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Eleni Giannoulatou
Eleni Giannoulatou
Verified email at victorchang.edu.au
Title
Cited by
Cited by
Year
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
29432011
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), 1341-1348, 2012
10452012
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
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
8202019
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), 205-212, 2014
5132014
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
4982018
Epidemiology and treatment of pulmonary arterial hypertension
EMT Lau, E Giannoulatou, DS Celermajer, M Humbert
Nature Reviews Cardiology 14 (10), 603-614, 2017
4132017
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
3512014
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 (1), 1418, 2013
3012013
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 (1), 5068, 2014
2772014
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
2262017
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
2192012
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 (1), 2924, 2013
1982013
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
1762013
Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection
D Adlam, TM Olson, N Combaret, JC Kovacic, SE Iismaa, A Al-Hussaini, ...
Journal of the American College of Cardiology 73 (1), 58-66, 2019
1742019
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
1702012
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
1662016
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), 352-355, 2012
1372012
Advances in the genetics of congenital heart disease: a clinician’s guide
GM Blue, EP Kirk, E Giannoulatou, GF Sholler, SL Dunwoodie, RP Harvey, ...
Journal of the American College of Cardiology 69 (7), 859-870, 2017
1362017
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
1272015
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