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Olga Jarinova
Olga Jarinova
University of Ottawa
Verified email at cheo.on.ca
Title
Cited by
Cited by
Year
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
JT 26. International Consortium for Blood Pressure Genome-Wide Association ...
Nature Genetics 478 (7367), 103-109, 2011
2283*2011
Human metabolic individuality in biomedical and pharmaceutical research
KJS Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, …CARDIoGRAM ...
Nature 477 (7362), 54-60, 2011
10822011
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
DCM Wain LV, Verwoert GC, O'Reilly PF, Shi G, Johnson T, …CARDIoGRAM ...
Nature Genetics 43 (10), 1005-1011, 2011
5022011
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ...
Nature communications 7 (1), 10023, 2016
4702016
Functional analysis of the chromosome 9p21. 3 coronary artery disease risk locus
O Jarinova, AFR Stewart, R Roberts, G Wells, P Lau, T Naing, C Buerki, ...
Arteriosclerosis, thrombosis, and vascular biology 29 (10), 1671-1677, 2009
4632009
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
GDGHC Lu X, Wang L, Chen S, He L, Yang X, CARDIoGRAM Consortium ...
Nature Genetics 44 (8), 890-894, 2012
3262012
Dysfunctional nitric oxide signalling increases risk of myocardial infarction
SH Erdmann J, Stark K, Esslinger UB, Rumpf PM,… CARDIoGRAM Consortium ...
Nature 504 (7490), 432-436, 2013
2752013
Evidence-based assessment of genes in dilated cardiomyopathy
E Jordan, L Peterson, T Ai, B Asatryan, L Bronicki, E Brown, R Celeghin, ...
Circulation 144 (1), 7-19, 2021
2592021
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations
E Demirkan A, van Duijn CM., Ugocsai P, Isaacs A, Pramstaller PP ...
PloS Genet 8 (2), e1002490, 2012
2382012
Regulatory roles of conserved intergenic domains in vertebrate Dlx bigene clusters
N Ghanem, O Jarinova, A Amores, Q Long, G Hatch, BK Park, ...
Genome research 13 (4), 533-543, 2003
2272003
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association …
ODCJ Sabater-Lleal M, Huang J, Chasman D, Naitza S, Dehghan A, Johnson AD ...
Circulation 128 (12), 1310-1324, 2013
1612013
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
ODCJ Ho JE, Chen WY, Chen MH, Larson MG, McCabe EL, Cheng S, Ghorbani A ...
Journal of Clinical Investigations 123 (10), 4208-18, 2013
1582013
Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the community.
VRS Kaess BM, Preis SR, Lieb W, Beiser AS, Yang Q, Chen TC, Hengstenberg C ...
Journal of American Heart Association 4 (3), e001544, 2015
1462015
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit
H Daoud, SM Luco, R Li, E Bareke, C Beaulieu, O Jarinova, N Carson, ...
Cmaj 188 (11), E254-E260, 2016
1072016
Genetic predisposition to higher blood pressure increases coronary artery disease risk
SAF Lieb W, Jansen H, Loley C, Pencina MJ, Nelson CP, …,CARDIoGRAM ...
Hypertension 61 (5), 995-1001, 0
92*
Chromosome 9p21 and coronary artery disease
R McPherson
New England Journal of Medicine 362 (18), 1736-1737, 2010
822010
Genetic analysis for a shared biological basis between migraine and coronary artery disease
BS Winsvold, CP Nelson, R Malik, P Gormley, V Anttila, J Vander Heiden, ...
Neurology: Genetics 1 (1), e10, 2015
782015
RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies
SAF Herder C, Peeters W, Illig T, Baumert J, de Kleijn DP,… CARDIoGRAM ...
PLoS One 6 (12), e25734, 2011
652011
Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay
H Daoud, D Zhang, F McMurray, A Yu, SM Luco, J Vanstone, O Jarinova, ...
Journal of medical genetics 53 (3), 200-207, 2016
622016
Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach
SM Harrison, JS Dolinksy, W Chen, CD Collins, S Das, JL Deignan, ...
Human mutation 39 (11), 1641-1649, 2018
552018
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