Articles

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
Journal Article (6211) 6211
Publication (839) 839
Book Review (631) 631
Book / eBook (454) 454
Dissertation (216) 216
Book Chapter (126) 126
Paper (103) 103
Conference Proceeding (96) 96
Newspaper Article (73) 73
Patent (47) 47
Magazine Article (36) 36
Report (14) 14
Trade Publication Article (6) 6
Government Document (4) 4
Data Set (3) 3
Reference (3) 3
Journal / eJournal (2) 2
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (3777) 3777
humans (2942) 2942
male (1661) 1661
female (1643) 1643
middle aged (946) 946
adult (917) 917
animals (916) 916
aged (758) 758
research (691) 691
article (665) 665
analysis (660) 660
abridged index medicus (591) 591
risk factors (496) 496
surgery (428) 428
adolescent (374) 374
studies (373) 373
cancer (370) 370
health aspects (351) 351
genetics & heredity (334) 334
genetic aspects (331) 331
mice (329) 329
oncology (323) 323
aged, 80 and over (298) 298
biochemistry & molecular biology (298) 298
genetics (287) 287
neurosciences (277) 277
treatment outcome (277) 277
risk (275) 275
research article (273) 273
child (270) 270
care and treatment (265) 265
pharmacology & pharmacy (248) 248
united states (245) 245
multidisciplinary sciences (243) 243
psychiatry (241) 241
cell biology (240) 240
children (240) 240
physiological aspects (240) 240
medicine (235) 235
genes (234) 234
genomics (224) 224
retrospective studies (223) 223
mortality (220) 220
management (218) 218
polymorphism, single nucleotide (218) 218
gene expression (216) 216
medicine & public health (216) 216
young adult (216) 216
disease (215) 215
mutation (212) 212
ecology (210) 210
proteins (209) 209
gastroenterology & hepatology (201) 201
time factors (201) 201
genotype (197) 197
diagnosis (194) 194
immunology (191) 191
expression (188) 188
usage (187) 187
prevalence (186) 186
population (185) 185
genomes (182) 182
genetic predisposition to disease (176) 176
biology (175) 175
case-control studies (171) 171
medical research (169) 169
science (167) 167
evolution (166) 166
rats (166) 166
diabetes (164) 164
methods (163) 163
endocrinology & metabolism (160) 160
physics (160) 160
epidemiology (159) 159
follow-up studies (159) 159
medicine, general & internal (159) 159
pediatrics (158) 158
cardiac & cardiovascular systems (155) 155
gastroenterology and hepatology (153) 153
therapy (152) 152
united-states (150) 150
prognosis (148) 148
psychology (148) 148
patients (145) 145
prevention (145) 145
association (142) 142
genome-wide association (140) 140
prospective studies (140) 140
algorithms (139) 139
genetic variation (139) 139
behavior (137) 137
genome-wide association study (137) 137
child, preschool (136) 136
cohort studies (136) 136
hematology (132) 132
phenotype (132) 132
microbiology (131) 131
physiology (131) 131
internal medicine (126) 126
molecular sequence data (123) 123
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (154) 154
Robarts - Stacks (150) 150
UofT at Mississauga - Stacks (47) 47
Collection Dvlpm't (Acquisitions) - Vendor file (43) 43
UTL at Downsview - May be requested (40) 40
UofT at Scarborough - Stacks (40) 40
Collection Dvlpm't (Acquisitions) - Closed Orders (31) 31
OISE - Stacks (23) 23
Trinity College (John W Graham) - Stacks (20) 20
Earth Sciences (Noranda) - Stacks (14) 14
St. Michael's College (John M. Kelly) - 2nd Floor (13) 13
Victoria University E.J. Pratt - Stacks (13) 13
Victoria University E.J. Pratt - Reference (10) 10
Law (Bora Laskin) - Stacks (9) 9
Providence Healthcare - Stacks (8) 8
Engineering & Comp. Sci. - Stacks (7) 7
Online Resources - Online (7) 7
Scarborough Hospital - Birchmount (6) 6
St. Michael's College (John M. Kelly) - 3rd Floor (6) 6
Royal Ontario Museum - Stacks (5) 5
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (5) 5
Holland Bloorview Kids Rehabilitation - Stacks (4) 4
Indust. Rel's & Hum. Resources (Newman) - Library use only (4) 4
Knox College (Caven) - Stacks (4) 4
Providence Healthcare - Reference (4) 4
Baycrest Hospital - Stacks (3) 3
Chemistry (A D Allen) - Stacks (3) 3
Criminology - Stacks (3) 3
Humber River Regional Hospital - Church Stacks (3) 3
Lakeridge Health Sciences - Oshawa (3) 3
New College (Ivey) - Stacks (3) 3
Thomas Fisher Rare Book - Rare Book (3) 3
University College (Laidlaw) - Stacks (3) 3
Architecture Landscape (Shore + Moffat) - Stacks (2) 2
Art - Library use only (2) 2
Credit Valley Hospital - Reserve desk (2) 2
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (2) 2
Dentistry (Harry R Abbott) - Stacks (2) 2
Gerstein Science - Reference (2) 2
Music - Stacks (2) 2
Pontifical Inst. Mediaeval Studies - Library use only (2) 2
Scarborough Hospital - General (2) 2
St. Michael's Hospital - Stacks (2) 2
Toronto East General Hospital - Stacks (2) 2
Trillium Health Centre - Reserve desk (2) 2
Trillium Health Centre - Stacks (2) 2
Trinity College (John W Graham) - Reference (2) 2
UofT at Mississauga - Reference (2) 2
UofT at Scarborough - Withdrawn (2) 2
Victoria University Emmanuel College - Stacks (2) 2
West Park Healthcare Centre - Hospital Department (2) 2
Astronomy & Astrophysics - Ask at library (1) 1
Business (Joseph L Rotman) - Stacks (1) 1
Criminology - Course Reserves (1) 1
Dentistry (Harry R Abbott) - Missing (1) 1
Faculty of Information - Stacks (1) 1
Gardiner Museum - Library use only (1) 1
Gerstein Science - Circulation Desk (1) 1
Humber River Regional Hospital - Finch Stacks (1) 1
Innis College - Stacks (1) 1
Institute for Christian Studies - Stacks (1) 1
Law (Bora Laskin) - Reserve desk (1) 1
Map & Data - Data & GIS (1) 1
Map & Data - Map Collection (1) 1
Mathematical Sciences - Stacks (1) 1
Music - Reference (1) 1
OISE - Curriculum Resources (1) 1
OISE - Reference (1) 1
OISE - Storage (1) 1
Physics - Stacks (1) 1
Providence Healthcare - Reserve desk (1) 1
Regis College - Reference (1) 1
Regis College - Stacks (1) 1
Reserve desk (1) 1
Robarts - Course Reserves (1) 1
Robarts - May be requested in 6-10 wks (1) 1
Robarts - Reference (1) 1
Robarts - Storage (1) 1
Royal Ontario Museum - Far Eastern (1) 1
Royal Ontario Museum - Periodical Stacks (1) 1
St Josephs Health Centre - Stacks (1) 1
St. Michael's College (John M. Kelly) - Reference (1) 1
St. Michael's Hospital - Circulation Desk (1) 1
Stacks (1) 1
Toronto East General Hospital - Online (1) 1
Toronto East General Hospital - Reference (1) 1
Trillium Health Centre - Online (1) 1
UofT Schools - Reference (1) 1
UofT at Mississauga - May be requested in 6-10 wks (1) 1
UofT at Mississauga - Missing (1) 1
UofT at Scarborough - Periodical Stacks (1) 1
Victoria University E.J. Pratt - Oversize (1) 1
Victoria University E.J. Pratt - Virginia Woolf (1) 1
West Park Healthcare Centre - Stacks (1) 1
Women's College Hospital - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (7216) 7216
Spanish (26) 26
French (20) 20
German (9) 9
Arabic (3) 3
Japanese (3) 3
Chinese (2) 2
Portuguese (2) 2
Ancient Greek (1) 1
Korean (1) 1
Latin (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text From HLA association to function
by Barrett, Jeffrey C
Nature Genetics, ISSN 1061-4036, 03/2012, Volume 44, Issue 3, pp. 235 - 236
A new study refines the association signals for rheumatoid arthritis susceptibility in the major histocompatibility complex (MHC) region to five amino-acid... 
RHEUMATOID-ARTHRITIS | MHC | RISK | MECHANISMS | GENETICS & HEREDITY | Arthritis, Rheumatoid - genetics | HLA-DRB1 Chains - genetics | Major Histocompatibility Complex - genetics | Humans | Models, Molecular | Amino Acid Substitution - genetics | HLA-DP beta-Chains - genetics | HLA-B Antigens - genetics | Histocompatibility antigens | Rheumatoid arthritis | HLA histocompatibility antigens | Physiological aspects | Genetic aspects | Research | Single nucleotide polymorphisms | Risk factors | Amino acids | Gene loci | Disease | Sample size | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
by Wright, Caroline F, Dr and Fitzgerald, Tomas W, MS and Jones, Wendy D, MBBS and Clayton, Stephen, MRes and McRae, Jeremy F, PhD and van Kogelenberg, Margriet, PhD and King, Daniel A, MD and Ambridge, Kirsty, BSc and Barrett, Daniel M, BSc and Bayzetinova, Tanya, BSc and Bevan, A Paul, PhD and Bragin, Eugene, MSc and Chatzimichali, Eleni A, PhD and Gribble, Susan, PhD and Jones, Philip, MSc and Krishnappa, Netravathi, MSc and Mason, Laura E, BSc and Miller, Ray, PhD and Morley, Katherine I, PhD and Parthiban, Vijaya, PhD and Prigmore, Elena, PhD and Rajan, Diana, MSc and Sifrim, Alejandro, PhD and Swaminathan, G Jawahar, PhD and Tivey, Adrian R, MSc and Middleton, Anna, PhD and Parker, Michael, Prof and Carter, Nigel P, PhD and Barrett, Jeffrey C, PhD and Hurles, Matthew E, PhD and FitzPatrick, David R, Prof and Firth, Helen V, DM and DDD Study and DDD study
Lancet, The, ISSN 0140-6736, 2015, Volume 385, Issue 9975, pp. 1305 - 1314
Summary Background Human genome sequencing has transformed our understanding of genomic variation and its relevance to health and disease, and is now starting... 
Internal Medicine | INTELLECTUAL DISABILITY | INCIDENTAL FINDINGS | EXOME | MEDICINE, GENERAL & INTERNAL | VARIANTS | SEQUENCE | UNIPARENTAL DISOMY | MUTATIONS | Humans | Child, Preschool | Incidental Findings | Infant | Male | Developmental Disabilities - genetics | Genome, Human - genetics | Information Dissemination | Specimen Handling | Phenotype | Adolescent | Female | Heterozygote | Genetic Variation - genetics | Genome-Wide Association Study - methods | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Medical research | Analysis | Genomics | Medicine, Experimental | Genetic research | Genomes | Nucleotide sequencing | DNA sequencing | Mutation | Medical diagnosis | Genes | Developmental disabilities | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Prevalence and architecture of de novo mutations in developmental disorders
by McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D'Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and De Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and Donnai, Dian and Donnelly, Deirdre and Donnelly, Carina and Douglas, Angela and Douzgou, Sofia and Duncan, Alexis and Eason, Jacqueline and Ellard, Sian and Ellis, Ian and Elmslie, Frances and Evans, Karenza and Everest, Sarah and Fendick, Tina and Fisher, Richard and Flinter, Frances and Foulds, Nicola and Fry, Andrew and Fryer, Alan and Gardiner, Carol and Gaunt, Lorraine and Ghali, Neeti and ... and Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important... 
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | Index Medicus | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Evaluating coverage of genome-wide association studies
by Barrett, Jeffrey C and Cardon, Lon R
Nature Genetics, ISSN 1061-4036, 06/2006, Volume 38, Issue 6, pp. 659 - 662
Genome-wide association studies involving hundreds of thousands of SNPs in thousands of cases and controls are now underway. The first of many analytical... 
POWER | LINKAGE DISEQUILIBRIUM | POLYMORPHISM | FUTURE | COMPLEX DISEASE | GENETICS & HEREDITY | Haplotypes | Likelihood Functions | Humans | Polymorphism, Single Nucleotide | Genome, Human | Case-Control Studies | Linkage Disequilibrium | Genetic markers | Usage | Genetic variation | Causes of | Physiological aspects | Research | Single nucleotide polymorphisms | Identification and classification | Genotype & phenotype | Success factors | Genomics | Research methodology | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
by Cleynen, Isabelle, PhD and Boucher, Gabrielle, MSc and Jostins, Luke, PhD and Schumm, L Philip, MA and Zeissig, Sebastian, PhD and Ahmad, Tariq, PhD and Andersen, Vibeke, Prof and Andrews, Jane M, Prof and Annese, Vito, MD and Brand, Stephan, Prof and Brant, Steven R, MD and Cho, Judy H, Prof and Daly, Mark J, Prof and Dubinsky, Marla, MD and Duerr, Richard H, Prof and Ferguson, Lynnette R, Prof and Franke, Andre, Prof and Gearry, Richard B, Prof and Goyette, Philippe, PhD and Hakonarson, Hakon, Prof and Halfvarson, Jonas, MD and Hov, Johannes R, PhD and Huang, Hailang, PhD and Kennedy, Nicholas A, PhD and Kupcinskas, Limas, Prof and Lawrance, Ian C, Prof and Lee, James C, PhD and Satsangi, Jack, Prof and Schreiber, Stephan, Prof and Théâtre, Emilie, PhD and van der Meulen-de Jong, Andrea E, MD and Weersma, Rinse K, Prof and Wilson, David C, Prof and Parkes, Miles, PhD and Vermeire, Severine, Prof and Rioux, John D, Prof and Mansfield, John, MD and Silverberg, Mark S, PhD and Radford-Smith, Graham, PhD and McGovern, Dermot P B, Prof and Barrett, Jeffrey C, Dr and Lees, Charlie W, Dr and Int Inflammatory Bowel Dis Genet and Örebro universitet and Institutionen för medicinska vetenskaper
Lancet, The, ISSN 0140-6736, 2016, Volume 387, Issue 10014, pp. 156 - 167
Summary Background Crohn's disease and ulcerative colitis are the two major forms of inflammatory bowel disease; treatment strategies have historically been... 
Internal Medicine | POPULATION | MEDICINE, GENERAL & INTERNAL | INFLAMMATORY-BOWEL-DISEASE | SUSCEPTIBILITY | FOLLOW-UP | CLASSIFICATION | RISK | INDUCTION | CLINICAL-COURSE | MAINTENANCE THERAPY | PRIMARY SCLEROSING CHOLANGITIS | Medicine, Experimental | Genetic research | Medical research | Genetic aspects | Colitis | Inflammatory bowel disease | Genotype & phenotype | Genetics | Colon | Family medical history | Crohns disease | Index Medicus | Abridged Index Medicus | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Gastroenterology and Hepatology | Gastroenterologi
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text The zebrafish reference genome sequence and its relationship to the human genome
by Howe, K and Clark, M.D and Torroja, C.F and Torrance, J and Berthelot, C and Muffato, M and Collins, J.E and Humphray, S and McLaren, K and Matthews, L and McLaren, S and Sealy, I and Caccamo, M and Churcher, C and Scott, C and Barrett, J.C and Koch, R and Rauch, G.J and White, S and Chow, W and Kilian, B and Quintais, L.T and Guerra-Assuncao, J.A and Zhou, Y and Gu, Y and Yen, J and Vogel, J.H and Eyre, T and Redmond, S and Banerjee, R and Chi, J and Fu, B and Langley, E and Maguire, S.F and Laird, G.K and Lloyd, D and Kenyon, E and Donaldson, S and Sehra, H and Almeida-King, J and Loveland, J and Trevanion, S and Jones, M and Quail, M and Willey, D and Hunt, A and Burton, J and Sims, S and McLay, K and Plumb, B and Davis, J and Clee, C and Oliver, K and Clark, R and Riddle, C and Elliot, D and Threadgold, G and Harden, G and Ware, D and Mortimore, B and Kerry, G and Heath, P and Phillimore, B and Tracey, A and Corby, N and Dunn, M and Johnson, C and Wood, J and Clark, S and Pelan, S and Griffiths, G and Smith, M and Glithero, R and Howden, P and Barker, N and Stevens, C and Harley, J and Holt, K and Panagiotidis, G and Lovell, J and Beasley, H and Henderson, C and Gordon, D and Auger, K and Wright, D and Collins, J and Raisen, C and Dyer, L and Leung, K and Robertson, L and Ambridge, K and Leongamornlert, D and McGuire, S and Gilderthorp, R and Griffiths, C and Manthravadi, D and Nichol, S and Barker, G and Whitehead, S and Kay, M and ...
Nature, ISSN 0028-0836, 2013, Volume 496, Issue 7446, pp. 498 - 503
Zebrafish have become a popular organism for the study of vertebrate gene function. The virtually transparent embryos of this species, and the ability to... 
DANIO-RERIO | EVOLUTION | GENE | MULTIDISCIPLINARY SCIENCES | FISH | VERTEBRATES | DUPLICATION | MUTATIONS | MAP | REVEALS | Conserved Sequence - genetics | Sex Determination Processes - genetics | Genomics | Humans | Molecular Sequence Annotation | Genome - genetics | Genes - genetics | Male | Genome, Human - genetics | Zebrafish - genetics | Meiosis - genetics | Pseudogenes - genetics | Reference Standards | Animals | Chromosomes - genetics | Female | Zebrafish Proteins - genetics | Evolution, Molecular | Physiological aspects | Genetic aspects | Research | Zebra fish | Human genetics | Proteins | Zebrafish | Genetics | Chromosomes | Genes | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights