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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 | 1101 | 2011 |
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 | 504 | 2011 |
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 | 489 | 2016 |
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 | 468 | 2009 |
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 | 330 | 2012 |
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 | 283 | 2021 |
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 | 279 | 2013 |
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 | 244 | 2012 |
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 | 228 | 2003 |
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 | 161 | 2013 |
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 | 160 | 2013 |
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 | 151 | 2015 |
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 | 109 | 2016 |
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 | 93* | |
Chromosome 9p21 and coronary artery disease R McPherson New England Journal of Medicine 362 (18), 1736-1737, 2010 | 83 | 2010 |
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 | 78 | 2015 |
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 | 65 | 2011 |
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 | 64 | 2016 |
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 | 58 | 2018 |