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
science & technology (26) 26
humans (25) 25
life sciences & biomedicine (25) 25
clinical neurology (19) 19
female (19) 19
male (19) 19
neurosciences & neurology (19) 19
neurology (18) 18
aged (17) 17
alzheimer disease - genetics (16) 16
aged, 80 and over (14) 14
alzheimer's disease (13) 13
genome-wide association study (10) 10
middle aged (10) 10
abridged index medicus (9) 9
biological and medical sciences (9) 9
dementia (9) 9
genotype (9) 9
medical sciences (9) 9
risk factors (9) 9
degenerative and inherited degenerative diseases of the nervous system. leukodystrophies. prion diseases (8) 8
genetic predisposition to disease (8) 8
neurosciences (8) 8
alzheimers disease (7) 7
polymorphism, single nucleotide (7) 7
alzheimer disease (6) 6
alzheimer disease - epidemiology (6) 6
genetics (6) 6
pathology (6) 6
alzheimer disease - diagnosis (5) 5
genomes (5) 5
medical and health sciences (5) 5
medicin och hälsovetenskap (5) 5
neurovetenskaper (5) 5
polymorphism, single nucleotide - genetics (5) 5
risk (5) 5
case-control studies (4) 4
clinical medicine (4) 4
cohort studies (4) 4
gene expression (4) 4
genetics & heredity (4) 4
genomics (4) 4
klinisk medicin (4) 4
medical research (4) 4
research (4) 4
age of onset (3) 3
alzheimer disease - pathology (3) 3
alzheimer’s disease (3) 3
apolipoproteins (3) 3
apolipoproteins e - genetics (3) 3
blood. blood coagulation. reticuloendothelial system (3) 3
consortia (3) 3
databases, factual (3) 3
fundamental and applied biological sciences. psychology (3) 3
genetic variation (3) 3
genetics of eukaryotes. biological and molecular evolution (3) 3
health risk assessment (3) 3
meta-analysis (3) 3
neuropsychological tests - standards (3) 3
pharmacology. drug treatments (3) 3
sex factors (3) 3
single nucleotide polymorphisms (3) 3
studies (3) 3
adult (2) 2
adult and adolescent clinical studies (2) 2
aligator (2) 2
alzheimer disease - cerebrospinal fluid (2) 2
amyloid beta-protein (2) 2
amyloid beta-protein precursor - genetics (2) 2
analysis (2) 2
apolipoprotein e (2) 2
apolipoprotein e4 - genetics (2) 2
basic medicine (2) 2
brain (2) 2
brain - pathology (2) 2
cholesterol metabolism (2) 2
chromosomes (2) 2
confidence intervals (2) 2
data collection - methods (2) 2
databases, factual - statistics & numerical data (2) 2
databases, genetic (2) 2
disorders of higher nervous function. focal brain diseases. central vestibular syndrome and deafness. brain stem syndromes (2) 2
endocytosis (2) 2
frontotemporal dementia - genetics (2) 2
gene frequency (2) 2
genes (2) 2
genetic aspects (2) 2
genetic variation - genetics (2) 2
genotype & phenotype (2) 2
genotypes (2) 2
geriatrics (2) 2
geriatrics & gerontology (2) 2
geriatrik (2) 2
health risks (2) 2
homozygote (2) 2
immune response (2) 2
information centers - organization & administration (2) 2
information dissemination (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Apolipoprotein E genotype and sex risk factors for Alzheimer disease: A meta-analysis
by Neu, Scott C and Pa, Judy and Kukull, Walter and Beekly, Duane and Kuzma, Amanda and Gangadharan, Prabhakaran and Wang, Li-San and Romero, Klaus and Arneric, Stephen P and Redolfi, Alberto and Orlandi, Daniele and Frisoni, Giovanni B and Au, Rhoda and Devine, Sherral and Auerbach, Sanford and Espinosa, Ana and Boada, Mercè and Ruiz, Agustín and Johnson, Sterling C and Koscik, Rebecca and Wang, Jiun-Jie and Hsu, Wen-Chuin and Chen, Yao-Liang and Toga, Arthur W
JAMA neurology, ISSN 2168-6149, 10/2017, Volume 74, Issue 10, pp. 1178 - 1189
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | Middle Aged | Risk Factors | Databases, Factual - statistics & numerical data | Logistic Models | Male | Sex Characteristics | Case-Control Studies | Apolipoproteins E - genetics | Aged, 80 and over | Alzheimer Disease - epidemiology | Female | Aged | Alzheimer Disease - genetics
Journal Article
Details down arrow
2. Full Text Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
by Naj, Adam C and Jun, Gyungah and Wang, Li-San and Buros, Jacqueline and Buxbaum, Joseph D and Jarvik, Gail P and Bird, Thomas D and Boeve, Bradley F and De Jager, Philip L and Schneider, Julie A and Younkin, Steven G and Kramer, Patricia and Hardy, John and Myers, Amanda J and Barmada, Michael M and Demirci, F Yesim and Baldwin, Clinton T and Green, Robert C and Rogaeva, Ekaterina and George-Hyslop, Peter St and Arnold, Steven E and Barber, Robert and Bigio, Eileen H and Bowen, James D and Boxer, Adam and Cairns, Nigel J and Carney, Regina M and Carroll, Steven L and Chui, Helena C and Corneveaux, Jason and Cotman, Carl W and Dekosky, Steven T and Dick, Malcolm and Faber, Kelley M and Ferris, Steven and Galasko, Douglas R and Ganguli, Mary and Gearing, Marla and Geschwind, Daniel H and Ghetti, Bernardino and Gilbert, John R and Giordani, Bruno and Glass, Jonathan D and Hamilton, Ronald L and Harrell, Lindy E and Head, Elizabeth and Honig, Lawrence S and Hyman, Bradley T and Jicha, Gregory A and Johnson, Nancy and Karlawish, Jason and Karydas, Anna and Kaye, Jeffrey A and Kim, Ronald and Lah, James J and Levey, Allan I and Lieberman, Andrew P and MacK, Wendy J and Marson, Daniel C and Mash, Deborah C and McCormick, Wayne C and McCurry, Susan M and McDavid, Andrew N and McKee, Ann C and Mesulam, Marsel and Parisi, Joseph E and Perl, Daniel P and Petersen, Ronald C and Poon, Wayne W and Rajbhandary, Ruchita A and Raskind, Murray and Ringman, John M and Roberson, Erik D and Rosenberg, Roger N and Sano, Mary and Schneider, Lon S and Smith, Charles D and Sonnen, Joshua A and Spina, Salvatore and Stern, Robert A and Tanzi, Rudolph E and Van Deerlin, Vivianna M and Vonsattel, Jean Paul and Weintraub, Sandra and Woltjer, Randall L and Cantwell, Laura B and Beekly, Duane and Lunetta, Kathryn L and Martin, Eden R and Kamboh, M Ilyas and Saykin, Andrew J and Reiman, Eric M and Morris, John C and Montine, Thomas J and Tsuang, Debby W and Hakonarson, Hakon and Kukull, Walter A and Haines, Jonathan L and Mayeux, Richard and Farrer, Lindsay A
Nature genetics, ISSN 1061-4036, 05/2011, Volume 43, Issue 5, pp. 436 - 443
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Neurology | Organic mental disorders. Neuropsychology | 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 | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Genetic Predisposition to Disease | Genome-Wide Association Study | Multigene Family | Cytoskeletal Proteins - genetics | Membrane Proteins - genetics | Humans | Databases, Genetic | Male | Antigens, CD - genetics | Antigens, Differentiation, Myelomonocytic - genetics | Genetic Variation | Receptor, EphA1 - genetics | Adaptor Proteins, Signal Transducing - genetics | Age of Onset | Aged, 80 and over | Female | Aged | Polymorphism, Single Nucleotide | Sialic Acid Binding Ig-like Lectin 3 | Alzheimer Disease - genetics | Cohort Studies | Conferences, meetings and seminars | Alzheimer's disease | Medical societies | Studies | Medical research | Genomes | Statistical methods | Alzheimers disease | Independent sample | Meta-analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
by Klei, Lambertus and Smith, Jill P and Neoptolemos, John P and Lerch, Markus M and Guda, Nalini M and Alkaade, Samer and Amann, Stephen T and Anderson, Michelle A and Baillie, John and Conwell, Darwin and Coté, Gregory A and Cotton, Peter B and DiSario, James and Farrer, Lindsay A and Forsmark, Chris E and Gardner, Timothy B and Greenhalf, William and Hartman, Douglas J and Papachristou, Georgios I and Romagnuolo, Joseph and Singh, Vijay P and Weiss, Frank Ulrich and Zarnescu, Narcis Octavian and O'Connell, Michael R and Roeder, Kathryn and Barmada, M Michael and Yadav, Dhiraj and Albert, Marilyn S and Albin, Roger L and Barber, Robert and Barnes, Lisa L and Beecham, Gary W and Beekly, Duane and Boxer, Adam and Carroll, Steven L and Chui, Helena C and Clark, David G and Cribbs, David H and Crocco, Elizabeth A and DeCarli, Charles and Demirci, F Yesim and Dick, Malcolm and Ertekin-Taner, Nilufer and Farlow, Martin R and Ferris, Steven and Frosch, Matthew P and Galasko, Douglas R and Ganguli, Mary and Gearing, Marla and Ghetti, Bernardino and Hakonarson, Hakon and Harrell, Lindy E and Head, Elizabeth and Honig, Lawrence S and Jin, Lee-Way and Jun, Gyungah and Kamboh, M Ilyas and Kaye, Jeffrey A and Kim, Ronald and Kowall, Neil W and Kramer, Joel H and Kukul, Walter A and LaFerla, Frank M and Levey, Allan I and Lin, Chiao-Feng and Lopez, Oscar L and Lunetta, Kathryn L and Lyketsos, Constantine G and MacK, Wendy J and Marson, Daniel C and Martin, Eden R and Martiniuk, Frank and Mash, Deborah C and Masliah, Eliezer and McKee, Ann C and Miller, Joshua W and Montine, Thomas J and Morris, John C and Murrel, Jill R and Olichney, John M and Peskind, Elaine and Raskind, Murray and Reitz, Christiane and Ringman, John M and Roberson, Erik D and Rosen, Howard J and Rosenberg, Roger N and Sano, Mary and Saykin, Andrew J and Schneider, Julie A and Schneider, Lon S and Sonnen, Joshua A and Troncoso, Juan C and Tsuang, Debby W and Valladares, Otto and Weintraub, Sandra and Woltjer, Randall L and Wright, Clinton B and Younkin, Steven G and Yu, Chang-En and Alzheimer's Dis Genetics Consortiu and Alzheimer's Disease Genetics Consortium
Nature genetics, ISSN 1061-4036, 12/2012, Volume 44, Issue 12, pp. 1349 - 1354
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Toxicology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Alcoholism | Psychopathology. Psychiatry | Addictive behaviors | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Alcoholism and acute alcohol poisoning | Claudins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Pancreatitis, Alcoholic - genetics | Gene Frequency | Humans | Male | Trypsinogen - genetics | Genetic Variation | Homozygote | Pancreatitis, Alcoholic - pathology | Sex Factors | Trypsin - genetics | Female | Mutation | Pancreatitis | Physiological aspects | Disease susceptibility | Research | Gene expression | Chromosomes | Risk factors | Proteins | Genealogy | Free radicals | Rodents | Genetics | Alcohol | Genomes | Pancreas | Health risk assessment | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Sex-specific association of apolipoprotein e with cerebrospinal fluid levels of tau
by Barnes, Lisa L and Thambisetty, Madhav and Beecham, Gary and Kunkle, Brian and Gifford, Katherine A and Bush, William S and Chibnik, Lori B and Mukherjee, Shubhabrata and Resnick, Susan M and Montine, Thomas J and Zetterberg, Henrik and Larson, Eric B and Johnson, Sterling C and Bennett, David A and Schneider, Julie A and Jefferson, Angela L and Abner, Erin and Adams, Perrie and Asthana, Sanjay and Baldwin, Clinton and Barber, Robert and Barral, Sandra and Bigio, Eileen and Bird, Thomas and Blacker, Deborah and Boeve, Bradley and Burke, James and Burns, Jeffrey and Buxbaum, Joseph and Cairns, Nigel and Cantwell, Laura and Cao, Chuanhai and Carlson, Chris and Carlsson, Cynthia and Carney, Regina and Cribbs, David and Crocco, Elizabeth and Evans, Denis and Faber, Kelley and Fallon, Kenneth and Farlow, Martin and Ferris, Steven and Foroud, Tatiana and Geschwind, Daniel and Gilbert, John and Goate, Alison and Graff-Radford, Neill and Green, Robert and Growdon, John and Hakonarson, Hakon and Hamilton-Nelson, Kara and Hardy, John and Honig, Lawrence and Huentelman, Matthew and Hulette, Christine and Hyman, Bradley and Jarvik, Gail and Jun, Gyungah and Kamboh, M. Ilyas and Kim, Ronald and Kowall, Neil and Kramer, Joel and Kuzma, Amanda and Lah, James and Leverenz, James and Levey, Allan and Li, Ge and Lipton, Richard and Lyketsos, Constantine and Malamon, John and Marson, Daniel and Martin, Eden and Mayeux, Richard and McCormick, Wayne and McKee, Ann and Miller, Bruce and Pericak-Vance, Margaret and Peskind, Elaine and Poon, Wayne and Qu, Liming and Reiman, Eric and Reisberg, Barry and Reitz, Christiane and Ringman, John and Roberson, Erik and Rosen, Howard and Saykin, Andrew and St George-Hyslop, Peter and Stern, Robert and Swerdlow, Russell and Tanzi, Rudolph and Trojanowski, John and Troncoso, Juan and Tsuang, Debby and Vardarajan, Badri and Wang, Li-San and Welsh-Bohmer, Kathleen and Wilhelmsen, Kirk and Woltjer, Randall and Wright, Clinton and Alzheimer's Dis Neuroimaging and Alzheimers Dis Genetics Consortium and Alzheimer’s Disease Genetics Consortium and the Alzheimer’s Disease Neuroimaging Initiative
JAMA neurology, ISSN 2168-6149, 08/2018, Volume 75, Issue 8, pp. 989 - 998
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurofibrillary Tangles - pathology | Peptide Fragments - cerebrospinal fluid | Plaque, Amyloid - pathology | Humans | Genotype | Male | tau Proteins - cerebrospinal fluid | Alzheimer Disease - cerebrospinal fluid | Phosphoproteins - cerebrospinal fluid | Plaque, Amyloid - cerebrospinal fluid | Alzheimer Disease - pathology | Plaque, Amyloid - genetics | Apolipoproteins E - genetics | Sex Factors | Aged, 80 and over | Amyloid beta-Peptides - cerebrospinal fluid | Female | Alzheimer Disease - genetics | Cohort Studies
Journal Article
Details down arrow
5. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: A genome-wide association study
by Reitz, Christiane and Kunkle, Brian W and Beecham, Gary W and Rajbhandary, Ruchita A and Wang, Li-San and Kauwe, John S. K and Myers, Amanda J and Bird, Thomas D and Rogaeva, Ekaterina and Demirci, F. Yesim and Cruchaga, Carlos and Kramer, Patricia L and Ertekin-Taner, Nilufer and Hardy, John and Green, Robert C and Larson, Eric B and St. George-Hyslop, Peter H and Buxbaum, Joseph D and Evans, Denis A and Schneider, Julie A and Lunetta, Kathryn L and Reiman, Eric M and De Jager, Philip L and Montine, Thomas J and Tsuang, Debby W and Kukull, Walter A and Foroud, Tatiana M and Martin, Eden R and Haines, Jonathan L and Farrer, Lindsay A and Schellenberg, Gerard D and Pericak-Vance, Margaret A and Albert, Marilyn S and Beach, Thomas G and Becker, James T and Beekly, Duane and Bigio, Eileen H and Burke, James R and Cairns, Nigel J and Chui, Helena C and Clark, David G and Crocco, Elizabeth A and DeKosky, Steven T and Duara, Ranjan and Faber, Kelley M and Farlow, Martin R and Ferris, Steven and Galasko, Douglas R and Ghetti, Bernardino and Gilbert, John R and Glass, Jonathan D and Hamilton, Ronald L and Harrell, Lindy E and Honig, Lawrence S and Hulette, Christine M and Jin, Lee-Way and Karydas, Anna and Kaye, Jeffrey A and Kowall, Neil W and Lah, James J and Levey, Allan I and Li, Ge and Lieberman, Andrew P and Lin, Chiao-Feng and Mash, Deborah C and Masliah, Elizer and McCormick, Wayne C and McCurry, Susan M and McKee, Ann C and Miller, Bruce L and Miller, Carol A and Miller, Joshua W and Murrell, Jill R and Pankratz, Vernon S and Parisi, Joseph E and Paulson, Henry L and Peskind, Elaine and Pierce, Aimee and Potter, Huntington and Quinn, Joseph F and Raj, Ashok and Raskind, Murray and Roberson, Erik D and Rosenberg, Roger N and Sano, Mary and Schneider, Lon S and Spina, Salvatore and Stern, Robert A and Tanzi, Rudolph E and Trojanowski, John Q and Troncoso, Juan C and Van Deerlin, Vivianna M and Vardarajan, Badri N and Vinters, Harry V and Weintraub, Sandra and Welsh-Bohmer, Kathleen A and Williamson, Jennifer and Wishnek, Sarah and Woltjer, Randall L and Yu, Lei and Alzheimer Dis Genetics Consortium and Alzheimer Disease Genetics Consortium
JAMA neurology, ISSN 2168-6149, 11/2014, Volume 71, Issue 11, pp. 1394 - 1404
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Prospective Studies | Humans | Middle Aged | Risk Factors | Genetic Loci - genetics | Genotype | Male | Age of Onset | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Alzheimer Disease - epidemiology | Female | Aged | Alzheimer Disease - genetics
Journal Article
Details down arrow
6. Full Text Assessment of the genetic variance of late-onset Alzheimer’s disease
by Ridge, Perry G and Hoyt, Kaitlyn B and Boehme, Kevin and Mukherjee, Shubhabrata and Crane, Paul K and Haines, Jonathan L and Mayeux, Richard and Farrer, Lindsay A and Pericak-Vance, Margaret A and Schellenberg, Gerard D and Kauwe, John S.K and Alzheimer's Disease Genetics Consortium (ADGC) and Alzheimer's Dis Genetics
Neurobiology of aging, ISSN 0197-4580, 2015, Volume 41, pp. 200.e13 - 200.e20
Neurology | Internal Medicine | Genetic variance | Genetics | Alzheimer's disease | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Geriatrics & Gerontology | Science & Technology | Genome-Wide Association Study | Datasets as Topic | Humans | Male | Risk | Membrane Glycoproteins - genetics | Amyloid beta-Protein Precursor - genetics | Aged, 80 and over | Female | Aged | Genetic Variation - genetics | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Receptors, Immunologic - genetics | Netrin Receptors | Receptors, Cell Surface - genetics | Analysis | Genomics | Amyloid beta-protein | Genetic research | Single nucleotide polymorphisms | Chromosomes | Epidemiology | Index Medicus | Alzheimer’s disease | Genetic Variance
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights