|Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis|
S Sawcer, G Hellenthal, M Pirinen, CCA Spencer, NA Patsopoulos, ...
Nature 476 (7359), 214, 2011
|Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls|
N Craddock, ME Hurles, N Cardin, RD Pearson, V Plagnol, S Robson, ...
Nature 464 (7289), 713, 2010
|Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity|
LC Tsoi, SL Spain, J Knight, E Ellinghaus, PE Stuart, F Capon, J Ding, ...
Nature genetics 44 (12), 1341, 2012
|Analysis of hundreds of cis-regulatory landscapes at high resolution in a single, high-throughput experiment|
JR Hughes, N Roberts, S McGowan, D Hay, E Giannoulatou, M Lynch, ...
Nature genetics 46 (2), 205, 2014
|Myelodysplastic syndromes are propagated by rare and distinct human cancer stem cells in vivo|
PS Woll, U Kjällquist, O Chowdhury, H Doolittle, DC Wedge, S Thongjuea, ...
Cancer cell 25 (6), 794-808, 2014
|Interferon-induced transmembrane protein-3 genetic variant rs12252-C is associated with severe influenza in Chinese individuals|
YH Zhang, Y Zhao, N Li, YC Peng, E Giannoulatou, RH Jin, HP Yan, ...
Nature communications 4, 1418, 2013
|Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins|
I Postmus, S Trompet, HA Deshmukh, MR Barnes, X Li, HR Warren, ...
Nature communications 5, 5068, 2014
|Smchd1-dependent and-independent pathways determine developmental dynamics of CpG island methylation on the inactive X chromosome|
AV Gendrel, A Apedaile, H Coker, A Termanis, I Zvetkova, J Godwin, ...
Developmental cell 23 (2), 265-279, 2012
|Early dynamic fate changes in haemogenic endothelium characterized at the single-cell level|
G Swiers, C Baumann, J O’Rourke, E Giannoulatou, S Taylor, A Joshi, ...
Nature communications 4, 2924, 2013
|Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error|
CY Cheng, M Schache, MK Ikram, TL Young, JA Guggenheim, V Vitart, ...
The American Journal of Human Genetics 93 (2), 264-277, 2013
|Pneumococcal genome sequencing tracks a vaccine escape variant formed through a multi-fragment recombination event|
T Golubchik, AB Brueggemann, T Street, RE Gertz Jr, CCA Spencer, T Ho, ...
Nature genetics 44 (3), 352, 2012
|Genome-wide association study implicates HLA-C* 01: 02 as a risk factor at the major histocompatibility complex locus in schizophrenia|
Irish Schizophrenia Genomics Consortium, ...
Biological psychiatry 72 (8), 620-628, 2012
|Epidemiology and treatment of pulmonary arterial hypertension|
EMT Lau, E Giannoulatou, DS Celermajer, M Humbert
Nature Reviews Cardiology 14 (10), 603, 2017
|Common variants in the HLA-DRB1–HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis|
M Fakiola, A Strange, HJ Cordell, EN Miller, M Pirinen, Z Su, A Mishra, ...
Nature genetics 45 (2), 208, 2013
|Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes|
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
|GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population|
E Giannoulatou, C Yau, S Colella, J Ragoussis, CC Holmes
Bioinformatics 24 (19), 2209-2214, 2008
|Male-lineage transmission of an acquired metabolic phenotype induced by grand-paternal obesity|
JE Cropley, SA Eaton, A Aiken, PE Young, E Giannoulatou, JWK Ho, ...
Molecular metabolism 5 (8), 699-708, 2016
|Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process|
H Springelkamp, R Höhn, A Mishra, PG Hysi, CC Khor, SJ Loomis, ...
Nature communications 5, 4883, 2014
|Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease|
GM Blue, EP Kirk, E Giannoulatou, SL Dunwoodie, JWK Ho, DCK Hilton, ...
Journal of the American College of Cardiology 64 (23), 2498-2506, 2014
|Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants|
R Malik, T Freilinger, BS Winsvold, V Anttila, J Vander Heiden, M Traylor, ...
Neurology 84 (21), 2132-2145, 2015