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

Search Articles

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (90) 90
Patent (25) 25
Publication (6) 6
Conference Proceeding (2) 2
Book Chapter (1) 1
Dissertation (1) 1
Magazine Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (63) 63
humans (57) 57
life sciences & biomedicine (51) 51
female (32) 32
genetic aspects (32) 32
genetics & heredity (28) 28
genome-wide association study (28) 28
male (28) 28
research (27) 27
biochemistry (26) 26
microbiology (26) 26
polymorphism, single nucleotide (26) 26
beer (24) 24
chemistry (24) 24
compositions or test papers therefor (24) 24
condition-responsive control in microbiological orenzymological processes (24) 24
enzymology (24) 24
measuring or testing processes involving enzymes, nucleicacids or microorganisms (24) 24
metallurgy (24) 24
mutation or genetic engineering (24) 24
processes of preparing such compositions (24) 24
spirits (24) 24
vinegar (24) 24
wine (24) 24
genomics (22) 22
genetics (21) 21
genetic predisposition to disease (20) 20
alleles (18) 18
case-control studies (17) 17
genotype (17) 17
middle aged (17) 17
risk factors (17) 17
compositions thereof (16) 16
culture media (16) 16
microorganisms or enzymes (16) 16
propagating, preserving or maintaining microorganisms (16) 16
polymorphism, single nucleotide - genetics (15) 15
adult (14) 14
genes (14) 14
genomes (13) 13
medical and health sciences (13) 13
aged (12) 12
medicin och hälsovetenskap (12) 12
studies (12) 12
biochemistry & molecular biology (11) 11
health aspects (11) 11
multidisciplinary sciences (11) 11
science & technology - other topics (11) 11
european continental ancestry group - genetics (10) 10
haplotypes (10) 10
meta-analysis (10) 10
cohort studies (9) 9
genetic variation (9) 9
medicine (9) 9
single nucleotide polymorphisms (9) 9
abridged index medicus (8) 8
clinical medicine (8) 8
genetic research (8) 8
klinisk medicin (8) 8
diabetes (7) 7
genetic predisposition to disease - genetics (7) 7
human genetics (7) 7
linkage disequilibrium (7) 7
phenotype (7) 7
physiological aspects (7) 7
association studies (6) 6
chromosomes (6) 6
endocrinology & metabolism (6) 6
gene expression (6) 6
gene frequency (6) 6
genome, human (6) 6
genome-wide association studies (6) 6
genome-wide association study - methods (6) 6
gwas (6) 6
medical research (6) 6
quality control (6) 6
adolescent (5) 5
aged, 80 and over (5) 5
analysis (5) 5
association studies articles (5) 5
bacteria (5) 5
biology (5) 5
diabetes mellitus, type 1 - genetics (5) 5
disease susceptibility (5) 5
electronic medical records (5) 5
endocrinology and diabetes (5) 5
endokrinologi och diabetes (5) 5
immune system (5) 5
immunology (5) 5
linear models (5) 5
medical genetics (5) 5
methods (5) 5
multiple sclerosis (5) 5
multiple sclerosis - genetics (5) 5
proteins (5) 5
quantitative trait loci (5) 5
quantitative trait loci - genetics (5) 5
risk (5) 5
type 1 diabetes (5) 5
united states (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Machiela, Mitchell J and Zhou, Weiyin and Sampson, Joshua N and Dean, Michael C and Jacobs, Kevin B and Black, Amanda and Brinton, Louise A and Chang, I-Shou and Chen, Chu and Chen, Constance and Chen, Kexin and Cook, Linda S and Crous Bou, Marta and De Vivo, Immaculata and Doherty, Jennifer and Friedenreich, Christine M and Gaudet, Mia M and Haiman, Christopher A and Hankinson, Susan E and Hartge, Patricia and Henderson, Brian E and Hong, Yun-Chul and Hosgood, H. Dean and Hsiung, Chao A and Hu, Wei and Hunter, David J and Jessop, Lea and Kim, Hee Nam and Kim, Yeul Hong and Kim, Young Tae and Klein, Robert and Kraft, Peter and Lan, Qing and Lin, Dongxin and Liu, Jianjun and Le Marchand, Loic and Liang, Xiaolin and Lissowska, Jolanta and Lu, Lingeng and Magliocco, Anthony M and Matsuo, Keitaro and Olson, Sara H and Orlow, Irene and Park, Jae Yong and Pooler, Loreall and Prescott, Jennifer and Rastogi, Radhai and Risch, Harvey A and Schumacher, Fredrick and Seow, Adeline and Setiawan, Veronica Wendy and Shen, Hongbing and Sheng, Xin and Shin, Min-Ho and Shu, Xiao-Ou and VanDen Berg, David and Wang, Jiu-Cun and Wentzensen, Nicolas and Wong, Maria Pik and Wu, Chen and Wu, Tangchun and Wu, Yi-Long and Xia, Lucy and Yang, Hannah P and Yang, Pan-Chyr and Zheng, Wei and Zhou, Baosen and Abnet, Christian C and Albanes, Demetrius and Aldrich, Melinda C and Amos, Christopher and Amundadottir, Laufey T and Berndt, Sonja I and Blot, William J and Bock, Cathryn H and Bracci, Paige M and Burdett, Laurie and Buring, Julie E and Butler, Mary A and Carreón, Tania and Chatterjee, Nilanjan and Chung, Charles C and Cook, Michael B and Cullen, Michael and Davis, Faith G and Ding, Ti and Duell, Eric J and Epstein, Caroline G and Fan, Jin-Hu and Figueroa, Jonine D and Fraumeni, Joseph F and Freedman, Neal D and Fuchs, Charles S and Gao, Yu-Tang and Gapstur, Susan M and Patiño-Garcia, Ana and Garcia-Closas, Montserrat and Gaziano, J. Michael and Giles, Graham G and Gillanders, Elizabeth M and ...
American journal of human genetics, ISSN 0002-9297, 03/2015, Volume 96, Issue 3, pp. 487 - 497
Journal Article
by Sandholm, Niina and Salem, Rany M and McKnight, Amy Jayne and Brennan, Eoin P and Forsblom, Carol and Isakova, Tamara and McKay, Gareth J and Williams, Winfred W and Sadlier, Denise M and Mäkinen, Ville-Petteri and Swan, Elizabeth J and Palmer, Cameron and Boright, Andrew P and Ahlqvist, Emma and Deshmukh, Harshal A and Keller, Benjamin J and Huang, Huateng and Ahola, Aila J and Fagerholm, Emma and Gordin, Daniel and Harjutsalo, Valma and He, Bing and Heikkilä, Outi and Hietala, Kustaa and Kytö, Janne and Lahermo, Päivi and Lehto, Markku and Lithovius, Raija and Österholm, Anne-May and Parkkonen, Maija and Pitkäniemi, Janne and Rosengård-Bärlund, Milla and Saraheimo, Markku and Sarti, Cinzia and Söderlund, Jenny and Soro-Paavonen, Aino and Syreeni, Anna and Thorn, Lena M and Tikkanen, Heikki and Tolonen, Nina and Tryggvason, Karl and Tuomilehto, Jaakko and Wadén, Johan and Gill, Geoffrey V and Prior, Sarah and Guiducci, Candace and Mirel, Daniel B and Taylor, Andrew and Hosseini, S. Mohsen and Parving, Hans-Henrik and Rossing, Peter and Tarnow, Lise and Ladenvall, Claes and Alhenc-Gelas, François and Lefebvre, Pierre and Rigalleau, Vincent and Roussel, Ronan and Tregouet, David-Alexandre and Maestroni, Anna and Maestroni, Silvia and Falhammar, Henrik and Gu, Tianwei and Möllsten, Anna and Cimponeriu, Danut and Ioana, Mihai and Mota, Maria and Mota, Eugen and Serafinceanu, Cristian and Stavarachi, Monica and Hanson, Robert L and Nelson, Robert G and Kretzler, Matthias and Colhoun, Helen M and Panduru, Nicolae Mircea and Gu, Harvest F and Brismar, Kerstin and Zerbini, Gianpaolo and Hadjadj, Samy and Marre, Michel and Groop, Leif and Lajer, Maria and Bull, Shelley B and Waggott, Daryl and Paterson, Andrew D and Savage, David A and Bain, Stephen C and Martin, Finian and Hirschhorn, Joel N and Godson, Catherine and Florez, Jose C and Groop, Per-Henrik and Maxwell, Alexander P and DCCT/EDIC Research Group and DCCT-EDIC Res Grp
PLoS genetics, ISSN 1553-7404, 09/2012, Volume 8, Issue 9, pp. e1002921 - e1002921
Journal Article
by Stewart, S E and Yu, D and Scharf, J M and Neale, B M and Fagerness, J A and Mathews, C A and Arnold, P D and Evans, P D and Gamazon, E R and Osiecki, L and McGrath, L and Haddad, S and Crane, J and Hezel, D and Illman, C and Mayerfeld, C and Konkashbaev, A and Liu, C and Pluzhnikov, A and Tikhomirov, A and Edlund, C K and Rauch, S L and Moessner, R and Falkai, P and Maier, W and Ruhrmann, S and Grabe, H-J and Lennertz, L and Wagner, M and Bellodi, L and Cavallini, M C and Richter, M A and Cook, E H and Kennedy, J L and Rosenberg, D and Stein, D J and Hemmings, S M J and Lochner, C and Azzam, A and Chavira, D A and Fournier, E and Garrido, H and Sheppard, B and Umaña, P and Murphy, D L and Wendland, J R and Veenstra-VanderWeele, J and Denys, D and Blom, R and Deforce, D and Van Nieuwerburgh, F and Westenberg, H G M and Walitza, S and Egberts, K and Renner, T and Miguel, E C and Cappi, C and Hounie, A G and Conceição do Rosário, M and Sampaio, A S and Vallada, H and Nicolini, H and Lanzagorta, N and Camarena, B and Delorme, R and Leboyer, M and Pato, C N and Pato, M T and Voyiaziakis, E and Heutink, P and Cath, D C and Posthuma, D and Smit, J H and Samuels, J and Bienvenu, O J and Cullen, B and Fyer, A J and Grados, M A and Greenberg, B D and McCracken, J T and Riddle, M A and Wang, Y and Coric, V and Leckman, J F and Bloch, M and Pittenger, C and Eapen, V and Black, D W and Ophoff, R A and Strengman, E and Cusi, D and Turiel, M and Frau, F and Macciardi, F and Gibbs, J R and Cookson, M R and Singleton, A and Hardy, J and Crenshaw, A T and Parkin, M A and ... and UK Brain Expression Database and North American Brain Expression Consortium and North Amer Brain Expression Consor
Molecular psychiatry, ISSN 1476-5578, 08/2012, Volume 18, Issue 7, pp. 788 - 798
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
Human genetics, ISSN 1432-1203, 10/2011, Volume 131, Issue 4, pp. 639 - 652
Journal Article
Molecular psychiatry, ISSN 1476-5578, 06/2009, Volume 14, Issue 8, pp. 755 - 763
Journal Article