X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (84748) 84748
Newspaper Article (189) 189
Book Chapter (185) 185
Magazine Article (62) 62
Newsletter (40) 40
Book / eBook (35) 35
Reference (19) 19
Dissertation (16) 16
Conference Proceeding (12) 12
Publication (10) 10
Book Review (3) 3
Streaming Video (2) 2
Trade Publication Article (2) 2
Transcript (2) 2
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (60853) 60853
female (32476) 32476
male (31370) 31370
genetics & heredity (31233) 31233
chromosomes (20824) 20824
animals (19951) 19951
chromosome mapping (16375) 16375
genetic aspects (15441) 15441
genes (15102) 15102
genetics (14793) 14793
adult (14659) 14659
research (13767) 13767
genomes (12644) 12644
genomics (12220) 12220
middle aged (11382) 11382
mutation (11366) 11366
molecular sequence data (10311) 10311
analysis (10308) 10308
biochemistry & molecular biology (10148) 10148
research article (10078) 10078
oncology (9821) 9821
gene expression (9720) 9720
base sequence (9540) 9540
dna (9113) 9113
cell biology (9048) 9048
in situ hybridization, fluorescence (8733) 8733
phenotype (8420) 8420
multidisciplinary sciences (8272) 8272
mice (8193) 8193
gene (8094) 8094
aged (7986) 7986
proteins (7983) 7983
expression (7904) 7904
deoxyribonucleic acid--dna (7341) 7341
child (7328) 7328
chromosome deletion (7310) 7310
genotype (6877) 6877
cancer (6827) 6827
life sciences (6555) 6555
genetic research (6516) 6516
pedigree (6327) 6327
polymerase chain reaction (6304) 6304
adolescent (6254) 6254
polymorphism, single nucleotide (6228) 6228
karyotyping (6141) 6141
alleles (5968) 5968
identification (5873) 5873
biology (5690) 5690
medicine (5651) 5651
translocation, genetic (5615) 5615
chromosome aberrations (5546) 5546
biotechnology & applied microbiology (5521) 5521
genetic markers (5438) 5438
evolution (5424) 5424
genetic linkage (5406) 5406
child, preschool (5079) 5079
physiological aspects (5043) 5043
amino acid sequence (4931) 4931
science (4851) 4851
genetic predisposition to disease (4688) 4688
haplotypes (4538) 4538
human genetics (4493) 4493
genome (4479) 4479
hematology (4426) 4426
mutations (4352) 4352
studies (4292) 4292
risk factors (4158) 4158
infant (4046) 4046
sequence analysis, dna (3999) 3999
genetic variation (3896) 3896
tumors (3801) 3801
phylogeny (3711) 3711
protein (3521) 3521
chromosomes, human, pair 7 (3377) 3377
chromatin (3358) 3358
pathology (3353) 3353
disease (3324) 3324
health aspects (3296) 3296
models, genetic (3264) 3264
quantitative trait loci (3255) 3255
dna methylation (3235) 3235
cloning, molecular (3196) 3196
aged, 80 and over (3180) 3180
pregnancy (3126) 3126
cytogenetics (3114) 3114
gene deletion (3100) 3100
comparative genomic hybridization (3086) 3086
prognosis (3084) 3084
association (3074) 3074
linkage (3074) 3074
molecular biology (3039) 3039
evolution, molecular (3013) 3013
biotechnology (3005) 3005
polymorphism (3002) 3002
deoxyribonucleic acid (2966) 2966
linkage disequilibrium (2925) 2925
cloning (2896) 2896
neurosciences (2893) 2893
evolutionary biology (2871) 2871
polymorphism, genetic (2870) 2870
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (18) 18
UofT at Mississauga - Stacks (6) 6
UofT at Scarborough - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Closed Orders (3) 3
St. Michael's College (John M. Kelly) - 2nd Floor (3) 3
Trinity College (John W Graham) - Stacks (3) 3
UTL at Downsview - May be requested (2) 2
Baycrest Hospital - Resident/Client Library (1) 1
Baycrest Hospital - Stacks (1) 1
Collection Dvlpm't (Acquisitions) - Cancelled Order (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Earth Sciences (Noranda) - Circulation Desk (1) 1
Earth Sciences (Noranda) - Oversize (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
Gerstein Science - Circulation Desk (1) 1
Gerstein Science - Reserve desk (1) 1
Law (Bora Laskin) - Stacks (1) 1
New College (Ivey) - Stacks (1) 1
Online Resources - Online (1) 1
Providence Healthcare - Stacks (1) 1
Regis College - Stacks (1) 1
St. Michael's College (John M. Kelly) - Stacks (1) 1
St. Michael's Hospital - 2nd Floor (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
University College (Laidlaw) - Stacks (1) 1
UofT Schools - Stacks (1) 1
UofT at Mississauga - Circulation Desk (1) 1
UofT at Mississauga - Not returned (1) 1
Victoria University E.J. Pratt - Circulation Desk (1) 1
Victoria University E.J. Pratt - Oversize (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (84633) 84633
Japanese (505) 505
Chinese (224) 224
German (124) 124
French (109) 109
Spanish (70) 70
Russian (63) 63
Polish (27) 27
Dutch (13) 13
Czech (10) 10
Italian (10) 10
Hungarian (7) 7
Portuguese (7) 7
Finnish (5) 5
Korean (5) 5
Danish (4) 4
Norwegian (4) 4
Ukrainian (4) 4
Hebrew (3) 3
Swedish (3) 3
Turkish (3) 3
Bulgarian (2) 2
Romanian (2) 2
Arabic (1) 1
Latin (1) 1
Latvian (1) 1
Serbian (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature genetics, ISSN 1546-1718, 2008, Volume 40, Issue 2, pp. 189 - 197
Blood concentrations of lipoproteins and lipids are heritable(1) risk factors for cardiovascular disease(2,3). Using genome-wide association data from three... 
GENERAL-POPULATION | PROTEIN | PLASMA-LEVELS | GENETICS & HEREDITY | HAPLOTYPES | HDL CHOLESTEROL | LIPASE | POLYMORPHISM | CORONARY-HEART-DISEASE | CONTRIBUTES | CARDIOVASCULAR RISK | Prospective Studies | Humans | Middle Aged | Male | RNA, Messenger - metabolism | Case-Control Studies | Genetic Variation | Chromosomes, Human, Pair 1 | Cholesterol, LDL - blood | Female | Gene Frequency | Liver - metabolism | Probability | Chromosomes, Human, Pair 8 | Genetic Markers | Cholesterol, HDL - genetics | Chromosomes, Human, Pair 7 | Sequence Analysis, DNA | Linkage Disequilibrium | Randomized Controlled Trials as Topic | Cholesterol, LDL - genetics | Chromosomes, Human, Pair 19 | Alleles | Triglycerides - blood | Cholesterol, HDL - blood | Aged | Polymorphism, Single Nucleotide | Triglycerides - genetics | Genome, Human | Cohort Studies | Type 2 diabetes | Proteolipids | Lipoproteins | Physiological aspects | Genetic aspects | Diagnosis | Research | Single nucleotide polymorphisms | Blood lipoproteins | Health aspects | Risk factors | Lipids | Gene loci | Triglycerides | Cholesterol | RNA | Liver | Pair 1 | Klinisk medicin | Single Nucleotide | HDL | genetics | LDL | Chromosomes | Pair 7 | Pair 8 | Human | Messenger | blood | Variation (Genetics) | Clinical Medicine | DNA | Pair 19 | metabolism | Sequence Analysis | Genome | Polymorphism
Journal Article
eLife, ISSN 2050-084X, 05/2015, Volume 4, Issue MAY
Journal Article
Nature (London), ISSN 1476-4687, 2009, Volume 462, Issue 7275, pp. 868 - 874
Journal Article
by Macé, Aurélien and Tuke, Marcus A and Deelen, Patrick and Kristiansson, Kati and Mattsson, Hannele and Nõukas, Margit and Sapkota, Yadav and Schick, Ursula and Porcu, Eleonora and Rüeger, Sina and McDaid, Aaron F and Porteous, David and Winkler, Thomas W and Salvi, Erika and Shrine, Nick and Liu, Xueping and Ang, Wei Q and Zhang, Weihua and Feitosa, Mary F and Venturini, Cristina and van der Most, Peter J and Rosengren, Anders and Wood, Andrew R and Beaumont, Robin N and Jones, Samuel E and Ruth, Katherine S and Yaghootkar, Hanieh and Tyrrell, Jessica and Havulinna, Aki S and Boers, Harmen and Mägi, Reedik and Kriebel, Jennifer and Müller-Nurasyid, Martina and Perola, Markus and Nieminen, Markku and Lokki, Marja-Liisa and Kähönen, Mika and Viikari, Jorma S and Geller, Frank and Lahti, Jari and Palotie, Aarno and Koponen, Päivikki and Lundqvist, Annamari and Rissanen, Harri and Bottinger, Erwin P and Afaq, Saima and Wojczynski, Mary K and Lenzini, Petra and Nolte, Ilja M and Sparsø, Thomas and Schupf, Nicole and Christensen, Kaare and Perls, Thomas T and Newman, Anne B and Werge, Thomas and Snieder, Harold and Spector, Timothy D and Chambers, John C and Koskinen, Seppo and Melbye, Mads and Raitakari, Olli T and Lehtimäki, Terho and Tobin, Martin D and Wain, Louise V and Sinisalo, Juha and Peters, Annette and Meitinger, Thomas and Martin, Nicholas G and Wray, Naomi R and Montgomery, Grant W and Medland, Sarah E and Swertz, Morris A and Vartiainen, Erkki and Borodulin, Katja and Männistö, Satu and Murray, Anna and Bochud, Murielle and Jacquemont, Sébastien and Rivadeneira, Fernando and Hansen, Thomas F and Oldehinkel, Albertine J and Mangino, Massimo and Province, Michael A and Deloukas, Panos and Kooner, Jaspal S and Freathy, Rachel M and Pennell, Craig and Feenstra, Bjarke and Strachan, David P and Lettre, Guillaume and Hirschhorn, Joel and Cusi, Daniele and Heid, Iris M and Hayward, Caroline and Männik, Katrin and Beckmann, Jacques S and Loos, Ruth J. F and Nyholt, Dale R and Metspalu, Andres and Eriksson, Johan G and ...
Nature communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, pp. 744 - 11
Journal Article
Journal Article
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 12, pp. 1355 - 1359
Journal Article
Stroke (1970), ISSN 0039-2499, 2014, Volume 45, Issue 11, pp. 3194 - 3199
Journal Article
Nature genetics, ISSN 1546-1718, 2015, Volume 47, Issue 8, pp. 911 - 916
Journal Article