UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.
Search Articles
The New England journal of medicine, ISSN 0028-4793, 01/2013, Volume 368, Issue 2, pp. 107 - 116
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Neurology | Organic mental disorders. Neuropsychology | General aspects | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Apolipoprotein E4 - genetics | Humans | Risk Factors | Cognition | Mutation, Missense | Genotyping Techniques | Sequence Analysis, DNA | Case-Control Studies | Iceland | Membrane Glycoproteins - genetics | Genetic Variation | Aged, 80 and over | Heterozygote | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Receptors, Immunologic - genetics | Genetic variation | Causes of | Genetic aspects | Research | Apolipoproteins | Alzheimer's disease | Health aspects | Genomes | Alzheimers disease | Older people | Age | Cognitive ability | Index Medicus | Abridged Index Medicus
Journal Article
Alzheimer's & dementia, ISSN 1552-5260, 07/2013, Volume 9, pp. P123 - P123
Journal Article
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 5, pp. 545 - 551
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Polymorphism, Single Nucleotide - genetics | Cognition Disorders - genetics | Genetic Loci | Genetic Markers | Alzheimer Disease - genetics | Dementia - genetics | Chromosomes, Human, Pair 12 - genetics | Hippocampus - physiopathology | Proteins | Neurology | Medical research | Genotype & phenotype | Ischemia | Education | Religious orders | Aging | Genetics | Genomes | Alzheimers disease | Index Medicus | Neuroscience | Cognitive science
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 02/2014, Volume 22, Issue 2, pp. 216 - 220
neurodegeneration | dementia | healthy cell bias | C18 | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Genetic Association Studies | Gene Frequency | Humans | Male | Risk | Alzheimer Disease - enzymology | Sex Characteristics | Case-Control Studies | Linkage Disequilibrium | Aromatase - genetics | Epistasis, Genetic | Interleukin-10 - genetics | Aged, 80 and over | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Odds Ratio | Neuroprotection | Cytokines | Neurodegenerative diseases | Estrogens | Childrens health | Sex | Systematic review | Gender differences | Epistasis | Breast cancer | Inflammation | Epidemiology | Post-menopause | Brain research | Hospitals | Womens health | Aromatase | Interleukin 10 | Interleukin 1 | Genetics | Alzheimers disease | Health risk assessment | Alzheimer's disease | Dementia | Index Medicus
Journal Article
Lancet neurology, ISSN 1474-4422, 10/2020, Volume 19, Issue 10, pp. 840 - 848
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Creutzfeldt-Jakob Syndrome - epidemiology | Creutzfeldt-Jakob Syndrome - diagnosis | Genetic Predisposition to Disease - genetics | Humans | Risk Factors | Genetic Loci - genetics | Polymorphism, Single Nucleotide - genetics | Creutzfeldt-Jakob Syndrome - genetics | Genetic Predisposition to Disease - epidemiology | Genome-Wide Association Study - methods | Genetic research | Genomics | Creutzfeldt-Jakob disease | Health care | Phenotypes | Transcription | Neurodegenerative diseases | Amino acid sequence | Genomes | Single-nucleotide polymorphism | Gene expression | Patients | Risk factors | Proteins | Genotyping | Surveillance | Tau protein | Progressive supranuclear palsy | Protein folding | Prions | Quality control | Heritability | Paralysis | Lipid metabolism | Prion protein | Health risk assessment | Index Medicus
Journal Article
Stroke (1970), ISSN 0039-2499, 02/2014, Volume 45, Issue 2, pp. 394 - 402
Genetic | Genetics | Risk assessment | Risk factors | Polymorphism | Clinical Neurology | Peripheral Vascular Disease | Neurosciences & Neurology | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Vascular diseases and vascular malformations of the nervous system | Medical sciences | Nervous system (semeiology, syndromes) | Prospective Studies | Humans | Middle Aged | Brain Ischemia - genetics | Male | Multilocus Sequence Typing | Case-Control Studies | Stroke - genetics | Genetic Variation | Aged, 80 and over | Adult | Female | Population | Stroke - epidemiology | Blood Pressure - physiology | Hypertension - epidemiology | Brain Ischemia - epidemiology | Genetic Predisposition to Disease | Genome-Wide Association Study | Reproducibility of Results | Risk Assessment | Risk Factors | Atrial Fibrillation - complications | Atrial Fibrillation - epidemiology | Coronary Artery Disease - complications | Sex Factors | Hypertension - complications | Polymorphism, Single Nucleotide - genetics | Aged | Coronary Artery Disease - epidemiology | Cohort Studies | Index Medicus | genetic | risk assessment | risk factors | polymorphism | genetics
Journal Article
Stroke (1970), ISSN 0039-2499, 02/2014, Volume 45, Issue 2, pp. 403 - 412
Genetic epidemiology | Stroke | Risk factors | Clinical Neurology | Peripheral Vascular Disease | Neurosciences & Neurology | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Vascular diseases and vascular malformations of the nervous system | Medical sciences | Nervous system (semeiology, syndromes) | Genetic Predisposition to Disease | Genome-Wide Association Study | Age Factors | Area Under Curve | Humans | Middle Aged | Risk Factors | European Continental Ancestry Group | Genotype | Male | Case-Control Studies | Stroke - genetics | Regression Analysis | Sex Factors | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Female | ROC Curve | Stroke - epidemiology | Aged | Cohort Studies | Index Medicus | stroke epidemiology | cardiovascular risk factors | population studies | genetic risk prediction | genetic epidemiology
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2015, Volume 23, Issue 6, pp. 837 - 843
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Dystrophin - genetics | Humans | Middle Aged | Adult | Female | Male | Cognition | Polymorphism, Single Nucleotide | Memory | Cognitive ability | Nervous system | Population studies | Epidemiology | Medical ethics | Muscular dystrophy | Studies | Genetic variance | Cognition & reasoning | Rodents | Reading comprehension | Population | Genetics | Mutation | Dystrophin | Index Medicus
Journal Article