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10084 (27) 27
index medicus (15) 15
cardiac & cardiovascular systems (13) 13
genetics (13) 13
peripheral vascular disease (11) 11
original (10) 10
risk factors (10) 10
genetics & heredity (9) 9
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10090 (7) 7
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10034 (6) 6
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protein (3) 3
risk (3) 3
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dk/atira/pure/researchoutput/pubmedpublicationtype/d016428 (2) 2
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Circulation, ISSN 0009-7322, 06/2019, Volume 139, Issue 24, pp. 2754 - 2764
BACKGROUND:There is great interest in widening the use of high-sensitivity cardiac troponins for population cardiovascular disease (CVD) and heart failure... 
Genetic aspects | Diagnosis | Cardiovascular diseases | Patient outcomes | troponin T | 10071 | risk factors | genetics | 10062 | 10084 | troponin | cardiovascular diseases | 10058 | Original s
Journal Article
Circulation. Cardiovascular Genetics, ISSN 1942-325X, 10/2016, Volume 9, Issue 5, pp. 419 - 425
Supplemental Digital Content is available in the text. 
10090 | mutation | 10084 | alternative splicing | Original | confusion | human | dilated cardiomyopathy
Journal Article
Circulation, ISSN 0009-7322, 04/2019, Volume 139, Issue 15, pp. 1786 - 1797
BACKGROUND:Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disorder characterized by myocardial fibrofatty replacement and an increased risk... 
death, sudden, cardiac | cardiomyopathies | arrhythmogenic right ventricular dysplasia | Cardiomyopathy | Patient outcomes | Heart ventricle, Left | Genetic aspects | Heart diseases | Health aspects | Risk factors | 10090 | 10084 | Original s | 10005
Journal Article
Stroke, ISSN 0039-2499, 02/2019, Volume 50, Issue 2, pp. 283 - 290
BACKGROUND AND PURPOSE—Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common monogenic form... 
leukoencephalopathy | migraine with aura | magnetic resonance imaging | brain | encephalopathy | Development and progression | CADASIL | Diagnosis | Statistics | Encephalopathy | Risk factors | 10084 | 10171 | Original Contributions | 10041 | 10173
Journal Article
Journal Article
Stroke, ISSN 0039-2499, 12/2017, Volume 49, Issue 1, pp. 54 - 61
BACKGROUND AND PURPOSE—A variant in the histone deacetylase 9 (HDAC9) gene is associated with large artery stroke. Therefore, inhibiting HDAC9 might offer a... 
genetics | secondary prevention | survival analysis | histone deacetylase | stroke | sodium valproate | TRIAL | ATHEROSCLEROSIS | PERIPHERAL VASCULAR DISEASE | CLINICAL NEUROLOGY | Index Medicus | 10084 | 10072 | Original Contributions | 10178 | 10188
Journal Article
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 08/2018, Volume 38, Issue 8, pp. 1837 - 1844
OBJECTIVE—Genome-wide association studies have revealed a robust association between genetic variation on chromosome 15q26.1 and coronary artery disease (CAD)... 
coronary artery disease | monocytes | macrophages | furin | polymorphism, single nucleotide | APOPTOSIS | ACTIVATION | WALL | ATHEROSCLEROSIS | polymorphism | LOCI | CLEAVAGE | PROPROTEIN CONVERTASES | ENZYME | single nucleotide | PERIPHERAL VASCULAR DISEASE | GROWTH-FACTOR | HEMATOLOGY | Index Medicus | 10081 | 10084 | 10189 | Basic Sciences
Journal Article
by Jones, G.T and Tromp, G and Kuivaniemi, H and Gretarsdottir, S and Baas, A.F and Giusti, B and Strauss, E and Hof, F.N. van 't and Webb, T.R and Erdman, R and Ritchie, M.D and Elmore, J.R and Verma, A and Pendergrass, S and Kullo, I.J and Ye, Z and Peissig, P.L and Gottesman, O and Verma, S.S and Malinowski, J and Rasmussen-Torvik, L.J and Borthwick, K.M and Smelser, D.T and Crosslin, D.R and Anade, M. de and Ryer, E.J and McCarty, C.A and Bottinger, E.P and Pacheco, J.A and Crawford, D.C and Carrell, D.S and Gerhard, G.S and Franklin, D.P and Carey, D.J and Phillips, V.L and Williams, M.J and Wei, W and Blair, R and Hill, A.A and Vasudevan, T.M and Lewis, D.R and Thomson, I.A and Krysa, J and Hill, G.B and Roake, J and Merriman, T.R and Oszkinis, G and Galora, S and Saracini, C and Abbate, R and Pulli, R and Pratesi, C and Saratzis, A and Verissimo, A.R and Bumpstead, S and Badger, S.A and Clough, R.E and Cockerill, G and Hafez, H and Scott, D.J and Futers, T.S and Romaine, S.P and Bridge, K and Griffin, K.J and Bailey, M.A and Smith, A and Thompson, M.M and Bockxmeer, F.M. van and Matthiasson, S.E and Thorleifsson, G and Thorsteinsdottir, U and Blankensteijn, J.D and Teijink, J.A and Wijmenga, C and Graaf, J. de and Kiemeney, L.A.L.M and Lindholt, J.S and Hughes, A and Bradley, D.T and Stirrups, K and Golledge, J and Norman, P.E and Powell, J.T and Humphries, S.E and Hamby, S.E and Goodall, A.H and Nelson, C.P and Sakalihasan, N and Courtois, A and Ferrell, R.E and Eriksson, P and Folkersen, L and Franco-Cereceda, A and Eicher, J.D and Johnson, A.D and Betsholtz, C and Ruusalepp, A and Franzen, O and Schadt, E.E and Bjorkegren, J.L and ... and Cardiogenics Consortium and Int Consortium Blood Pressure and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet and Vaskulärbiologi
Circulation Research, ISSN 0009-7330, 2017, Volume 120, Issue 2, pp. 341 - 353
RATIONALE: Abdominal aortic aneurysm (AAA) is a complex disease with both genetic and environmental risk factors. Together, 6 previously identified risk loci... 
computational biology | meta-analysis | genetics | aortic aneurysm abdominal | matrix metalloproteinases | genome-wide association study | C-REACTIVE PROTEIN | TRANSCRIPTION FACTORS | CARDIAC & CARDIOVASCULAR SYSTEMS | SEQUENCE VARIANT | aortic aneurysm, abdominal | SUSCEPTIBILITY LOCI | ELECTRONIC MEDICAL-RECORDS | HUMAN PREFRONTAL CORTEX | DENSITY-LIPOPROTEIN CHOLESTEROL | PERIPHERAL VASCULAR DISEASE | CANDIDATE GENE ASSOCIATION | HEMATOLOGY | RECEPTOR-RELATED PROTEIN-1 | CORONARY-ARTERY-DISEASE | Aortic Aneurysm, Abdominal - diagnosis | Genetic Predisposition to Disease - genetics | Humans | Genetic Loci - genetics | Genome-Wide Association Study - trends | Aortic Aneurysm, Abdominal - genetics | Genetic Variation - genetics | Aortic Aneurysm, Abdominal - epidemiology | Genetic Predisposition to Disease - epidemiology | Genome-Wide Association Study - methods | Diabetes mellitus | Coronary artery | Aneurysm | Aneurysms | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Risk factors | Gelatinase B | Chromosome 1 | Interleukin 6 | Interleukin 6 receptors | Aorta | Lipoprotein (low density) receptors | Blood pressure | Chromosome 13 | Heritability | Cardiovascular diseases | Heart diseases | Index Medicus | 10082 | Clinical Track | 10084 | 10185 | 10195 | 10014 | Medical and Health Sciences | Hematology | Medicin och hälsovetenskap | Klinisk medicin | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | aortic aneurysm | Hematologi | abdominal
Journal Article