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1. Full Text Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci
by Saxena, Richa and Elbers, Clara C and Guo, Yiran and Peter, Inga and Gaunt, Tom R and Mega, Jessica L and Lanktree, Matthew B and Tare, Archana and Castillo, Berta Almoguera and Li, Yun R and Johnson, Toby and Bruinenberg, Marcel and Gilbert-Diamond, Diane and Rajagopalan, Ramakrishnan and Voight, Benjamin F and Balasubramanyam, Ashok and Barnard, John and Bauer, Florianne and Baumert, Jens and Bhangale, Tushar and Böhm, Bernhard O and Braund, Peter S and Burton, Paul R and Chandrupatla, Hareesh R and Clarke, Robert and Cooper-DeHoff, Rhonda M and Crook, Errol D and Davey-Smith, George and Day, Ian N and de Boer, Anthonius and de Groot, Mark C.H and Drenos, Fotios and Ferguson, Jane and Fox, Caroline S and Furlong, Clement E and Gibson, Quince and Gieger, Christian and Gilhuijs-Pederson, Lisa A and Glessner, Joseph T and Goel, Anuj and Gong, Yan and Grant, Struan F.A and Grobbee, Diederick E and Hastie, Claire and Humphries, Steve E and Kim, Cecilia E and Kivimaki, Mika and Kleber, Marcus and Meisinger, Christa and Kumari, Meena and Langaee, Taimour Y and Lawlor, Debbie A and Li, Mingyao and Lobmeyer, Maximilian T and Maitland-van der Zee, Anke-Hilse and Meijs, Matthijs F.L and Molony, Cliona M and Morrow, David A and Murugesan, Gurunathan and Musani, Solomon K and Nelson, Christopher P and Newhouse, Stephen J and O'Connell, Jeffery R and Padmanabhan, Sandosh and Palmen, Jutta and Patel, Sanjey R and Pepine, Carl J and Pettinger, Mary and Price, Thomas S and Rafelt, Suzanne and Ranchalis, Jane and Rasheed, Asif and Rosenthal, Elisabeth and Ruczinski, Ingo and Shah, Sonia and Shen, Haiqing and Silbernagel, Günther and Smith, Erin N and Spijkerman, Annemieke W.M and Stanton, Alice and Steffes, Michael W and Thorand, Barbara and Trip, Mieke and van der Harst, Pim and van der A, Daphne L and van Iperen, Erik P.A and van Setten, Jessica and van Vliet-Ostaptchouk, Jana V and Verweij, Niek and Wolffenbuttel, Bruce H.R and Young, Taylor and Zafarmand, M. Hadi and Zmuda, Joseph M and Boehnke, Michael and Altshuler, David and McCarthy, Mark and Kao, W.H. Linda and Pankow, James S and Cappola, Thomas P and Sever, Peter and ... and the Look AHEAD Research Group and DIAGRAM consortium and PROCARDIS and Diagram Consortium and ASCOT Investigators and Look AHEAD Res Grp and Look AHEAD Research Group
American journal of human genetics, ISSN 0002-9297, 03/2012, Volume 90, Issue 3, pp. 410 - 425
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Diabetes. Impaired glucose tolerance | Medical genetics | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Genetic Predisposition to Disease | Follow-Up Studies | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Genotype | Male | Genetic Loci | Case-Control Studies | Young Adult | Diabetes Mellitus, Type 2 - ethnology | Ethnic Groups | Adolescent | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Genotype & phenotype | Genetics | Gene loci | Diabetes | Minority & ethnic groups | Meta-analysis | Index Medicus | Reviews | Genotyping | Diabetes mellitus | Ethnic groups | Clinical trials | Population studies | Single-nucleotide polymorphism | Genetic factors | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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2. Full Text A meta-Analysis of Alzheimer's disease brain transcriptomic data
by Patel, Hamel and Dobson, Richard J.B and Newhouse, Stephen J
Journal of Alzheimer's disease, ISSN 1387-2877, 2019, Volume 68, Issue 4, pp. 1635 - 1656
Human | Meta-Analysis | Mental disorders | Neuropathology | Gene expression | Alzheimer's disease | Neurodegenerative disorders | Microarray analysis | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Cerebellum | Brain | Frontal lobe | Identification methods | Genes | Mental health | Disorders | Schizophrenia | Bipolar disorder | Mapping | Mental depression | Proteins | Replicating | Pathways | Plaques | Temporal lobe | Therapeutic applications | Brain mapping | Metabolism | Ribonucleic acid--RNA | DNA microarrays | Reproducibility | Parietal lobe | Index Medicus
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3. Full Text Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
by Nicolas, Aude and Kenna, Kevin P and Renton, Alan E and Ticozzi, Nicola and Faghri, Faraz and Chia, Ruth and Dominov, Janice A and Kenna, Brendan J and Nalls, Mike A and Keagle, Pamela and Rivera, Alberto M and van Rheenen, Wouter and Murphy, Natalie A and van Vugt, Joke J.F.A and Geiger, Joshua T and Van der Spek, Rick A and Pliner, Hannah A and Shankaracharya and Smith, Bradley N and Marangi, Giuseppe and Topp, Simon D and Abramzon, Yevgeniya and Gkazi, Athina Soragia and Eicher, John D and Kenna, Aoife and Logullo, Francesco O and Simone, Isabella and Logroscino, Giancarlo and Salvi, Fabrizio and Bartolomei, Ilaria and Borghero, Giuseppe and Murru, Maria Rita and Costantino, Emanuela and Pani, Carla and Puddu, Roberta and Caredda, Carla and Piras, Valeria and Tranquilli, Stefania and Cuccu, Stefania and Corongiu, Daniela and Melis, Maurizio and Milia, Antonio and Marrosu, Francesco and Marrosu, Maria Giovanna and Floris, Gianluca and Cannas, Antonino and Capasso, Margherita and Caponnetto, Claudia and Mancardi, Gianluigi and Origone, Paola and Mandich, Paola and Conforti, Francesca L and Mora, Gabriele and Marinou, Kalliopi and Sideri, Riccardo and Penco, Silvana and Mosca, Lorena and Lunetta, Christian and Pinter, Giuseppe Lauria and Corbo, Massimo and Riva, Nilo and Carrera, Paola and Volanti, Paolo and Mandrioli, Jessica and Fini, Nicola and Fasano, Antonio and Tremolizzo, Lucio and Arosio, Alessandro and Ferrarese, Carlo and Trojsi, Francesca and Tedeschi, Gioacchino and Monsurrò, Maria Rosaria and Piccirillo, Giovanni and Femiano, Cinzia and Ticca, Anna and Ortu, Enzo and La Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Sabatelli, Mario and Zollino, Marcella and Conte, Amelia and Luigetti, Marco and Lattante, Serena and Marangi, Giuseppe and Santarelli, Marialuisa and Petrucci, Antonio and Pugliatti, Maura and Pirisi, Angelo and Parish, Leslie D and Occhineri, Patrizia and Giannini, Fabio and Battistini, Stefania and Benigni, Michele and Cau, Tea B and Loi, Daniela and Calvo, Andrea and Moglia, Cristina and Brunetti, Maura and Barberis, Marco and ... and Project MinE ALS Sequencing Consortium and ALS Sequencing Consortium and Genomic Translation for ALS Care (GTAC) Consortium and NYGC ALS Consortium and ITALSGEN Consortium and Answer ALS Foundation and Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium and SLAGEN Consortium and French ALS Consortium and Genomic Translation ALS Care GTAC and Clinical Res ALS Related Disorders and Project MinE ALS Sequencing Consor and Answer ALS Fdn
Neuron (Cambridge, Mass.), ISSN 0896-6273, 03/2018, Volume 97, Issue 6, pp. 1268 - 1283.e6
WGS | GWAS | WES | KIF5A | ALS | axonal transport | cargo | no | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amino Acid Sequence | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Amyotrophic Lateral Sclerosis - diagnosis | Male | Young Adult | Aged, 80 and over | Kinesin - genetics | Adult | Female | Aged | Genome-Wide Association Study - methods | Amyotrophic Lateral Sclerosis - epidemiology | Cohort Studies | Loss of Function Mutation - genetics | Genetic research | Genes | Analysis | Genomics | Phenotypes | Disease | Neurodegenerative diseases | Pathogenesis | Homeostasis | Amyotrophic lateral sclerosis | Genomes | Risk factors | Consortia | Hereditary spastic paraplegia | Proteins | Paraplegia | Charcot-Marie-Tooth disease | Cytoskeleton | Mutation | Spastic paraplegia | Index Medicus | Life Sciences
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4. Full Text Blood Pressure Loci Identified with a Gene-Centric Array
by Johnson, Toby and Gaunt, Tom R and Newhouse, Stephen J and Padmanabhan, Sandosh and Tomaszewski, Maciej and Kumari, Meena and Morris, Richard W and Tzoulaki, Ioanna and O'Brien, Eoin T and Poulter, Neil R and Sever, Peter and Shields, Denis C and Thom, Simon and Wannamethee, Sasiwarang G and Whincup, Peter H and Brown, Morris J and Connell, John M and Dobson, Richard J and Howard, Philip J and Mein, Charles A and Onipinla, Abiodun and Shaw-Hawkins, Sue and Zhang, Yun and Smith, George Davey and Day, Ian N.M and Lawlor, Debbie A and Goodall, Alison H and Fowkes, F. Gerald and Abecasis, Gonçalo R and Elliott, Paul and Gateva, Vesela and Braund, Peter S and Burton, Paul R and Nelson, Christopher P and Tobin, Martin D and van der Harst, Pim and Glorioso, Nicola and Neuvrith, Hani and Salvi, Erika and Staessen, Jan A and Stucchi, Andrea and Devos, Nabila and Jeunemaitre, Xavier and Plouin, Pierre-François and Tichet, Jean and Juhanson, Peeter and Org, Elin and Putku, Margus and Sõber, Siim and Veldre, Gudrun and Viigimaa, Margus and Levinsson, Anna and Rosengren, Annika and Thelle, Dag S and Hastie, Claire E and Hedner, Thomas and Lee, Wai K and Melander, Olle and Wahlstrand, Björn and Hardy, Rebecca and Wong, Andrew and Cooper, Jackie A and Palmen, Jutta and Chen, Li and Stewart, Alexandre F.R and Wells, George A and Westra, Harm-Jan and Wolfs, Marcel G.M and Clarke, Robert and Franzosi, Maria Grazia and Goel, Anuj and Hamsten, Anders and Lathrop, Mark and Peden, John F and Seedorf, Udo and Watkins, Hugh and Ouwehand, Willem H and Sambrook, Jennifer and Stephens, Jonathan and Casas, Juan-Pablo and Drenos, Fotios and Holmes, Michael V and Kivimaki, Mika and Shah, Sonia and Shah, Tina and Talmud, Philippa J and Whittaker, John and Wallace, Chris and Delles, Christian and Laan, Maris and Kuh, Diana and Humphries, Steve E and Nyberg, Fredrik and Cusi, Daniele and Roberts, Robert and Newton-Cheh, Christopher and Franke, Lude and Stanton, Alice V and Dominiczak, Anna F and Farrall, Martin and ... and The Global BPgen Consortium and The Cardiogenics Consortium and Global BPgen Consortium and Cardiogenics Consortium and Institutionen för medicin, avdelningen för samhällsmedicin och folkhälsa and Institute of Medicine and Göteborgs universitet and Gothenburg University and Institutionen för medicin, avdelningen för invärtesmedicin and Institute of Medicine, School of Public Health and Community Medicine and Sahlgrenska Academy and Sahlgrenska akademin and Institutionen för medicin, avdelningen för akut och kardiovaskulär medicin and Institute of Medicine, Department of Emergeny and Cardiovascular Medicine and Institute of Medicine, Department of Internal Medicine and Institutionen för medicin
American journal of human genetics, ISSN 0002-9297, 12/2011, Volume 89, Issue 6, pp. 688 - 700
COMMON VARIANTS | POPULATION | QUANTITATIVE-TRAIT LOCI | LINKAGE DISEQUILIBRIUM | METAANALYSIS | ANGIOTENSINOGEN | CARDIOVASCULAR-DISEASE | SUSCEPTIBILITY LOCI | ESSENTIAL-HYPERTENSION | UMCG Approved | GENOME-WIDE ASSOCIATION | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Haplotypes | Genome-Wide Association Study | Oligonucleotide Array Sequence Analysis | Plasma Membrane Calcium-Transporting ATPases - genetics | Blood Pressure - genetics | Gene Frequency | Humans | Middle Aged | Male | Gene Expression Profiling | Genetic Loci | Sequence Analysis, DNA | Case-Control Studies | Linkage Disequilibrium | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Receptors, Atrial Natriuretic Factor - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Hypertension - genetics | Measurement | Hypertension | Causes of | Blood pressure | Genetic aspects | Research | Single nucleotide polymorphisms | Cardiovascular diseases | Genetic regulation | Risk factors | Genotype & phenotype | Cardiovascular disease | Chromatin | Gene loci | Gene expression | Index Medicus | Kardiologi | Medicinsk genetik | Medical Genetics | Cardiac and Cardiovascular Systems | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Public Health, Global Health, Social Medicine and Epidemiology
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5. Full Text High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
by Eyre, Steve and Bowes, John and Diogo, Dorothee and Lee, Annette and Barton, Anne and Martin, Paul and Zhernakova, Alexana and Stahl, Eli and Viatte, Sebastien and McAllister, Kate and Amos, Christopher I and Padyukov, Leonid and Toes, Rene E. M and Huizinga, Tom W. J and Wijmenga, Cisca and Trynka, Gosia and Franke, Lude and Westra, Harm-Jan and Alfredsson, Lars and Hu, Xinli and Sandor, Cynthia and de Bakker, Paul I. W and Davila, Sonia and Khor, Chiea Chuen and Heng, Khai Koon and Anews, Robert and Edkins, Sarah and Hunt, Sarah E and Langford, Cordelia and Symmons, Deborah and Concannon, Pat and Onengut-Gumuscu, Suna and Rich, Stephen S and Deloukas, Panos and Gonzalez-Gay, Miguel A and Roiguez-Roiguez, Luis and Arlsetig, Lisbeth and Martin, Javier and Rantapaa-Dahlqvist, Solbritt and Plenge, Robert M and Raychaudhuri, Soumya and Klareskog, Lars and Gregersen, Peter K and Worthington, Jane and Biol Rheumatoid Arthrit Genetics G and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate
Nature genetics, ISSN 1061-4036, 12/2012, Volume 44, Issue 12, pp. 1336 - 1340
INTERLEUKIN-6 RECEPTOR | RISK LOCI | METAANALYSIS | CORONARY-HEART-DISEASE | EXPRESSION | ASSOCIATION | UMCG Approved | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Diseases of the osteoarticular system | Inflammatory joint diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Methods, theories and miscellaneous | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Oligonucleotide Array Sequence Analysis | Autoantibodies - blood | Humans | Male | Genetic Loci | Chromosome Mapping - instrumentation | Arthritis, Rheumatoid - genetics | Chromosome Mapping - methods | Female | Polymorphism, Single Nucleotide | Autoantibodies - genetics | Rheumatoid arthritis | Physiological aspects | Genetic aspects | Disease susceptibility | Single nucleotide polymorphisms | Research | Chromosomes | Studies | Medical research | Autoimmune diseases | Index Medicus | Medicin och hälsovetenskap
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