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Molecular psychiatry, ISSN 1359-4184, 12/2013, Volume 18, Issue 12, pp. 1315 - 1323
de novo mutation | anomalous dopamine efflux | autism spectrum disorder | dopamine | Drosophila melanogaster | transporter | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Humans | Risk Factors | Child, Preschool | Child Development Disorders, Pervasive - physiopathology | Male | Dopamine Plasma Membrane Transport Proteins - genetics | Drosophila melanogaster - genetics | Mutation, Missense - genetics | Motor Activity - genetics | Animals | Child Development Disorders, Pervasive - genetics | Dopamine - physiology | Dopaminergic Neurons - physiology | Homeostasis - genetics | Dopamine | Gene mutations | Pervasive developmental disorders | Genetic aspects | Research | Nucleotide sequencing | Properties | Risk factors | DNA sequencing | Autism | Index Medicus
Journal Article
Molecular psychiatry, ISSN 1359-4184, 04/2012, Volume 17, Issue 4, pp. 402 - 411
structural variation | synaptic transmission | neurotransmission | glutamatergic signaling | autism | copy-number variation | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Genotyping Techniques - psychology | Genetic Predisposition to Disease - genetics | Synaptic Transmission - genetics | Humans | Child, Preschool | Male | DNA Copy Number Variations - genetics | Synapses - genetics | Genome-Wide Association Study - statistics & numerical data | Nerve Tissue Proteins - genetics | Case-Control Studies | Phenotype | Animals | Child Development Disorders, Pervasive - genetics | Adolescent | Adult | Female | Mice | Genome-Wide Association Study - methods | Genotyping Techniques - methods | Child | Psychological aspects | Autism | Genetic variation | Physiological aspects | Neural transmission | Genetic aspects | Health aspects | Synapses | Index Medicus | Original
Journal Article
Journal of autism and developmental disorders, ISSN 0162-3257, 5/2017, Volume 47, Issue 5, pp. 1314 - 1322
Pediatrics | Child and School Psychology | Neurosciences | Public Health | Family peer advocate | Psychology | Minority | Caregiver stress | Autism spectrum disorder | Psychology, Developmental | Social Sciences | Caregivers | Stress Variables | Intervention | Stress Management | Program Validation | Hispanic American Students | Autism | Randomized Controlled Trials | Pervasive Developmental Disorders | Family Programs | Models | African American Students | Program Effectiveness | Single-Blind Method | Stress, Psychological - therapy | Caregivers - psychology | Humans | Child, Preschool | Peer Group | Male | Patient Acceptance of Health Care - psychology | Health Knowledge, Attitudes, Practice | Hispanic Americans - psychology | Family Therapy | Parents - psychology | Mental Health Services | Autism Spectrum Disorder - nursing | Quality of Life | Adult | Female | Child | African Americans - psychology | Psychological aspects | Care and treatment | Research | Behavior | Pervasive developmental disorders | Caretaker syndrome | Mental disorders | Health services | Service provision | Hispanic Americans | Mental health | Families & family life | Retention | Hispanic people | Empowerment | Carers | Parents & parenting | Advocacy | Family support | Ethnic groups | Mental health services | Diagnosis | Children | Helpseeking | Autistic spectrum disorders | Efficacy | Autistic children | Minority & ethnic groups | Stress | Quality of life | Children & youth | Service delivery | Studies | Quantitative psychology | Developmental disabilities | Index Medicus
Journal Article
Molecular psychiatry, ISSN 1359-4184, 08/2013, Volume 18, Issue 8, pp. 889 - 897
therapeutics | amyloid | autophagy | Alzheimer's disease | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Organic mental disorders. Neuropsychology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Biological and medical sciences | Medical sciences | Neuropharmacology | Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) | Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer | Neurology | Psychopharmacology | Pharmacology. Drug treatments | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Psychopathology. Psychiatry | Neuroprotective Agents - therapeutic use | Peptide Fragments - metabolism | TOR Serine-Threonine Kinases - metabolism | Microtubule-Associated Proteins - metabolism | Cells, Cultured | Alzheimer Disease - drug therapy | Mice, Transgenic | Cognition - drug effects | Autophagy - drug effects | Alzheimer Disease - pathology | Brain - drug effects | Brain - metabolism | Dose-Response Relationship, Drug | Animals | Neuroprotective Agents - pharmacology | Autophagy-Related Protein 5 | Signal Transduction - drug effects | Amyloid beta-Peptides - metabolism | Indoles - pharmacology | Indoles - therapeutic use | Mice | alpha-Synuclein - metabolism | Alzheimer Disease - psychology | Autophagy (Cytology) | Reports | Care and treatment | Models | Research | Index Medicus | Alzheimer’s disease
Journal Article
Molecular psychiatry, ISSN 1359-4184, 2002, Volume 7, Issue 3, pp. 311 - 316
Journal Article
Molecular psychiatry, ISSN 1359-4184, 06/2013, Volume 18, Issue 6, pp. 635 - 636
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | DNA Methylation | Mental Disorders - pathology | Animals | Paternal Age | Mice | Mice, Inbred Strains | Brain - physiology | Disease Models, Animal | Physiological aspects | Fathers | Mental illness | Risk factors | Age | Index Medicus
Journal Article
The American journal of pathology, ISSN 0002-9440, 2000, Volume 156, Issue 1, pp. 15 - 20
Neurology | Biological and medical sciences | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
Molecular psychiatry, ISSN 1359-4184, 09/2010, Volume 15, Issue 9, pp. 954 - 968
MULTILOCUS GENOTYPE DATA | autistic disorder | CANDIDATE GENES | SPECTRUM DISORDERS | CHROMOSOME 7Q | UMCG Approved | PERVASIVE DEVELOPMENTAL DISORDERS | GENOME | disease susceptibility | chromosome 7 | LINKED MENTAL-RETARDATION | chromosome 2 | LINKAGE ANALYSES | ARRAY-CGH | MUTATIONS | single nucleotide polymorphisms | linkage disequilibrium | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Autistic Disorder - genetics | Genetic Predisposition to Disease | Humans | Genotype | Male | Gene Dosage | Chromosomes, Human, Pair 7 | Linkage Disequilibrium | Chromosomes, Human, Pair 2 | Genetic Variation | Endopeptidases - genetics | Adult | Female | Polymorphism, Single Nucleotide | GTPase-Activating Proteins - genetics | Child | Autism | Genetic aspects | Research | Single nucleotide polymorphisms | Genetic susceptibility | Risk factors | Index Medicus | Original
Journal Article
Clinical genetics, ISSN 0009-9163, 10/2017, Volume 92, Issue 4, pp. 415 - 422
array‐CGH | developmental delay | CNV | genomic disorders | autism spectrum disorder | intellectual disability | array-CGH | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Association Studies | Genomics | Humans | Intellectual Disability - pathology | Child, Preschool | Chromosomal Position Effects - genetics | Infant | Male | DNA Copy Number Variations - genetics | Developmental Disabilities - genetics | DNA-Binding Proteins - genetics | Intellectual Disability - genetics | Young Adult | Developmental Disabilities - pathology | Phenotype | Comparative Genomic Hybridization | Pedigree | Adolescent | Chromosome Aberrations | Adult | Female | Child | Sequence Deletion - genetics | Proteins | Genetic research | Cytogenetics | Autism | Analysis | Genes | Pathogenicity | Position effects | Intellectual disabilities | Copy number | Data processing | Hybridization | Developmental disabilities | Index Medicus
Journal Article
Molecular psychiatry, ISSN 1359-4184, 2003, Volume 8, Issue 2, pp. 186 - 194
Autism | Sodium channel | Genetic susceptibility | Neurogenetics | Calmodulin | Chr 2 | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Autistic Disorder - genetics | Haplotypes | Protein Structure, Tertiary | Cell Line | Genetic Predisposition to Disease | Exons | Introns | Humans | Family Health | Male | Nerve Tissue Proteins - genetics | NAV1.1 Voltage-Gated Sodium Channel | Nerve Tissue Proteins - chemistry | Sodium Channels - chemistry | Pedigree | Base Sequence | NAV1.3 Voltage-Gated Sodium Channel | Female | Sodium Channels - genetics | NAV1.2 Voltage-Gated Sodium Channel | Index Medicus
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