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 (61) 61
life sciences & biomedicine (43) 43
humans (42) 42
genome-wide association study (24) 24
male (23) 23
genetics & heredity (22) 22
female (20) 20
medicin och hälsovetenskap (20) 20
polymorphism, single nucleotide (20) 20
multidisciplinary sciences (18) 18
science & technology - other topics (18) 18
genetic aspects (15) 15
genome-wide association (14) 14
gene expression (13) 13
genetics (13) 13
genomes (13) 13
medical and health sciences (13) 13
biochemistry & molecular biology (11) 11
genotype (11) 11
research (11) 11
diabetes (10) 10
genes (10) 10
loci (10) 10
middle aged (10) 10
adult (9) 9
epidemiology (9) 9
genetic loci (9) 9
health aspects (9) 9
medical genetics (9) 9
risk factors (9) 9
animals (8) 8
case-control studies (8) 8
disease (8) 8
genetic predisposition to disease (8) 8
genetic variation (8) 8
metaanalysis (8) 8
mice (8) 8
software (8) 8
studies (8) 8
analysis (7) 7
basic medicine (7) 7
biology (7) 7
body mass index (7) 7
computational biology (7) 7
genetic research (7) 7
genomics (7) 7
medicinsk genetik (7) 7
medicinska och farmaceutiska grundvetenskaper (7) 7
obesity (7) 7
physiological aspects (7) 7
science (7) 7
aged (6) 6
bioinformatics (6) 6
gene expression profiling (6) 6
life sciences (6) 6
meta-analysis (6) 6
obesity - genetics (6) 6
phenotype (6) 6
variants (6) 6
biotechnology & applied microbiology (5) 5
clinical medicine (5) 5
development and progression (5) 5
diabetes mellitus (5) 5
genetic association studies (5) 5
genome-wide association studies (5) 5
health risk assessment (5) 5
human genetics (5) 5
identification and classification (5) 5
mathematical & computational biology (5) 5
metabolism (5) 5
methods (5) 5
pathways (5) 5
protein interaction mapping (5) 5
stem cells (5) 5
transcriptome (5) 5
type 2 diabetes (5) 5
abridged index medicus (4) 4
association studies (4) 4
association studies articles (4) 4
biochemical research methods (4) 4
biological and medical sciences (4) 4
cell differentiation (4) 4
common snps (4) 4
data processing (4) 4
diabetis (4) 4
expression (4) 4
gene expression regulation (4) 4
gene-expression (4) 4
genome-wide association study - methods (4) 4
glycemic traits (4) 4
heart (4) 4
human height (4) 4
immunology (4) 4
internet (4) 4
klinisk medicin (4) 4
mass spectrometry (4) 4
mathematics (4) 4
medicine (4) 4
metabolites (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 Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes
by Lohmueller, Kirk E and Sparsø, Thomas and Li, Qibin and Andersson, Ehm and Korneliussen, Thorfinn and Albrechtsen, Anders and Banasik, Karina and Grarup, Niels and Hallgrimsdottir, Ingileif and Kiil, Kristoffer and Kilpeläinen, Tuomas O and Krarup, Nikolaj T and Pers, Tune H and Sanchez, Gaston and Hu, Youna and DeGiorgio, Michael and Jørgensen, Torben and Sandbæk, Annelli and Lauritzen, Torsten and Brunak, Søren and Kristiansen, Karsten and Li, Yingrui and Hansen, Torben and Wang, Jun and Nielsen, Rasmus and Pedersen, Oluf
American journal of human genetics, ISSN 0002-9297, 12/2013, Volume 93, Issue 6, pp. 1072 - 1086
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Association Studies | Diabetes Mellitus, Type 2 - genetics | Humans | Open Reading Frames | Computational Biology | European Continental Ancestry Group | Genotype | Models, Statistical | Exome | Genetic Variation | Denmark | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Type 2 diabetes | Genetic code | Genetic variation | Physiological aspects | Genetic research | Genetic aspects | Research | Nucleotide sequencing | Population genetics | DNA sequencing | Biological variation | Mutation | Diabetes | Simulation | Genes | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Gene set analysis for interpreting genetic studies
by Pers, Tune H
Human molecular genetics, ISSN 0964-6906, 10/2016, Volume 25, Issue 2, pp. R133 - R140
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text A molecular census of arcuate hypothalamus and median eminence cell types
by Campbell, John N and Macosko, Evan Z and Fenselau, Henning and Pers, Tune H and Lyubetskaya, Anna and Tenen, Danielle and Goldman, Melissa and Verstegen, Anne M. J and Resch, Jon M and McCarroll, Steven A and Rosen, Evan D and Lowell, Bradford B and Tsai, Linus T
Nature neuroscience, ISSN 1097-6256, 02/2017, Volume 20, Issue 3, pp. 484 - 496
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genome-Wide Association Study | Peptide Fragments - metabolism | Orexins - metabolism | Arcuate Nucleus of Hypothalamus - metabolism | Ependymoglial Cells - metabolism | Male | Mice, Transgenic | Gene Expression Profiling | Agouti-Related Protein - metabolism | Pro-Opiomelanocortin - physiology | Obesity - metabolism | Leptin - physiology | Peptide Fragments - physiology | Pro-Opiomelanocortin - metabolism | Median Eminence - anatomy & histology | Animals | Arcuate Nucleus of Hypothalamus - anatomy & histology | Agouti-Related Protein - physiology | Female | Mice | Neurons - metabolism | Energy Metabolism - physiology | Median Eminence - metabolism | Somatostatin - metabolism | Physiological aspects | Research | Intermedin | Gene expression | Analysis | Leptin | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
by Miraoui, Hichem and Dwyer, Andrew A and Sykiotis, Gerasimos P and Plummer, Lacey and Chung, Wilson and Feng, Bihua and Beenken, Andrew and Clarke, Jeff and Pers, Tune H and Dworzynski, Piotr and Keefe, Kimberley and Niedziela, Marek and Raivio, Taneli and Crowley, William F and Seminara, Stephanie B and Quinton, Richard and Hughes, Virginia A and Kumanov, Philip and Young, Jacques and Yialamas, Maria A and Hall, Janet E and Van Vliet, Guy and Chanoine, Jean-Pierre and Rubenstein, John and Mohammadi, Moosa and Tsai, Pei-San and Sidis, Yisrael and Lage, Kasper and Pitteloud, Nelly
American journal of human genetics, ISSN 0002-9297, 05/2013, Volume 92, Issue 5, pp. 725 - 743
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Immunohistochemistry | Surface Plasmon Resonance | Dual Specificity Phosphatase 6 - genetics | Genetic Predisposition to Disease - genetics | Genetic Association Studies | Membrane Proteins - genetics | Humans | Computational Biology | Fibroblast Growth Factors - genetics | Molecular Sequence Data | Male | Mutation - genetics | Nerve Tissue Proteins - genetics | Receptors, Interleukin - genetics | Sequence Analysis, DNA | Hypogonadism - genetics | Sequence Homology | Algorithms | Animals | Base Sequence | Inheritance Patterns - genetics | Female | Mice | Intracellular Signaling Peptides and Proteins - genetics | Physiological aspects | Genetic research | Genetic aspects | Research | Gene mutations | Hypogonadism | Proteins | Genetic disorders | Mutation | Gene expression | Bioinformatics | Genes | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Biological interpretation of genome-wide association studies using predicted gene functions
by Pers, Tune H and Karjalainen, Juha M and Chan, Yingleong and Westra, Harm-Jan and Wood, Anew R and Yang, Jian and Lui, Julian C and Vedantam, Sailaja and Gustafsson, Stefan and Esko, Tonu and Frayling, Tim and Speliotes, Elizabeth K and Boehnke, Michael and Raychaudhuri, Soumya and Fehrmann, Rudolf S. N and Hirschhorn, Joel N and Franke, Lude and Genetic Invest ANthropometric Trai and Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature communications, ISSN 2041-1723, 2015, Volume 6, Issue 1, pp. 5890 - 5890
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genome-Wide Association Study - methods | Software | Index Medicus | Medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease
by Maguire, Lillias H and Handelman, Samuel K and Du, Xiaomeng and Chen, Yanhua and Pers, Tune H and Speliotes, Elizabeth K
Nature genetics, ISSN 1061-4036, 10/2018, Volume 50, Issue 10, pp. 1359 - 1365
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Humans | Middle Aged | Male | Genetic Loci | Genome-Wide Association Study - statistics & numerical data | Case-Control Studies | Diverticular Diseases - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Diverticular Diseases - epidemiology | Genome-Wide Association Study - methods | Quantitative Trait Loci | United Kingdom - epidemiology | Genome-wide association studies | Care and treatment | Genetic susceptibility | Colorectal diseases | Development and progression | Research | Quantitative trait loci | Gastrointestinal diseases | Genetic research | Genetic aspects | Health aspects | Identification and classification | Methods | Medical research | Genomics | Stem cells | Medicine, Experimental | Disease susceptibility | Genomes | Mesenchyme | Genes | Association analysis | Smooth muscle | Biology | Intestinal motility | Immunity | Cell adhesion & migration | Hernia | Connective tissues | Etiology | Intestine | Cell adhesion | Extracellular matrix | Colon | Bioinformatics | Age | Codes | Gene expression | Disease control | Loci | Morbidity | Studies | Collagen | Mutation | Index Medicus | diverticulosis | genomics | diverticular disease | diverticulitis | genome-wide association study
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text SNPsnap: A Web-based tool for identification and annotation of matched SNPs
by Pers, Tune H and Timshel, Pascal and Hirschhorn, Joel N
Bioinformatics, ISSN 1367-4803, 07/2015, Volume 31, Issue 3, pp. 418 - 420
Statistics & Probability | Biochemistry & Molecular Biology | Physical Sciences | Computer Science, Interdisciplinary Applications | Life Sciences & Biomedicine | Technology | Biochemical Research Methods | Computer Science | Mathematics | Biotechnology & Applied Microbiology | Science & Technology | Mathematical & Computational Biology | Genome-Wide Association Study | Humans | Molecular Sequence Annotation | Polymorphism, Single Nucleotide - genetics | Software | Internet | Linkage Disequilibrium | Index Medicus | Enrichment | Annotations | Genes | World Wide Web | Biological | Servers | Bioinformatics | Contact | Applications Notes
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text scVAE: variational auto-encoders for single-cell gene expression data
by Gronbech, Christopher Heje and Vording, Maximillian Fornitz and Timshel, Pascal N and Sonderby, Casper Kaae and Pers, Tune H and Winther, Ole
BIOINFORMATICS, ISSN 1367-4803, 08/2020, Volume 36, Issue 16, pp. 4415 - 4422
Statistics & Probability | Biochemistry & Molecular Biology | Physical Sciences | Computer Science, Interdisciplinary Applications | Life Sciences & Biomedicine | Technology | Biochemical Research Methods | Computer Science | Mathematics | Biotechnology & Applied Microbiology | Science & Technology | Mathematical & Computational Biology | Likelihood Functions | Gene Expression Profiling | Software | Sequence Analysis, RNA | Single-Cell Analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights