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The New England journal of medicine, ISSN 1533-4406, 08/2017, Volume 377, Issue 9, pp. 839 - 848
Journal Article
by van Zuydam, Natalie R and Ahlqvist, Emma and Sandholm, Niina and Deshmukh, Harshal and Rayner, N. William and Abdalla, Moustafa and Ladenvall, Claes and Ziemek, Daniel and Fauman, Eric and Robertson, Neil R and McKeigue, Paul M and Valo, Erkka and Forsblom, Carol and Harjutsalo, Valma and Perna, Annalisa and Rurali, Erica and Marcovecchio, M. Loredana and Igo, Robert P and Salem, Rany M and Perico, Norberto and Lajer, Maria and Käräjämäki, Annemari and Imamura, Minako and Kubo, Michiaki and Takahashi, Atsushi and Sim, Xueling and Liu, Jianjun and van Dam, Rob M and Jiang, Guozhi and Tam, Claudia H.T and Luk, Andrea O.Y and Lee, Heung Man and Lim, Cadmon K.P and Szeto, Cheuk Chun and So, Wing Yee and Chan, Juliana C.N and Ang, Su Fen and Dorajoo, Rajkumar and Wang, Ling and Clara, Tan Si Hua and McKnight, Amy-Jayne and Duffy, Seamus and Pezzolesi, Marcus G and Marre, Michel and Gyorgy, Beata and Hadjadj, Samy and Hiraki, Linda T and Ahluwalia, Tarunveer S and Almgren, Peter and Schulz, Christina-Alexandra and Orho-Melander, Marju and Linneberg, Allan and Christensen, Cramer and Witte, Daniel R and Grarup, Niels and Brandslund, Ivan and Melander, Olle and Paterson, Andrew D and Tregouet, David and Maxwell, Alexander P and Lim, Su Chi and Ma, Ronald C.W and Tai, E Shyong and Maeda, Shiro and Lyssenko, Valeriya and Tuomi, Tiinamaija and Krolewski, Andrzej S and Rich, Stephen S and Hirschhorn, Joel N and Florez, Jose C and Dunger, David and Pedersen, Oluf and Hansen, Torben and Rossing, Peter and Remuzzi, Giuseppe and Brosnan, Mary Julia and Palmer, Colin N.A and Groop, Per-Henrik and Colhoun, Helen M and Groop, Leif C and McCarthy, Mark I and Warren 3 and Genetics of Kidneys in Diabetes (GoKinD) Study Group and Hong Kong Diabetes Registry Theme-based Research Scheme Project Group and Diabetes Control and Complications Trial (DCCT)/Epidemiology of Diabetes Interventions and Complications (EDIC) Research Group and GENIE (GEnetics of Nephropathy an International Effort) Consortium and Finnish Diabetic Nephropathy Study (FinnDiane) and SUrrogate markers for Micro- and Macrovascular hard endpoints for Innovative diabetes Tools (SUMMIT) Consortium and SUrrogate Markers Micro Macrovascu and Warren 3 Genetics Kidneys Diabet and Hong Kong Diabet Registry Theme and Finnish Diabetic Nephropathy Study and Epidemiology Diabet Interventions and Diabet Control Complications Trial and GENIE GEnetics Nephropathy Int and SUMMIT Consortium and GENIE (Genetics of Nepropathy an International Effort) Consortium
Diabetes (New York, N.Y.), ISSN 1939-327X, 07/2018, Volume 67, Issue 7, pp. 1414 - 1427
Identification of sequence variants robustly associated with predisposition to diabetic kidney disease (DKD) has the potential to provide insights into the... 
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Diabetic Nephropathies - genetics | Male | Renal Insufficiency, Chronic - complications | Case-Control Studies | Diabetes Mellitus, Type 2 - epidemiology | Kidney Failure, Chronic - genetics | Renal Insufficiency, Chronic - epidemiology | Kidney Failure, Chronic - epidemiology | Kidney Failure, Chronic - complications | Renal Insufficiency, Chronic - genetics | Aged, 80 and over | Adult | Female | Aged | Diabetic Nephropathies - epidemiology | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 2 - complications | Type 2 diabetes | Genome-wide association studies | Usage | Research | Diabetic nephropathies | Genotype & phenotype | Phenotypes | Kidneys | Diabetes mellitus | Replication | Genomes | Diabetes | Kidney diseases | Diabetes mellitus (non-insulin dependent) | Quantitative analysis | Glomerular filtration rate | Index Medicus | Abridged Index Medicus | Metabolomics | Genetics | 0103 | Proteomics | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Medicinsk genetik | Medical Genetics | Endokrinologi och diabetes | Kidney Failure, Chronic/complications | Endocrinology and Diabetes | Diabetic Nephropathies/epidemiology | Basic Medicine | Renal Insufficiency, Chronic/complications | Diabetes Mellitus, Type 2/complications | Clinical Medicine | Medicinska och farmaceutiska grundvetenskaper
Journal Article
by Stacey, Simon N and Sulem, Patrick and Jonasdottir, Aslaug and Masson, Gisli and Gudmundsson, Julius and Gudbjartsson, Daniel F and Magnusson, Olafur T and Gudjonsson, Sigurjon A and Sigurgeirsson, Bardur and Thorisdottir, Kristin and Ragnarsson, Rafn and Benediktsdottir, Kristrun R and Nexø, Bjørn A and Tjønneland, Anne and Overvad, Kim and Rudnai, Peter and Gurzau, Eugene and Koppova, Kvetoslava and Hemminki, Kari and Corredera, Cristina and Fuentelsaz, Victoria and Grasa, Pilar and Navarrete, Sebastian and Fuertes, Fernando and García-Prats, Maria D and Sanambrosio, Enrique and Panadero, Angeles and De Juan, Ana and Garcia, Almudena and Rivera, Fernando and Planelles, Dolores and Soriano, Virtudes and Requena, Celia and Aben, Katja K and van Rossum, Michelle M and Cremers, Ruben G H M and van Oort, Inge M and van Spronsen, Dick-Johan and Schalken, Jack A and Peters, Wilbert H M and Helfand, Brian T and Donovan, Jenny L and Hamdy, Freddie C and Badescu, Daniel and Codreanu, Ovidiu and Jinga, Mariana and Csiki, Irma E and Constantinescu, Vali and Badea, Paula and Mates, Ioan N and Dinu, Daniela E and Constantin, Adrian and Mates, Dana and Kristjansdottir, Sjofn and Agnarsson, Bjarni A and Jonsson, Eirikur and Barkardottir, Rosa B and Einarsson, Gudmundur V and Sigurdsson, Fridbjorn and Moller, Pall H and Stefansson, Tryggvi and Valdimarsson, Trausti and Johannsson, Oskar T and Sigurdsson, Helgi and Jonsson, Thorvaldur and Jonasson, Jon G and Tryggvadottir, Laufey and Rice, Terri and Hansen, Helen M and Xiao, Yuanyuan and Lachance, Daniel H and O′Neill, Brian Patrick and Kosel, Matthew L and Decker, Paul A and Thorleifsson, Gudmar and Johannsdottir, Hrefna and Helgadottir, Hafdis T and Sigurdsson, Asgeir and Steinthorsdottir, Valgerdur and Lindblom, Annika and Sandler, Robert S and Keku, Temitope O and Banasik, Karina and Jørgensen, Torben and Witte, Daniel R and Hansen, Torben and Pedersen, Oluf and Jinga, Viorel and Neal, David E and Catalona, William J and Wrensch, Margaret and Wiencke, John and Jenkins, Robert B and Nagore, Eduardo and Vogel, Ulla and Kiemeney, Lambertus A and Kumar, Rajiv and Mayordomo, José I and Olafsson, Jon H and Kong, Augustine and ... and Swedish Low-risk Colorectal Cancer Study Group and Swedish Low-Risk Colorectal Canc
Nature genetics, ISSN 1546-1718, 09/2011, Volume 43, Issue 11, pp. 1098 - 1103
Journal Article
by Al Olama, Ali Amin and Kote-Jarai, Zsofia and Berndt, Sonja I and Conti, David V and Schumacher, Fredrick and Han, Ying and Benlloch, Sara and Hazelett, Dennis J and Wang, Zhaoming and Saunders, Ed and Leongamornlert, Daniel and Lindstrom, Sara and Jugurnauth-Little, Sara and Dadaev, Tokhir and Tymrakiewicz, Malgorzata and Stram, Daniel O and Rand, Kristin and Wan, Peggy and Stram, Alex and Sheng, Xin and Pooler, Loreall C and Park, Karen and Xia, Lucy and Tyrer, Jonathan and Kolonel, Laurence N and Le Marchand, Loic and Hoover, Robert N and Machiela, Mitchell J and Yeager, Merideth and Burdette, Laurie and Chung, Charles C and Hutchinson, Amy and Yu, Kai and Goh, Chee and Ahmed, Mahbubl and Govindasami, Koveela and Guy, Michelle and Tammela, Teuvo L J and Auvinen, Anssi and Wahlfors, Tiina and Schleutker, Johanna and Visakorpi, Tapio and Leinonen, Katri A and Xu, Jianfeng and Aly, Markus and Donovan, Jenny and Travis, Ruth C and Key, Tim J and Siddiq, Afshan and Canzian, Federico and Khaw, Kay-Tee and Takahashi, Atsushi and Kubo, Michiaki and Pharoah, Paul and Pashayan, Nora and Weischer, Maren and Nordestgaard, Borge G and Nielsen, Sune F and Klarskov, Peter and Røder, Martin Andreas and Iversen, Peter and Thibodeau, Stephen N and McDonnell, Shannon K and Schaid, Daniel J and Stanford, Janet L and Kolb, Suzanne and Holt, Sarah and Knudsen, Beatrice and Coll, Antonio Hurtado and Gapstur, Susan M and Diver, W Ryan and Stevens, Victoria L and Maier, Christiane and Luedeke, Manuel and Herkommer, Kathleen and Rinckleb, Antje E and Strom, Sara S and Pettaway, Curtis and Yeboah, Edward D and Tettey, Yao and Biritwum, Richard B and Adjei, Andrew A and Tay, Evelyn and Truelove, Ann and Niwa, Shelley and Chokkalingam, Anand P and Cannon-Albright, Lisa and Cybulski, Cezary and Wokołorczyk, Dominika and Kluźniak, Wojciech and Park, Jong and Sellers, Thomas and Lin, Hui-Yi and Isaacs, William B and Partin, Alan W and Brenner, Hermann and Dieffenbach, Aida Karina and Stegmaier, Christa and Chen, Constance and Giovannucci, Edward L and ... and The PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and The Breast and Prostate Cancer Cohort Consortium (BPC3) and The COGS (Collaborative Oncological Gene-environment Study) Consortium and The GAME-ON/ELLIPSE Consortium and Practical Prostate Canc Associatio and GAME-ON ELLIPSE Consortium and Breast Prostate Canc Cohort Consor and COGS Consortium and Breast and Prostate Cancer Cohort Consortium (BPC3) and GAME-ON/ELLIPSE Consortium and COGS (Collaborative Oncological Gene-environment Study) Consortium and PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium
Nature genetics, ISSN 1546-1718, 09/2014, Volume 46, Issue 10, pp. 1103 - 1109
Journal Article
by Gravel, S and Henn, B. M and Gutenkunst, R. N and Indap, A. R and Marth, G. T and Clark, A. G and Yu, F and Gibbs, R. A and Bustamante, C. D and Altshuler, D. L and Durbin, R. M and Abecasis, G. R and Bentley, D. R and Chakravarti, A and Collins, F. S and De La Vega, F. M and Donnelly, P and Egholm, M and Flicek, P and Gabriel, S. B and Knoppers, B. M and Lander, E. S and Lehrach, H and Mardis, E. R and McVean, G. A and Nickerson, D. A and Peltonen, L and Schafer, A. J and Sherry, S. T and Wang, J and Wilson, R. K and Deiros, D and Metzker, M and Muzny, D and Reid, J and Wheeler, D and Li, J and Jian, M and Li, G and Li, R and Liang, H and Tian, G and Wang, B and Wang, W and Yang, H and Zhang, X and Zheng, H and Ambrogio, L and Bloom, T and Cibulskis, K and Fennell, T. J and Jaffe, D. B and Shefler, E and Sougnez, C. L and Gormley, N and Humphray, S and Kingsbury, Z and Koko-Gonzales, P and Stone, J and McKernan, K. J and Costa, G. L and Ichikawa, J. K and Lee, C. C and Sudbrak, R and Borodina, T. A and Dahl, A and Davydov, A. N and Marquardt, P and Mertes, F and Nietfeld, W and Rosenstiel, P and Schreiber, S and Soldatov, A. V and Timmermann, B and Tolzmann, M and Affourtit, J and Ashworth, D and Attiya, S and Bachorski, M and Buglione, E and Burke, A and Caprio, A and Celone, C and Clark, S and Conners, D and Desany, B and Gu, L and Guccione, L and Kao, K and Kebbel, A and Knowlton, J and Labrecque, M and McDade, L and Mealmaker, C and Minderman, M and Nawrocki, A and Niazi, F and Pareja, K and Ramenani, R and Riches, D and ... and The 1000 Genomes Project and 1000 Genomes Project
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 07/2011, Volume 108, Issue 29, pp. 11983 - 11988
Journal Article
by Helgadottir, Anna and Gretarsdottir, Solveig and Thorleifsson, Gudmar and Holm, Hilma and Patel, Riyaz S and Gudnason, Thorarinn and Jones, Gregory T and van Rij, Andre M and Eapen, Danny J and Baas, Annette F and Tregouet, David-Alexandre and Morange, Pierre-Emmanuel and Emmerich, Joseph and Lindblad, Bengt and Gottsäter, Anders and Kiemeny, Lambertus A and Lindholt, Jes S and Sakalihasan, Natzi and Ferrell, Robert E and Carey, David J and Elmore, James R and Tsao, Philip S and Grarup, Niels and Jørgensen, Torben and Witte, Daniel R and Hansen, Torben and Pedersen, Oluf and Pola, Roberto and Gaetani, Eleonora and Magnadottir, Hulda B and Wijmenga, Cisca and Tromp, Gerard and Ronkainen, Antti and Ruigrok, Ynte M and Blankensteijn, Jan D and Mueller, Thomas and Wells, Philip S and Corral, Javier and Soria, Jose Manuel and Souto, Juan Carlos and Peden, John F and Jalilzadeh, Shapour and Mayosi, Bongani M and Keavney, Bernard and Strawbridge, Rona J and Sabater-Lleal, Maria and Gertow, Karl and Baldassarre, Damiano and Nyyssönen, Kristiina and Rauramaa, Rainer and Smit, Andries J and Mannarino, Elmo and Giral, Philippe and Tremoli, Elena and de Faire, Ulf and Humphries, Steve E and Hamsten, Anders and Haraldsdottir, Vilhelmina and Olafsson, Isleifur and Magnusson, Magnus K and Samani, Nilesh J and Levey, Allan I and Markus, Hugh S and Kostulas, Konstantinos and Dichgans, Martin and Berger, Klaus and Kuhlenbäumer, Gregor and Ringelstein, E. Bernd and Stoll, Monika and Seedorf, Udo and Rothwell, Peter M and Powell, Janet T and Kuivaniemi, Helena and Onundarson, Pall T and Valdimarsson, Einar and Matthiasson, Stefan E and Gudbjartsson, Daniel F and Thorgeirsson, Guðmundur and Quyyumi, Arshed A and Watkins, Hugh and Farrall, Martin and Thorsteinsdottir, Unnur and Stefansson, Kari
Journal of the American College of Cardiology, ISSN 0735-1097, 08/2012, Volume 60, Issue 8, pp. 722 - 729
Objectives The purpose of this study is investigate the effects of variants in the apolipoprotein(a) gene ( LPA ) on vascular diseases with different... 
Cardiovascular | Internal Medicine | atherosclerosis | genetic | association | thrombosis | lipoprotein(a) | INTIMA-MEDIA THICKNESS | RISK-FACTORS | METAANALYSIS | MYOCARDIAL-INFARCTION | UMCG Approved | VASCULAR-DISEASE | WOMEN | PERIPHERAL ARTERIAL-DISEASE | ISCHEMIC-STROKE | SEVERITY | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Severity of Illness Index | Myocardial Infarction - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Apolipoproteins A - genetics | Angiography | Carotid Intima-Media Thickness | Intracranial Aneurysm - genetics | Atherosclerosis - genetics | Humans | Risk Factors | Brain Ischemia - genetics | African Americans - genetics | Linear Models | Logistic Models | Aortic Aneurysm, Abdominal - genetics | Stroke - genetics | Venous Thromboembolism - genetics | Peripheral Arterial Disease - genetics | Age of Onset | Coronary Artery Disease - genetics | Polymorphism, Single Nucleotide | Odds Ratio | Medical colleges | Neurosciences | Stock options | Genes | Aneurysms | Coronary heart disease | Biometry | Lipoprotein A | Anopheles | Atherosclerosis | Medical genetics | Genetic research | Genetic aspects | Diabetes | Thromboembolism | Cardiology | Public health | Dementia | Stroke | Medical imaging | Values | Cardiovascular disease | Apolipoproteins | Thrombosis | Studies | Confidence intervals | Coronary vessels | Blood pressure | Drug therapy | Age | Methods | Index Medicus | Abridged Index Medicus | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article