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Molecular psychiatry, ISSN 1359-4184, 03/2014, Volume 19, Issue 3, pp. 351 - 357
Alzheimer's disease (AD) | Apolipoprotein E (APOE) | Amyloid | Butyrylcholinesterase (BCHE) | Florbetapir (AV-45) | Genomewide association study (GWAS) | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Neurology | Organic mental disorders. Neuropsychology | 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 | Geriatrics | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Butyrylcholinesterase - genetics | Aniline Compounds | Humans | Middle Aged | Male | Positron-Emission Tomography | Cerebral Cortex - diagnostic imaging | Cerebral Cortex - metabolism | Plaque, Amyloid - diagnostic imaging | Functional Neuroimaging | Ethylene Glycols | Apolipoproteins E - genetics | Aged, 80 and over | Cognitive Dysfunction - genetics | Female | Plaque, Amyloid - metabolism | Aged | Alzheimer Disease - genetics | Physiological aspects | Research | Alzheimer's disease | Psychiatric research | Amyloid beta-protein | Index Medicus | genome-wide association study (GWAS) | florbetapir (AV-45) | Alzheimer’s disease (AD) | amyloid | butyrylcholinesterase (BCHE) | apolipoprotein E (APOE)
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Stroke (1970), ISSN 0039-2499, 01/2013, Volume 44, Issue 1, pp. S26 - S28
Whole exome sequencing | Rare variant | Intracranial aneurysm | DNA - genetics | Exome - genetics | Genome-Wide Association Study | Animals | Intracranial Aneurysm - genetics | Pedigree | Humans | Exons - genetics | Intracranial Aneurysm - epidemiology | Genome, Human | Sequence Analysis, DNA | Index Medicus
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Nature reviews. Gastroenterology & hepatology, ISSN 1759-5045, 08/2013, Volume 10, Issue 8, pp. 487 - 494
Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Receptor, Muscarinic M2 - genetics | Aldehyde Dehydrogenase, Mitochondrial | Humans | Risk Factors | Aldehyde Dehydrogenase - genetics | G Protein-Coupled Inwardly-Rectifying Potassium Channels - genetics | Alcoholism - epidemiology | Proteins - genetics | Receptors, GABA-A - genetics | Alcohol Dehydrogenase - genetics | Liver - physiology | Alcoholism - genetics | Alcoholism - physiopathology | Complications and side effects | Genetic variation | Alcoholism | Causes of | Physiological aspects | Genetic aspects | Research | Index Medicus
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Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 9, pp. 989 - +
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Humans | Risk Factors | Genotype | Polymorphism, Single Nucleotide | Genetic Loci | Parkinson Disease - genetics | Genome-Wide Association Study - methods | Case-Control Studies | Genome-wide association studies | Parkinson's disease | Genetic aspects | Single nucleotide polymorphisms | Identification and classification | Methods | Risk factors | Studies | Genealogy | Parkinsons disease | Quality control | DNA methylation | Statistical methods | Genomes | Health risk assessment | Meta-analysis | Index Medicus
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Mayo Clinic proceedings, ISSN 0025-6196, 2016, Volume 92, Issue 2, pp. 292 - 305
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Precision Medicine - standards | Humans | High-Throughput Nucleotide Sequencing - methods | Nervous System Diseases - genetics | Nervous System Diseases - diagnosis | Precision Medicine - methods | High-Throughput Nucleotide Sequencing - standards | Nervous System Diseases - therapy | Usage | Nervous system diseases | Nucleotide sequencing | Diagnosis | Exome sequencing | DNA sequencing | Index Medicus | Abridged Index Medicus
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NeuroImage (Orlando, Fla.), ISSN 1053-8119, 11/2010, Volume 53, Issue 3, pp. 1051 - 1063
Neuroimaging | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Radiology, Nuclear Medicine & Medical Imaging | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Genotype | Male | Cognition Disorders - genetics | Magnetic Resonance Imaging | Phenotype | Apolipoproteins E - genetics | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Quantitative Trait Loci | Cluster Analysis | Databases, Factual | Studies | Genotype & phenotype | Automation | Medical imaging | Genomics | Genetics | Genomes | Public private partnerships | Index Medicus | Alzheimer's disease
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Common genetic determinants of vitamin D insufficiency: a genome-wide association study
The Lancet (British edition), ISSN 0140-6736, 2010, Volume 376, Issue 9736, pp. 180 - 188
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | General aspects | Medical sciences | Immunoassay | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Vitamin D Deficiency - genetics | United States | Europe | Humans | International Cooperation | Chromosomes, Human, Pair 4 | Linkage Disequilibrium | Vitamin D - blood | Canada | Homozygote | Vitamin D Deficiency - prevention & control | Vitamin D - genetics | Vitamin D Deficiency - blood | Heterozygote | Vitamin D - analogs & derivatives | Chromosomes, Human, Pair 11 | Polymorphism, Single Nucleotide | Seasons | Dietary Supplements | Cohort Studies | Vitamin D deficiency | Genetic aspects | Research | Genetic variation | Risk factors | Studies | Medical research | Vitamin D | Nutrition | Index Medicus | Abridged Index Medicus | Endokrinologi och diabetes | Endocrinology and Diabetes
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