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Molecular psychiatry, ISSN 1359-4184, 01/2015, Volume 20, Issue 10, pp. 1232 - 1239
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Genetic Association Studies | Humans | Middle Aged | Self Report | African Americans - genetics | Male | Sleep - genetics | Dyssomnias - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Quantitative trait loci | Genome-wide association studies | Genetic aspects | Sleep | Health aspects | Identification and classification | Attention deficit hyperactivity disorder | Genomes | Metabolism | Loci | Chromosome 2 | Morbidity | Consortia | Genetic variance | Gene frequency | Alleles | Cardiovascular diseases | Chromosomes | Pax8 protein | Thyroid | Index Medicus | Genome-wide association study
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Translational psychiatry, ISSN 2158-3188, 2017, Volume 7, Issue 4, pp. e1109 - e1109
Life Sciences & Biomedicine | Psychiatry | Science & Technology | Iceland - epidemiology | Humans | Middle Aged | Magnetic Resonance Imaging - methods | Male | Temporal Lobe - anatomy & histology | Developmental Disabilities - genetics | Functional Neuroimaging - methods | Functional Neuroimaging - standards | Temporal Lobe - diagnostic imaging | Intellectual Disability - genetics | Young Adult | Dyscalculia - genetics | Cognition - physiology | Adult | Female | Chromosome Deletion | Neuropsychological Tests - standards | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Dyslexia - genetics | Phenotype | Adolescent | Chromosome Aberrations | Heterozygote | Aged | Index Medicus | Original
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Science (American Association for the Advancement of Science), ISSN 0036-8075, 6/2013, Volume 340, Issue 6139, pp. 1467 - 1471
Medical research | Phenotypes | Psychology | REPORTS | Personality traits | Genetic research | Research facilities | Genetics | Epidemiology | Research universities | Educational attainment | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genome-Wide Association Study | Endophenotypes | Humans | Female | Male | Cognition | Educational Status | Polymorphism, Single Nucleotide | Genetic Loci | Multifactorial Inheritance | Academic achievement | Genetic aspects | Research | Single nucleotide polymorphisms | Genetic variation | Genomics | Science education | Index Medicus | Single Nucleotide | Medicinsk genetik | Medical Genetics | Psykiatri | Psychiatry | Polymorphism
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GWAS for executive function and processing speed suggests involvement of the CADM2 gene
Molecular psychiatry, ISSN 1359-4184, 02/2016, Volume 21, Issue 2, pp. 189 - 197
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | gamma-Aminobutyric Acid | Cell Adhesion Molecules - genetics | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Cell Adhesion Molecules - physiology | Genetic Association Studies | Introns | Genomics | Humans | Middle Aged | Male | Executive Function - physiology | Neuropsychological Tests | Aged, 80 and over | Cognition - physiology | Female | Aged | Genetic Variation - genetics | Polymorphism, Single Nucleotide | Cohort Studies | GABA | Physiological aspects | Genetic aspects | Single nucleotide polymorphisms | Research | Diagnosis | Dementia | Index Medicus
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BMJ, ISSN 0959-8138, 2011, Volume 342, Issue 7794, pp. 425 - 425
RESEARCH | Disease risk | Coronary artery disease | Medical genetics | Predisposing factors | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Coronary Disease - blood | Prospective Studies | Gene Frequency | Humans | Middle Aged | Risk Factors | Male | C-Reactive Protein - genetics | C-Reactive Protein - metabolism | Coronary Disease - genetics | Mendelian Randomization Analysis | Polymorphism, Single Nucleotide - genetics | Female | Cardiovascular disease | Genetic markers | Causality | RecA protein | Meta-analysis | Index Medicus | Abridged Index Medicus | Medicin och hälsovetenskap
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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Nature (London), ISSN 0028-0836, 10/2014, Volume 514, Issue 7520, pp. 92 - 97
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Age Factors | Diabetes Mellitus, Type 2 - genetics | Humans | Genetic Loci - genetics | Parents | Male | Cardiovascular Diseases - genetics | Obesity - genetics | Europe - ethnology | Female | Ribonucleoproteins - genetics | Hypothalamo-Hypophyseal System - physiology | Child | Body Mass Index | Genome-Wide Association Study | Calcium-Binding Proteins | Membrane Proteins - genetics | Menarche - genetics | Intercellular Signaling Peptides and Proteins - genetics | Potassium Channels, Tandem Pore Domain - genetics | Ovary - physiology | Receptors, Retinoic Acid - metabolism | Genomic Imprinting - genetics | Proteins - genetics | Breast Neoplasms - genetics | Adolescent | Alleles | Polymorphism, Single Nucleotide - genetics | Quantitative Trait Loci - genetics | Receptors, GABA-B - metabolism | Allelomorphism | Menarche | Physiological aspects | Genome-wide association studies | Genetic aspects | Vitamin A | Puberty | Menstruation | Acids | Genomes | Mutation | Chromosomes | Girls | Age | Index Medicus | Medicin och hälsovetenskap
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