Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (407) 407
Newspaper Article (126) 126
Conference Proceeding (66) 66
Publication (65) 65
Book / eBook (41) 41
Book Chapter (34) 34
Book Review (28) 28
Patent (18) 18
Dissertation (13) 13
Magazine Article (10) 10
Web Resource (6) 6
Compact Disc (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (194) 194
humans (156) 156
female (77) 77
male (76) 76
genetic aspects (58) 58
research (58) 58
risk factors (58) 58
genetics (57) 57
article (54) 54
genetics & heredity (48) 48
polymorphism, single nucleotide (46) 46
cardiac & cardiovascular systems (45) 45
medical and health sciences (44) 44
medicin och hälsovetenskap (44) 44
middle aged (44) 44
genome-wide association study (43) 43
adult (42) 42
abridged index medicus (41) 41
genetic predisposition to disease (40) 40
cardiovascular disease (39) 39
studies (39) 39
analysis (38) 38
genomes (34) 34
aged (32) 32
genome-wide association (32) 32
risk (31) 31
phenotype (30) 30
animals (29) 29
cardiovascular (29) 29
computer science (29) 29
genomics (28) 28
cardiovascular diseases (26) 26
diabetes (26) 26
artificial intelligence (25) 25
atherosclerosis (25) 25
genetic variation (25) 25
clinical medicine (24) 24
disease (24) 24
health aspects (24) 24
insulin resistance (24) 24
klinisk medicin (24) 24
algorithms (23) 23
association (23) 23
case-control studies (23) 23
genes (23) 23
genotype (23) 23
optimization (23) 23
schizophrenia (23) 23
cholesterol (22) 22
hypercholesterolemia (22) 22
multidisciplinary sciences (22) 22
polymorphism, single nucleotide - genetics (22) 22
population (21) 21
cardiology (20) 20
endocrinology & metabolism (20) 20
internal medicine (20) 20
mice (20) 20
peripheral vascular disease (20) 20
gene expression (19) 19
usage (19) 19
coronary heart disease (18) 18
endocrinology and diabetes (18) 18
endokrinologi och diabetes (18) 18
evolutionary computation (18) 18
genetic research (18) 18
meta-analysis (18) 18
variants (18) 18
computer science, theory & methods (17) 17
metaanalysis (17) 17
physics (17) 17
risk assessment (17) 17
type 2 diabetes (17) 17
calculating (16) 16
computing (16) 16
coronary-artery-disease (16) 16
counting (16) 16
physiological aspects (16) 16
psychiatry (16) 16
single nucleotide polymorphisms (16) 16
biology (15) 15
care and treatment (15) 15
glucose (15) 15
hypertension (15) 15
loci (15) 15
schizophrenia - genetics (15) 15
algorithm analysis and problem complexity (14) 14
alleles (14) 14
familial hypercholesterolemia (14) 14
heart attacks (14) 14
low density lipoproteins (14) 14
research article (14) 14
susceptibility loci (14) 14
adolescent (13) 13
biochemistry & molecular biology (13) 13
epidemiology (13) 13
genetic algorithms (13) 13
genetic predisposition to disease - genetics (13) 13
heart-disease (13) 13
medicine (13) 13
methods (13) 13
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (16) 16
Online Resources - Online (14) 14
UTL at Downsview - May be requested (10) 10
UofT at Scarborough - Stacks (6) 6
Collection Dvlpm't (Acquisitions) - Closed Orders (5) 5
Victoria University E.J. Pratt - Stacks (4) 4
OISE - Stacks (3) 3
Thomas Fisher Rare Book - Rare Book (3) 3
UofT at Mississauga - Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Music - Stacks (2) 2
Pontifical Inst. Mediaeval Studies - Library use only (2) 2
Trinity College (John W Graham) - Stacks (2) 2
Gerstein Science - Stacks (1) 1
Indust. Rel's & Hum. Resources (Newman) - Library use only (1) 1
Law (Bora Laskin) - Stacks (1) 1
Music - Circulation Desk (1) 1
OISE - Curriculum Resources (1) 1
Pontifical Inst. Mediaeval Studies - Oversize (1) 1
Robarts - May be requested in 6-10 wks (1) 1
Robarts - Storage (1) 1
Royal Ontario Museum - Far Eastern Reference (1) 1
St. Augustine's Seminary - Reference (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
Trinity College (John W Graham) - Reference (1) 1
Trinity College (John W Graham) - Wycliffe Storage (1) 1
University College (Laidlaw) - Stacks (1) 1
UofT at Scarborough - Withdrawn (1) 1
Victoria University CRRS - Library use only (1) 1
Victoria University E.J. Pratt - Reference (1) 1
Victoria University Emmanuel College - Reference (1) 1
Victoria University Emmanuel College - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Distinguishing Coevolution from Covicariance in an Obligate Pollination Mutualism: Asynchronous Divergence in Joshua Tree and its Pollinators
by Christopher Irwin Smith and William K. W. Godsoe and Shantel Tank and Jeremy B. Yoder and Olle Pellmyr
Evolution, ISSN 0014-3820, 2008, Volume 62, Issue 10, pp. 2676 - 2687
Abstract Obligate pollination mutualisms-–in which both plants and their pollinators are reliant upon one another for reproduction-–represent some of the most... 
Bouse Embayment | pollination | coevolution | cospeciation | yucca moth | Biogeography | yucca | vicariance | Pollinating insects | Gene flow | Chloroplasts | Phylogenetics | Evolution | Moths | Coevolution | Genetic mutation | Mutualism | Pollination | Yucca | Yucca moth | Vicariance | Cospeciation | DIVERSIFICATION | FIG | MITOCHONDRIAL-DNA EVOLUTION | TIME DEPENDENCY | AGAVACEAE | YUCCA-BREVIFOLIA | RATES | EVOLUTIONARY BIOLOGY | ORIGIN | GENETICS & HEREDITY | ECOLOGY | LEPIDOPTERA | LIKELIHOOD | Geography | DNA, Chloroplast - chemistry | Yucca - physiology | Phylogeny | Sequence Analysis, DNA | Moths - genetics | Animals | Genetic Speciation | Bayes Theorem | Moths - physiology | Mutation | Yucca - genetics | Evolution, Molecular | Usage | Cladistic analysis | Analysis | Mutualism (Biology) | Research | Pollination by insects | Studies | Butterflies & moths | Plant reproduction | Flowers & plants | Evolutionary biology | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
by Lange, Leslie A and Lange, Ethan M and Lange, Christoph and Hu, Youna and Zhang, Qunyuan and Zhang, Ji and Zhang, He and Xue, Chenyi and Schmidt, Ellen M and Tang, Hua and Tang, Zheng-Zheng and Bizon, Chris and Smith, Nicholas L and Smith, Joshua D and Smith, Albert V and Turner, Emily H and Jun, Goo and Kang, Hyun Min and Peloso, Gina and Auer, Paul L and Auer, Paul and Li, Kuo-ping and Li, Mingyao and Li, Yun and Li, Bingshan and Li, Dalin and Flannick, Jason and Fuchsberger, Christian and Gaulton, Kyle and Lindgren, Cecilia and Locke, Adam and Manning, Alisa and Sim, Xueling and Rivas, Manuel A and Holmen, Oddgeir L and Gottesman, Omri and Lu, Yingchang and Ruderfer, Douglas and Stahl, Eli A and Duan, Qing and Durda, Peter and Durda, J. Peter and Jiao, Shuo and Isaacs, Aaron and Hofman, Albert and Bis, Joshua C and Bis, Joshua and Correa, Adolfo and Griswold, Michael E and Jakobsdottir, Johanna and Schreiner, Pamela and Schreiner, Pamela J and Feitosa, Mary F and Huffman, Jennifer E and Crosby, Jacy and Wassel, Chrstina L and Wassel, Christina L and Do, Ron and Franceschini, Nora and Martin, Lisa and Martin, Lisa W and Martin, Thomas R and Robinson, Jennifer G and Assimes, Themistocles L and Crosslin, David R and Rosenthal, Elisabeth A and Tsai, Michael Y and Tsai, Michael and Rieder, Mark J and Farlow, Deborah N and Folsom, Aaron R and Lumley, Thomas and Fox, Ervin R and Fox, Caroline S and Fox, P. Keolu and Fox, Ervin and Carlson, Christopher S and Peters, Ulrike and Jackson, Rebecca D and Jackson, Rebecca and van Duijn, Cornelia M and Uitterlinden, André G and Levy, Daniel and Rotter, Jerome I and Taylor, Herman A and Taylor, Kira C and Taylor, Kent and Gudnason, Vilmundur and Siscovick, David S and Fornage, Myriam and Borecki, Ingrid B and Hayward, Caroline and Rudan, Igor and Chen, Wei-Min and Chen, Y. Eugene and Chen, Donna T and Chen, Ida Y and Bottinger, Erwin P and Loos, Ruth J.F and Sætrom, Pål and ... and NHLBI Grand Opportunity Exome Sequ and NHLBI Grand Opportunity Exome Sequencing Project and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
The American Journal of Human Genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 233 - 245
Elevated low-density lipoprotein cholesterol (LDL-C) is a treatable, heritable risk factor for cardiovascular disease. Genome-wide association studies (GWASs)... 
OBJECTIVES | HEART-DISEASE | DESIGN | PLASMA | SUSCEPTIBILITY | GENETICS & HEREDITY | ATHEROSCLEROSIS | RISK | DENSITY-LIPOPROTEIN-CHOLESTEROL | ABSORPTION | SPECTRUM | Dyslipidemias - genetics | Genetic Code | Follow-Up Studies | Humans | Middle Aged | Male | Proprotein Convertases - genetics | Exome | Dyslipidemias - blood | Serine Endopeptidases - genetics | Adult | Female | Receptors, LDL - genetics | Genome-Wide Association Study | Gene Frequency | Genotype | Sequence Analysis, DNA | Cholesterol, LDL - genetics | Phenotype | Apolipoproteins E - blood | Apolipoproteins E - genetics | Aged | Polymorphism, Single Nucleotide | Cohort Studies | Lipase - genetics | Proprotein Convertase 9 | Genetic code | Genetic variation | Physiological aspects | Genetic research | Cholesterol, LDL | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Genotype & phenotype | Low density lipoprotein | Genes | Cholesterol | Risk factors | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Analysis of shared heritability in common disorders of the brain
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Index Medicus | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
by Speliotes, Elizabeth and Willer, Cristen and Berndt, Sonja and Monda, Keri and Thorleifsson, Gudmar and Jackson, Anne and Allen, H.L and Lindgren, Cecilia and Luan, J and Mägi, Reedik and Randall, Joshua and Vedantam, Sailaja and Winkler, Thomas and Qi, Lu and Workalemahu, Tsegaselassie and Heid, Iris and Steinthorsdottir, Valgerdur and Stringham, Heather and Wheeler, Eleanor and Wood, Anew and Ferreira, Teresa and Weyant, Robert and Segrè, Ayellet and Eestrada, Karol and Liang, Liming and Nemesh, James and Park, J.H and Gustafsson, Stefan and Kilpeläinen, Tuomas and Yang, Joanna and Bouatia-Naji, Nabila and Eesko, Tõnu and Feitosa, Mary Furlan and Kutalik, Zoltán and Mangino, Massimo and Raychaudhuri, Soumya and Scherag, Ane and Smith, Albert Vernon and Welch, Ryan and Zhao, Jing Hua and Aben, Katja and Absher, Devin and Amin, Najaf and Dixon, Anna and Fisher, Eeva and Glazer, Nicole and Goddard, Michael and Heard-Costa, Nancy and Hoesel, Volker and Hottenga, Jouke Jan and Johansson, Åsa and Johnson, Toby and Ketkar, Shamika and Lamina, Claudia and Li, Shengxu and Moffatt, Miriam and Myers, Richard and Narisu, Narisu and Perry, John and Peters, Marjolein and Preuss, Michael and Ripatti, Samuli and Rivadeneira Ramirez, Fernando and Sandholt, Camilla and Scott, Laura and Timpson, Nicholas and Tyrer, Jonathan and Wingerden, Sophie and White, Charles and Wiklund, Freik and Barlassina, Christina and Chasman, Daniel and Cooper, Matthew and Jansson, J.O and Lawrence, Robert and Pellikka, Niina and Prokopenko, Inga and Shi, Jianxin and Thiering, Eelisabeth and Alavere, Helene and Alibrandi, Maria and Almgren, Peter and Arnold, Alice and Aspelund, Thor and Atwood, Larry and Balkau, Beverley and Balmforth, Anthony and Bennett, Amanda and Ben-Shlomo, Y and Bergman, Richard and Bergmann, Sven and Biebermann, Heike and Blakemore, Alexana and Boes, Tanja and Bonnycastle, Lori and Bornstein, Stefan and Brown, Morris and Buchanan, Thomas and Busonero, F and Campbell, Harry and ... and MAGIC and Procardis Consortium and on behalf of Procardis Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 11/2010, Volume 42, Issue 11, pp. 937 - 948
textabstractObesity is globaLy prevalent and highly heritable, but its underlying genetic factors remain largely elusive. To identify genetic loci for obesity... 
COMMON VARIANTS | GLUCOSE-HOMEOSTASIS | FTO GENE | GENETICS & HEREDITY | EARLY-ONSET | MELANOCORTIN-4 RECEPTOR GENE | RISK | GASTRIC-INHIBITORY POLYPEPTIDE | ADULT OBESITY | FAT MASS | GENOME-WIDE ASSOCIATION | Body Mass Index | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Humans | Body Size - genetics | Chromosome Mapping | Polymorphism, Single Nucleotide | Body Weight - genetics | Obesity - genetics | Body Height - genetics | Measurement | Body mass index | Obesity | Genetic aspects | Research | Risk factors | Studies | Medical research | Hospitals | Biomedical research | Councils | Risk assessment | Genetics | Society | Charitable foundations | Public health | Index Medicus | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Hundreds of variants clustered in genomic loci and biological pathways affect human height
by Allen, H.L and Estrada Gil, Karol and Lettre, Guillaume and Berndt, Sonja and Rivadeneira Ramirez, Fernando and Willer, Cristen and Jackson, Anne and Vedantam, Sailaja and Raychaudhuri, Soumya and Ferreira, Teresa and Wood, Anew and Weyant, Robert and Segrè, Ayellet and Speliotes, Elizabeth and Wheeler, Eleanor and Soranzo, Nicole and Park, J.H and Yang, Joanna and Gudbjartsson, Daniel and Heard-Costa, Nancy and Randall, Joshua and Qi, Lu and Smith, Albert Vernon and Mägi, Reedik and Pastinen, Tomi and Liang, Liming and Heid, Iris and Luan, J and Thorleifsson, Gudmar and Winkler, Thomas and Goddard, Michael and Lo, K.S and Palmer, Cameron and Workalemahu, Tsegaselassie and Aulchenko, Yurii and Johansson, Åsa and Zillikens, Carola and Feitosa, Mary Furlan and Esko, Tõnu and Johnson, Toby and Ketkar, Shamika and Kraft, Peter and Mangino, Massimo and Prokopenko, Inga and Absher, Devin and Albrecht, Eva and Ernst, Florian and Glazer, Nicole and Hayward, Caroline and Hottenga, Jouke Jan and Jacobs, Kevin and Knowles, Joshua and Kutalik, Zoltán and Monda, Keri and Polasek, Ozren and Preuss, Michael and Rayner, Nigel William and Robertson, Neil and Steinthorsdottir, Valgerdur and Tyrer, Jonathan and Voight, Benjamin and Wiklund, Freik and Xu, Jianfeng and Zhao, Jing Hua and Nyholt, Dale and Pellikka, Niina and Perola, Markus and Perry, John and Surakka, Ida and Tammesoo, M.L and Altmaier, Elizabeth and Amin, Najaf and Aspelund, Thor and Bhangale, Tushar and Boucher, Gabrielle and Chasman, Daniel and Chen, Constance and Coin, Lachlan and Cooper, Matthew and Dixon, Anna and Gibson, Quince and Grundberg, Elin and Hao, Ke and Junttila, Juhani and Kaplan, Robert and Kettunen, Johannes and König, Inke and Kwan, Tony and Lawrence, Robert and Levinson, Douglas and Lorentzon, Mattias and McKnight, Barbara and Morris, Anew and Müller, Martina and Ngwa, J.S and Purcell, Shaun and Rafelt, Suzanne and Salem, Rany and Salvi, Erika and Sanna, Serena and ... and Procardis Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature: international weekly journal of science, ISSN 0028-0836, 10/2010, Volume 467, Issue 7317, pp. 832 - 838
textabstractMost common human traits and diseases have a polygenic pattern of inheritance: DNA sequence variants at many genetic loci influence the phenotype.... 
COMMON VARIANTS | POPULATION | DISEASES | WIDE ASSOCIATION ANALYSIS | MULTIDISCIPLINARY SCIENCES | GROWTH | SNPS | TRAITS | HERITABILITY | ADULT | STRATIFICATION | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Metabolic Networks and Pathways - genetics | Phenotype | Humans | Genetic Loci - genetics | Polymorphism, Single Nucleotide - genetics | Body Height - genetics | Chromosomes, Human, Pair 3 - genetics | Genome, Human - genetics | Confidence intervals | Genetics | Independent sample | Meta-analysis | Index Medicus | Life Sciences | Naturvetenskap | Natural Sciences | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights