X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3914) 3914
Book Review (986) 986
Publication (560) 560
Book Chapter (122) 122
Book / eBook (38) 38
Conference Proceeding (16) 16
Dissertation (10) 10
Data Set (3) 3
Magazine Article (1) 1
Newspaper Article (1) 1
Trade Publication Article (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (2845) 2845
neurodevelopmental disorders (2658) 2658
humans (2022) 2022
neurosciences (1417) 1417
autism (1357) 1357
female (1312) 1312
male (1215) 1215
animals (1137) 1137
brain (941) 941
children (727) 727
schizophrenia (726) 726
mutation (713) 713
child (709) 709
psychiatry (656) 656
mental disorders (652) 652
genetics & heredity (633) 633
mice (630) 630
analysis (593) 593
genes (565) 565
article (526) 526
research (523) 523
genetic aspects (517) 517
gene expression (499) 499
genetics (498) 498
proteins (496) 496
pregnancy (463) 463
multidisciplinary sciences (445) 445
neurology (441) 441
neurons (438) 438
adolescent (427) 427
risk factors (421) 421
pediatrics (414) 414
medicine (412) 412
child, preschool (407) 407
adult (402) 402
phenotype (386) 386
neuroscience (384) 384
autism spectrum disorder (378) 378
cortex (366) 366
biochemistry & molecular biology (364) 364
disease models, animal (356) 356
research article (354) 354
disorders (332) 332
health aspects (325) 325
epilepsy (320) 320
science (320) 320
phenotypes (317) 317
nervous system (314) 314
intellectual disability (312) 312
neurodevelopmental disorder (310) 310
cognitive ability (308) 308
autism spectrum disorders (306) 306
genomes (303) 303
behavior (301) 301
clinical neurology (298) 298
mutations (295) 295
rodents (289) 289
neurodevelopmental disorders - genetics (279) 279
medical research (278) 278
studies (278) 278
expression (270) 270
psychology (269) 269
genomics (264) 264
animal models (256) 256
infant (254) 254
cell biology (251) 251
mouse model (246) 246
age (242) 242
gene (242) 242
intellectual disabilities (224) 224
medicine, experimental (221) 221
young adult (217) 217
physiological aspects (214) 214
rats (213) 213
biology (204) 204
cognition (203) 203
pharmacology & pharmacy (200) 200
etiology (199) 199
development and progression (198) 198
nervous system diseases (198) 198
rett syndrome (197) 197
abnormalities (195) 195
hippocampus (194) 194
brain - metabolism (193) 193
gene-expression (193) 193
brain research (192) 192
magnetic resonance imaging (192) 192
disease (190) 190
diagnosis (189) 189
biology and life sciences (184) 184
social behavior (183) 183
attention deficit disorder (181) 181
review (181) 181
stem cells (180) 180
dna methylation (178) 178
attention deficit hyperactivity disorder (175) 175
de-novo mutations (175) 175
clonal deletion (174) 174
epigenetics (172) 172
mice, inbred c57bl (172) 172
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (18) 18
UofT at Scarborough - Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
OISE - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
UofT at Mississauga - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Music - Protected Material (1) 1
Music - Stacks (1) 1
Online Resources - Online (1) 1
Scarborough Hospital - General (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (4012) 4012
Japanese (13) 13
Spanish (12) 12
German (11) 11
French (9) 9
Chinese (2) 2
Croatian (1) 1
Dutch (1) 1
Italian (1) 1
Russian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by De Rubeis, Silvia and He, Xin and Goldberg, Arthur P and Poultney, Christopher S and Samocha, Kaitlin and Cicek, A. Ercument and Kou, Yan and Liu, Li and Fromer, Menachem and Walker, Susan and Singh, Tarjinder and Klei, Lambertus and Kosmicki, Jack and Fu, Shih-Chen and Aleksic, Branko and Biscaldi, Monica and Bolton, Patrick F and Brownfeld, Jessica M and Cai, Jinlu and Campbell, Nicholas G and Carracedo, Angel and Chahrour, Maria H and Chiocchetti, Andreas G and Coon, Hilary and Crawford, Emily L and Crooks, Lucy and Curran, Sarah R and Dawson, Geraldine and Duketis, Eftichia and Fernandez, Bridget A and Gallagher, Louise and Geller, Evan and Guter, Stephen J and Hill, R. Sean and Ionita-Laza, Iuliana and Gonzalez, Patricia Jimenez and Kilpinen, Helena and Klauck, Sabine M and Kolevzon, Alexander and Lee, Irene and Lei, Jing and Lehtimäki, Terho and Lin, Chiao-Feng and Ma'ayan, Avi and Marshall, Christian R and McInnes, Alison L and Neale, Benjamin and Owen, Michael J and Ozaki, Norio and Parellada, Mara and Parr, Jeremy R and Purcell, Shaun and Puura, Kaija and Rajagopalan, Deepthi and Rehnström, Karola and Reichenberg, Abraham and Sabo, Aniko and Sachse, Michael and Sanders, Stephan J and Schafer, Chad and Schulte-Rüther, Martin and Skuse, David and Stevens, Christine and Szatmari, Peter and Tammimies, Kristiina and Valladares, Otto and Voran, Annette and Wang, Li-San and Weiss, Lauren A and Willsey, A. Jeremy and Yu, Timothy W and Yuen, Ryan K. C and Cook, Edwin H and Freitag, Christine M and Gill, Michael and Hultman, Christina M and Lehner, Thomas and Palotie, Aarno and Schellenberg, Gerard D and Sklar, Pamela and State, Matthew W and Sutcliffe, James S and Walsh, Christopher A and Scherer, Stephen W and Zwick, Michael E and Barrett, Jeffrey C and Cutler, David J and Roeder, Kathryn and Devlin, Bernie and Daly, Mark J and Buxbaum, Joseph D and Homozygosity Mapping Collaborative and DDD Study and Autism Sequencing Consortium and UK10K Consortium and Homozygosity Mapping Collaborative for Autism and The Autism Sequencing Consortium and The DDD Study
Nature, ISSN 0028-0836, 11/2014, Volume 515, Issue 7526, pp. 209 - 215
Journal Article
Journal Article
Neuron, ISSN 0896-6273, 12/2018, Volume 100, Issue 5, pp. 1014 - 1016
Mutations in the chromodomain helicase DNA-binding 2 ( ) gene have been found in patients with a range of neurodevelopmental disorders. In this issue of ,... 
DE-NOVO MUTATIONS | NEUROSCIENCES | Animals | Memory, Long-Term | Neurons | Humans | Mice | Mutation | DNA-Binding Proteins - genetics | Neurogenesis | Genes | Brain | Synaptogenesis | Cortex | Gene expression | Neurodevelopmental disorders | Cell adhesion & migration | Haploinsufficiency | DNA helicase | Autism | Convulsions & seizures | Stem cells
Journal Article
Neuropsychopharmacology, ISSN 0893-133X, 12/2017, Volume 42, Issue 13, pp. 2516 - 2526
cThe fundamental role of the brain-specific myelin transcription factor 1-like (MYT1L) gene in cases of intellectual disability and in the etiology of... 
TRANSCRIPTION FACTORS | CELLS | DIFFERENTIATION ID1 | PSYCHIATRY | ID PROTEINS | SCHIZOPHRENIA | NEUROSCIENCES | REGION | 2P25.3 | DISORDER | NEUROGENESIS | PHARMACOLOGY & PHARMACY | BRAIN-FUNCTION | Humans | Male | Neoplasm Proteins - metabolism | Hippocampus - diagnostic imaging | Gene Knockdown Techniques | Basic Helix-Loop-Helix Transcription Factors - metabolism | HEK293 Cells | Adult | Female | Hippocampus - growth & development | Gene Expression | Genetic Association Studies | Organ Size | Inhibitor of Differentiation Proteins - metabolism | Transcription Factors - genetics | Inhibitor of Differentiation Protein 1 - metabolism | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Hippocampus - metabolism | Magnetic Resonance Imaging | Neurogenesis - physiology | Hippocampus - anatomy & histology | Polymorphism, Single Nucleotide | Neural Stem Cells - metabolism | Memory - physiology | Potentiation | Neuroimaging | Brain | Regulators | Id1 protein | Intellectual disabilities | Genes | Neurodevelopmental disorders | Neurogenesis | Etiology | Synaptic transmission | Neurodegeneration | Helix-loop-helix proteins | Medical imaging | Myelin | Long-term potentiation | Gene expression | Neurology | DNA microarrays | Life span | Stem cells | Neural stem cells | Differentiation | Hippocampus | Cancer | Index Medicus | Life Sciences | Neurons and Cognition | Original
Journal Article
Human Mutation, ISSN 1059-7794, 08/2019, Volume 40, Issue 8, pp. 1013 - 1029
SATB2 ‐associated syndrome (SAS) is an autosomal dominant neurodevelopmental disorder caused by alterations in the SATB2 gene. Here we present a review of... 
associated syndrome | genotype‐phenotype correlation | pathogenic variants | SATB2 | whole exome sequencing | SATB2-associated syndrome | genotype-phenotype correlation | GENETICS & HEREDITY | Genetic aspects | Codon | Genes | Analysis | Animal models | Phenotypes | Reviews | Nonsense mutation | Coding | Stop codon | Neurodevelopmental disorders | Genotypes | Hereditary diseases | Index Medicus
Journal Article
Annals of Neurology, ISSN 0364-5134, 11/2018, Volume 84, Issue 5, pp. 788 - 795
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2015, Volume 10, Issue 8, pp. e0129631 - e0129631
Journal Article
eLife, ISSN 2050-084X, 02/2019, Volume 8
A long non-coding RNA called lnc-NR2F1 regulates several neuronal genes, including some involved in autism and intellectual disabilities. 
LONG NONCODING RNAS | EVOLUTION | BIOLOGY | Autism | RNA | Neurons | Physiological aspects | Genetic aspects | Genetic regulation | Health aspects | Mental retardation | Proteins | Coding | Intellectual disabilities | Fibroblasts | Mutation | Gene expression | Non-coding RNA
Journal Article
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 09/2019, Volume 180, Issue 6, pp. 365 - 376
Journal Article