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2015, ISBN 9782503535265, 160 pages
Book
Nature genetics, ISSN 1061-4036, 06/2012, Volume 44, Issue 6, pp. 670 - 5
COMMON VARIANTS | PR INTERVAL | REPLICATION | CHROMOSOME 4Q25 | DILATED CARDIOMYOPATHY | MUTATIONS | PROTEINS | UMCG Approved | PACEMAKER CHANNEL | GENOME-WIDE ASSOCIATION | CAVEOLIN-1 | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Cardiology. Vascular system | Heart | Cardiac dysrhythmias | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Humans | Middle Aged | Risk Factors | Asian Continental Ancestry Group - genetics | Child, Preschool | Infant | Male | Genetic Loci | Atrial Fibrillation - genetics | Young Adult | Adolescent | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Child | Infant, Newborn | Gene mutations | Atrial fibrillation | Disease susceptibility | Genetic aspects | Research | Health aspects | Risk factors | Cardiac arrhythmia | Signal transduction | Musculoskeletal system | Genealogy | Genetics | Genomes | Gene loci | Mutation | Chromosomes | Methods | Meta-analysis | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 06/2017, Volume 49, Issue 6, pp. 946 - 952
VISUALIZATION | GENETIC-VARIATION | METAANALYSIS | SNP | ANNOTATION | SUSCEPTIBILITY | RISK | BURDEN | GENOME-WIDE ASSOCIATION | TOOL | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | African Americans - genetics | Genetic Loci | Atrial Fibrillation - genetics | Quantitative Trait Loci | Pharmaceutical research | Genetic variation | Atrial fibrillation | Genetic research | Genetic aspects | Forecasts and trends | Drug discovery | Identification and classification | Risk factors | Heart | Cardiac arrhythmia | Thoracic surgery | Target recognition | Laboratories | Syngeneic grafts | Genes | Genomics | Risk | Genomes | Remodeling | Epidemiology | Fibrillation | Electrocardiography | Genetics | Cardiology | Heart diseases | Public health | Heart failure | Stroke | Genealogy | Internal medicine | Mortality | Loci | Meta-analysis | Medicine | Studies | Hospitals | Death | Gene loci | Index Medicus | population genetics | gene-expression | genome-wide association studies | Genetik | Biological Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
Journal Article
JAMA oncology, ISSN 2374-2437, 02/2017, Volume 3, Issue 5, pp. 636 - 651
Life Sciences & Biomedicine | Oncology | Science & Technology | Mendelian Randomization Analysis - methods | Risk Assessment - methods | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Humans | Middle Aged | Male | Telomere Homeostasis - genetics | Cardiovascular Diseases - genetics | Neoplasms - genetics | Aged, 80 and over | Germ-Line Mutation | Adult | Female | Aged | Polymorphism, Single Nucleotide | Telomere - genetics | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 09/2018, Volume 50, Issue 9, pp. 1225 - 1233
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Ethnic Groups - genetics | Humans | Transcriptome | Atrial Fibrillation - ethnology | Atrial Fibrillation - genetics | Genome-Wide Association Study - methods | Quantitative Trait Loci | Case-Control Studies | Genome-wide association studies | Usage | Genetic aspects | Research | Atrial fibrillation | Heart | Cardiac arrhythmia | Disease | Genes | Genomics | Genomes | Gene expression | Drug development | Muscle contraction | Loci | Ethnic factors | Meta-analysis | Quantitative trait loci | Consortia | Fibrillation | Pathways | Mutation | Bioinformatics | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
2011, ISBN 0962336416, 471
Book
Nature genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 524 - 537
HUMAN GENETIC-VARIATION | SMALL-VESSEL DISEASE | SUDDEN CARDIAC DEATH | SUSCEPTIBILITY LOCI | WHITE-MATTER HYPERINTENSITIES | ISCHEMIC-STROKE | COMPLEX TRAITS | CORONARY-ARTERY-DISEASE | HEMORRHAGIC STROKE | ATRIAL-FIBRILLATION | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Epigenesis, Genetic | Humans | Risk Factors | Computational Biology | Databases, Genetic | Male | Genetic Loci | Gene Regulatory Networks | Stroke - physiopathology | INDEL Mutation | Stroke - genetics | Linkage Disequilibrium | Stroke - classification | Female | Models, Genetic | Polymorphism, Single Nucleotide | Stroke | Genes | Health risks | Risk | Cardiovascular disease | Genomes | Genetic diversity | Regression analysis | Loci | Meta-analysis | Consortia | Pleiotropy | Etiology | Blood pressure | Thromboembolism | Bioinformatics | Asians | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
2001, Bettie Allison Rand lectures in art history, ISBN 0807826413, x, 188 pages
Book