Articles

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

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (6) 6
science & technology (6) 6
female (5) 5
life sciences & biomedicine (5) 5
male (5) 5
biological and medical sciences (3) 3
case-control studies (3) 3
epidemiology (3) 3
genetic aspects (3) 3
genome-wide association study (3) 3
genomes (3) 3
genotype (3) 3
medical research (3) 3
medical sciences (3) 3
polymorphism, single nucleotide (3) 3
adult and adolescent clinical studies (2) 2
aging (2) 2
alleles (2) 2
biochemistry & molecular biology (2) 2
cardiovascular disease (2) 2
complex traits (2) 2
coronary heart disease (2) 2
coronary vessels (2) 2
councils (2) 2
diabetes (2) 2
genetic predisposition to disease (2) 2
genetic variation (2) 2
genetics (2) 2
genetics & heredity (2) 2
genetics and genomics (2) 2
genetics of disease (2) 2
kidney stones (2) 2
medical genetics (2) 2
medicine (2) 2
meta-analysis (2) 2
metabolites (2) 2
middle aged (2) 2
oligonucleotide array sequence analysis (2) 2
population genetics (2) 2
psychiatry (2) 2
psychology. psychoanalysis. psychiatry (2) 2
psychopathology. psychiatry (2) 2
public health and epidemiology (2) 2
research (2) 2
risk (2) 2
science (2) 2
single nucleotide polymorphisms (2) 2
abridged index medicus (1) 1
adults (1) 1
allergy and immunology (1) 1
ankyrins - genetics (1) 1
anticholesteremic agents - therapeutic use (1) 1
apolipoproteins (1) 1
association studies (1) 1
association studies articles (1) 1
biological psychiatry (1) 1
biomarkers (1) 1
bipolar disorder (1) 1
bipolar disorder - genetics (1) 1
bipolar disorders (1) 1
blood cholesterol (1) 1
calcium channels, l-type - genetics (1) 1
cardiology. vascular system (1) 1
cardiovascular diseases (1) 1
cardiovascular disorders (1) 1
care and treatment (1) 1
carrier proteins (1) 1
children (1) 1
cholesterol (1) 1
cholesterol, ldl - blood (1) 1
cholesterol, ldl - drug effects (1) 1
cholesterol, ldl - genetics (1) 1
chromosome deletion (1) 1
chromosome disorders - complications (1) 1
chromosome disorders - genetics (1) 1
chromosome mapping (1) 1
chromosome replication (1) 1
chromosomes, human, pair 10 (1) 1
chromosomes, human, pair 2 - genetics (1) 1
chromosomes, human, pair 6 - genetics (1) 1
chromosomes, human, pair 9 (1) 1
chromosomes, human, pair 9 - genetics (1) 1
cnv (1) 1
cohort studies (1) 1
computational biology (1) 1
confidence intervals (1) 1
consortia (1) 1
coronary artery (1) 1
coronary artery disease (1) 1
coronary artery disease - genetics (1) 1
coronary disease - genetics (1) 1
coronary disease - prevention & control (1) 1
deoxyribonucleic acid (1) 1
deoxyribonucleic acid--dna (1) 1
dna (1) 1
dna copy number variations - genetics (1) 1
environmental health (1) 1
european continental ancestry group - genetics (1) 1
eye diseases (1) 1
female; genetic variation; genome-wide association study; gout/etiology; humans; male; uric acid/blood ; colaus study (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 Genomewide Association Analysis of Coronary Artery Disease
by Samani, Nilesh J and Erdmann, Jeanette and Hall, Alistair S and Hengstenberg, Christian and Mangino, Massimo and Mayer, Bjoern and Dixon, Richard J and Meitinger, Thomas and Braund, Peter and Wichmann, H.-Erich and Barrett, Jennifer H and König, Inke R and Stevens, Suzanne E and Szymczak, Silke and Tregouet, David-Alexandre and Iles, Mark M and Pahlke, Friedrich and Pollard, Helen and Lieb, Wolfgang and Cambien, Francois and Fischer, Marcus and Ouwehand, Willem and Blankenberg, Stefan and Balmforth, Anthony J and Baessler, Andrea and Ball, Stephen G and Strom, Tim M and Brænne, Ingrid and Gieger, Christian and Deloukas, Panos and Tobin, Martin D and Ziegler, Andreas and Thompson, John R and Schunkert, Heribert and Cardiogenics Consortium and WTCCC and WTCCC and the Cardiogenics Consortium
The New England journal of medicine, ISSN 0028-4793, 08/2007, Volume 357, Issue 5, pp. 443 - 453
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Cardiology. Vascular system | Heart | Biological and medical sciences | General aspects | Medical sciences | Coronary heart disease | Myocardial Infarction - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genotype | Male | Risk | Genetic Markers | Chromosomes, Human, Pair 6 - genetics | Chromosomes, Human, Pair 2 - genetics | Chromosomes, Human, Pair 9 - genetics | Coronary Artery Disease - genetics | Female | Polymorphism, Single Nucleotide | Genome, Human | Cardiovascular disease | Gene loci | Heart attacks | Coronary vessels | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia
by Grozeva, Detelina and Conrad, Donald F and Barnes, Chris P and Hurles, Matthew and Owen, Michael J and O'Donovan, Michael C and Craddock, Nick and Kirov, George and WTCCC
Schizophrenia research, ISSN 0920-9964, 2011, Volume 135, Issue 1, pp. 1 - 7
Psychiatry | Schizophrenia | CNV | WTCCC | Life Sciences & Biomedicine | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Psychoses | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Chromosome Deletion | Genetic Predisposition to Disease | Humans | Chromosome Disorders - complications | Genotype | Male | DNA Copy Number Variations - genetics | Microarray Analysis - statistics & numerical data | Schizophrenia - epidemiology | Case-Control Studies | Schizophrenia - genetics | Female | United Kingdom - epidemiology | Chromosome Disorders - genetics | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample
by Green, E.K and Hamshere, M and Forty, L and Gordon-Smith, K and Fraser, C and Russell, E and Grozeva, D and Kirov, G and Holmans, P and Moran, J.L and Purcell, S and Sklar, P and Owen, M.J and O'donovan, M.C and Jones, L and Jones, I.R and Craddock, N and WTCCC
Molecular psychiatry, ISSN 1359-4184, 12/2013, Volume 18, Issue 12, pp. 1302 - 1307
PGC-BD | genome-wide significant association | rs3818253 | bipolar disorder | immunoChip | rs7296288 | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Miscellaneous | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Mood disorders | Biological and medical sciences | Medical sciences | Bipolar disorders | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Oligonucleotide Array Sequence Analysis | Humans | Middle Aged | Male | Genotyping Techniques | Bipolar Disorder - genetics | Case-Control Studies | Calcium Channels, L-Type - genetics | Ankyrins - genetics | Alleles | Polymorphism, Single Nucleotide - genetics | Female | Chromosome replication | Bipolar disorder | Genotype | Genetic aspects | Research | Single nucleotide polymorphisms | Identification and classification | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125b in the TwinsUK cohort
by Nag, Abhishek and Venturini, Cristina and Small, Kerrin S and Young, Terri L and Viswanathan, Ananth C and Mackey, David A and Hysi, Pirro G and Hammond, Christopher and Int Glaucoma Genetics Consortium and International Glaucoma Genetics Consortium
Human molecular genetics, ISSN 0964-6906, 2014, Volume 23, Issue 12, pp. 3343 - 3348
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Vesicular Transport Proteins - metabolism | Humans | Vesicular Transport Proteins - genetics | Male | United Kingdom | Chromosomes, Human, Pair 9 | Intraocular Pressure - genetics | Female | Glaucoma - pathology | Polymorphism, Single Nucleotide | Glaucoma - genetics | Twins | Cohort Studies | Index Medicus | Association Studies
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
by Kolz, Melanie and Johnson, Toby and Sanna, Serena and Teumer, Alexander and Vitart, Veronique and Perola, Markus and Mangino, Massimo and Albrecht, Eva and Wallace, Chris and Farrall, Martin and Johansson, Åsa and Dimas, Antigone and Aulchenko, Yurii and Beckmann, Jacques and Bergmann, Sven and Bochud, Murielle and Brown, Morris and Campbell, Harry and Connell, John and Dominiczak, Anna and Homuth, Georg and Lamina, Claudia and McCarthy, Mark and Meitinger, Thomas and Mooser, Vincent and Munroe, Patricia and Nauck, Matthias and Peden, John and Prokisch, Holger and Salo, Perttu and Salomaa, Veikko and Samani, Nilesh and Schlessinger, David and Uda, Manuela and Waeber, Gérard and Waterworth, Dawn and Wang-Sattler, Rui and Wright, Alan and Adamski, Jerzy and Whitfield, John and Gyllensten, Ulf and Wilson, James and Rudan, Igor and Pramstaller, Peter Paul and Watkins, Hugh and Doering, Angela and Wichmann, Erich and Spector, Timothy and Peltonen, Leena Johanna and Völzke, Henry and Nagaraja, Ramaiah and Vollenweider, Peter and Caulfield, Mark and Illig, Thomas and Gieger, Christian and Völker, Uwe and ENGAGE Consortium and KORA Study and EUROSPAN Consortium and PROCARDIS Consortium and WTCCC and for the EUROSPAN Consortium and for the PROCARDIS Consortium and for the ENGAGE Consortium and for the KORA Study and for the WTCCC
PLoS genetics, ISSN 1553-7390, 06/2009, Volume 5, Issue 6, pp. e1000504 - e1000504
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Variation | Genome-Wide Association Study | Humans | Female | Male | Uric Acid - blood | Gout - etiology | Prevention | Hyperuricemia | Care and treatment | Carrier proteins | Genetic variation | Physiological aspects | Genetic aspects | Research | Uric acid | Health aspects | Index Medicus | Medical research | Metabolites | Councils | Deoxyribonucleic acid | DNA | Aging | Genomes | Diabetes | Epidemiology | Meta-analysis | Kidney stones
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease-A Mendelian Randomisation Study
by Linsel-Nitschke, Patrick and Goetz, Anika and Erdmann, Jeanette and Braenne, Ingrid and Braund, Peter and Hengstenberg, Christian and Stark, Klaus and Fischer, Marcus and Schreiber, Stefan and El Mokhtari, Nour Eddine and Schaefer, Arne and Schrezenmeier, Juergen and Rubin, Diana and Hinney, Anke and Reinehr, Thomas and Roth, Christian and Ortlepp, Jan and Hanrath, Peter and Hall, Alistair S and Mangino, Massimo and Lieb, Wolfgang and Lamina, Claudia and Heid, Iris M and Doering, Angela and Gieger, Christian and Peters, Annette and Meitinger, Thomas and Wichmann, H. -Erich and Koenig, Inke R and Ziegler, Andreas and Kronenberg, Florian and Samani, Nilesh J and Schunkert, Heribert and Cardiogenics Consortium and WTCCC and Wellcome Trust Case Control Consortium (WTCCC) and for the Wellcome Trust Case Control Consortium (WTCCC) and the Cardiogenics Consortium
PloS one, ISSN 1932-6203, 08/2008, Volume 3, Issue 8, pp. e2986 - e2986
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Receptors, LDL - genetics | Oligonucleotide Array Sequence Analysis | Risk Assessment | Humans | Risk Factors | Cholesterol, LDL - drug effects | Chromosome Mapping | Random Allocation | Case-Control Studies | Genetic Variation | Cholesterol, LDL - genetics | Coronary Disease - prevention & control | Anticholesteremic Agents - therapeutic use | Coronary Disease - genetics | Cholesterol, LDL - blood | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 10 | Medical research | Hypercholesterolemia | Blood cholesterol | Low density lipoproteins | Genes | Medicine, Experimental | Genetic research | Genetics | Genetic aspects | Single nucleotide polymorphisms | Coronary heart disease | Risk factors | Lipoproteins (low density) | Risk | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Gene polymorphism | Epidemiology | Consortia | Confidence intervals | Randomization | Population | Lipoprotein (low density) receptors | Children | Heart diseases | Statistical analysis | Mortality | Coronary artery | Health risks | Environmental health | Genetic diversity | Regression analysis | Metabolism | LDLR gene | Apolipoproteins | Coronary artery disease | Low density lipoprotein | Cholesterol | Studies | Genetic variance | Hospitals | Coronary vessels | Alleles | Biomarkers | Receptor density | Adults | Mutation | Polymorphism | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text A Genome-wide Assessment of the Genetic Basis of Type 1 Diabetes
by Plagnol, Vincent, Mr, JDRF/WT DIL, University of Cambridge, Cambridge, England and Clayton, David, Professor, JDRF/WT Diabetes and Inflammation Laboratory, Cambridge, England and Dunger, David, Department of Pediatric, University of Cambridge, Cambridge, England and Downes, Kate, JDRF/WT Diabetes and Inflammation Laboratory, Cambridge, England and Leung, Hin-Tak, JDRF/WT Diabetes and Inflammation Laboratory, Cambridge, England and Smyth, Deborah, JDRF/WT Diabetes and Inflammation Laboratory, Cambridge, England and Stevens, Helen, JDRF/WT Diabetes and Inflammation Laboratory, Cambridge, England and Walker, Neil, Mr, JDRF/WT Diabetes and Inflammation Laboratory, Cambridge, England and WTCCC, Wellcome Trust Case Control Consortium, http://www.wtccc.org.uk/, Wellcome Trust, Cambridge, England and Todd, John, Professor, JDRF/WT Diabetes and Inflammation Laboratory, Cambridge, England and WTCCC, Wellcome Trust Case Control Consortium
Clinical immunology (Orlando, Fla.), ISSN 1521-6616, 2006, Volume 123, pp. S136 - S136
Allergy and Immunology
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations
: e1000504
by Melanie Kolz and Toby Johnson and Serena Sanna and Alexander Teumer and Veronique Vitart and Markus Perola and Massimo Mangino and Eva Albrecht and Chris Wallace and Martin Farrall and Åsa Johansson and Dale R Nyholt and Yurii Aulchenko and Jacques S Beckmann and Sven Bergmann and Murielle Bochud and Morris Brown and Harry Campbell and John Connell and Anna Dominiczak and Georg Homuth and Claudia Lamina and Mark I McCarthy and Thomas Meitinger and Vincent Mooser and Patricia Munroe and Matthias Nauck and John Peden and Holger Prokisch and Perttu Salo and Veikko Salomaa and Nilesh J Samani and David Schlessinger and Manuela Uda and Uwe Völker and Gérard Waeber and Dawn Waterworth and Rui Wang-Sattler and Alan F Wright and Jerzy Adamski and John B Whitfield and Ulf Gyllensten and James F Wilson and Igor Rudan and Peter Pramstaller and Hugh Watkins and Angela Doering and H-Erich Wichmann and Tim D Spector and Leena Peltonen and Henry Völzke and Ramaiah Nagaraja and Peter Vollenweider and Mark Caulfield and Thomas Illig and Christian Gieger and for the EUROSPAN Consortium and for the ENGAGE Consortium and for the PROCARDIS Consortium and for the KORA Study and for the WTCCC
PLoS genetics, ISSN 1553-7390, 06/2009, Volume 5, Issue 6
Medical research | Metabolites | Councils | Aging | Genomes | Diabetes | Epidemiology | Deoxyribonucleic acid--DNA | Meta-analysis | Kidney stones
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Correction: Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study
by Linsel-Nitschke, Patrick and Götz, Anika and Erdmann, Jeanette and Braenne, Ingrid and Braund, Peter and Hengstenberg, Christian and Stark, Klaus and Fischer, Marcus and Schreiber, Stefan and El Mokhtari, Nour Eddine and Schaefer, Arne and Schrezenmeir, Jürgen and Rubin, Diana and Hinney, Anke and Reinehr, Thomas and Roth, Christian and Ortlepp, Jan and Hanrath, Peter and Hall, Alistair S and Mangino, Massimo and Lieb, Wolfgang and Lamina, Claudia and Heid, Iris M and Doering, Angela and Gieger, Christian and Peters, Annette and Meitinger, Thomas and Wichmann, H.-Erich and König, Inke R and Ziegler, Andreas and Kronenberg, Florian and Samani, Nilesh J and Schunkert, Heribert and for the Wellcome Trust Case Control Consortium (WTCCC) and the Cardiogenics Consortium
PloS one, ISSN 1932-6203, 09/2008, Volume 3, Issue 9
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.