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American journal of medical genetics. Part B, Neuropsychiatric genetics, ISSN 1552-4841, 07/2016, Volume 171, Issue 5, pp. 650 - 675
animal models | genetic association studies | aggression | epigenetics | Genetics & Heredity | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Aggression - physiology | Neuroendocrine Cells | Dopamine | Genetic Association Studies | Serotonin | Humans | Risk Factors | Aggression - psychology | Gene-Environment Interaction | Behavior, Animal | Animals | Epigenesis, Genetic - genetics | Social Behavior | Genome-Wide Association Study - methods | Genetic research | Epigenetic inheritance | Analysis | Index Medicus
Journal Article
European child & adolescent psychiatry, ISSN 1018-8827, 3/2010, Volume 19, Issue 3, pp. 169 - 178
Autistic disorder | Linkage | Copy number variation | Medicine & Public Health | Mutation | Psychiatry | Whole genome association | Pediatrics | Social Sciences | Life Sciences & Biomedicine | Psychology | Psychology, Developmental | Science & Technology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Diseases in Twins - genetics | Humans | Chromosome Mapping | Genetic Counseling | Child Development Disorders, Pervasive - psychology | Child Development Disorders, Pervasive - genetics | DNA Mutational Analysis | Genetic Markers - genetics | Adolescent | Child Development Disorders, Pervasive - diagnosis | DNA Copy Number Variations - physiology | Cytogenetic Analysis | Child | Autism | Anopheles | Genetic counseling | Oncology, Experimental | Medical genetics | Psychotherapy | Genetic aspects | Research | Cancer | Index Medicus | Review
Journal Article
American journal of human genetics, ISSN 0002-9297, 05/2009, Volume 84, Issue 5, pp. 605 - 616
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Nijmegen Breakage Syndrome - pathology | Genetic Predisposition to Disease | Tumor Suppressor Proteins - metabolism | Signal Transduction | Cell Survival | Humans | Radiation Tolerance | Cell Cycle Proteins - metabolism | Cells, Cultured | DNA Repair Enzymes - genetics | Ataxia Telangiectasia Mutated Proteins | DNA-Binding Proteins - genetics | Nijmegen Breakage Syndrome - genetics | DNA-Binding Proteins - deficiency | DNA-Binding Proteins - metabolism | DNA Repair Enzymes - metabolism | Germ-Line Mutation | Adult | Female | Heterozygote | DNA Damage | Chromosomal Instability | DNA Repair Enzymes - deficiency | Protein-Serine-Threonine Kinases - metabolism | Medical colleges | Immunoglobulins | Molecular genetics | Nuclear radiation | DNA damage | DNA synthesis | Automated teller machines | Mental illness | Proteins | Genetic disorders | Mutation | Medical disorders | Genes | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Human genetics, ISSN 0340-6717, 6/2014, Volume 133, Issue 6, pp. 781 - 792
Human Genetics | Gene Function | Molecular Medicine | Biomedicine | Metabolic Diseases | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Child Development Disorders, Pervasive - metabolism | Calcium-Calmodulin-Dependent Protein Kinase Type 4 - metabolism | Humans | Child, Preschool | Male | Fragile X Mental Retardation Protein - metabolism | Genotyping Techniques | Calcium-Calmodulin-Dependent Protein Kinase Type 4 - genetics | Neuronal Plasticity - genetics | Female | Child | Genetic Predisposition to Disease | Signal Transduction | Child Development Disorders, Pervasive - pathology | Risk Factors | Gene Expression Regulation | European Continental Ancestry Group | Child Development Disorders, Pervasive - genetics | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Alleles | Protein Binding | Fragile X Mental Retardation Protein - genetics | Polymorphism, Single Nucleotide | Adaptor Proteins, Signal Transducing - metabolism | Child Development Disorders, Pervasive - ethnology | Autism | Family | RNA | Genes | Genomics | Risk factors | Index Medicus | Calcium-Calmodulin-Dependent Protein Kinase Type 4 | Psychiatrics and mental health | Fragile X Mental Retardation Protein | Life Sciences | Human health and pathology | Adaptor Proteins, Signal Transducing | Neuronal Plasticity | Child Development Disorders, Pervasive | Cognitive science | Medicin och hälsovetenskap
Journal Article
Journal of Neural Transmission, ISSN 0300-9564, 9/2014, Volume 121, Issue 9, pp. 1107 - 1116
Neurology | Common variant | Neurosciences | Repetitive behaviour | Medicine & Public Health | High-functioning autism | Association analysis | Transmission disequilibrium testing | Pharmacology/Toxicology | Psychiatry | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Psychiatric Status Rating Scales | Child Development Disorders, Pervasive - genetics | Humans | Female | Logistic Models | Male | Polymorphism, Single Nucleotide | Genotyping Techniques | Child | Nucleocytoplasmic Transport Proteins - genetics | Cohort Studies | Autism | RNA | Glutamate | Risk factors | Index Medicus
Journal Article