X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (796) 796
Publication (139) 139
Patent (118) 118
Conference Proceeding (103) 103
Book / eBook (58) 58
Newspaper Article (56) 56
Book Review (50) 50
Magazine Article (11) 11
Dissertation (9) 9
Book Chapter (4) 4
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 (458) 458
humans (441) 441
male (297) 297
female (288) 288
aged (176) 176
genetics & heredity (172) 172
middle aged (169) 169
neurosciences (163) 163
adult (148) 148
alzheimer disease - genetics (137) 137
clinical neurology (134) 134
genotype (121) 121
alzheimer's disease (118) 118
article (110) 110
genetics (106) 106
aged, 80 and over (100) 100
genome-wide association study (100) 100
genetic predisposition to disease (97) 97
risk factors (96) 96
polymorphism, single nucleotide (94) 94
genetic aspects (89) 89
psychiatry (89) 89
genome-wide association (80) 80
risk (80) 80
dementia (76) 76
research (75) 75
human necessities (73) 73
diagnosis (72) 72
neurology (70) 70
genes (69) 69
abridged index medicus (68) 68
genomics (65) 65
mutation (63) 63
association (62) 62
hygiene (60) 60
medical or veterinary science (60) 60
genomes (58) 58
pedigree (56) 56
polymorphism, single nucleotide - genetics (56) 56
alleles (55) 55
identification (55) 55
case-control studies (54) 54
disease (53) 53
physics (53) 53
analysis (52) 52
alzheimers disease (50) 50
european continental ancestry group - genetics (50) 50
gene (50) 50
genetic linkage (50) 50
biochemistry & molecular biology (47) 47
metaanalysis (46) 46
adolescent (45) 45
animals (45) 45
parkinson's disease (44) 44
genetic research (43) 43
surgery (43) 43
african americans - genetics (42) 42
chromosome mapping (42) 42
common variants (41) 41
medical research (41) 41
gene frequency (40) 40
genetic variation (40) 40
phenotype (40) 40
apolipoproteins e - genetics (39) 39
chemistry (39) 39
population (39) 39
haplotypes (38) 38
parkinson disease - genetics (37) 37
age of onset (36) 36
genetic markers (36) 36
geriatrics & gerontology (36) 36
loci (35) 35
multidisciplinary sciences (35) 35
age (34) 34
alzheimer disease - epidemiology (34) 34
genetic predisposition to disease - genetics (34) 34
linkage disequilibrium (34) 34
african americans (33) 33
linkage (33) 33
research article (32) 32
brain (31) 31
metallurgy (31) 31
neurodegenerative diseases (31) 31
proteins (31) 31
single nucleotide polymorphisms (31) 31
biochemistry (30) 30
epidemiology (30) 30
expression (30) 30
gene expression (30) 30
mice (30) 30
studies (30) 30
susceptibility (30) 30
testing (30) 30
aging (29) 29
cohort studies (29) 29
hematology (29) 29
medical colleges (29) 29
young adult (29) 29
alzheimer disease (28) 28
alzheimers-disease (28) 28
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (18) 18
UTL at Downsview - May be requested (15) 15
Online Resources - Online (6) 6
Gerstein Science - Stacks (5) 5
St. Michael's College (John M. Kelly) - 3rd Floor (5) 5
Royal Ontario Museum - Far Eastern (4) 4
Knox College (Caven) - Stacks (2) 2
Massey College (Robertson Davies) - Rare Book (2) 2
Regis College - Stacks (2) 2
St. Michael's College (John M. Kelly) - 2nd Floor (2) 2
Thomas Fisher Rare Book - Rare Book (2) 2
Victoria University Emmanuel College - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
Gardiner Museum - Library use only (1) 1
Indust. Rel's & Hum. Resources (Newman) - Library use only (1) 1
Institute for Christian Studies - Stacks (1) 1
Royal Ontario Museum - Rare Book (1) 1
St. Augustine's Seminary - Stacks (1) 1
Trinity College (John W Graham) - Storage (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1104) 1104
French (124) 124
German (19) 19
Spanish (18) 18
Italian (3) 3
Russian (2) 2
Chinese (1) 1
Dutch (1) 1
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


eBook
Encephale, ISSN 0013-7006, 02/2009, Volume 35, Issue 1, pp. 43 - 51
First-rank symptoms of schizophrenia have been related to an impaired sense of agency (the sense of causing and controlling an action). The sense of agency is... 
Sense of body | Schizophrenia | First-rank symptoms | Self-recognition | Sense of agency
Journal Article
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Index Medicus | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
Journal Article
1975, ISBN 0292790058, xvii, 99
Book
Neurobiology of Aging, ISSN 0197-4580, 01/2017, Volume 49, pp. 217.e1 - 217.e4
Journal Article
Nature, ISSN 0028-0836, 04/2017, Volume 544, Issue 7650, pp. 357 - 361
Journal Article
Nature Physics, ISSN 1745-2473, 12/2010, Volume 6, Issue 12, pp. 947 - 950
The signature of coherent coupling between two quantum states is an anticrossing in their energies as one is swept through the other. In single semiconductor... 
OPTICAL-SPECTRUM | PHYSICS, MULTIDISCIPLINARY | ENTANGLED PHOTON PAIRS | Semiconductors | Quantum dots | Quantum physics | Electric fields | Particle physics | Splitting | Coherence | Control systems | Joining | Photons | Excitation | Signatures
Journal Article
Journal Article
Journal Article
PLoS Medicine, ISSN 1549-1277, 03/2017, Volume 14, Issue 3, pp. e1002258 - e1002258
Background Identifying individuals at risk for developing Alzheimer disease (AD) is of utmost importance. Although genetic studies have identified... 
MEDICINE, GENERAL & INTERNAL | METAANALYSIS | VARIANTS | HISPANICS | LOCI | AFRICAN-AMERICANS | ONSET | NEUROPATHOLOGIC ASSESSMENT | PREDICTION | LIFE | United States - epidemiology | Humans | Middle Aged | Genotype | Male | Apolipoproteins E - metabolism | Multifactorial Inheritance | Apolipoproteins E - genetics | Aged, 80 and over | Alzheimer Disease - epidemiology | Female | Geriatric Assessment - methods | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Longitudinal Studies | Psychological aspects | Physiological aspects | Genetic aspects | Disease susceptibility | Diagnosis | Research | Single nucleotide polymorphisms | Alzheimer's disease | Risk factors | Brain | Parkinson's disease | Computational neuroscience | Colleges & universities | Disorders | Cognitive ability | Nervous system | Single-nucleotide polymorphism | Cerebrospinal fluid | Epidemiology | Incidence | Consortia | Genetics | Ophthalmology | Public health | Movement disorders | Neurodegenerative diseases | Addictions | Apolipoproteins | Survival analysis | Neurology | Hospitals | Editors | Computer applications | Predictions | Radiology | Biomarkers | Clinical medicine | Health risk assessment | Polygenic inheritance | Transporter | Neuroimaging | Neurosciences | Mental disorders | Mental health | Science | African Americans | Apolipoprotein E | Dementia disorders | Division | Heart diseases | Medical imaging | Statistical analysis | Health | Diabetes mellitus | Health risks | Breast cancer | Decision analysis | Adhesion | Medicine | Addiction | Breast | Psychiatry | Manganese | Cancer | Index Medicus
Journal Article
by Sims, Rebecca and Van Der Lee, Sven J and Naj, Adam C and Bellenguez, Céline and Badarinarayan, Nandini and Jakobsdottir, Johanna and Kunkle, Brian W and Boland, Anne and Raybould, Rachel and Bis, Joshua C and Martin, Eden R and Grenier-Boley, Benjamin and Heilmann-Heimbach, Stefanie and Chouraki, Vincent and Kuzma, Amanda B and Sleegers, Kristel and Vronskaya, Maria and Ruiz, Agustin and Graham, Robert R and Olaso, Robert and Hoffmann, Per and Grove, Megan L and Vardarajan, Badri N and Hiltunen, Mikko and Nöthen, Markus M and White, Charles C and Hamilton-Nelson, Kara L and Epelbaum, Jacques and Maier, Wolfgang and Choi, Seung-Hoan and Beecham, Gary W and Dulary, Cécile and Herms, Stefan and Smith, Albert V and Funk, Cory C and Derbois, Céline and Forstner, Andreas J and Ahmad, Shahzad and Li, Hongdong and Bacq, Delphine and Harold, Denise and Satizabal, Claudia L and Valladares, Otto and Squassina, Alessio and Thomas, Rhodri and Brody, Jennifer A and Qu, Liming and Sánchez-Juan, Pascual and Morgan, Taniesha and Wolters, Frank J and Zhao, Yi and Garcia, Florentino Sanchez and Denning, Nicola and Fornage, Myriam and Malamon, John and Naranjo, Maria Candida Deniz and Majounie, Elisa and Mosley, Thomas H and Dombroski, Beth and Wallon, David and Lupton, Michelle K and Dupuis, Josée and Whitehead, Patrice and Fratiglioni, Laura and Medway, Christopher and Jian, Xueqiu and Mukherjee, Shubhabrata and Keller, Lina and Brown, Kristelle and Lin, Honghuang and Cantwell, Laura B and Panza, Francesco and McGuinness, Bernadette and Moreno-Grau, Sonia and Burgess, Jeremy D and Solfrizzi, Vincenzo and Proitsi, Petra and Adams, Hieab H and Allen, Mariet and Seripa, Davide and Pastor, Pau and Cupples, L Adrienne and Price, Nathan D and Hannequin, Didier and Frank-García, Ana and Levy, Daniel and Chakrabarty, Paramita and Caffarra, Paolo and Giegling, Ina and Beiser, Alexa S and Giedraitis, Vilmantas and Hampel, Harald and Garcia, Melissa E and Wang, Xue and Lannfelt, Lars and Mecocci, Patrizia and Eiriksdottir, Gudny and Crane, Paul K and Pasquier, Florence and Boccardi, Virginia and ... and EADI and GERAD PERADES and ARUKConsortium and CHARGE and ADGC and GERAD/PERADES, CHARGE, ADGC, EADI and ARUK Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 09/2017, Volume 49, Issue 9, pp. 1373 - 1384
Journal Article