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
humans (22) 22
science & technology (22) 22
life sciences & biomedicine (19) 19
neurology (19) 19
alzheimer's disease (15) 15
female (14) 14
male (14) 14
aged (12) 12
neurosciences (12) 12
genetics (11) 11
genome-wide association study (11) 11
medicin och hälsovetenskap (11) 11
neurosciences & neurology (11) 11
alzheimer disease - genetics (10) 10
aged, 80 and over (9) 9
polymorphism, single nucleotide (9) 9
risk factors (9) 9
clinical neurology (8) 8
genetic aspects (8) 8
medical and health sciences (8) 8
polymorphism, single nucleotide - genetics (8) 8
dementia (7) 7
genetics & heredity (7) 7
middle aged (7) 7
epidemiology (6) 6
genetic predisposition to disease (6) 6
genetic research (6) 6
medicinska och farmaceutiska grundvetenskaper (6) 6
neurodegenerative diseases (6) 6
psychiatry (6) 6
biological and medical sciences (5) 5
clinical medicine (5) 5
epistasis (5) 5
genetic loci (5) 5
genomics (5) 5
klinisk medicin (5) 5
adult (4) 4
alzheimers disease (4) 4
analysis (4) 4
apolipoprotein e4 - genetics (4) 4
basic medicine (4) 4
biochemistry & molecular biology (4) 4
case-control studies (4) 4
cognition (4) 4
cohort studies (4) 4
educational status (4) 4
genetic predisposition to disease - genetics (4) 4
genetic variation (4) 4
genotype (4) 4
medical sciences (4) 4
nervous system (4) 4
neurodegeneration (4) 4
neurovetenskaper (4) 4
polymorphism (4) 4
aligator (3) 3
cardiovascular system & cardiology (3) 3
cholesterol metabolism (3) 3
creutzfeldt-jakob disease (3) 3
creutzfeldt-jakob syndrome - epidemiology (3) 3
endocytosis (3) 3
gene frequency (3) 3
genetic association studies (3) 3
genomes (3) 3
health aspects (3) 3
hypertension (3) 3
immune response (3) 3
medical research (3) 3
medicinsk genetik (3) 3
multidisciplinary sciences (3) 3
mutation (3) 3
netherlands (3) 3
neurologi (3) 3
neuroscience (3) 3
pathway analysis (3) 3
phenotype (3) 3
phenotypes (3) 3
proteins (3) 3
research (3) 3
science & technology - other topics (3) 3
single nucleotide (3) 3
single-nucleotide polymorphism (3) 3
stroke - genetics (3) 3
ubiquitination (3) 3
weighted gene co-expression network analysis (3) 3
[scco.neur]cognitive science/neuroscience (2) 2
academic achievement (2) 2
adult and adolescent clinical studies (2) 2
aging (2) 2
alzheimer disease (2) 2
alzheimer disease - epidemiology (2) 2
alzheimer's risk (2) 2
alzheimer’s disease (2) 2
amyloid beta-peptides - blood (2) 2
amyloid beta-protein precursor - genetics (2) 2
apolipoproteins (2) 2
biology (2) 2
biometry (2) 2
cognitive ability (2) 2
cognitive science (2) 2
consortia (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Variant of TREM2 Associated with the Risk of Alzheimer's Disease
by Jonsson, Thorlakur and Jonsson, Palmi V and Stefansson, Hreinn and Stefansson, Kari and Steinberg, Stacy and Jonsdottir, Ingileif and Snaedal, Jon and Bjornsson, Sigurbjorn and Huttenlocher, Johanna and Levey, Allan I and Lah, James J and Rujescu, Dan and Hampel, Harald and Giegling, Ina and Andreassen, Ole A and Engedal, Knut and Ulstein, Ingun and Djurovic, Srdjan and Ibrahim-Verbaas, Carla and Hofman, Albert and Ikram, M. Arfan and van Duijn, Cornelia M and Thorsteinsdottir, Unnur and Kong, Augustine
The New England journal of medicine, ISSN 0028-4793, 01/2013, Volume 368, Issue 2, pp. 107 - 116
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Neurology | Organic mental disorders. Neuropsychology | General aspects | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Apolipoprotein E4 - genetics | Humans | Risk Factors | Cognition | Mutation, Missense | Genotyping Techniques | Sequence Analysis, DNA | Case-Control Studies | Iceland | Membrane Glycoproteins - genetics | Genetic Variation | Aged, 80 and over | Heterozygote | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Receptors, Immunologic - genetics | Genetic variation | Causes of | Genetic aspects | Research | Apolipoproteins | Alzheimer's disease | Health aspects | Genomes | Alzheimers disease | Older people | Age | Cognitive ability | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text F1–01–02: APOE‐stratified genome‐wide association analysis reveals differential effects by APOE status and potential new risk loci for Alzheimer's disease
by Ibrahim‐Verbaas, Carla
Alzheimer's & dementia, ISSN 1552-5260, 07/2013, Volume 9, pp. P123 - P123
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Common variants at 12q14 and 12q24 are associated with hippocampal volume
by Bis, Joshua C and Decarli, Charles and Smith, Albert Vernon and van der Lijn, Fedde and Crivello, Fabrice and Fornage, Myriam and Debette, Stephanie and Shulman, Joshua M and Schmidt, Helena and Srikanth, Velandai and Schuur, Maaike and Yu, Lei and Choi, Seung-Hoan and Sigurdsson, Sigurdur and Verhaaren, Benjamin F. J and DeStefano, Anita L and Lambert, Jean-Charles and Jack, Clifford R and Struchalin, Maksim and Stankovich, Jim and Ibrahim-Verbaas, Carla A and Fleischman, Debra and Zijdenbos, Alex and den Heijer, Tom and Mazoyer, Bernard and Coker, Laura H and Enzinger, Christian and Danoy, Patrick and Amin, Najaf and Arfanakis, Konstantinos and van Buchem, Mark A and de Bruijn, Renée F. A. G and Beiser, Alexa and Dufouil, Carole and Huang, Juebin and Cavalieri, Margherita and Thomson, Russell and Niessen, Wiro J and Chibnik, Lori B and Gislason, Gauti K and Hofman, Albert and Pikula, Aleksana and Amouyel, Philippe and Freeman, Kevin B and Phan, Thanh G and Oostra, Ben A and Stein, Jason L and Medland, Sarah E and Vasquez, Alejano Arias and Hibar, Derrek P and Cohorts Heart Aging Res Genomic Ep and Enhancing Neuro Imaging Genetics M and Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium and Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium and Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium and the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 5, pp. 545 - 551
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Polymorphism, Single Nucleotide - genetics | Cognition Disorders - genetics | Genetic Loci | Genetic Markers | Alzheimer Disease - genetics | Dementia - genetics | Chromosomes, Human, Pair 12 - genetics | Hippocampus - physiopathology | Proteins | Neurology | Medical research | Genotype & phenotype | Ischemia | Education | Religious orders | Aging | Genetics | Genomes | Alzheimers disease | Index Medicus | Neuroscience | Cognitive science
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text The sex-specific associations of the aromatase gene with Alzheimer's disease and its interaction with IL10 in the Epistasis Project
by Medway, Christopher and Combarros, Onofre and Cortina-Borja, Mario and Butler, Helen and Ibrahim-Verbaas, Carla and Bruijn, Renée and Koudstaal, Peter and Tikka-Kleemola, Päivi and Ikram, Arfan and Mateo, Ignacio and Sanchez-Juan, Pascual and Lehmann, Michael and Heun, Reinhard and Kölsch, Heike and Deloukas, Panagiotis and Hammond, Naomi and Coto, Eliecer and Alvarez, Victoria and Kehoe, Patrick and Barber, Rachel and Wilcock, Gordon and Brown, K and Belbin, Olivia and Warden, Donald and Smith, A.D and Morgan, Kevin
European journal of human genetics : EJHG, ISSN 1018-4813, 02/2014, Volume 22, Issue 2, pp. 216 - 220
neurodegeneration | dementia | healthy cell bias | C18 | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Genetic Association Studies | Gene Frequency | Humans | Male | Risk | Alzheimer Disease - enzymology | Sex Characteristics | Case-Control Studies | Linkage Disequilibrium | Aromatase - genetics | Epistasis, Genetic | Interleukin-10 - genetics | Aged, 80 and over | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Odds Ratio | Neuroprotection | Cytokines | Neurodegenerative diseases | Estrogens | Childrens health | Sex | Systematic review | Gender differences | Epistasis | Breast cancer | Inflammation | Epidemiology | Post-menopause | Brain research | Hospitals | Womens health | Aromatase | Interleukin 10 | Interleukin 1 | Genetics | Alzheimers disease | Health risk assessment | Alzheimer's disease | Dementia | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
by Jones, Emma and Hummerich, Holger and Viré, Emmanuelle and Uphill, James and Dimitriadis, Athanasios and Speedy, Helen and Campbell, Tracy and Norsworthy, Penny and Quinn, Liam and Whitfield, Jerome and Linehan, Jacqueline and Jaunmuktane, Zane and Brandner, Sebastian and Jat, Parmjit and Nihat, Akin and How Mok, Tze and Ahmed, Parvin and Collins, Steven and Stehmann, Christiane and Sarros, Shannon and Kovacs, Gabor G and Geschwind, Michael D and Golubjatnikov, Aili and Frontzek, Karl and Budka, Herbert and Aguzzi, Adriano and Karamujić-Čomić, Hata and van der Lee, Sven J and Ibrahim-Verbaas, Carla A and van Duijn, Cornelia M and Sikorska, Beata and Golanska, Ewa and Liberski, Pawel P and Calero, Miguel and Calero, Olga and Sanchez-Juan, Pascual and Salas, Antonio and Martinón-Torres, Federico and Bouaziz-Amar, Elodie and Haïk, Stéphane and Laplanche, Jean-Louis and Brandel, Jean-Phillipe and Amouyel, Phillipe and Lambert, Jean-Charles and Parchi, Piero and Bartoletti-Stella, Anna and Capellari, Sabina and Poleggi, Anna and Ladogana, Anna and Pocchiari, Maurizio and Aneli, Serena and Matullo, Giuseppe and Knight, Richard and Zafar, Saima and Zerr, Inga and Booth, Stephanie and Coulthart, Michael B and Jansen, Gerard H and Glisic, Katie and Blevins, Janis and Gambetti, Pierluigi and Safar, Jiri and Appleby, Brian and Collinge, John and Mead, Simon
Lancet neurology, ISSN 1474-4422, 10/2020, Volume 19, Issue 10, pp. 840 - 848
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Creutzfeldt-Jakob Syndrome - epidemiology | Creutzfeldt-Jakob Syndrome - diagnosis | Genetic Predisposition to Disease - genetics | Humans | Risk Factors | Genetic Loci - genetics | Polymorphism, Single Nucleotide - genetics | Creutzfeldt-Jakob Syndrome - genetics | Genetic Predisposition to Disease - epidemiology | Genome-Wide Association Study - methods | Genetic research | Genomics | Creutzfeldt-Jakob disease | Health care | Phenotypes | Transcription | Neurodegenerative diseases | Amino acid sequence | Genomes | Single-nucleotide polymorphism | Gene expression | Patients | Risk factors | Proteins | Genotyping | Surveillance | Tau protein | Progressive supranuclear palsy | Protein folding | Prions | Quality control | Heritability | Paralysis | Lipid metabolism | Prion protein | Health risk assessment | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies
by Malik, Rainer and Bevan, Steve and Nalls, Michael and Holliday, Elizabeth and Devan, William and Cheng, Yu-Ching and Ibrahim-Verbaas, Carla and Verhaaren, Benjamin and Bis, Joshua and Joon, Aron and Stefano, Anita and Fornage, Myriam and Psaty, Bruce and Ikram, Arfan and Launer, Lenore and Duijn, Cornelia and Sharma, Pankaj and Mitchell, Braxton and Rosand, Jonathan and Meschia, James F and Levi, Christopher and Rothwell, Peter and Sudlow, Cathie and Markus, Hugh and Seshai, Sudha and Kubisch, Christian and Wellcome Trust Case Control and Wellcome Trust Case Control Consortium 2
Stroke (1970), ISSN 0039-2499, 02/2014, Volume 45, Issue 2, pp. 394 - 402
Genetic | Genetics | Risk assessment | Risk factors | Polymorphism | Clinical Neurology | Peripheral Vascular Disease | Neurosciences & Neurology | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Vascular diseases and vascular malformations of the nervous system | Medical sciences | Nervous system (semeiology, syndromes) | Prospective Studies | Humans | Middle Aged | Brain Ischemia - genetics | Male | Multilocus Sequence Typing | Case-Control Studies | Stroke - genetics | Genetic Variation | Aged, 80 and over | Adult | Female | Population | Stroke - epidemiology | Blood Pressure - physiology | Hypertension - epidemiology | Brain Ischemia - epidemiology | Genetic Predisposition to Disease | Genome-Wide Association Study | Reproducibility of Results | Risk Assessment | Risk Factors | Atrial Fibrillation - complications | Atrial Fibrillation - epidemiology | Coronary Artery Disease - complications | Sex Factors | Hypertension - complications | Polymorphism, Single Nucleotide - genetics | Aged | Coronary Artery Disease - epidemiology | Cohort Studies | Index Medicus | genetic | risk assessment | risk factors | polymorphism | genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Predicting stroke through genetic risk functions the CHARGE risk score project
by Ibrahim-Verbaas, Carla and Fornage, Myriam and Bis, Joshua and Choi, Seung-Hoan and Psaty, Bruce and Meigs, James and Rao, Madhu and Nalls, Michael and Fontes, Michel and O'Donnell, Christopher and Kathiresan, Sekar and Ehret, Georg and Fox, Caroline and Malik, Rainer and Kubisch, Christian and Schmidt, Reinhold and Lahti, Jari and Heckbert, Susan and Lumley, Thomas and Rice, Kenneth and Rotter, Jerome and Taylor, Kent and Folsom, Aaron and Boerwinkle, Eric and Rosamond, Wayne and Shahar, Eyal and Gottesman, Rebecca and Koudstaal, Peter and Amin, Najaf and Wieberdink, Renske and Dehghan, Abbas and Hofman, Albert and Uitterlinden, Ané and DeStefano, Anita and Debette, Stéphanie and Xue, Luting and Beiser, Alexa and Wolf, Philip and DeCarli, Charles and Ikram, Arfan and Seshai, Sudha and Mosley, Thomas and Longstreth, W.T and Duijn, Cornelia and Launer, Lenore
Stroke (1970), ISSN 0039-2499, 02/2014, Volume 45, Issue 2, pp. 403 - 412
Genetic epidemiology | Stroke | Risk factors | Clinical Neurology | Peripheral Vascular Disease | Neurosciences & Neurology | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Vascular diseases and vascular malformations of the nervous system | Medical sciences | Nervous system (semeiology, syndromes) | Genetic Predisposition to Disease | Genome-Wide Association Study | Age Factors | Area Under Curve | Humans | Middle Aged | Risk Factors | European Continental Ancestry Group | Genotype | Male | Case-Control Studies | Stroke - genetics | Regression Analysis | Sex Factors | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Female | ROC Curve | Stroke - epidemiology | Aged | Cohort Studies | Index Medicus | stroke epidemiology | cardiovascular risk factors | population studies | genetic risk prediction | genetic epidemiology
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text The dystrophin gene and cognitive function in the general population
by Vojinović, Dina and Adams, Hieab and Lee, Sven and Ibrahim-Verbaas, Carla and Brouwer, Rutger and van den hout, Mirjam and Oole, Edwin and van Rooij, Jeroen and Uitterlinden, Ané and Hofman, Albert and IJcken, Wilfred and Aartsma-Rus, Annemieke and Van Ommen, Gert-Jan B and Ikram, Arfan and Duijn, Cornelia and Amin, Najaf
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2015, Volume 23, Issue 6, pp. 837 - 843
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Dystrophin - genetics | Humans | Middle Aged | Adult | Female | Male | Cognition | Polymorphism, Single Nucleotide | Memory | Cognitive ability | Nervous system | Population studies | Epidemiology | Medical ethics | Muscular dystrophy | Studies | Genetic variance | Cognition & reasoning | Rodents | Reading comprehension | Population | Genetics | Mutation | Dystrophin | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights