Eleni Giannoulatou
Eleni Giannoulatou
Verified email at victorchang.edu.au
TitleCited byYear
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
18162011
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
7502010
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
6332012
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
2592014
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
1902014
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
1682013
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
1422014
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
1242012
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
1162013
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
912013
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
822012
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
792012
Common variants in the HLA-DRB1HLA-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
752013
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
712008
Epidemiology and treatment of pulmonary arterial hypertension
EMT Lau, E Giannoulatou, DS Celermajer, M Humbert
Nature Reviews Cardiology 14 (10), 603, 2017
662017
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
652014
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
622014
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
602015
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
582016
NAD deficiency, congenital malformations, and niacin supplementation
H Shi, A Enriquez, M Rapadas, EMMA Martin, R Wang, J Moreau, CK Lim, ...
New England Journal of Medicine 377 (6), 544-552, 2017
502017
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Articles 1–20