Fortune, OS Burren, E Schofield, JA Todd, C Wallace
Human molecular genetics 24 (12), 3305-3313, 2015
1402015
Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene
LJ Davison, C Wallace, JD Cooper, NF Cope, NK Wilson, DJ Smyth, ...
Human molecular genetics 21 (2), 322-333, 2012
1282012
T1DBase: update 2011, organization and presentation of large-scale data sets for type 1 diabetes research
OS Burren, EC Adlem, P Achuthan, M Christensen, RMR Coulson, ...
Nucleic acids research 39 (suppl_1), D997-D1001, 2010
1062010
Genetics of Type 1 Diabetes in Finland, Simmonds MJ, Heward JM, Gough SC, Wellcome Trust Case Control Consortium, Dunger DB, Wicker LS, Clayton DG: Robust associations of four …
JA Todd, NM Walker, JD Cooper, DJ Smyth, K Downes, V Plagnol, ...
Nat Genet 39 (7), 857-864, 2007
1042007
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
T Lorenzini, M Fliegauf, N Klammer, N Frede, M Proietti, A Bulashevska, ...
Journal of Allergy and Clinical Immunology 146 (4), 901-911, 2020
962020
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