Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
life sciences & biomedicine (61) 61
science & technology (61) 61
humans (55) 55
animals (30) 30
male (30) 30
autism (29) 29
neurosciences (29) 29
biological and medical sciences (28) 28
female (28) 28
neurosciences & neurology (26) 26
medical sciences (23) 23
biochemistry & molecular biology (20) 20
psychiatry (17) 17
research (17) 17
genetic aspects (16) 16
genetic predisposition to disease (15) 15
genetics & heredity (15) 15
mice (15) 15
psychology. psychoanalysis. psychiatry (15) 15
psychopathology. psychiatry (15) 15
mental disorders (12) 12
mutation (12) 12
neurology (12) 12
autistic disorder - genetics (11) 11
child (11) 11
child clinical studies (11) 11
developmental disorders (11) 11
fundamental and applied biological sciences. psychology (11) 11
infantile autism (11) 11
alzheimer's disease (10) 10
child, preschool (10) 10
genes (10) 10
genetic variation (10) 10
genomes (10) 10
risk factors (10) 10
adult (9) 9
analysis (9) 9
autism spectrum disorder (9) 9
physiological aspects (9) 9
cells, cultured (8) 8
degenerative and inherited degenerative diseases of the nervous system. leukodystrophies. prion diseases (8) 8
genetics (8) 8
genomics (8) 8
polymorphism, single nucleotide (8) 8
proteins (8) 8
schizophrenia (8) 8
brain - metabolism (7) 7
cell biology (7) 7
gene expression (7) 7
phenotype (7) 7
alzheimer disease - metabolism (6) 6
behavioral sciences (6) 6
disease models, animal (6) 6
genetic predisposition to disease - genetics (6) 6
genome-wide association study (6) 6
linkage disequilibrium (6) 6
mice, transgenic (6) 6
nerve tissue proteins - genetics (6) 6
psychology (6) 6
psychology, developmental (6) 6
social sciences (6) 6
studies (6) 6
transfection (6) 6
adult and adolescent clinical studies (5) 5
case-control studies (5) 5
child development disorders, pervasive - genetics (5) 5
genetics of eukaryotes. biological and molecular evolution (5) 5
genotype (5) 5
internal medicine (5) 5
middle aged (5) 5
nerve tissue proteins - metabolism (5) 5
neurons - metabolism (5) 5
phosphorylation (5) 5
rats (5) 5
schizophrenia - genetics (5) 5
adolescent (4) 4
aged (4) 4
alzheimer disease - genetics (4) 4
amyloid beta-protein precursor - metabolism (4) 4
autistic disorder (4) 4
behavior (4) 4
care and treatment (4) 4
chromosome mapping (4) 4
cohort studies (4) 4
dentistry (4) 4
family health (4) 4
gene deletion (4) 4
human genetics (4) 4
kv channel-interacting proteins (4) 4
medicin och hälsovetenskap (4) 4
neurons - cytology (4) 4
original (4) 4
original article (4) 4
pedigree (4) 4
pervasive developmental disorders (4) 4
repressor proteins (4) 4
transmission disequilibrium test (4) 4
aged, 80 and over (3) 3
aging - metabolism (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder
by Hamilton, P.J and Campbell, N.G and Sharma, S and Erreger, K and Herborg Hansen, F and Saunders, C and Belovich, A.N and Daly, M.J and Gibbs, R.A and Boerwinkle, E and Buxbaum, J.D and Cook, E.H and Devlin, B and Lim, E.T and Neale, B.M and Roeder, K and Sabo, A and Schellenberg, G.D and Stevens, C and Sutcliffe, J.S and Sahai, M.A and Cook, E.H and Gether, U and Mchaourab, H.S and Matthies, H.J.G and Sutcliffe, J.S and Galli, A and NIH ARRA Autism Sequencing Consort and NIH ARRA Autism Sequencing Consortium
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
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Rare structural variation of synapse and neurotransmission genes in autism
by Gai, X and Xie, H.M and Perin, J.C and Takahashi, N and Murphy, K and Wenocur, A.S and D'arcy, M and O'Hara, R.J and Goldmuntz, E and Grice, D.E and Shaikh, T.H and Hakonarson, H and Buxbaum, J.D and Elia, J and White, P.S
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
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Examining the Efficacy of a Family Peer Advocate Model for Black and Hispanic Caregivers of Children with Autism Spectrum Disorder
by Jamison, J M and Fourie, E and Siper, P M and Trelles, M P and George-Jones, Julia and Buxbaum Grice, A and Krata, J and Holl, E and Shaoul, J and Hernandez, B and Mitchell, L and McKay, M M and Buxbaum, J D and Kolevzon, Alexander
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
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model
by Steele, J.W and Lachenmayer, M.L and Ju, S and Stock, A and Liken, J and Kim, S.H and Delgado, L.M and Alfaro, I.E and Bernales, S and Verdile, G and Bharadwaj, P and Gupta, V and Barr, R and Friss, A and Dolios, G and Wang, R and Ringe, D and Fraser, P and Westaway, D and St George-Hyslop, P.H and Szabo, P and Relkin, N.R and Buxbaum, J.D and Glabe, C.G and Protter, A.A and Martins, R.N and Ehrlich, M.E and Petsko, G.A and Yue, Z and Gandy, S
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
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Association between a GABRB3 polymorphism and autism
by Buxbaum, J.D and Silverman, J.M and Smith, C.J and Greenberg, D.A and Kilifarski, M and Reichert, J and Cook Jr, E.H and Fang, Y and Song, C.-Y and Vitale, R
Molecular psychiatry, ISSN 1359-4184, 2002, Volume 7, Issue 3, pp. 311 - 316
Autism | Transmission disequilibrium test (TDT) | Epilepsy | γ-aminobutyric acid type-A receptor β3 subunit | Linkage analysis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: Implications for neuropsychiatric disease
by Smith, R.G and Reichenberg, A and Kember, R.L and Buxbaum, J.D and Schalkwyk, L.C and Fernandes, C and Mill, J
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
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Intraneuronal Aβ42 Accumulation in Human Brain
by Gouras, Gunnar K and Tsai, Julia and Naslund, Jan and Vincent, Bruno and Edgar, Mark and Checler, Frederic and Greenfield, Jeffrey P and Haroutunian, Vahram and Buxbaum, Joseph D and Xu, Huaxi and Greengard, Paul and Relkin, Norman R
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
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility
by Maestrini, E and Pagnamenta, A. T and Lamb, J. A and Bacchelli, E and Sykes, N. H and Sousa, I and Toma, C and Barnby, G and Butler, H and Winchester, L and Scerri, T. S and Minopoli, F and Reichert, J and Cai, G and Buxbaum, J. D and Korvatska, O and Schellenberg, G. D and Dawson, G and de Bildt, A and Minderaa, R. B and Mulder, E. J and Morris, A. P and Bailey, A. J and Monaco, A. P and IMGSAC
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
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes
by Di Gregorio, E and Riberi, E and Belligni, E.F and Biamino, E and Spielmann, M and Ala, U and Calcia, A and Bagnasco, I and Carli, D and Gai, G and Giordano, M and Guala, A and Keller, R and Mandrile, G and Arduino, C and Maffè, A and Naretto, V.G and Sirchia, F and Sorasio, L and Ungari, S and Zonta, A and Zacchetti, G and Talarico, F and Pappi, P and Cavalieri, S and Giorgio, E and Mancini, C and Ferrero, M and Brussino, A and Savin, E and Gandione, M and Pelle, A and Giachino, D.F and De Marchi, M and Restagno, G and Provero, P and Cirillo Silengo, M and Grosso, E and Buxbaum, J.D and Pasini, B and De Rubeis, S and Brusco, A and Ferrero, G.B
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
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Sodium channels SCN1A, SCN2A and SCN3A in familial autism
by Weiss, L.A and Escayg, A and Kearney, J.A and Trudeau, M and MacDonald, B.T and Mori, M and Reichert, J and Buxbaum, J.D and Meisler, M.H
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
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights