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Cell (Cambridge), ISSN 0092-8674, 06/2018, Volume 173, Issue 7, pp. 1705 - 1715.e16
Journal Article
American journal of human genetics, ISSN 0002-9297, 06/2018, Volume 102, Issue 6, pp. 1185 - 1194
Genetics(clinical) | Humans | Databases, Genetic | accuracy | schizophrenia | Haplotypes/genetics | Likelihood Functions | Polymorphism, Single Nucleotide/genetics | biasedness | genome-wide SNPs | Body Height/genetics | Computer Simulation | linkage disequilibrium score regression | Adult | Genetics | genetic correlation | Linkage Disequilibrium/genetics | Schizophrenia/genetics | height | body mass index | Genotype | SNP heritability | Regression Analysis | Phenotype | Inheritance Patterns/genetics | Genome, Human | genomic restricted maximum likelihood
Journal Article
Molecular psychiatry, ISSN 1359-4184, 05/2018, Volume 23, Issue 5, pp. 1181 - 1188
Journal Article
European neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S713 - S713
Journal Article
European neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S713 - S713
Journal Article
Nature communications, ISSN 2041-1723, 11/2017, Volume 8, Issue 1, pp. 1826 - 11
Journal Article | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Crohn Disease - genetics | Computational Biology - methods | Genetic Predisposition to Disease | Genome-Wide Association Study - instrumentation | Humans | Databases, Genetic | Molecular Sequence Annotation - methods | Chromosome Mapping - instrumentation | Linkage Disequilibrium | Chromosome Mapping - methods | Internet | Genome, Human | Genome-Wide Association Study - methods | Quantitative Trait Loci | Chromatin - genetics | Quantitative trait loci | Genotype & phenotype | Biological effects | Chromatin | Annotations | Visual aids | Coding | Linkage disequilibrium | Gene loci | Gene expression | Gene mapping | Data interpretation | Index Medicus
Journal Article
Biological psychiatry (1969), ISSN 0006-3223, 01/2021, Volume 89, Issue 1, pp. 41 - 53
Pathway analysis | molQTL | Polygenicity | Gene-set analysis | Genome-wide association study | Functional genomics | Biological Psychiatry | Anopheles | Chromatin | Nervous system diseases | Neurosciences | Analysis | Genomics | Genes | Development and progression | Genetic aspects | Methylation | Coercive interrogation | Methods | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 07/2018, Volume 50, Issue 7, pp. 912 - 919
Genetics | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Humans | Middle Aged | Adolescent | Female | Male | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Intelligence - genetics | Quantitative Trait Loci | Brain - physiology | Brain | Chromatin | Neurosciences | Intelligence | Synaptogenesis | Mental disorders | Genomics | Genes | Cognitive ability | Schizophrenia | Association analysis | Nervous system | Identification | Mapping | Genomes | Genetic effects | Annotations | Coding | Genetic analysis | Neostriatum | Alzheimer's disease | Bioinformatics | Neurodegenerative diseases | Neurons | Attention deficit hyperactivity disorder | Causation | Gene expression | Spiny neurons | Loci | Educational attainment | Meta-analysis | Quantitative trait loci | Neurological diseases | Studies | Pyramidal cells | Gene loci | Gene mapping | Alzheimers disease | Hippocampus | Index Medicus | Medicin och hälsovetenskap
Journal Article
Neuron (Cambridge, Mass.), ISSN 0896-6273, 06/2017, Volume 94, Issue 6, pp. 1101 - 1111.e7
structural variation | genetics | copy number variation | CNTN6 | Tourette Syndrome | NRXN1 | tic disorders | neurodevelopmental disorders | SNP GENOTYPING DATA | GENETICS | HIDDEN-MARKOV MODEL | NEUREXINS | COHORT | PREVALENCE | ASSOCIATION | OBSESSIVE-COMPULSIVE DISORDER | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Tourette Syndrome - genetics | Contactins - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Genotype | Male | Nerve Tissue Proteins - genetics | Case-Control Studies | Cell Adhesion Molecules, Neuronal - genetics | DNA Copy Number Variations | Young Adult | Adolescent | Adult | Female | Odds Ratio | Child | Tourette's syndrome | Nervous system diseases | Genomics | Obsessive compulsive disorder | Working groups | Mental disorders | Copy number | Circuits | Genes | Cortex | Schizophrenia | Genomes | Single-nucleotide polymorphism | Cases (containers) | Loci | Studies | Consortia | Attention Deficit Hyperactivity Disorder | Genetics | Gilles de la Tourette syndrome | Tourette syndrome | Index Medicus
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Full Text
Meta-analysis of the heritability of human traits based on fifty years of twin studies
Nature genetics, ISSN 1061-4036, 2015, Volume 47, Issue 7, pp. 702 - +
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genetic Association Studies | Twins, Monozygotic - genetics | Humans | Models, Genetic | Gene-Environment Interaction | Genetic Heterogeneity | Twins, Dizygotic - genetics | Cluster Analysis | Chromosome mapping | Genetic variation | Innovations | Genetic aspects | Heritability | Twins | Identification and classification | Studies | Design | Sample size | Authorship | Genes | Older people | Classification | Population | Research | Metabolism | Estimates | Index Medicus | Medicin och hälsovetenskap
Journal Article
Nature reviews. Genetics, ISSN 1471-0056, 2016, Volume 17, Issue 6, pp. 353 - 364
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Computational Biology - methods | Algorithms | Humans | Polymorphism, Single Nucleotide - genetics | Gene Expression Profiling | Software | Models, Statistical | Genome-Wide Association Study - methods | Genomics - methods | Genome-wide association studies | Gene expression | Observations | Genetic variation | Identification and classification | Methods | Index Medicus
Journal Article
Neuron (Cambridge, Mass.), ISSN 0896-6273, 05/2017, Volume 94, Issue 3, pp. 486 - 499.e9
gene discovery | TIC Genetics | de novo variants | Tourette disorder | Tourette syndrome | TSAICG | whole-exome sequencing | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Tourette Syndrome - genetics | Genetic Predisposition to Disease | Humans | Parents | Male | Phosphoproteins - genetics | Sequence Analysis, DNA | Genetic Variation | Proteins - genetics | Adult | Female | Fibronectins - genetics | Mutation | Cadherins - genetics | Odds Ratio | Child | Intracellular Signaling Peptides and Proteins - genetics | Cell Cycle Proteins | Cohort Studies | Receptors, Cell Surface - genetics | Tourette's syndrome | Fibronectins | Epidermal growth factor | Genes | Obsessive compulsive disorder | Pathogenesis | Genomics | Genomes | Cadherin | Neurodevelopmental disorders | Fibronectin | Studies | Consortia | Celsr3 protein | Signal transduction | Autism | Coding | Attention Deficit Hyperactivity Disorder | Quality control | Genetics | Gilles de la Tourette syndrome | Siblings | Index Medicus
Journal Article