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 (176) 176
humans (123) 123
life sciences & biomedicine (105) 105
female (78) 78
male (71) 71
genetics & heredity (65) 65
genomes (58) 58
risk factors (58) 58
polymorphism, single nucleotide (56) 56
biological and medical sciences (55) 55
genetic aspects (54) 54
genome-wide association study (54) 54
research (54) 54
genetic predisposition to disease (51) 51
genetic variation (44) 44
middle aged (42) 42
iceland (41) 41
multidisciplinary sciences (41) 41
physics (41) 41
science & technology - other topics (41) 41
medical sciences (39) 39
medicin och hälsovetenskap (38) 38
adult (37) 37
genetics (37) 37
physical sciences (36) 36
aged (35) 35
fundamental and applied biological sciences. psychology (35) 35
high energy physics - lattice (34) 34
genetics of eukaryotes. biological and molecular evolution (33) 33
case-control studies (29) 29
medical and health sciences (28) 28
physiological aspects (28) 28
genotype (25) 25
gene expression (23) 23
physics, particles & fields (22) 22
alleles (21) 21
health aspects (21) 21
polymorphism, single nucleotide - genetics (21) 21
european continental ancestry group - genetics (20) 20
genes (20) 20
gene frequency (19) 19
studies (19) 19
aged, 80 and over (18) 18
genomics (18) 18
high energy physics - theory (18) 18
diabetes (17) 17
haplotypes (17) 17
clinical medicine (16) 16
genome, human (16) 16
physics - high energy physics - lattice (16) 16
risk (16) 16
single nucleotide polymorphisms (16) 16
biochemistry & molecular biology (15) 15
diabetes mellitus, type 2 - genetics (15) 15
genome-wide association studies (15) 15
klinisk medicin (15) 15
phenotype (15) 15
body mass index (14) 14
medical genetics (14) 14
mutation (14) 14
astronomy & astrophysics (13) 13
cohort studies (13) 13
adolescent (12) 12
cardiovascular disease (12) 12
chromosomes (12) 12
disease (12) 12
exact sciences and technology (12) 12
general (12) 12
genotype & phenotype (12) 12
odds ratio (12) 12
chromosome mapping (11) 11
genetic loci (11) 11
health risks (11) 11
loci (11) 11
medicine (11) 11
neurology (11) 11
osteoarthritis (11) 11
physics, nuclear (11) 11
population (11) 11
analysis (10) 10
base sequence (10) 10
basic medicine (10) 10
linkage disequilibrium (10) 10
medical research (10) 10
medicinska och farmaceutiska grundvetenskaper (10) 10
science (10) 10
cardiovascular system & cardiology (9) 9
epidemiology (9) 9
genetic predisposition to disease - genetics (9) 9
meta-analysis (9) 9
molecular sequence data (9) 9
obesity (9) 9
quantitative trait loci (9) 9
type 2 diabetes (9) 9
usage (9) 9
association studies (8) 8
biology (8) 8
cancer (8) 8
cardiology. vascular system (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits
by Styrkarsdottir, Unnur and Thorleifsson, Gudmar and Sulem, Patrick and Gudbjartsson, Daniel F and Sigurdsson, Asgeir and Jonasdottir, Aslaug and Jonasdottir, Adalbjorg and Oddsson, Asmundur and Helgason, Agnar and Magnusson, Olafur T and Walters, G. Bragi and Frigge, Michael L and Helgadottir, Hafdis T and Johannsdottir, Hrefna and Bergsteinsdottir, Kristin and Ogmundsdottir, Margret H and Center, Jacqueline R and Nguyen, Tuan V and Eisman, John A and Christiansen, Claus and Steingrimsson, Erikur and Jonasson, Jon G and Tryggvadottir, Laufey and Eyjolfsson, Gudmundur I and Theodors, Asgeir and Jonsson, Thorvaldur and Ingvarsson, Thorvaldur and Olafsson, Isleifur and Rafnar, Thorunn and Kong, Augustine and Sigurdsson, Gunnar and Masson, Gisli and Thorsteinsdottir, Unnur and Stefansson, Kari
Nature (London), ISSN 0028-0836, 2013, Volume 497, Issue 7450, pp. 517 - 520
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Receptors, G-Protein-Coupled - metabolism | Carcinoma, Squamous Cell - genetics | Humans | Male | Bone Density - genetics | Iceland | Female | Biliary Tract Neoplasms - genetics | Water-Electrolyte Imbalance - genetics | Menarche - genetics | Osteoporotic Fractures - genetics | Down-Regulation - genetics | Mice, Knockout | Phenotype | Animals | Receptors, G-Protein-Coupled - deficiency | Skin Neoplasms - genetics | Testosterone - analysis | Denmark | Heterozygote | Mice | Receptors, G-Protein-Coupled - genetics | Australia | Codon, Nonsense - genetics | Receptors, G-Protein-Coupled - chemistry | Bones | Genetic aspects | Health aspects | Density | Mutation (Biology) | Osteoporosis | Brain-derived neurotrophic factor | Genes | Bone density | Genomes | Mutation | Age | Cancer | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
by Swaminathan, Bhairavi and Thorleifsson, Gudmar and Jöud, Magnus and Ali, Mina and Johnsson, Ellinor and Ajore, Ram and Sulem, Patrick and Halvarsson, Britt-Marie and Eyjolfsson, Gudmundur and Haraldsdottir, Vilhelmina and Hultman, Christina and Ingelsson, Erik and Kristinsson, Sigurdur Y and Kähler, Anna K and Lenhoff, Stig and Masson, Gisli and Mellqvist, Ulf-Henrik and Månsson, Robert and Nelander, Sven and Olafsson, Isleifur and Sigurdardottir, Olof and Steingrimsdóttir, Hlif and Vangsted, Annette and Vogel, Ulla and Waage, Anders and Nahi, Hareth and Gudbjartsson, Daniel F and Rafnar, Thorunn and Turesson, Ingemar and Gullberg, Urban and Stefánsson, Kári and Hansson, Markus and Thorsteinsdóttir, Unnur and Nilsson, Björn
Nature communications, ISSN 2041-1723, 05/2015, Volume 6, Issue 1, pp. 7213 - 7213
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Proteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Immunoglobulin G - blood | Meningitis, Bacterial - genetics | Humans | Immunoglobulin A - blood | Transcriptional Elongation Factors - genetics | Multiple Myeloma - genetics | Index Medicus | Medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Genetics of gene expression and its effect on disease
by Emilsson, Valur and Thorleifsson, Gudmar and Zhang, Bin and Leonardson, Amy S and Zink, Florian and Zhu, Jun and Carlson, Sonia and Helgason, Agnar and Walters, G. Bragi and Gunnarsdottir, Steinunn and Mouy, Magali and Steinthorsdottir, Valgerdur and Eiriksdottir, Gudrun H and Bjornsdottir, Gyda and Reynisdottir, Inga and Gudbjartsson, Daniel and Helgadottir, Anna and Jonasdottir, Aslaug and Jonasdottir, Adalbjorg and Styrkarsdottir, Unnur and Gretarsdottir, Solveig and Magnusson, Kristinn P and Stefansson, Hreinn and Fossdal, Ragnheidur and Kristjansson, Kristleifur and Gislason, Hjortur G and Stefansson, Tryggvi and Leifsson, Bjorn G and Thorsteinsdottir, Unnur and Lamb, John R and Gulcher, Jeffrey R and Reitman, Marc L and Kong, Augustine and Schadt, Eric E and Stefansson, Kari
Nature (London), ISSN 0028-0836, 03/2008, Volume 452, Issue 7186, pp. 423 - 428
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Obesity | Biological and medical sciences | Metabolic diseases | Medical sciences | Humans | Middle Aged | Male | Gene Expression Profiling | Blood - metabolism | Obesity - genetics | Iceland | Lod Score | Adipose Tissue - metabolism | Aged, 80 and over | Adult | Female | Waist-Hip Ratio | Body Mass Index | European Continental Ancestry Group - genetics | Gene Expression Regulation - genetics | Sample Size | Animals | Adolescent | Polymorphism, Single Nucleotide - genetics | Aged | Mice | Genome, Human | Cohort Studies | Quantitative Trait Loci - genetics | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Identification of sequence variants influencing immunoglobulin levels
by Jonsson, Stefan and Sveinbjornsson, Gardar and de Lapuente Portilla, Aitzkoa Lopez and Swaminathan, Bhairavi and Plomp, Rosina and Dekkers, Gillian and Ajore, Ram and Ali, Mina and Bentlage, Arthur E. H and Elmér, Evelina and Eyjolfsson, Gudmundur I and Gudjonsson, Sigurjon A and Gullberg, Urban and Gylfason, Arnaldur and Halldorsson, Bjarni V and Hansson, Markus and Holm, Hilma and Johansson, Åsa and Johnsson, Ellinor and Jonasdottir, Aslaug and Ludviksson, Bjorn R and Oddsson, Asmundur and Olafsson, Isleifur and Olafsson, Sigurgeir and Sigurdardottir, Olof and Sigurdsson, Asgeir and Stefansdottir, Lilja and Masson, Gisli and Sulem, Patrick and Wuhrer, Manfred and Wihlborg, Anna-Karin and Thorleifsson, Gudmar and Gudbjartsson, Daniel F and Thorsteinsdottir, Unnur and Vidarsson, Gestur and Jonsdottir, Ingileif and Nilsson, Björn and Stefansson, Kari
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 8, pp. 1182 - 1191
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Immunity, Humoral - genetics | Hematopoiesis - genetics | Male | Immunoglobulins - genetics | Iceland | Immunoglobulin Isotypes - genetics | Genetic Variation | Sweden | Female | Polymorphism, Single Nucleotide | Immunoglobulin Class Switching - genetics | Cohort Studies | Physiological aspects | Immunoglobulins | Genetic aspects | Research | Genetic variation | Genomics | Immunoglobulin M | Haplotypes | Adaptive systems | Pathogenesis | Genes | Immunoglobulin G | Genomes | Gene deletion | Immunoglobulin A | Immunity | Blood | Clonal deletion | Immunity (humoral) | Immune system | Blood & organ donations | Blood cells | Health risks | Principal components analysis | Loci | Switching | Class switching | Studies | Fc receptors | Heavy chains | Histocompatibility antigen HLA | Production capacity | Autoimmune diseases | Runx3 protein | Index Medicus | Basic Medicine | Immunologi inom det medicinska området | Medical and Health Sciences | Medicin och hälsovetenskap | Immunology in the medical area | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma
by Gudmar Thorleifsson and Kristinn P. Magnusson and Patrick Sulem and G. Bragi Walters and Daniel F. Gudbjartsson and Hreinn Stefansson and Thorlakur Jonsson and Adalbjorg Jonasdottir and Aslaug Jonasdottir and Gerdur Stefansdottir and Gisli Masson and Gudmundur A. Hardarson and Hjorvar Petursson and Arsaell Arnarsson and Mehdi Motallebipour and Ola Wallerman and Claes Wadelius and Jeffrey R. Gulcher and Unnur Thorsteinsdottir and Augustine Kong and Fridbert Jonasson and Kari Stefansson
Science (American Association for the Advancement of Science), ISSN 0036-8075, 9/2007, Volume 317, Issue 5843, pp. 1397 - 1400
Glaucoma | Haplotypes | Adipose tissues | Exons | Exfoliation syndrome | P values | Reports | Genotypes | Exfoliation | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Gene Expression | Genetic Predisposition to Disease | Glaucoma, Open-Angle - genetics | Humans | Genotype | Male | Chi-Square Distribution | Case-Control Studies | Iceland | Amino Acid Oxidoreductases - genetics | Adipose Tissue - metabolism | Female | Polymorphism, Single Nucleotide | Glaucoma - genetics | Exfoliation Syndrome - genetics | Causes of | Genomes | Research | Risk factors | Blindness | Ophthalmology | Genes | Genomics | Polymorphism | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Rate of de novo mutations and the importance of father's age to disease risk
by Kong, Augustine and Frigge, Michael L and Masson, Gisli and Besenbacher, Soren and Sulem, Patrick and Magnusson, Gisli and Gudjonsson, Sigurjon A and Sigurdsson, Asgeir and Jonasdottir, Aslaug and Jonasdottir, Adalbjorg and Wong, Wendy S. W and Sigurdsson, Gunnar and Walters, G. Bragi and Steinberg, Stacy and Helgason, Hannes and Thorleifsson, Gudmar and Gudbjartsson, Daniel F and Helgason, Agnar and Magnusson, Olafur Th and Thorsteinsdottir, Unnur and Stefansson, Kari
Nature (London), ISSN 0028-0836, 08/2012, Volume 488, Issue 7412, pp. 471 - 475
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Human | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Iceland - epidemiology | Paternal Age | Humans | Middle Aged | Male | Spermatozoa - metabolism | Mothers | Autistic Disorder - etiology | Selection, Genetic - genetics | Young Adult | Schizophrenia - genetics | Adult | Female | Autistic Disorder - genetics | Genetic Predisposition to Disease | Chromosomes, Human - genetics | Risk Factors | Mutation Rate | Autistic Disorder - epidemiology | Schizophrenia - epidemiology | Sequence Analysis, DNA | Genome, Human - genetics | Schizophrenia - etiology | Pedigree | Polymorphism, Single Nucleotide - genetics | Ovum - metabolism | Schizophrenia | Genetic aspects | Research | Gene mutations | Health aspects | Risk factors | Haplotypes | Confidence intervals | Autism | Demographics | Genetics | Genomes | Fathers | Mutation | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text A community-driven global reconstruction of human metabolism
by Thiele, Ines and Swainston, Neil and Fleming, Ronan M. T and Hoppe, Aneas and Sahoo, Swagatika and Aurich, Maike K and Haraldsdottir, Hulda and Mo, Monica L and Rolfsson, Ottar and Stobbe, Miranda D and Thorleifsson, Stefan G and Agren, Rasmus and Bölling, Christian and Bordel, Sergio and Chavali, Arvind K and Dobson, Paul and Dunn, Warwick B and Endler, Lukas and Hala, David and Hucka, Michael and Hull, Duncan and Jameson, Daniel and Jamshidi, Neema and Jonsson, Jon J and Juty, Nick and Keating, Sarah and Nookaew, Intawat and Le Novère, Nicolas and Malys, Naglis and Mazein, Alexander and Papin, Jason A and Price, Nathan D and Selkov, Evgeni and Sigurdsson, Martin I and Simeonidis, Evangelos and Sonnenschein, Nikolaus and Smallbone, Kieran and Sorokin, Anatoly and van Beek, Johannes H. G. M and Weichart, Dieter and Goryanin, Igor and Nielsen, Jens and Westerhoff, Hans V and Kell, Douglas B and Mendes, Peo and Palsson, Bernhard Ø
Nature biotechnology, ISSN 1087-0156, 2013, Volume 31, Issue 5, pp. 419 - 425
Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Models, Biological | Proteome - metabolism | Computer Simulation | Databases, Protein | Humans | Metabolome - physiology | Physiological aspects | Host-parasite relationships | Disease transmission | Research | Metabolism | Computers | Models | Index Medicus | Microbiology | Mikrobiologi
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Variant of transcription factor 7-like 2 ( TCF7L2 ) gene confers risk of type 2 diabetes
by Jonsdottir, Thorbjorg and Walters, G Bragi and Saemundsdottir, Jona and Thorsteinsdottir, Unnur and Bagger, Yu and Wilensky, Robert L and Sainz, Jesus and Styrkarsdottir, Unnur and Benediktsson, Rafn and Gylfason, Arnaldur and Palsdottir, Ebba and Gulcher, Jeffrey R and Grant, Struan F A and Gudmundsdottir, Thorunn and Kong, Augustine and Gudnason, Vilmundur and Helgadottir, Anna and Rader, Daniel J and Sigurdsson, Gunnar and Reilly, Muredach P and Manolescu, Andrei and Stefansson, Kari and Emilsson, Valur and Stefansson, Hreinn and Reynisdottir, Inga and Magnusson, Kristinn P and Christiansen, Claus and Thorleifsson, Gudmar and Helgason, Agnar
Nature genetics, ISSN 1061-4036, 03/2006, Volume 38, Issue 3, pp. 320 - 323
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Diabetes. Impaired glucose tolerance | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Genetic Predisposition to Disease | Introns | Diabetes Mellitus, Type 2 - genetics | Gene Frequency | Humans | Molecular Sequence Data | Reference Values | Chromosome Mapping | Transcription Factor 7-Like 2 Protein | Denmark | TCF Transcription Factors - genetics | Chromosomes, Human, Pair 10 | Genetic Carrier Screening | Microsatellite Repeats | Cohort Studies | Type 2 diabetes | Genetic variation | Physiological aspects | Causes of | Genetic aspects | DNA binding proteins | Research | Health aspects | Genotype & phenotype | Population | Diabetes | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights