UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (23) 23
humans (22) 22
life sciences & biomedicine (17) 17
genome-wide association study (15) 15
genomes (15) 15
risk factors (14) 14
polymorphism, single nucleotide (12) 12
atherosclerosis (11) 11
female (10) 10
male (10) 10
middle aged (10) 10
aged (9) 9
abridged index medicus (7) 7
cardiovascular disease (7) 7
cardiovascular diseases (7) 7
cohort studies (7) 7
genetic predisposition to disease (7) 7
heart diseases (7) 7
medical and health sciences (7) 7
medicin och hälsovetenskap (7) 7
genetics (6) 6
heart rate (6) 6
multidisciplinary sciences (6) 6
quantitative trait loci (6) 6
science (6) 6
science & technology - other topics (6) 6
adult (5) 5
arteriosclerosis (5) 5
atherosclerosis - genetics (5) 5
blood pressure (5) 5
clinical neurology (5) 5
coronary artery disease (5) 5
gene expression (5) 5
genetics & heredity (5) 5
genomics (5) 5
neurology (5) 5
neurosciences & neurology (5) 5
single-nucleotide polymorphism (5) 5
stroke (5) 5
studies (5) 5
animals (4) 4
basic medicine (4) 4
cardiac and cardiovascular systems (4) 4
cholesterol (4) 4
clinical medicine (4) 4
gene sequencing (4) 4
genetic aspects (4) 4
genetic variation (4) 4
genome-wide association study - methods (4) 4
health risk assessment (4) 4
heart (4) 4
hispanic americans (4) 4
kardiologi (4) 4
klinisk medicin (4) 4
loci (4) 4
low density lipoprotein (4) 4
medical genetics (4) 4
medicinsk genetik (4) 4
minority & ethnic groups (4) 4
research (4) 4
stroke - genetics (4) 4
triglycerides (4) 4
adolescent (3) 3
aged, 80 and over (3) 3
biochemistry, genetics and molecular biology (3) 3
cardiac & cardiovascular systems (3) 3
cardiovascular system (3) 3
cardiovascular system & cardiology (3) 3
chemistry (3) 3
cholesterol, ldl - blood (3) 3
european continental ancestry group - genetics (3) 3
gene frequency (3) 3
gene loci (3) 3
genealogy (3) 3
general & internal medicine (3) 3
genetic loci (3) 3
genetic research (3) 3
genome-wide association (3) 3
genotype (3) 3
health aspects (3) 3
health risks (3) 3
lipids (3) 3
lipoproteins (3) 3
medical imaging (3) 3
meta-analysis (3) 3
metaanalysis (3) 3
mortality (3) 3
neurosciences (3) 3
phenotype (3) 3
physics and astronomy (3) 3
research article (3) 3
young adult (3) 3
3111 biomedicine (2) 2
african americans (2) 2
age (2) 2
aortic valve stenosis - genetics (2) 2
apolipoproteins (2) 2
atherosclerosis - epidemiology (2) 2
atherosclerosis - ethnology (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The New England journal of medicine, ISSN 1533-4406, 02/2013, Volume 368, Issue 6, pp. 503 - 512
Journal Article
Journal Article
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 11/2014, Volume 312, Issue 17, pp. 1764 - 1771
Journal Article
Arthritis & rheumatology (Hoboken, N.J.), ISSN 2326-5191, 06/2017, Volume 69, Issue 6, pp. 1294 - 1305
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 2017, Volume 69, Issue 24, pp. 2941 - 2948
Abstract Background Mitral annular calcium (MAC), commonly identified by cardiac imaging, is associated with cardiovascular events and predisposes to the... 
Cardiovascular | Internal Medicine | mitral valve | lipids | Mendelian randomization | single nucleotide polymorphism | prevention | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Calcinosis - genetics | Calcinosis - diagnosis | Genetic Predisposition to Disease | Prospective Studies | Follow-Up Studies | Humans | Middle Aged | Risk Factors | Male | Tomography, X-Ray Computed | Incidence | Mitral Valve Insufficiency - diagnosis | Mitral Valve Insufficiency - genetics | Polymorphism, Genetic | Genetic Variation | Mitral Valve - diagnostic imaging | Triglycerides - blood | Female | Aged | Triglycerides - genetics | Calcinosis - metabolism | Mitral Valve Insufficiency - metabolism | Medical colleges | Pharmacogenetics | Genetic research | Triglycerides | Research institutes | Cardiology | Epidemiology | Biometry | Public health | Analysis | Calcification (ectopic) | Heart | Calcium | Hispanic Americans | Stenosis | Lipids | Cardiovascular disease | Risk factors | Consortia | Randomization | Imaging | Atherosclerosis | Regurgitation | Genetics | Robustness | Rheumatic heart disease | Heart diseases | Age | Mitral valve | Sensitivity analysis | Medical imaging | Metabolism | Gene expression | Apolipoproteins | Minority & ethnic groups | Estimates | Low density lipoprotein | Cholesterol | Studies | Pleiotropy | Sensitivity | Ethnicity | Womens health | Arteriosclerosis | Calcification | Determinants | Replication | Health risk assessment | Index Medicus | Abridged Index Medicus
Journal Article
by Traylor, Matthew and Malik, Rainer and Nalls, Mike A and Cotlarciuc, Ioana and Radmanesh, Farid and Thorleifsson, Gudmar and Hanscombe, Ken B and Langefeld, Carl and Saleheen, Danish and Rost, Natalia S and Yet, Idil and Spector, Tim D and Bell, Jordana T and Hannon, Eilis and Mill, Jonathan and Chauhan, Ganesh and Debette, Stephanie and Bis, Joshua C and Longstreth, W.T and Ikram, M. Arfan and Launer, Lenore J and Seshadri, Sudha and Hamilton-Bruce, Monica Anne and Jimenez-Conde, Jordi and Cole, John W and Schmidt, Reinhold and Słowik, Agnieszka and Lemmens, Robin and Lindgren, Arne and Melander, Olle and Grewal, Raji P and Sacco, Ralph L and Rundek, Tatjana and Rexrode, Kathryn and Arnett, Donna K and Johnson, Julie A and Benavente, Oscar R and Wasssertheil-Smoller, Sylvia and Lee, Jin-Moo and Pulit, Sara L and Wong, Quenna and Rich, Stephen S and de Bakker, Paul I.W and McArdle, Patrick F and Woo, Daniel and Anderson, Christopher D and Xu, Huichun and Heitsch, Laura and Fornage, Myriam and Jern, Christina and Stefansson, Kari and Thorsteinsdottir, Unnur and Gretarsdottir, Solveig and Lewis, Cathryn M and Sharma, Pankaj and Sudlow, Cathie L.M and Rothwell, Peter M and Boncoraglio, Giorgio B and Thijs, Vincent and Levi, Chris and Meschia, James F and Rosand, Jonathan and Kittner, Steven J and Mitchell, Braxton D and Dichgans, Martin and Worrall, Bradford B and Markus, Hugh S and on behalf of the International Stroke Genetics Consortium and METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium and UK Young Lacunar DNA Study and NINDS Stroke Genetics Network and METASTROKE and Neurology Working Grp CHARGE Conso and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Institutionen för biomedicin, avdelningen för patologi and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Pathology and Sahlgrenska Academy
Annals of neurology, ISSN 0364-5134, 03/2017, Volume 81, Issue 3, pp. 383 - 394
Journal Article
Nature genetics, ISSN 1546-1718, 10/2019, Volume 51, Issue 11, pp. 1580 - 1587
...] , Xiaoling Zhang [sup.4] [sup.5] [sup.6] , Florian Wunderer [sup.7] [sup.8] , Albert V. Smith [sup.9] [sup.10] , Quenna Wong [sup.11] , Sonali Pechlivanis [sup.12... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Muscle, Smooth, Vascular - metabolism | Atherosclerosis - genetics | Humans | Middle Aged | Vascular Calcification - genetics | Male | Aorta - metabolism | GTPase-Activating Proteins - metabolism | Repressor Proteins - physiology | Vascular Calcification - metabolism | Female | Repressor Proteins - metabolism | Atherosclerosis - pathology | Genetic Predisposition to Disease | Genome-Wide Association Study | Histone Deacetylases - genetics | Mice, Inbred C57BL | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Vascular Calcification - pathology | Atherosclerosis - metabolism | Mice, Knockout | Aorta - pathology | Muscle, Smooth, Vascular - pathology | Phenotype | Animals | Muscle Contraction | Aged | Mice | Polymorphism, Single Nucleotide | GTPase-Activating Proteins - genetics | Histone Deacetylases - physiology | Cohort Studies | Evaluation | Genome-wide association studies | Smooth muscle | Genetic aspects | Single nucleotide polymorphisms | Cardiovascular diseases | Health aspects | Risk factors | Calcification (ectopic) | Heart | Phenotypes | Hispanic Americans | Muscles | African Americans | Genomes | Thorax | Single-nucleotide polymorphism | Gene expression | Muscle contraction | Loci | Abdomen | Meta-analysis | Proteins | Signal transduction | Arteriosclerosis | Coronary vessels | Atherosclerosis | Calcification | Aorta | Gene loci | Inhibition | Index Medicus
Journal Article
by Pulit, Sara L and McArdle, Patrick F and Wong, Quenna and Malik, Rainer and Gwinn, Katrina and Achterberg, Sefanja and Algra, Ale and Amouyel, Philippe and Anderson, Christopher D and Arnett, Donna K and Arsava, Ethem Murat and Attia, John and Ay, Hakan and Bartz, Traci M and Battey, Thomas and Benavente, Oscar R and Bevan, Steve and Biffi, Alessandro and Bis, Joshua C and Blanton, Susan H and Boncoraglio, Giorgio B and Brown, Robert D and Burgess, Annette I and Carrera, Caty and Chapman Smith, Sherita N and Chasman, Daniel I and Chauhan, Ganesh and Chen, Wei-Min and Cheng, Yu-Ching and Chong, Michael and Cloonan, Lisa K and Cole, John W and Cotlarciuc, Ioana and Cruchaga, Carlos and Cuadrado-Godia, Elisa and Dave, Tushar and Dawson, Jesse and Debette, Stéphanie and Delavaran, Hossein and Dell, Cameron A and Dichgans, Martin and Doheny, Kimberly F and Dong, Chuanhui and Duggan, David J and Engström, Gunnar and Evans, Michele K and Pallejà, Xavier Estivill and Faul, Jessica D and Fernández-Cadenas, Israel and Fornage, Myriam and Frossard, Philippe M and Furie, Karen and Gamble, Dale M and Gieger, Christian and Giese, Anne-Katrin and Giralt-Steinhauer, Eva and González, Hector M and Goris, An and Gretarsdottir, Solveig and Grewal, Raji P and Grittner, Ulrike and Gustafsson, Stefan and Han, Buhm and Hankey, Graeme J and Heitsch, Laura and Higgins, Peter and Hochberg, Marc C and Holliday, Elizabeth and Hopewell, Jemma C and Horenstein, Richard B and Howard, George and Ikram, M Arfan and Ilinca, Andreea and Ingelsson, Erik and Irvin, Marguerite R and Jackson, Rebecca D and Jern, Christina and Conde, Jordi Jiménez and Johnson, Julie A and Jood, Katarina and Kahn, Muhammad S and Kaplan, Robert and Kappelle, L Jaap and Kardia, Sharon L R and Keene, Keith L and Kissela, Brett M and Kleindorfer, Dawn O and Koblar, Simon and Labovitz, Daniel and Launer, Lenore J and Laurie, Cathy C and Laurie, Cecelia A and Lee, Cue Hyunkyu and Lee, Jin-Moo and Lehm, Manuel and Lemmens, Robin and Levi, Christopher and Leys, Didier and Lindgren, Arne and Longstreth, W T and ... and International Stroke Genetics Consortium (ISGC) and NINDS Stroke Genetics Network (SiGN) and NINDS Stroke Genetics Network SiGN and ISGC and Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering and Institute of Neuroscience and Physiology and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Pathology and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy and Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation and Institutionen för biomedicin, avdelningen för patologi and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi
Lancet neurology, ISSN 1474-4422, 2016, Volume 15, Issue 2, pp. 174 - 184
Journal Article