フォロー
Thorsten Kessler
Thorsten Kessler
Deutsches Herzzentrum München
確認したメール アドレス: dhm.mhn.de
タイトル
引用先
引用先
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature genetics 47 (10), 1121-1130, 2015
26102015
Large-scale association analysis identifies new risk loci for coronary artery disease
CARDIoGRAMplusC4D Consortium, P Deloukas, S Kanoni, C Willenborg, ...
Nature genetics 45 (1), 25-33, 2013
17952013
Diagnostic yield and clinical utility of sequencing familial hypercholesterolemia genes in patients with severe hypercholesterolemia
AV Khera, HH Won, GM Peloso, KS Lawson, TM Bartz, X Deng, ...
Journal of the American College of Cardiology 67 (22), 2578-2589, 2016
9692016
Multi-ethnic genome-wide association study for atrial fibrillation
C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ...
Nature genetics 50 (9), 1225-1233, 2018
6932018
Association analyses based on false discovery rate implicate new loci for coronary artery disease
CP Nelson, A Goel, AS Butterworth, S Kanoni, TR Webb, E Marouli, ...
Nature genetics 49 (9), 1385-1391, 2017
6682017
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
5502022
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
Myocardial Infarction Genetics Consortium Investigators
New England Journal of Medicine 371 (22), 2072-2082, 2014
4802014
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
4232016
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
KG Aragam, T Jiang, A Goel, S Kanoni, BN Wolford, DS Atri, EM Weeks, ...
Nature genetics 54 (12), 1803-1815, 2022
4092022
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
M Dichgans, R Malik, IR König, J Rosand, R Clarke, S Gretarsdottir, ...
Stroke 45 (1), 24-36, 2014
3992014
A decade of genome-wide association studies for coronary artery disease: the challenges ahead
J Erdmann, T Kessler, L Munoz Venegas, H Schunkert
Cardiovascular research 114 (9), 1241-1257, 2018
3662018
Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease
TR Webb, J Erdmann, KE Stirrups, NO Stitziel, NGD Masca, H Jansen, ...
Journal of the American College of Cardiology 69 (7), 823-836, 2017
2632017
Phenotypic characterization of genetically lowered human lipoprotein (a) levels
CA Emdin, AV Khera, P Natarajan, D Klarin, HH Won, GM Peloso, ...
Journal of the American College of Cardiology 68 (25), 2761-2772, 2016
2312016
Predictors of permanent pacemaker implantations and new-onset conduction abnormalities with the SAPIEN 3 balloon-expandable transcatheter heart valve
O Husser, C Pellegrini, T Kessler, C Burgdorf, H Thaller, NP Mayr, ...
JACC: Cardiovascular Interventions 9 (3), 244-254, 2016
1962016
Association of rare and common variation in the lipoprotein lipase gene with coronary artery disease
AV Khera, HH Won, GM Peloso, C O’Dushlaine, D Liu, NO Stitziel, ...
Jama 317 (9), 937-946, 2017
1952017
The impact of genome‐wide association studies on the pathophysiology and therapy of cardiovascular disease
T Kessler, B Vilne, H Schunkert
EMBO molecular medicine 8 (7), 688-701, 2016
1882016
Pro-angiogenic macrophage phenotype to promote myocardial repair
B Ferraro, G Leoni, R Hinkel, S Ormanns, N Paulin, A Ortega-Gomez, ...
Journal of the American College of Cardiology 73 (23), 2990-3002, 2019
1642019
ADAMTS-7 inhibits re-endothelialization of injured arteries and promotes vascular remodeling through cleavage of thrombospondin-1
T Kessler, L Zhang, Z Liu, X Yin, Y Huang, Y Wang, Y Fu, M Mayr, Q Ge, ...
Circulation 131 (13), 1191-1201, 2015
1502015
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
Interleukin 1 Genetics Consortium
The Lancet Diabetes & Endocrinology 3 (4), 243-253, 2015
1222015
Associations of autozygosity with a broad range of human phenotypes
DW Clark, Y Okada, KHS Moore, D Mason, N Pirastu, I Gandin, ...
Nature communications 10 (1), 4957, 2019
1172019
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