X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (523) 523
Publication (34) 34
Book / eBook (4) 4
Book Review (4) 4
Conference Proceeding (2) 2
Patent (2) 2
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (237) 237
male (172) 172
female (166) 166
cardiac & cardiovascular systems (123) 123
middle aged (120) 120
aged (114) 114
risk factors (101) 101
genetics (90) 90
adult (77) 77
risk (77) 77
polymorphism, single nucleotide (71) 71
medical and health sciences (67) 67
medicin och hälsovetenskap (66) 66
genome-wide association study (65) 65
genetic aspects (59) 59
mortality (59) 59
genetics & heredity (57) 57
genetic predisposition to disease (54) 54
research (53) 53
case-control studies (52) 52
studies (52) 52
cardiovascular disease (49) 49
myocardial infarction (49) 49
genome-wide association (48) 48
aged, 80 and over (47) 47
cardiovascular (46) 46
genomes (44) 44
internal medicine (44) 44
genotype (43) 43
coronary artery disease (42) 42
coronary artery disease - genetics (40) 40
clinical medicine (38) 38
klinisk medicin (37) 37
treatment outcome (37) 37
medical research (36) 36
abridged index medicus (34) 34
medicine (34) 34
metaanalysis (34) 34
myocardial infarction - genetics (34) 34
analysis (33) 33
cardiology (33) 33
coronary heart disease (33) 33
echocardiography (33) 33
implantation (33) 33
myocardial-infarction (33) 33
association (32) 32
heart valve diseases (32) 32
atherosclerosis (31) 31
peripheral vascular disease (30) 30
replacement (30) 30
disease (29) 29
genomics (29) 29
loci (29) 29
phenotype (29) 29
expression (28) 28
gene expression (28) 28
genes (28) 28
heart (28) 28
stenosis (28) 28
body mass index (27) 27
medicine, general & internal (27) 27
prospective studies (27) 27
aorta (26) 26
heart-disease (26) 26
medical genetics (26) 26
multidisciplinary sciences (26) 26
patients (26) 26
aortic valve (25) 25
heart failure (25) 25
polymorphism, single nucleotide - genetics (25) 25
single nucleotide polymorphisms (25) 25
endocrinology and diabetes (24) 24
endokrinologi och diabetes (24) 24
genetic variation (24) 24
health aspects (24) 24
heart attacks (24) 24
meta-analysis (24) 24
polymorphism (24) 24
time factors (24) 24
aortic valve stenosis - surgery (23) 23
gene frequency (23) 23
physiological aspects (23) 23
prognosis (23) 23
transcatheter aortic valve replacement (23) 23
cholesterol (22) 22
diabetes (22) 22
medicinsk genetik (22) 22
outcomes (22) 22
population (22) 22
cardiac and cardiovascular systems (21) 21
follow-up studies (21) 21
heart diseases (21) 21
hypertension (21) 21
kardiologi (21) 21
stroke (21) 21
coronary vessels (20) 20
electrocardiography (20) 20
research article (20) 20
transcatheter aortic valve implantation (20) 20
consortia (19) 19
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Lancet (British edition), ISSN 0140-6736, 2014, Volume 383, Issue 9933, pp. 1990 - 1998
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2007, Volume 357, Issue 5, pp. 443 - 453
Journal Article
by Surakka, Ida and Horikoshi, Momoko and Mägi, Reedik and Sarin, Antti-Pekka and Mahajan, Anubha and Lagou, Vasiliki and Marullo, Letizia and Ferreira, Teresa and Miraglio, Benjamin and Timonen, Sanna and Kettunen, Johannes and Pirinen, Matti and Karjalainen, Juha and Thorleifsson, Gudmar and Hägg, Sara and Hottenga, Jouke-Jan and Isaacs, Aaron and Ladenvall, Claes and Beekman, Marian and Esko, Tõnu and Ried, Janina S and Nelson, Christopher P and Willenborg, Christina and Gustafsson, Stefan and Westra, Harm-Jan and Blades, Matthew and de Craen, Anton J M and de Geus, Eco J and Deelen, Joris and Grallert, Harald and Hamsten, Anders and Havulinna, Aki S and Hengstenberg, Christian and Houwing-Duistermaat, Jeanine J and Hyppönen, Elina and Karssen, Lennart C and Lehtimäki, Terho and Lyssenko, Valeriya and Magnusson, Patrik K E and Mihailov, Evelin and Müller-Nurasyid, Martina and Mpindi, John-Patrick and Pedersen, Nancy L and Penninx, Brenda W J H and Perola, Markus and Pers, Tune H and Peters, Annette and Rung, Johan and Smit, Johannes H and Steinthorsdottir, Valgerdur and Tobin, Martin D and Tsernikova, Natalia and van Leeuwen, Elisabeth M and Viikari, Jorma S and Willems, Sara M and Willemsen, Gonneke and Schunkert, Heribert and Erdmann, Jeanette and Samani, Nilesh J and Kaprio, Jaakko and Lind, Lars and Gieger, Christian and Metspalu, Andres and Slagboom, P Eline and Groop, Leif and van Duijn, Cornelia M and Eriksson, Johan G and Jula, Antti and Salomaa, Veikko and Boomsma, Dorret I and Power, Christine and Raitakari, Olli T and Ingelsson, Erik and Järvelin, Marjo-Riitta and Thorsteinsdottir, Unnur and Franke, Lude and Ikonen, Elina and Kallioniemi, Olli and Pietiäinen, Vilja and Lindgren, Cecilia M and Stefansson, Kari and Palotie, Aarno and McCarthy, Mark I and Morris, Andrew P and Prokopenko, Inga and Ripatti, Samuli and ENGAGE Consortium
Nature genetics, ISSN 1546-1718, 2015, Volume 47, Issue 6, pp. 589 - 597
Journal Article
by Horikoshi, Momoko and Mӓgi, Reedik and Bunt, Martijn and Surakka, Ida and Sarin, A.-P and Mahajan, Anubha and Marullo, Letizia and Thorleifsson, Gudmar and Hӓgg, Sara and Hottenga, Jouke Jan and Ladenvall, Claes and Ried, Janina and Winkler, Thomas W and Willems, Sara and Pervjakova, Natalia and Esko, Tõnu and Beekman, Marian and Nelson, Christopher P and Willenborg, Christina and Wiltshire, Steven and Ferreira, Teresa and Fernandez, Juan and Gaulton, Kyle and Steinthorsdottir, Valgerdur and Hamsten, Anders and Magnusson, Patrik K. E and Willemsen, Gonneke and Milaneschi, Yuri and Robertson, Neil R and Groves, Christopher and Bennett, Amanda and Lehtimӓki, Terho and Viikari, Jorma and Rung, Johan and Lyssenko, Valeriya and Perola, Markus and Heid, Iris and Herder, Christian and Grallert, Harald and Müller-Nurasyid, Martina and Roden, Michael and Hypponen, Elina and Isaacs, Aaron and Leeuwen, Elisa and Karssen, Lennart and Mihailov, Evelin and Houwing-Duistermaat, Jeanine and De Craen, Anton J. M and Deelen, Joris and Havulinna, Aki and Blades, Matthew and Hengstenberg, Christian and Erdmann, Jeanette and Schunkert, Heribert and Kaprio, Jaakko and Tobin, Martin and Samani, Nilesh and Lind, Lars and Salomaa, Veikko and Lindgren, Cecilia M and Slagboom, Eline and Metspalu, Anes and Duijn, Cornelia and Eriksson, Johan G and Peters, Annette and Gieger, Christian and Jula, Antti and Groop, Leif and Raitakari, Olli T and Power, Christopher and Penninx, Brenda and Geus, Eco and Smit, Johannes and Boomsma, Dorret and Pedersen, Nancy L and Ingelsson, Erik and Thorsteinsdottir, Unnur and Zwart, John-Anker and Ripatti, Samuli and Prokopenko, Inga and McCarthy, Mark and Morris, Anew and Engage Consortium and ENGAGE Consortium
PLoS genetics, ISSN 1553-7390, 01/2015, Volume 11, Issue 7, p. e1005230
Journal Article
by Soranzo, Nicole and Spector, Tim D and Mangino, Massimo and Kühnel, Brigitte and Rendon, Augusto and Teumer, Alexander and Willenborg, Christina and Wright, Benjamin and Chen, Li and Li, Mingyao and Salo, Perttu and Voight, Benjamin F and Burns, Philippa and Laskowski, Roman A and Xue, Yali and Menzel, Stephan and Altshuler, David and Bradley, John R and Bumpstead, Suzannah and Burnett, Mary-Susan and Devaney, Joseph and Döring, Angela and Elosua, Roberto and Epstein, Stephen E and Erber, Wendy and Falchi, Mario and Garner, Stephen F and Ghori, Mohammed J R and Goodall, Alison H and Gwilliam, Rhian and Hakonarson, Hakon H and Hall, Alistair S and Hammond, Naomi and Hengstenberg, Christian and Illig, Thomas and König, Inke R and Knouff, Christopher W and McPherson, Ruth and Melander, Olle and Mooser, Vincent and Nauck, Matthias and Nieminen, Markku S and O'Donnell, Christopher J and Peltonen, Leena and Potter, Simon C and Prokisch, Holger and Rader, Daniel J and Rice, Catherine M and Roberts, Robert and Salomaa, Veikko and Sambrook, Jennifer and Schreiber, Stefan and Schunkert, Heribert and Schwartz, Stephen M and Serbanovic-Canic, Jovana and Sinisalo, Juha and Siscovick, David S and Stark, Klaus and Surakka, Ida and Stephens, Jonathan and Thompson, John R and Völker, Uwe and Völzke, Henry and Watkins, Nicholas A and Wells, George A and Wichmann, H-Erich and Van Heel, David A and Tyler-Smith, Chris and Thein, Swee Lay and Kathiresan, Sekar and Perola, Markus and Reilly, Muredach P and Stewart, Alexandre F R and Erdmann, Jeanette and Samani, Nilesh J and Meisinger, Christa and Greinacher, Andreas and Deloukas, Panos and Ouwehand, Willem H and Gieger, Christian
Nature genetics, ISSN 1546-1718, 2009, Volume 41, Issue 11, pp. 1182 - 1190
Journal Article
PloS one, ISSN 1932-6203, 2008, Volume 3, Issue 8, p. e2986
..., Leicester, United Kingdom Christian Hengstenberg Affiliation: Klinik und Poliklinik für Innere Medizin II, Universität Regensburg, Regensburg, Germany Klaus Stark... 
METAANALYSIS | THERAPY | EVENTS | MULTIDISCIPLINARY SCIENCES | PHENOTYPE | POLYMORPHISM | HYPERCHOLESTEROLEMIA | PREVALENCE | ASSOCIATION | Receptors, LDL - genetics | Oligonucleotide Array Sequence Analysis | Risk Assessment | Humans | Risk Factors | Cholesterol, LDL - drug effects | Chromosome Mapping | Random Allocation | Case-Control Studies | Genetic Variation | Cholesterol, LDL - genetics | Coronary Disease - prevention & control | Anticholesteremic Agents - therapeutic use | Coronary Disease - genetics | Cholesterol, LDL - blood | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 10 | Medical research | Hypercholesterolemia | Blood cholesterol | Low density lipoproteins | Genes | Medicine, Experimental | Genetic research | Genetics | Genetic aspects | Single nucleotide polymorphisms | Coronary heart disease | Risk factors | Lipoproteins (low density) | Risk | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Gene polymorphism | Epidemiology | Consortia | Confidence intervals | Randomization | Population | Lipoprotein (low density) receptors | Children | Heart diseases | Statistical analysis | Mortality | Coronary artery | Health risks | Environmental health | Genetic diversity | Regression analysis | Metabolism | LDLR gene | Apolipoproteins | Coronary artery disease | Low density lipoprotein | Cholesterol | Studies | Genetic variance | Hospitals | Coronary vessels | Alleles | Biomarkers | Receptor density | Adults | Mutation | Polymorphism
Journal Article
by Webb, Thomas R and Erdmann, Jeanette and Stirrups, Kathleen E and Stitziel, Nathan O and Masca, Nicholas G.D and Jansen, Henning and Kanoni, Stavroula and Nelson, Christopher P and Ferrario, Paola G and König, Inke R and Eicher, John D and Johnson, Andrew D and Hamby, Stephen E and Betsholtz, Christer and Ruusalepp, Arno and Franzén, Oscar and Schadt, Eric E and Björkegren, Johan L.M and Weeke, Peter E and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenborg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S.F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Pier A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian and El-Mokhtari, Nour Eddine and Franke, Andre and Heilmann, Stefanie and Hengstenberg, Christian and Hoffmann, Per and Holmen, Oddgeir L and Hveem, Kristian and Jansson, Jan-Håkan and Jöckel, Karl-Heinz and Kessler, Thorsten and Kriebel, Jennifer and Laugwitz, Karl L and Marouli, Eirini and Martinelli, Nicola and McCarthy, Mark I and Van Zuydam, Natalie R and Meisinger, Christa and Esko, Tõnu and Mihailov, Evelin and Escher, Stefan A and Alver, Maris and Moebus, Susanne and Morris, Andrew D and Virtamo, Jarma and Nikpay, Majid and Olivieri, Oliviero and Provost, Sylvie and AlQarawi, Alaa and Robertson, Neil R and Akinsansya, Karen O and Reilly, Dermot F and Vogt, Thomas F and Yin, Wu and Asselbergs, Folkert W and Kooperberg, Charles and Jackson, Rebecca D and Stahl, Eli and Müller-Nurasyid, Martina and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Chowdhury, Rajiv and Salomaa, Veikko and Ford, Ian and Jukema, J. Wouter and Amouyel, Philippe and Kontto, Jukka and Nordestgaard, Børge G and Ferrières, Jean and Saleheen, Danish and Sattar, Naveed and Surendran, Praveen and Wagner, Aline and Young, Robin and Howson, Joanna M.M and ... and Wellcome Trust Case Control Consortium and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators and MORGAM Investigators and Wellcome Trust Case Control and Myocardial Infarction Genetics
Journal of the American College of Cardiology, ISSN 0735-1097, 2017, Volume 69, Issue 7, pp. 823 - 836
Abstract Background Genome-wide association studies have so far identified 56 loci associated with risk of coronary artery disease (CAD). Many CAD loci show... 
Cardiovascular | Internal Medicine | expression quantitative trait loci | genetics | genome-wide association | single nucleotide polymorphism | cholesteryl ester transfer protein | SR-BI | CARDIAC & CARDIOVASCULAR SYSTEMS | METAANALYSIS | CETP MASS | SUSCEPTIBILITY | RISK | PHOSPHOLIPASE A | VARIANT | SCAVENGER RECEPTOR | ABDOMINAL AORTIC-ANEURYSM | Genome-Wide Association Study | Gene Frequency | Humans | Coronary Artery Disease - genetics | Female | Male | Coronary Artery Disease - epidemiology | Genetic Pleiotropy | Polymorphism, Single Nucleotide | Genetic Loci | Odds Ratio | Case-Control Studies | Coronary heart disease | Analysis | Genealogy | Cardiovascular disease | Genomes | Metabolism | Gene expression | Blood | Risk factors | Studies | Celiac disease | Lipoproteins | Coronary vessels | Rheumatoid arthritis | Quality control | Calcification | Diabetes | Bioinformatics | LD, linkage disequilibrium | CETP, cholesteryl ester transfer protein | eQTL, expression quantitative trait locus | CAD, coronary artery disease | GWAS, genome-wide association study | BMI, body mass index | SNP, single nucleotide polymorphism | HDL, high-density lipoprotein | LDL, low-density lipoprotein | Original Investigation | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article