X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (16805) 16805
Publication (2232) 2232
Book Review (1764) 1764
Book Chapter (167) 167
Conference Proceeding (97) 97
Magazine Article (41) 41
Book / eBook (38) 38
Dissertation (34) 34
Government Document (5) 5
Newspaper Article (4) 4
Web Resource (4) 4
Newsletter (3) 3
Data Set (2) 2
Reference (2) 2
Journal / eJournal (1) 1
Streaming Video (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (14299) 14299
humans (11143) 11143
male (6867) 6867
female (6842) 6842
genetics & heredity (6681) 6681
genetics (4927) 4927
genetic linkage (4899) 4899
linkage disequilibrium (4683) 4683
genetic aspects (4192) 4192
linkage (4107) 4107
genotype (3983) 3983
polymorphism, single nucleotide (3448) 3448
chromosome mapping (3416) 3416
adult (3387) 3387
research (3314) 3314
genetic predisposition to disease (3236) 3236
middle aged (2980) 2980
genomics (2945) 2945
animals (2904) 2904
genes (2839) 2839
phenotype (2648) 2648
quantitative trait loci (2644) 2644
linkage analysis (2563) 2563
pedigree (2528) 2528
analysis (2510) 2510
genomes (2279) 2279
haplotypes (2256) 2256
association (2220) 2220
alleles (2088) 2088
genetic markers (2019) 2019
biochemistry & molecular biology (1987) 1987
aged (1838) 1838
genetic research (1758) 1758
risk factors (1742) 1742
lod score (1724) 1724
research article (1720) 1720
mutation (1644) 1644
gene frequency (1613) 1613
psychiatry (1553) 1553
genome-wide association study (1531) 1531
article (1520) 1520
population (1473) 1473
adolescent (1470) 1470
models, genetic (1455) 1455
genetic variation (1450) 1450
gene (1424) 1424
genome-wide association (1409) 1409
case-control studies (1381) 1381
neurosciences (1371) 1371
polymorphism (1365) 1365
studies (1352) 1352
disease (1324) 1324
chromosomes (1320) 1320
child (1318) 1318
genome, human (1303) 1303
single nucleotide polymorphisms (1250) 1250
polymorphism, single nucleotide - genetics (1213) 1213
genome (1201) 1201
loci (1194) 1194
schizophrenia (1153) 1153
single-nucleotide polymorphism (1136) 1136
genetic predisposition to disease - genetics (1117) 1117
physiological aspects (1078) 1078
identification (1062) 1062
microsatellite repeats (1047) 1047
life sciences (1045) 1045
human genetics (1039) 1039
risk (1024) 1024
susceptibility (1002) 1002
family (997) 997
medicine (995) 995
multidisciplinary sciences (979) 979
complex traits (927) 927
expression (924) 924
population genetics (923) 923
polymorphism, genetic (909) 909
gene expression (898) 898
mice (893) 893
locus (867) 867
schizophrenia - genetics (847) 847
endocrinology & metabolism (830) 830
abridged index medicus (821) 821
susceptibility locus (799) 799
quantitative genetics (788) 788
science (782) 782
health aspects (759) 759
biology (753) 753
genetic linkage - genetics (742) 742
bipolar disorder (730) 730
evolutionary biology (730) 730
molecular sequence data (725) 725
genome scan (724) 724
biotechnology & applied microbiology (719) 719
gene mapping (697) 697
genotype & phenotype (696) 696
biotechnology (689) 689
quantitative trait, heritable (683) 683
aged, 80 and over (680) 680
mutations (676) 676
quantitative trait loci - genetics (671) 671
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (22) 22
UofT at Mississauga - Stacks (7) 7
Online Resources - Online (6) 6
UofT at Scarborough - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Closed Orders (3) 3
Robarts - Stacks (3) 3
UTL at Downsview - May be requested (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Providence Healthcare - Stacks (2) 2
Credit Valley Hospital - Stacks (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Faculty of Information - Stacks (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Law (Bora Laskin) - Stacks (1) 1
May be requested (1) 1
Pontifical Inst. Mediaeval Studies - Library use only (1) 1
Providence Healthcare - Reserve desk (1) 1
Royal Ontario Museum - Stacks (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
Trinity College (John W Graham) - Stacks (1) 1
UTL at Downsview - Pharmacy (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (16967) 16967
Chinese (26) 26
French (21) 21
German (21) 21
Spanish (13) 13
Swedish (6) 6
Japanese (3) 3
Polish (3) 3
Turkish (2) 2
Afrikaans (1) 1
Czech (1) 1
Dutch (1) 1
Hungarian (1) 1
Korean (1) 1
Lithuanian (1) 1
Portuguese (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2014, Genetics of cardiovascular disease : genetic interactions in a multifactorial disease
Web Resource
Bioinformatics, ISSN 1367-4803, 1/2010, Volume 26, Issue 2, pp. 259 - 262
Journal Article
Journal Article
by Burton, Paul R and Clayton, David G and Cardon, Lon R and Craddock, Nick and Deloukas, Panos and Duncanson, Audrey and Kwiatkowski, Dominic P and McCarthy, Mark I and Ouwehand, Willem H and Samani, Nilesh J and Todd, John A and Donnelly, Peter and Barrett, Jeffrey C and Davison, Dan and Easton, Doug and Evans, David M and Leung, Hin-Tak and Marchini, Jonathan L and Morris, Andrew P and Spencer, Chris C.A and Tobin, Martin D and Attwood, Antony P and Boorman, James P and Cant, Barbara and Everson, Ursula and Hussey, Judith M and Jolley, Jennifer D and Knight, Alexandra S and Koch, Kerstin and Meech, Elizabeth and Nutland, Sarah and Prowse, Christopher V and Stevens, Helen E and Taylor, Niall C and Walters, Graham R and Walker, Neil M and Watkins, Nicholas A and Winzer, Thilo and Jones, Richard W and McArdle, Wendy L and Ring, Susan M and Strachan, David P and Pembrey, Marcus and Breen, Gerome and Clair, David St and Caesar, Sian and Gordon-Smith, Katharine and Jones, Lisa and Fraser, Christine and Green, Elaine K and Grozeva, Detelina and Hamshere, Marian L and Holmans, Peter A and Jones, Ian R and Kirov, George and Moskivina, Valentina and Nikolov, Ivan and O'Donovan, Michael C and Owen, Michael J and Collier, David A and Elkin, Amanda and Farmer, Anne and Williamson, Richard and McGuffin, Peter and Young, Allan H and Ferrier, I. Nicol and Ball, Stephen G and Balmforth, Anthony J and Barrett, Jennifer H and Bishop, Timothy D and Iles, Mark M and Maqbool, Azhar and Yuldasheva, Nadira and Hall, Alistair S and Braund, Peter S and Dixon, Richard J and Mangino, Massimo and Stevens, Suzanne and Thompson, John R and Bredin, Francesca and Tremelling, Mark and Parkes, Miles and Drummond, Hazel and Lees, Charles W and Nimmo, Elaine R and Satsangi, Jack and Fisher, Sheila A and Forbes, Alastair and Lewis, Cathryn M and Onnie, Clive M and Prescott, Natalie J and Sanderson, Jeremy and Matthew, Christopher G and Barbour, Jamie and Mohiuddin, M. Khalid and Todhunter, Catherine E and Mansfield, John C and Ahmad, Tariq and Cummings, Fraser R and Jewell, Derek P and ... and Breast Cancer Susceptibility Collaboration (UK) and Wellcome Trust Case Control Consortium and Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering Committee and Australo-Anglo-American Spondylitis Consortium (TASC) and The Australo-Anglo-American Spondylitis Consortium (TASC)
Nature Genetics, ISSN 1061-4036, 11/2007, Volume 39, Issue 11, pp. 1329 - 1337
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2003, Volume 73, Issue 1, pp. 34 - 48
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2008, Volume 40, Issue 2, pp. 204 - 210
Systemic lupus erythematosus (SLE) is a common systemic autoimmune disease with complex etiology but strong clustering in families (λS = ∼30). We performed a... 
RHEUMATOID-ARTHRITIS | HUMAN SLE | METAANALYSIS | DISEASE | GENETICS & HEREDITY | RISK | POLYMORPHISM | LINKAGE | EXPRESSION | Haplotypes | Confidence Intervals | Area Under Curve | Humans | HLA Antigens - genetics | Case-Control Studies | Genetic Variation | Chromosomes, Human, Pair 3 | CD11b Antigen - genetics | Chromosomes, Human, Pair 1 | Lupus Erythematosus, Systemic - immunology | Female | Odds Ratio | Intracellular Signaling Peptides and Proteins - genetics | Genetic Predisposition to Disease | Protein Tyrosine Phosphatase, Non-Receptor Type 22 - genetics | Risk Factors | Protein-Serine-Threonine Kinases - genetics | Interferon Regulatory Factors - genetics | European Continental Ancestry Group | Logistic Models | Genetic Markers | Chromosomes, Human, Pair 6 | Nerve Tissue Proteins - genetics | Linkage Disequilibrium | Lupus Erythematosus, Systemic - genetics | Alleles | Chromosomes, Human, Pair 16 | ROC Curve | STAT4 Transcription Factor - genetics | Chromosomes, Human, Pair 11 | Polymorphism, Single Nucleotide | Genome, Human | Cohort Studies | Genetic aspects | Systemic lupus erythematosus | Research | Single nucleotide polymorphisms | Identification and classification | Lupus | Autoimmune diseases | Genomics | Index Medicus | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
Journal Article
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2010, Volume 49, Issue 9, pp. 898 - 905.e3
Journal Article
Journal Article
Journal Article