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Nature neuroscience, ISSN 1097-6256, 10/2016, Volume 19, Issue 11, pp. 1426 - 1428
Journal Article
Genome medicine, ISSN 1756-994X, 07/2016, Volume 8, Issue 1, pp. 78 - 78
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Psychotic Disorders - diagnosis | Genome-Wide Association Study | Quantitative Trait, Heritable | Rett Syndrome - diagnosis | Humans | Genotype | Genetic Pleiotropy | Arthritis, Rheumatoid - pathology | Genetic Variation | Arthritis, Rheumatoid - genetics | Phenotype | Psychotic Disorders - genetics | Animals | Epistasis, Genetic | Rett Syndrome - pathology | Psychotic Disorders - pathology | Models, Genetic | Quantitative Trait Loci | Rett Syndrome - genetics | Arthritis, Rheumatoid - diagnosis | Type 2 diabetes | Pleiotropy | Care and treatment | Genomics | Genetic aspects | Research | Risk factors | Editing | Cardiovascular disease | Genomes | Gene expression | Medicine | Studies | Genotype & phenotype | Body mass index | Coronary vessels | Rheumatoid arthritis | DNA methylation | Mutation | Diabetes | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Nature neuroscience, ISSN 1097-6256, 2014, Volume 17, Issue 6, pp. 782 - 790
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Mental Disorders - genetics | Genetic Predisposition to Disease - genetics | Animals | Genomics | Humans | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Mental Disorders - diagnosis | Genetic aspects | Research | Genetic variation | Mental illness | Risk factors | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 05/2018, Volume 50, Issue 5, pp. 635 - 637
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Autism Spectrum Disorder | Genome-Wide Association Study | High-Throughput Nucleotide Sequencing | Humans | Medical research | Genomics | Genetic research | Medicine, Experimental | Genomes | Genetic aspects | Nucleotide sequencing | DNA sequencing | Studies | Hypotheses | Annotations | Disease | Families & family life | Mutation | Gene sequencing
Journal Article
Nature (London), ISSN 0028-0836, 2013, Volume 502, Issue 7469, pp. 93 - 95
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Selection, Genetic | Reproduction - genetics | Genotype | Male | Mating Preference, Animal - physiology | Polymorphism, Genetic | Genetic Variation | Phenotype | Animals | Survival Analysis | Female | Horns | Receptors, G-Protein-Coupled - genetics | Confidence intervals | Genotype & phenotype | Animal reproduction | Population | Sheep | Gene loci | Males | Success | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 07/2016, Volume 48, Issue 7, pp. 718 - 724
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Age Factors | Paternal Age | Genetic Markers - genetics | Humans | Risk Factors | Male | Mutation - genetics | Child | Autistic Disorder - etiology | Schizophrenia - etiology | Gene mutations | Father and child | Aging | Development and progression | Genetic aspects | Mental illness | Population genetics | Identification and classification | Health aspects | Methods | Mental disorders | Schizophrenia | Genomes | Studies | Autism | Hypotheses | Liability | Fathers | Mutation | Behavior | Health risk assessment | Public health | Age | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 2018, Volume 50, Issue 8, pp. 1112 - 1121
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Middle Aged | Male | Educational Status | Multifactorial Inheritance | Phenotype | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Cohort Studies | Cell interaction | Genome-wide association studies | Usage | Analysis | Multifactorial traits | Research | Health education | Brain | Phenotypes | Dosage compensation | Sample size | Cognitive ability | Association analysis | Genomes | Single-nucleotide polymorphism | Gene expression | Estimates | Environmental effects | Educational attainment | Meta-analysis | Consortia | Education | X Chromosomes | Genetic analysis | Heritability | Index Medicus | Clinical Medicine | Obstetrics, Gynecology and Reproductive Medicine | Reproduktionsmedicin och gynekologi | Klinisk medicin
Journal Article
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Genome-wide association study identifies 74 loci associated with educational attainment
Nature (London), ISSN 0028-0836, 05/2016, Volume 533, Issue 7604, pp. 539 - 542
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genome-Wide Association Study | Gene Expression Regulation - genetics | Humans | Molecular Sequence Annotation | Computational Biology | Fetus - metabolism | United Kingdom | Cognition | Educational Status | Bipolar Disorder - genetics | Gene-Environment Interaction | Brain - metabolism | Schizophrenia - genetics | Polymorphism, Single Nucleotide - genetics | Alzheimer Disease - genetics | Quantitative trait loci | Academic achievement | Genome-wide association studies | Genetic aspects | Observations | Studies | Genomes | Gene expression | Genes | Educational attainment | Meta-analysis | Index Medicus | Quantitative Finance | Obstetrics, Gynecology and Reproductive Medicine | Reproduktionsmedicin och gynekologi
Journal Article
Nature genetics, ISSN 1061-4036, 03/2013, Volume 45, Issue 3, pp. 234 - 238
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Autistic Disorder - genetics | Genetic Predisposition to Disease | Schizophrenia - genetics | Genetic Association Studies | Pedigree | Humans | Exons - genetics | Mutation | Open Reading Frames - genetics | Genetic Linkage | Quantitative genetics | Gene mutations | Genetic variation | Neuropsychiatry | Nucleotide sequencing | Research | Methods | DNA sequencing | Proteins | Studies | Genetics | Genes | Index Medicus
Journal Article
Lancet neurology, ISSN 1474-4422, 12/2019, Volume 18, Issue 12, pp. 1091 - 1102
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Phenotypes | Parkinson's disease | Neurodegenerative diseases | Genomics | Parkinsons disease | Cognitive ability | Clinical trials | Genomes | Single-nucleotide polymorphism | Gene expression | Putamen | Risk factors | Datasets | Studies | Prediction models | DNA methylation | Aging | Heritability | Movement disorders | Index Medicus
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