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
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Newspaper Article (4016) 4016
Journal Article (2038) 2038
Report (279) 279
Book Chapter (87) 87
Transcript (79) 79
Magazine Article (75) 75
Book Review (55) 55
Patent (55) 55
Book / eBook (47) 47
Dissertation (25) 25
Web Resource (17) 17
Publication (16) 16
Trade Publication Article (15) 15
Conference Proceeding (14) 14
Data Set (5) 5
Reference (5) 5
Paper (1) 1
Streaming Video (1) 1
Video Recording (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (853) 853
life sciences & biomedicine (687) 687
humans (655) 655
cern lhc coll (539) 539
experimental results (536) 536
experiment (478) 478
physics (475) 475
female (446) 446
p p: scattering (429) 429
high energy physics - experiment (428) 428
particle physics (409) 409
p p: colliding beams (401) 401
physics - high energy physics - experiment (382) 382
male (339) 339
hep (277) 277
high energy physics (274) 274
cms (272) 272
gev-cms (229) 229
[phys.hexp]physics [physics]/high energy physics - experiment [hep-ex] (219) 219
adult (210) 210
presidents (202) 202
middle aged (197) 197
biological and medical sciences (195) 195
13000 gev-cms (186) 186
criminal investigations (183) 183
phenomenology (182) 182
medical sciences (179) 179
physics of elementary particles and fields (167) 167
research (164) 164
trump, donald j (163) 163
aged (159) 159
hadron-hadron scattering (145) 145
abridged index medicus (142) 142
background (137) 137
physical sciences (132) 132
analysis (130) 130
nuclear experiment (129) 129
risk factors (129) 129
murders & murder attempts (124) 124
social sciences (121) 121
political campaigns (117) 117
trials (117) 117
politics (115) 115
child (114) 114
presidential elections (107) 107
scattering [p p] (106) 106
social networks (105) 105
health aspects (104) 104
adolescent (103) 103
oncology (99) 99
animals (93) 93
colliding beams [p p] (91) 91
mass dependence (91) 91
cancer (90) 90
channel cross section: upper limit (87) 87
women (87) 87
transverse momentum: missing-energy (86) 86
genetics & heredity (85) 85
pediatrics (84) 84
hospitals (83) 83
supersymmetry (81) 81
weather (81) 81
studies (79) 79
infant (78) 78
cern lab (76) 76
candidates (75) 75
rain (75) 75
genetic aspects (74) 74
particle physics - experiment (74) 74
physics, particles & fields (72) 72
obama, barack (67) 67
aged, 80 and over (66) 66
armed forces (66) 66
infant, newborn (66) 66
mutation (66) 66
students (66) 66
astrophysics (65) 65
care and treatment (65) 65
local elections (65) 65
8000 gev-cms (64) 64
child, preschool (64) 64
governors (64) 64
muon: pair production (64) 64
professional basketball (64) 64
sex crimes (64) 64
political parties (63) 63
public, environmental & occupational health (63) 63
transverse momentum dependence (63) 63
channel cross section: branching ratio: upper limit (62) 62
treatment outcome (62) 62
colleges & universities (61) 61
general & internal medicine (61) 61
hep-ex (61) 61
medicin och hälsovetenskap (61) 61
children & youth (60) 60
kinematics (60) 60
mass spectrum: (59) 59
neurosciences & neurology (59) 59
prime ministers (59) 59
court hearings & proceedings (58) 58
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Online Resources - Online (17) 17
Robarts - Stacks (13) 13
Collection Dvlpm't (Acquisitions) - Vendor file (5) 5
Gerstein Science - Stacks (4) 4
St. Michael's College (John M. Kelly) - 2nd Floor (3) 3
UTL at Downsview - May be requested (3) 3
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Dentistry (Harry R Abbott) - Stacks (2) 2
Gerstein Science - Theses (2) 2
Scarborough Hospital - Birchmount (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
UofT at Mississauga - Stacks (2) 2
UofT at Scarborough - Stacks (2) 2
Art - Library use only (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Law (Bora Laskin) - Stacks (1) 1
Media Commons - Microtexts (1) 1
New College (Ivey) - Stacks (1) 1
OISE - Stacks (1) 1
Pontifical Inst. Mediaeval Studies - Library use only (1) 1
Providence Healthcare - Stacks (1) 1
Robarts - Reference (1) 1
St. Michael's College (John M. Kelly) - Audio Visual (1) 1
Trinity College (John W Graham) - Reference (1) 1
UTL at Downsview - Stacks (1) 1
UofT at Mississauga - Reference (1) 1
Victoria University E.J. Pratt - Reference (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (6802) 6802
French (27) 27
German (9) 9
Spanish (6) 6
Chinese (3) 3
Korean (3) 3
Arabic (1) 1
Irish (1) 1
Japanese (1) 1
Latin (1) 1
Norwegian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Christine Brooke-Rose: an algorithmic appreciation
by Walsh, Joanna
Textual practice, ISSN 0950-236X, 02/2018, Volume 32, Issue 2, pp. 201 - 203
Arts & Humanities | Literature | Women | Brooke-Rose, Christine (1923-2012) | Algorithms | British & Irish literature | Writers
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
by Weiner, Daniel J and Wigdor, Emilie M and Ripke, Stephan and Walters, Raymond K and Kosmicki, Jack A and Grove, Jakob and Samocha, Kaitlin E and Goldstein, Jacqueline I and Okbay, Aysu and Bybjerg-Grauholm, Jonas and Werge, Thomas and Hougaard, David M and Taylor, Jacob and Skuse, David and Devlin, Bernie and Anney, Richard and Sanders, Stephan J and Bishop, Somer and Mortensen, Preben Bo and Børglum, Anders D and Smith, George Davey and Daly, Mark J and Robinson, Elise B and Bækvad-Hansen, Marie and Dumont, Ashley and Hansen, Christine and Hansen, Thomas F and Howrigan, Daniel and Mattheisen, Manuel and Moran, Jennifer and Mors, Ole and Nordentoft, Merete and Nørgaard-Pedersen, Bent and Poterba, Timothy and Poulsen, Jesper and Stevens, Christine and Anttila, Verneri and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A. Jeremy and Wijsman, Ellen M and Wassink, Thomas H and Psychiat Genomics Consortium and iPSYCH-Broad Autism Grp and iPSYCH-Broad Autism Group and Psychiatric Genomics Consortium Autism Group and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Nature genetics, ISSN 1061-4036, 07/2017, Volume 49, Issue 7, pp. 978 - 985
Genetics | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Autism Spectrum Disorder - genetics | Sequence Deletion | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Risk Factors | Family Health | Genetics, Behavioral | Male | Educational Status | Intelligence - genetics | Multifactorial Inheritance | Intellectual Disability - genetics | Genetic Variation | Phenotype | Ethnic Groups - genetics | Schizophrenia - genetics | Autism Spectrum Disorder - epidemiology | Adult | Female | Child | Cohort Studies | Family | Genetic aspects | Genetic transformation | Research | Risk factors | Pervasive developmental disorders | Mental disorders | Intellectual disabilities | Disorders | Schizophrenia | Risk | Genomes | Cases (containers) | Subgroups | Educational attainment | Children & youth | Proteins | Studies | Consortia | Autism | Parents & parenting | Etiology | Population | Mutation | Children | Psychiatry | Index Medicus | Life Sciences | Neurons and Cognition | Neurologi | disease | biology | insights | variants | de-novo | Neurology | mutations | general-population | genetic risk | genome-wide association | loci
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Using Whole-Exome Sequencing to Identify Inherited Causes of Autism
by Yu, Timothy W and Chahrour, Maria H and Coulter, Michael E and Jiralerspong, Sarn and Okamura-Ikeda, Kazuko and Ataman, Bulent and Schmitz-Abe, Klaus and Harmin, David A and Adli, Mazhar and Malik, Athar N and D’Gama, Alissa M and Lim, Elaine T and Sanders, Stephan J and Mochida, Ganesh H and Partlow, Jennifer N and Sunu, Christine M and Felie, Jillian M and Rodriguez, Jacqueline and Nasir, Ramzi H and Ware, Janice and Joseph, Robert M and Hill, R. Sean and Kwan, Benjamin Y and Al-Saffar, Muna and Mukaddes, Nahit M and Hashmi, Asif and Balkhy, Soher and Gascon, Generoso G and Hisama, Fuki M and LeClair, Elaine and Poduri, Annapurna and Oner, Ozgur and Al-Saad, Samira and Al-Awadi, Sadika A and Bastaki, Laila and Ben-Omran, Tawfeg and Teebi, Ahmad S and Al-Gazali, Lihadh and Eapen, Valsamma and Stevens, Christine R and Rappaport, Leonard and Gabriel, Stacey B and Markianos, Kyriacos and State, Matthew W and Greenberg, Michael E and Taniguchi, Hisaaki and Braverman, Nancy E and Morrow, Eric M and Walsh, Christopher A
Neuron (Cambridge, Mass.), ISSN 0896-6273, 01/2013, Volume 77, Issue 2, pp. 259 - 273
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Autistic Disorder - genetics | Humans | Cells, Cultured | Child, Preschool | Rats | Male | Young Adult | Exome - genetics | Animals | Pedigree | Adolescent | Female | Autistic Disorder - diagnosis | Genome-Wide Association Study - methods | Child | Sequence Analysis, DNA - methods | Cohort Studies | Navy-yards and naval stations | Enzymes | Medical colleges | Genetic disorders | Orphans | Neurons | Genes | Diseases | Autism | Armed Forces | Gene mutations | Genetics | Genetic aspects | Children | Studies | Design | Parents & parenting | Families & family life | Genomes | Mutation | Behavior | Experiments | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Two decades beyond BRCA1/2: Homologous recombination, hereditary cancer risk and a target for ovarian cancer therapy
by Walsh, Christine S
Gynecologic oncology, ISSN 0090-8258, 2015, Volume 137, Issue 2, pp. 343 - 350
Hematology, Oncology and Palliative Medicine | Obstetrics and Gynecology | BRCA1 | PARP inhibitor synthetic lethality | Genetic testing | BRCA2 | Homologous recombination | Oncology | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Ovarian Neoplasms - diagnosis | Humans | Cell Line, Tumor | Female | Homologous Recombination | Molecular Targeted Therapy | Genetic Testing - methods | Ovarian Neoplasms - drug therapy | BRCA2 Protein - genetics | Antimitotic agents | Chemotherapy | Genetic aspects | Antineoplastic agents | Health aspects | Sugars | Risk factors | Monosaccharides | Ovarian cancer | Cancer | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text An evidence assessment tool for ecosystem services and conservation studies
by Anne-Christine Mupepele and Jessica C. Walsh and William J. Sutherland and Carsten F. Dormann
Ecological applications, ISSN 1051-0761, 7/2016, Volume 26, Issue 5, pp. 1295 - 1301
quantification | valuation | quality checklist | rigour | governance | Rigour | Quality checklist | Quantification | Governance | Valuation | Environmental Sciences & Ecology | Ecology | Life Sciences & Biomedicine | Science & Technology | Environmental Sciences | Decision Making | Reproducibility of Results | Ecosystem | Environmental Monitoring - standards | Humans | Environmental Monitoring - methods | Conservation of Natural Resources | Research Design | Decision-making | Ecosystem services | Research | Conservation of natural resources | Analysis | Environmental protection | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Synaptic, transcriptional and chromatin genes disrupted in autism
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 The Autism Sequencing Consortium and The DDD Study and Homozygosity Mapping Collaborative for Autism
Nature (London), ISSN 0028-0836, 11/2014, Volume 515, Issue 7526, pp. 209 - 215
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Gene mutations | Analysis | Pervasive developmental disorders | Research | Genetic transcription | Nucleotide sequencing | Health aspects | DNA sequencing | Studies | Autism | Neurosciences | Chromatin | Mutation | Genes | Index Medicus | Medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text The Cult of St Katherine of Alexandria in Early Medieval Europe
by Christine Walsh
05/2017, Church, Faith and Culture in the Medieval West, ISBN 9780754658610, 244
European History | Greek | Religious History | Late Antiquity & Byzantium | Medieval History 400-1500 | Christian hagiography | Christian saints | Christian women saints
eBook
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Who is at risk after risk reduction?
by Walsh, Christine S
Cancer, ISSN 0008-543X, 03/2018, Volume 124, Issue 5, pp. 884 - 887
Life Sciences & Biomedicine | Oncology | Science & Technology | Complications and side effects | Research | Gynecology, Operative | BRCA mutations | Peritonitis | Risk factors | Reduction | BRCA1 protein | Surgery | Health risks | Risk reduction | Risk | Breast cancer | Peritoneum | Cancer | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights