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 (68) 68
life sciences & biomedicine (62) 62
humans (60) 60
female (43) 43
male (41) 41
genetics (35) 35
genetics & heredity (35) 35
middle aged (35) 35
aged (33) 33
adult (28) 28
risk factors (28) 28
polymorphism, single nucleotide (26) 26
electronic health records (25) 25
genome-wide association study (24) 24
genetic aspects (23) 23
genomics (22) 22
phenotype (22) 22
research (21) 21
genetic predisposition to disease (18) 18
aged, 80 and over (15) 15
case-control studies (15) 15
electronic medical records (15) 15
genes (15) 15
genetic variation (15) 15
genotype (14) 14
medical records (14) 14
atherosclerosis (13) 13
analysis (12) 12
genomes (12) 12
research article (11) 11
single-nucleotide polymorphism (11) 11
cardiac & cardiovascular systems (10) 10
cardiovascular disease (10) 10
cardiovascular system & cardiology (10) 10
biochemistry & molecular biology (9) 9
biological and medical sciences (9) 9
body mass index (9) 9
genetic research (9) 9
human genetics (9) 9
alleles (8) 8
cohort studies (8) 8
gene frequency (8) 8
genotype & phenotype (8) 8
haplotypes (8) 8
mathematical & computational biology (8) 8
medical research (8) 8
abridged index medicus (7) 7
adolescent (7) 7
cholesterol (7) 7
heart diseases (7) 7
linkage disequilibrium (7) 7
medical sciences (7) 7
medicine (7) 7
molecular medicine (7) 7
polymorphism, single nucleotide - genetics (7) 7
age (6) 6
arteriosclerosis (6) 6
atherosclerosis - genetics (6) 6
biomedicine (6) 6
epidemiology (6) 6
european continental ancestry group - genetics (6) 6
fundamental and applied biological sciences. psychology (6) 6
gene function (6) 6
genome, human (6) 6
genome-wide association studies (6) 6
genome-wide association study - methods (6) 6
health aspects (6) 6
heart (6) 6
lipids (6) 6
metabolic diseases (6) 6
multidisciplinary sciences (6) 6
phenotypes (6) 6
science & technology - other topics (6) 6
studies (6) 6
usage (6) 6
algorithms (5) 5
cancer (5) 5
cardiology. vascular system (5) 5
cardiovascular diseases (5) 5
child (5) 5
coronary artery disease (5) 5
coronary artery disease - genetics (5) 5
coronary vessels (5) 5
genetic disorders (5) 5
genetic epidemiology (5) 5
genetic markers (5) 5
genetic predisposition to disease - genetics (5) 5
genetics of eukaryotes. biological and molecular evolution (5) 5
genotypes (5) 5
medicine, experimental (5) 5
physiological aspects (5) 5
science (5) 5
surgery (5) 5
young adult (5) 5
abdominal aortic aneurysm (4) 4
african continental ancestry group - genetics (4) 4
age of onset (4) 4
care and treatment (4) 4
cholesterol, ldl - blood (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
by Denny, Joshua C and Bastarache, Lisa and Ritchie, Marylyn D and Carroll, Robert J and Zink, Raquel and Mosley, Jonathan D and Field, Julie R and Pulley, Jill M and Ramirez, Andrea H and Bowton, Erica and Basford, Melissa A and Carrell, David S and Peissig, Peggy L and Kho, Abel N and Pacheco, Jennifer A and Rasmussen, Luke V and Crosslin, David R and Crane, Paul K and Pathak, Jyotishman and Bielinski, Suzette J and Pendergrass, Sarah A and Xu, Hua and Hindorff, Lucia A and Li, Rongling and Manolio, Teri A and Chute, Christopher G and Chisholm, Rex L and Larson, Eric B and Jarvik, Gail P and Brilliant, Murray H and Mccarty, Catherine A and Kullo, Iftikhar J and Haines, Jonathan L and Crawford, Dana C and Masys, Daniel R and Roden, Dan M
Nature biotechnology, ISSN 1087-0156, 12/2013, Volume 31, Issue 12, pp. 1102 - 1110
Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Electronic Health Records - statistics & numerical data | Medical Record Linkage - methods | Genetic Predisposition to Disease - genetics | Phenotype | Chromosome Mapping - methods | Humans | Polymorphism, Single Nucleotide - genetics | Genome-Wide Association Study - statistics & numerical data | Genetic Predisposition to Disease - epidemiology | Genome-Wide Association Study - methods | Data Mining - methods | Medical records | Usage | Disease susceptibility | Genetic aspects | Research | Genomics | Genotype & phenotype | Data analysis | Electronic health records | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text The phenotypic legacy of admixture between modern humans and Neandertals
by Simonti, Corinne N and Vernot, Benjamin and Bastarache, Lisa and Bottinger, Erwin and Carrell, David S and Chisholm, Rex L and Crosslin, David R and Hebbring, Scott J and Jarvik, Gail P and Kullo, Iftikhar J and Li, Rongling and Pathak, Jyotishman and Ritchie, Marylyn D and Roden, Dan M and Verma, Shefali S and Tromp, Gerard and Prato, Jeffrey D and Bush, William S and Akey, Joshua M and Denny, Joshua C and Capra, John A
Science (American Association for the Advancement of Science), ISSN 0036-8075, 02/2016, Volume 351, Issue 6274, pp. 737 - 741
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Haplotypes | European Continental Ancestry Group - genetics | Disease - genetics | Humans | Neanderthals - genetics | Depression - genetics | Genetic Variation | Phenotype | Animals | Keratosis, Actinic - genetics | Alleles | Genome, Human | Evolution, Molecular | Neanderthals | Genetic aspects | Nucleotide sequencing | Observations | Methods | DNA sequencing | Genotype & phenotype | Genomes | Hominids | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Joint Linkage and Association Analysis with Exome Sequence Data Implicates SLC25A40 in Hypertriglyceridemia
by Rosenthal, Elisabeth A and Ranchalis, Jane and Crosslin, David R and Burt, Amber and Brunzell, John D and Motulsky, Arno G and Nickerson, Deborah A and Wijsman, Ellen M and Jarvik, Gail P and NHLBI GO Exome Sequencing Project
American journal of human genetics, ISSN 0002-9297, 12/2013, Volume 93, Issue 6, pp. 1035 - 1045
Genetic Predisposition to Disease | Hypertriglyceridemia - genetics | Genetic Association Studies | Humans | Middle Aged | Hypertriglyceridemia - metabolism | Male | Chromosomes, Human, Pair 7 | Mitochondrial Membrane Transport Proteins - genetics | Exome | Young Adult | Phenotype | Chromosomes, Human, Pair 17 | Adolescent | Triglycerides - blood | Aged, 80 and over | Adult | Female | Aged | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Child | Genetic Linkage | Hyperlipidemia | Genetic variation | Physiological aspects | Genetic research | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Cardiovascular disease | Triglycerides | Genes | Risk factors | Genetic linkage | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Complement Receptor 1 Gene Variants Are Associated with Erythrocyte Sedimentation Rate
by Kullo, Iftikhar J and Ding, Keyue and Shameer, Khader and McCarty, Catherine A and Jarvik, Gail P and Denny, Joshua C and Ritchie, Marylyn D and Ye, Zi and Crosslin, David R and Chisholm, Rex L and Manolio, Teri A and Chute, Christopher G
American journal of human genetics, ISSN 0002-9297, 07/2011, Volume 89, Issue 1, pp. 131 - 138
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Blood Sedimentation | Humans | Middle Aged | Immunity, Innate - genetics | Databases, Genetic | Genetic Association Studies - methods | Genotype | Male | Receptors, Complement - metabolism | Receptors, Complement 3b - metabolism | Receptors, Complement - genetics | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Receptors, Complement 3b - genetics | Binding Sites | Electronic Health Records | Cohort Studies | Usage | Genetic variation | Genetic aspects | Research | Erythrocyte sedimentation rate | Coronary heart disease | Risk factors | Proteins | Biological variation | Electronic health records | Binding sites | Erythrocytes | Index Medicus | Report
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects
by Shameer, Khader and Shameer, Khader and Denny, Joshua C and Denny, Joshua C and Ding, Keyue and Ding, Keyue and Jouni, Hayan and Jouni, Hayan and Crosslin, David R and Crosslin, David R and de Andrade, Mariza and de Andrade, Mariza and Chute, Christopher G and Chute, Christopher G and Peissig, Peggy and Peissig, Peggy and Pacheco, Jennifer A and Pacheco, Jennifer A and Li, Rongling and Li, Rongling and Bastarache, Lisa and Bastarache, Lisa and Kho, Abel N and Kho, Abel N and Ritchie, Marylyn D and Ritchie, Marylyn D and Masys, Daniel R and Masys, Daniel R and Chisholm, Rex L and Chisholm, Rex L and Larson, Eric B and Larson, Eric B and McCarty, Catherine A and McCarty, Catherine A and Roden, Dan M and Roden, Dan M and Jarvik, Gail P and Jarvik, Gail P and Kullo, Iftikhar J and Kullo, Iftikhar J
Human genetics, ISSN 0340-6717, 1/2014, Volume 133, Issue 1, pp. 95 - 109
Human Genetics | Gene Function | Molecular Medicine | Biomedicine | Metabolic Diseases | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Meta-Analysis as Topic | Chromosomes, Human - genetics | Humans | Middle Aged | Male | Genetic Pleiotropy | Genetic Loci | Cardiovascular Diseases - genetics | Thrombopoiesis - genetics | Phenotype | Platelet Count | Hemostasis | Aged, 80 and over | Mean Platelet Volume | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Proteins | Medical records | Genomes | Genes | Genomics | Index Medicus | Cancer
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants
by Namjou, Bahram and Stanaway, Ian B and Lingren, Todd and Mentch, Frank D and Benoit, Barbara and Dikilitas, Ozan and Niu, Xinnan and Shang, Ning and Shoemaker, Ashley H and Carey, David J and Mirshahi, Tooraj and Singh, Rajbir and Nestor, Jordan G and Hakonarson, Hakon and Denny, Joshua C and Crosslin, David R and Jarvik, Gail P and Kullo, Iftikhar J and Williams, Marc S and Harley, John B and eMERGE Network
International Journal of Obesity, ISSN 0307-0565, 2020, Volume 45, Issue 1, pp. 155 - 169
Obesity | Cell receptors | Genetic variation | Genetic research | Genetic aspects | Research | Health aspects | Risk factors | Haplotypes | Diabetes mellitus | Melanocortin | Homeostasis | Melanocortin MC4 receptors | Genomes | Regression analysis | Energy balance | Body mass index | Nephropathy | Genotyping | Body mass | Food intake | Body size | Renal failure | Diabetes mellitus (non-insulin dependent) | Index Medicus | Development
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival
by Kim, Daniel Seung, BS and Kim, Jerry H., MD, MPH and Burt, Amber A., MS and Crosslin, David R., PhD and Burnham, Nancy, MSN and Kim, Cecilia E., BS and McDonald-McGinn, Donna M., MS and Zackai, Elaine H., MD and Nicolson, Susan C., MD and Spray, Thomas L., MD and Stanaway, Ian B., BS and Nickerson, Deborah A., PhD and Heagerty, Patrick J., PhD and Hakonarson, Hakon, MD, PhD and Gaynor, J. William, MD and Jarvik, Gail P., MD, PhD
The Journal of thoracic and cardiovascular surgery, ISSN 0022-5223, 2015, Volume 151, Issue 4, pp. 1147 - 1151.e4
Cardiothoracic Surgery | congenital heart disease | genetics | copy number variation | survival | Cardiac & Cardiovascular Systems | Respiratory System | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Surgery | Science & Technology | Predictive Value of Tests | Prospective Studies | Heart Defects, Congenital - surgery | Humans | Child, Preschool | Infant | Male | Case-Control Studies | DNA Copy Number Variations | Heart Defects, Congenital - genetics | Time Factors | Polymerase Chain Reaction | Female | Child | Genetic Predisposition to Disease | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Heart Transplantation | Gene Dosage | Genetic Markers | Chi-Square Distribution | Disease-Free Survival | Phenotype | Heart Defects, Congenital - diagnosis | Electronic Health Records | Congenital heart disease | Genetic disorders | Analgesics | Heart diseases | Genomics | Medical genetics | Analysis | Medical records | Epidemiology | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network
by Crosslin, David R and Crosslin, David R and McDavid, Andrew and McDavid, Andrew and Weston, Noah and Weston, Noah and Nelson, Sarah C and Nelson, Sarah C and Zheng, Xiuwen and Zheng, Xiuwen and Hart, Eugene and Hart, Eugene and de Andrade, Mariza and de Andrade, Mariza and Kullo, Iftikhar J and Kullo, Iftikhar J and McCarty, Catherine A and McCarty, Catherine A and Doheny, Kimberly F and Doheny, Kimberly F and Pugh, Elizabeth and Pugh, Elizabeth and Kho, Abel and Kho, Abel and Hayes, M Geoffrey and Hayes, M Geoffrey and Pretel, Stephanie and Pretel, Stephanie and Saip, Alexander and Saip, Alexander and Ritchie, Marylyn D and Ritchie, Marylyn D and Crawford, Dana C and Crawford, Dana C and Crane, Paul K and Crane, Paul K and Newton, Katherine and Newton, Katherine and Li, Rongling and Li, Rongling and Mirel, Daniel B and Mirel, Daniel B and Crenshaw, Andrew and Crenshaw, Andrew and Larson, Eric B and Larson, Eric B and Carlson, Chris S and Carlson, Chris S and Jarvik, Gail P and Jarvik, Gail P and Med Records Genomics eMERGE and Electronic Medical Records and Genomics (eMERGE) Network and The electronic Medical Records and Genomics (eMERGE) Network
Human genetics, ISSN 0340-6717, 4/2012, Volume 131, Issue 4, pp. 639 - 652
Gene Function | Human Genetics | Molecular Medicine | Biomedicine | Metabolic Diseases | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Middle Aged | Male | Genome-Wide Association Study - statistics & numerical data | Genetic Variation | Medical Records - statistics & numerical data | Aged, 80 and over | Adult | Female | Leukocyte Count | African Continental Ancestry Group - genetics | Neoplasm Proteins - genetics | Principal Component Analysis | European Continental Ancestry Group - genetics | Gene Frequency | European Continental Ancestry Group - statistics & numerical data | Genotype | Mediator Complex - genetics | Genome, Human - genetics | Proteasome Endopeptidase Complex - genetics | Alleles | Aged | Polymorphism, Single Nucleotide | Duffy Blood-Group System - genetics | Genome-Wide Association Study - methods | Receptors, Cell Surface - genetics | Blood cell count | Genomics | Genetic aspects | Index Medicus | Inflammatory bowel diseases | electronic medical records | Association analysis | Crohn's disease | Leukocytes (neutrophilic) | Single-nucleotide polymorphism | Leukocytes | Chemokine receptors | Chromosome 1 | Promoters | Asthma | Duffy antigen | genomics | Blood groups | chromosome 17
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network
by Namjou, Bahram and Lingren, Todd and Huang, Yongbo and Parameswaran, Sreeja and Cobb, Beth L and Stanaway, Ian B and Connolly, John J and Mentch, Frank D and Benoit, Barbara and Niu, Xinnan and Wei, Wei-Qi and Carroll, Robert J and Pacheco, Jennifer A and Harley, Isaac T. W and Divanovic, Senad and Carrell, David S and Larson, Eric B and Carey, David J and Verma, Shefali and Ritchie, Marylyn D and Gharavi, Ali G and Murphy, Shawn and Williams, Marc S and Crosslin, David R and Jarvik, Gail P and Kullo, Iftikhar J and Hakonarson, Hakon and Li, Rongling and Xanthakos, Stavra A and Harley, John B and eMERGE Network and The eMERGE Network
BMC medicine, ISSN 1741-7015, 07/2019, Volume 17, Issue 1, pp. 135 - 135
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Genomics - statistics & numerical data | Community Networks - organization & administration | Humans | Middle Aged | Male | Electronic Health Records - organization & administration | Case-Control Studies | Genomics - organization & administration | Adult | Female | Body Mass Index | Genetic Predisposition to Disease | Genome-Wide Association Study