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1. Full Text Genome-wide association analysis identifies 13 new risk loci for schizophrenia
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K. E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Levinson, Douglas F and Gejman, Pablo V and Laurent, Claudine and Mowry, Bryan J and O'Donovan, Michael C and Pulver, Ann E and Schwab, Sibylle G and Wildenauer, Dieter B and Dudbridge, Frank and Shi, Jianxin and Albus, Margot and Alexander, Madeline and Campion, Dominique and Cohen, David and Dikeos, Dimitris and Duan, Jubao and Eichhammer, Peter and Godard, Stephanie and Hansen, Mark and Lerer, F. Bernard and Liang, Kung-Yee and Maier, Wolfgang and Mallet, Jacques and Nertney, Deborah A and Nestadt, Gerald and Norton, Nadine and Papadimitriou, George N and Ribble, Robert and Sanders, Alan R and Silverman, Jeremy M and Walsh, Dermot and Williams, Nigel M and Wormley, Brandon and Arranz, Maria J and Bakker, Steven and Bender, Stephan and Bramon, Elvira and Collier, David and Crespo-Facorro, Benedicto and Hall, Jeremy and Iyegbe, Conrad and Jablensky, Assen and Kahn, Rene S and Kalaydjieva, Luba and Lawrie, Stephen and Lewis, Cathryn M and ... and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 10, pp. 1150 - 1159
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Sweden | Schizophrenia - genetics | Humans | Female | Male | Polymorphism, Single Nucleotide | Case-Control Studies | Schizophrenia | Genetic aspects | Single nucleotide polymorphisms | Research | Risk factors | Studies | Councils | Sample size | Genomics | Genomes | Chromosomes | Index Medicus | Medicinsk genetik | Hälsovetenskap | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Psykiatri | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Klinisk medicin
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2. Full Text The impact of low-frequency and rare variants on lipid levels
by Surakka, Ida and Horikoshi, Momoko and Mägi, Reedik and Sarin, A.-P 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 and Nelson, Christopher P and Willenborg, Christina and Gustafsson, Stefan and Westra, Harm-Jan and Blades, Matthew and De Craen, Anton J. M and Geus, Eco and Deelen, Joris and Grallert, Harald and Hamsten, Anders and Havulinna, Aki and Hengstenberg, Christian and Houwing-Duistermaat, Jeanine and Hypponen, Elina and Karssen, Lennart and Lehtimäki, Terho and Lyssenko, Valeriya and Magnusson, Patrik and Mihailov, Evelin and Müller-Nurasyid, Martina and Mpindi, John-Patrick and Pedersen, Nancy L and Penninx, Brenda and Perola, Markus and Pers, Tune and Peters, Annette and Rung, Johan and Smit, Johannes and Steinthorsdottir, Valgerdur and Tobin, Martin and Tsernikova, Natalia and Leeuwen, Elisa and Viikari, Jorma and Willems, Sara and Willemsen, Gonneke and Schunkert, Heribert and Erdmann, Jeanette and Samani, Nilesh and Kaprio, Jaakko and Lind, Lars and Gieger, Christian and Metspalu, Anes and Slagboom, Eline and Groop, Leif and Duijn, Cornelia and Eriksson, Johan G and Jula, Antti and Salomaa, Veikko and Boomsma, Dorret and Power, Christopher and Raitakari, Olli T and Ingelsson, Erik and Jarvelin, Marjo-Riitta and Thorsteinsdottir, Unnur and Franke, Lude and Ikonen, Elina and Kallioniemi, Olli and Pietiäinen, Vilja and Lindgren, Cecilia M and Zwart, John-Anker and Palotie, Aarno and McCarthy, Mark and Morris, Anew and Prokopenko, Inga and Ripatti, Samuli and ENGAGE Consortium
Nature genetics, ISSN 1061-4036, 01/2015, Volume 47, Issue 6, pp. 589 - 597
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Dyslipidemias - genetics | Genome-Wide Association Study | Gene Frequency | Humans | Lipid Metabolism - genetics | Polymorphism, Single Nucleotide | Genetic Loci | Mutation, Missense | Sequence Analysis, DNA | Linkage Disequilibrium | Genetic aspects | Single nucleotide polymorphisms | Lipid metabolism | Identification and classification | Health aspects | Studies | Design | Lipids | Agreements | Cholesterol | Index Medicus | Clinical Medicine | Endokrinologi och diabetes | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
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3. Full Text A polygenic burden of rare disruptive mutations in schizophrenia
by Purcell, Shaun M and Moran, Jennifer L and Fromer, Menachem and Ruderfer, Douglas and Solovieff, Nadia and Roussos, Panos and O'Dushlaine, Colm and Chambert, Kimberly and Bergen, Sarah E and Kähler, Anna and Duncan, Laramie and Stahl, Eli and Genovese, Giulio and Fernández, Esperanza and Collins, Mark O and Komiyama, Noboru H and Choudhary, Jyoti S and Magnusson, Patrik K. E and Banks, Eric and Shakir, Khalid and Garimella, Kiran and Fennell, Tim and Depristo, Mark and Grant, Seth G. N and Haggarty, Stephen J and Gabriel, Stacey and Scolnick, Edward M and Lander, Eric S and Hultman, Christina M and Sullivan, Patrick F and McCarroll, Steven A and Sklar, Pamela
Nature (London), ISSN 0028-0836, 2014, Volume 506, Issue 7487, pp. 185 - 190
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Autistic Disorder - genetics | Disks Large Homolog 4 Protein | Multifactorial Inheritance - genetics | Genome-Wide Association Study | Cytoskeletal Proteins - genetics | Membrane Proteins - genetics | Humans | Male | DNA Copy Number Variations - genetics | Fragile X Mental Retardation Protein - metabolism | Mutation - genetics | Nerve Tissue Proteins - genetics | Intellectual Disability - genetics | Receptors, N-Methyl-D-Aspartate - genetics | Schizophrenia - genetics | Female | Calcium Channels - genetics | Intracellular Signaling Peptides and Proteins - genetics | Psychological aspects | Schizophrenia | Genetic aspects | Gene mutations | Health aspects | Multifactorial traits | Studies | Confidence intervals | Algorithms | Disease | Genes | Population | Bipolar disorder | Genomes | Mutation | Health risk assessment | Index Medicus | Medicin och hälsovetenskap
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4. Full Text Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
by Ferreira, Manuel A and Vonk, Judith M and Baurecht, Hansjörg and Marenholz, Ingo and Tian, Chao and Hoffman, Joshua D and Helmer, Quinta and Tillander, Annika and Ullemar, Vilhelmina and Van Dongen, Jenny and Lu, Yi and Rüschendorf, Franz and Esparza-Gordillo, Jorge and Medway, Chris W and Mountjoy, Edward and Burrows, Kimberley and Hummel, Oliver and Grosche, Sarah and Brumpton, Ben M and Witte, John S and Hottenga, Jouke-Jan and Willemsen, Gonneke and Zheng, Jie and Rodríguez, Elke and Hotze, Melanie and Franke, Andre and Revez, Joana A and Beesley, Jonathan and Matheson, Melanie C and Dharmage, Shyamali C and Bain, Lisa M and Fritsche, Lars G and Gabrielsen, Maiken E and Balliu, Brunilda and Nielsen, Jonas B and Zhou, Wei and Hveem, Kristian and Langhammer, Arnulf and Holmen, Oddgeir L and Løset, Mari and Abecasis, Goncalo R and Willer, Cristen J and Arnold, Andreas and Homuth, Georg and Schmidt, Carsten O and Thompson, Philip J and Martin, Nicholas G and Duffy, David L and Novak, Natalija and Schulz, Holger and Karrasch, Stefan and Gieger, Christian and Strauch, Konstantin and Melles, Ronald B and Hinds, David A and Hübner, Norbert and Weidinger, Stephan and Magnusson, Patrik K. E and Jansen, Rick and Jorgenson, Eric and Lee, Young-Ae and Boomsma, Dorret I and Almqvist, Catarina and Karlsson, Robert and Koppelman, Gerard H and Paternoster, Lavinia and 23andMe Res Team and BIOS consortium and LifeLines Cohort Study and AAGC collaborators and 23andMe Research Team
Nature genetics, ISSN 1061-4036, 12/2017, Volume 49, Issue 12, pp. 1752 - 1757
RHINITIS | ATOPIC-DERMATITIS | VARIANTS | TRANSCRIPTOME | HUMAN-CELLS | COHORT | LD SCORE REGRESSION | IDENTIFICATION | GENOME-WIDE ASSOCIATION | TWIN | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Eczema - genetics | Genetic Predisposition to Disease - genetics | Phenotype | Rhinitis, Allergic, Seasonal - genetics | Humans | Risk Factors | Hypersensitivity - genetics | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Asthma - genetics | Genome-wide association studies | Genetic variation | Eczema | Genetic aspects | Health aspects | Hay-fever | Risk factors | Methods | Asthma | Hay | Disease | Transcription | Rhinitis | Genes | Risk sharing | Genomes | Dermatitis | Immunity | Genetic effects | Atopic dermatitis | Allergic rhinitis | DNA methylation | Skin diseases | Age | CpG islands | Health risks | Risk analysis | Gene expression | Allergies | Biological activity | Hay fever | Studies | Heritability | Methylation | Index Medicus | Medicin och hälsovetenskap
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5. Full Text Identification of seven loci affecting mean telomere length and their association with disease
by Codd, Veryan and Nelson, Christopher P and Albrecht, Eva and Mangino, Massimo and Deelen, Joris and Buxton, Jessica L and Hottenga, Jouke Jan and Fischer, Krista and Esko, Tonu and Surakka, Ida and Broer, Linda and Nyholt, Dale R and Mateo Leach, Irene and Salo, Perttu and Hagg, Sara and Matthews, Mary K and Palmen, Jutta and Norata, Giuseppe D and O'Reilly, Paul F and Saleheen, Danish and Amin, Najaf and Balmforth, Anthony J and Beekman, Marian and de Boer, Rudolf A and Bohringer, Stefan and Braund, Peter S and Burton, Paul R and de Craen, Anton J. M and Denniff, Matthew and Dong, Yanbin and Douroudis, Konstantinos and Dubinina, Elena and Eriksson, Johan G and Garlaschelli, Katia and Guo, Dehuang and Hartikainen, Anna-Liisa and Henders, Anjali K and Houwing-Duistermaat, Jeanine J and Kananen, Laura and Karssen, Lennart C and Kettunen, Johannes and Klopp, Norman and Lagou, Vasiliki and van Leeuwen, Elisabeth M and Madden, Pamela A and Maegi, Reedik and Verweij, Niek and van Veldhuisen, Dirk J and van Gilst, Wiek H and van der Harst, Pim and CARDIoGRAM Consortium and CARDIoGRAM consortium
Nature genetics, ISSN 1061-4036, 04/2013, Volume 45, Issue 4, pp. 422 - 427
VARIANTS | SUSCEPTIBILITY | CARDIOVASCULAR-DISEASE | ATHEROSCLEROSIS | RISK | DYSFUNCTION | STRESS | CANCER | CORONARY-ARTERY-DISEASE | FIBROBLASTS | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Disease - genetics | Humans | Risk Factors | Genetic Loci - genetics | Male | Case-Control Studies | Telomerase - genetics | Female | Biomarkers, Tumor - genetics | Leukocytes - metabolism | Telomere - genetics | DNA polymerases | Physiological aspects | Telomeres | Genetic aspects | Research | Aging | Genetics | Gene therapy | Chromosomes | Deoxyribonucleic acid--DNA | Index Medicus | Medicin och hälsovetenskap
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6. Full Text Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs
by Hemani, Gibran and Yang, Jian and Vinkhuyzen, Anna and Powell, Joseph E and Willemsen, Gonneke and Hottenga, Jouke-Jan and Abdellaoui, Abdel and Mangino, Massimo and Valdes, Ana M and Medland, Sarah E and Madden, Pamela A and Heath, Andrew C and Henders, Anjali K and Nyholt, Dale R and de Geus, Eco J.C and Magnusson, Patrik K.E and Ingelsson, Erik and Montgomery, Grant W and Spector, Timothy D and Boomsma, Dorret I and Pedersen, Nancy L and Martin, Nicholas G and Visscher, Peter M
American journal of human genetics, ISSN 0002-9297, 11/2013, Volume 93, Issue 5, pp. 865 - 875
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Body Mass Index | Genetics, Population | Quantitative Trait, Heritable | Humans | Genotype | Male | Body Height - genetics | Phenotype | Alleles | Female | Models, Genetic | Polymorphism, Single Nucleotide | Genome, Human | Quantitative Trait Loci | Genetic Linkage | Siblings | Quantitative genetics | Body mass index | Genetic aspects | Research | Gene expression | Genomes | Mutation | Genomics | Index Medicus | Medicin och hälsovetenskap
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7. Full Text Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
by Day, Felix R and Thompson, Deborah J and Helgason, Hannes and Chasman, Daniel I and Finucane, Hilary and Sulem, Patrick and Ruth, Katherine S and Whalen, Sean and Sarkar, Abhishek K and Albrecht, Eva and Altmaier, Elisabeth and Amini, Marzyeh and Barbieri, Caterina M and Boutin, Thibaud and Campbell, Archie and Demerath, Ellen and Giri, Ayush and He, Chunyan and Hottenga, Jouke J and Karlsson, Robert and Kolcic, Ivana and Loh, Po-Ru and Lunetta, Kathryn L and Mangino, Massimo and Marco, Brumat and McMahon, George and Medland, Sarah E and Nolte, Ilja M and Noordam, Raymond and Nutile, Teresa and Paternoster, Lavinia and Perjakova, Natalia and Porcu, Eleonora and Rose, Lynda M and Schraut, Katharina E and Segre, Ayellet V and Smith, Albert V and Stolk, Lisette and Teumer, Alexander and Anulis, Irene L and Bandinelli, Stefania and Beckmann, Matthias W and Benitez, Javier and Bergmann, Sven and Franke, Lude and Hartman, Catharina A and Oldehinkel, Albertine J and Wolffenbuttel, Bruce H. R and Alizadeh, Behrooz Z and Snieder, Harold and Endometrial Canc Accoc Consortium and InterAct Consortium and PRACTICAl Consortium and kConFab AOCS Investigators and LifeLines Cohort Study and Ovarian Canc Accoc Consortium and kConFab/AOCS Investigators and Ovarian Cancer Association Consortium and PRACTICAL consortium and Endometrial Cancer Association Consortium and The InterAct Consortium and The LifeLines Cohort Study
Nature genetics, ISSN 1061-4036, 06/2017, Volume 49, Issue 6, pp. 834 - 841
REGRESSION | METAANALYSIS | METABOLISM | GROWTH | BODY-MASS INDEX | LOCI | WIDE ASSOCIATION | MENDELIAN RANDOMIZATION | TRAITS | INHERITANCE | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Body Mass Index | Genomic Imprinting | Genetic Predisposition to Disease | Genome-Wide Association Study | Calcium-Binding Proteins | Age Factors | Membrane Proteins - genetics | Menarche - genetics | Humans | Risk Factors | Intercellular Signaling Peptides and Proteins - genetics | Databases, Genetic | Male | Puberty - genetics | Neoplasms - genetics | Adolescent | Female | Ribonucleoproteins - genetics | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Genetic variation | Menarche | Genetic aspects | Gene expression | Health aspects | Carcinogenesis | Risk factors | Enrichment | Transcription | Laboratories | Genomics | Genes | Risk | Genomes | Tissues | Preadipocyte factor 1 | Epidemiology | Variance | Complexity | Body mass index | Mens health | Randomization | Coding | Genetics | Trends | Children | Endometrium | Public health | Age | Medical research | Puberty | Internal medicine | Gynecology | Health risks | Time measurement | Obstetrics | Diseases | Medicine | Studies | Hospitals | Body mass | Womens health | Men | Breast | Links | Heritability | Polygenic inheritance | Prostate cancer | Prostate | Endocrinology | Cancer | Index Medicus | InterAct Consortium | AOCS Investigators | PRACTICAL consortium | Endometrial Cancer Association Consortium | Ovarian Cancer Association Consortium | LifeLines Cohort Study | kConFab | Medicin och hälsovetenskap
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