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Nature genetics, ISSN 1546-1718, 2016, Volume 48, Issue 10, pp. 1279 - 1283
We describe a reference panel of 64,976 human haplotypes at 39,235,157 SNPs constructed using whole-genome sequence data from 20 studies of predominantly... 
POPULATION | RARE VARIANTS | SEQUENCE | GENOME-WIDE ASSOCIATION | Studies | Datasets | Haplotypes | Consortia | Accuracy | Genealogy | Researchers | Genomics | Collaboration | Genomes | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Lancet, The, ISSN 0140-6736, 2017, Volume 389, pp. S53 - S53
Abstract Background A genetic overlap between type 2 diabetes and depression has been reported in twin studies, but the finding has not been replicated with... 
Internal Medicine | Type 2 diabetes | Genomics | Genetic aspects | Medical research | Analysis | Depression, Mental | Medicine, Experimental
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 02/2017, Volume 25, Issue 2, pp. 240 - 245
Journal Article
PLoS medicine, ISSN 1549-1676, 2019, Volume 16, Issue 12, p. e1002982
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 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
PLoS genetics, ISSN 1553-7404, 2018, Volume 14, Issue 12, p. e1007813
Journal Article
PLoS genetics, ISSN 1553-7404, 2019, Volume 15, Issue 10, p. e1008405
...Author(s): Jenny C. Censin 1,2, Sanne A. E. Peters 3,4, Jonas Bovijn 1,2, Teresa Ferreira 1, Sara L. Pulit 1,5,6, Reedik Magi 7, Anubha Mahajan 2,8, Michael V... 
MENDELIAN RANDOMIZATION ANALYSIS | DIABETES-MELLITUS | WAIST CIRCUMFERENCE | CARDIOMETABOLIC TRAITS | FATTY LIVER-DISEASE | INSTRUMENTAL VARIABLES | GENETICS & HEREDITY | CARDIOVASCULAR-DISEASE | BODY-MASS INDEX | GENETIC-VARIANTS | CORONARY-HEART-DISEASE | Pulmonary Disease, Chronic Obstructive - mortality | Blood Pressure - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Male | Pulmonary Disease, Chronic Obstructive - pathology | Obesity - genetics | Cause of Death | Neoplasms | Coronary Artery Disease - pathology | Mendelian Randomization Analysis | Female | Obesity - mortality | Waist-Hip Ratio | Diabetes Mellitus, Type 2 - complications | Pulmonary Disease, Chronic Obstructive - genetics | Body Mass Index | Genome-Wide Association Study | Stroke | Obesity - complications | Risk Factors | Coronary Artery Disease - mortality | Pulmonary Disease, Chronic Obstructive - complications | Adiposity - genetics | Obesity - pathology | Coronary Artery Disease - complications | Diabetes Mellitus, Type 2 - mortality | Coronary Artery Disease - genetics | Aged | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 2 - pathology | Type 2 diabetes | Obesity | Liver diseases | Communicable diseases | Liver | Lung cancer | Mortality | United Kingdom | Coronary heart disease | Stroke (Disease) | Body mass index | Chronic kidney failure | Analysis | Colorectal cancer | Cardiovascular disease | Genomes | Epidemiology | Population genetics | Fatty liver | Ischemia | Chronic obstructive pulmonary disease | Blood pressure | Diabetes mellitus (non-insulin dependent) | Heart diseases | Public health | Lung diseases | Coronary artery | Big Data | Sex differences | Gender differences | Breast cancer | Hip | Medicine | Studies | Genetic variance | Womens health | Obstructive lung disease | Renal failure | Death | Software | Diabetes | Kidney diseases | Health risk assessment | Methods
Journal Article
by Gusarova, Viktoria and O’Dushlaine, Colm and Teslovich, Tanya M and Benotti, Peter N and Mirshahi, Tooraj and Gottesman, Omri and Van Hout, Cristopher V and Murray, Michael F and Mahajan, Anubha and Nielsen, Jonas B and Fritsche, Lars and Wulff, Anders Berg and Gudbjartsson, Daniel F and Sjögren, Marketa and Emdin, Connor A and Scott, Robert A and Lee, Wen-Jane and Small, Aeron and Kwee, Lydia C and Dwivedi, Om Prakash and Prasad, Rashmi B and Bruse, Shannon and Lopez, Alexander E and Penn, John and Marcketta, Anthony and Leader, Joseph B and Still, Christopher D and Kirchner, H. Lester and Mirshahi, Uyenlinh L and Wardeh, Amr H and Hartle, Cassandra M and Habegger, Lukas and Fetterolf, Samantha N and Tusie-Luna, Teresa and Morris, Andrew P and Holm, Hilma and Steinthorsdottir, Valgerdur and Sulem, Patrick and Thorsteinsdottir, Unnur and Rotter, Jerome I and Chuang, Lee-Ming and Damrauer, Scott and Birtwell, David and Brummett, Chad M and Khera, Amit V and Natarajan, Pradeep and Orho-Melander, Marju and Flannick, Jason and Lotta, Luca A and Willer, Cristen J and Holmen, Oddgeir L and Ritchie, Marylyn D and Ledbetter, David H and Murphy, Andrew J and Borecki, Ingrid B and Reid, Jeffrey G and Overton, John D and Hansson, Ola and Groop, Leif and Shah, Svati H and Kraus, William E and Rader, Daniel J and Chen, Yii-Der I and Hveem, Kristian and Wareham, Nicholas J and Kathiresan, Sekar and Melander, Olle and Stefansson, Kari and Nordestgaard, Børge G and Tybjærg-Hansen, Anne and Abecasis, Goncalo R and Altshuler, David and Florez, Jose C and Boehnke, Michael and McCarthy, Mark I and Yancopoulos, George D and Carey, David J and Shuldiner, Alan R and Baras, Aris and Dewey, Frederick E and Gromada, Jesper
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 2252 - 11
Angiopoietin-like 4 (ANGPTL4) is an endogenous inhibitor of lipoprotein lipase that modulates lipid levels, coronary atherosclerosis risk, and nutrient... 
HEART-DISEASE | REMNANT CHOLESTEROL | PLASMA-LIPIDS | MULTIDISCIPLINARY SCIENCES | MICE | ANGIOPOIETIN-LIKE PROTEIN-4 | LIPOPROTEIN-LIPASE | HAN CHINESE | CHINESE POPULATION | GENOME-WIDE ASSOCIATION | ADIPOSE-TISSUE | Diabetes Mellitus, Type 2 - genetics | Humans | Homeostasis | Male | Diabetes Mellitus, Type 2 - metabolism | Case-Control Studies | Genetic Variation | Diabetes Mellitus, Type 2 - etiology | Female | Lipoprotein Lipase - metabolism | Genetic Association Studies | Mice, Inbred C57BL | Risk Factors | Gene Silencing | Angiopoietin-like 4 Protein - deficiency | Mice, Knockout | Whole Exome Sequencing | Animals | Insulin Resistance - genetics | Angiopoietin-like 4 Protein - metabolism | Heterozygote | Mice | Blood Glucose - metabolism | Amino Acid Substitution | Angiopoietin-like 4 Protein - genetics | Deactivation | Angiopoietin | Diabetes mellitus | Health risks | Risk reduction | Risk | Lipoprotein lipase | Glucose | Lipase | Inactivation | Insulin | Proteins | Confidence intervals | Sensitivity | Nutrient loss | Rodents | Arteriosclerosis | Atherosclerosis | Genetics | Diabetes | Diabetes mellitus (non-insulin dependent) | Medicinsk genetik | Basic Medicine | Medical Genetics | Clinical Medicine | Medical and Health Sciences | Endokrinologi och diabetes | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Endocrinology and Diabetes
Journal Article