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
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (488) 488
Publication (52) 52
Patent (11) 11
Conference Proceeding (8) 8
Newspaper Article (3) 3
Book Chapter (2) 2
Dissertation (1) 1
Streaming Audio (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (295) 295
life sciences & biomedicine (250) 250
humans (245) 245
female (189) 189
male (173) 173
aged (152) 152
medicin och hälsovetenskap (121) 121
aged, 80 and over (103) 103
risk factors (98) 98
middle aged (75) 75
research (74) 74
medical and health sciences (72) 72
biological and medical sciences (70) 70
genome-wide association study (67) 67
epidemiology (60) 60
medical sciences (58) 58
genetics (57) 57
adult (55) 55
cohort studies (53) 53
iceland - epidemiology (51) 51
studies (49) 49
genetics & heredity (48) 48
polymorphism, single nucleotide (47) 47
genetic aspects (46) 46
aging (44) 44
medicine (44) 44
cardiovascular disease (40) 40
genomes (40) 40
health aspects (40) 40
meta-analysis (39) 39
analysis (38) 38
abridged index medicus (36) 36
clinical medicine (36) 36
cardiovascular diseases (34) 34
neurosciences & neurology (34) 34
prospective studies (33) 33
iceland (32) 32
klinisk medicin (32) 32
multidisciplinary sciences (32) 32
physiological aspects (32) 32
research article (32) 32
science & technology - other topics (32) 32
genomics (30) 30
mortality (30) 30
endocrinology & metabolism (29) 29
medical research (29) 29
neurosciences (29) 29
age (28) 28
body mass index (28) 28
diabetes (28) 28
genetic predisposition to disease (28) 28
older people (27) 27
obesity (26) 26
fundamental and applied biological sciences. psychology (24) 24
genotype (24) 24
heart (24) 24
cardiovascular system & cardiology (23) 23
phenotype (23) 23
rheumatology (23) 23
age factors (22) 22
animals (22) 22
health risk assessment (22) 22
magnetic resonance imaging (22) 22
medicinska och farmaceutiska grundvetenskaper (22) 22
oncology (22) 22
physical sciences (22) 22
polymorphism, single nucleotide - genetics (22) 22
science (22) 22
cross-sectional studies (21) 21
european continental ancestry group - genetics (21) 21
general & internal medicine (21) 21
medicinsk genetik (21) 21
public health (21) 21
adolescent (20) 20
basic medicine (20) 20
clinical neurology (20) 20
coronary heart disease (20) 20
genetic variation (20) 20
medical genetics (20) 20
neurology (20) 20
biochemistry & molecular biology (19) 19
cardiac & cardiovascular systems (19) 19
chemistry (19) 19
sex factors (19) 19
usage (19) 19
health sciences (18) 18
medicine, general & internal (18) 18
prevalence (18) 18
biochemistry (17) 17
blood pressure (17) 17
genes (17) 17
genetic loci (17) 17
genome-wide association studies (17) 17
nutrition & dietetics (17) 17
tumors (17) 17
alleles (16) 16
atherosclerosis (16) 16
biomarkers - blood (16) 16
follow-up studies (16) 16
osteoporosis (16) 16
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Novel loci associated with usual sleep duration: The CHARGE Consortium Genome-Wide Association Study
by Gottlieb, Daniel J and Hek, Karin and Chen, T.-H and Watson, N.F and Eiriksdottir, Gudny and Byrne, E.M and Cornelis, Marilyn and Warby, S.C and Bandinelli, S and Cherkas, Lynn and Evans, Daniel and Grabe, Hans Jörgen and Lahti, Jari and Li, Man and Lehtimäki, Terho and Lumley, Thomas and Marciante, Kristin and Perusse, Louis and Psaty, Bruce and Robbins, J and Tranah, Gregory and Vink, J.M and Wilk, J.B and Stafford, J.M and Bellis, Claire and Biffar, R and Bouchard, Claude and Cade, B and Curhan, Gary and Eriksson, J and Ewert, R and Ferrucci, Luigi and Fülöp, T and Gehrman, Philip and Goodloe, Robert and Harris, Tamara and Heath, Anew C and Hernandez, Dena and Hofman, Albert and Hottenga, Jouke Jan and Hunter, David and Jensen, Majken K and Johnson, Anew and Kähönen, Mika and Kao, Wen and Kraft, Peter and Larkin, E.K and Lauderdale, D.S and Luik, Annemarie and Medici, M and Montgomery, Grant W and Palotie, A and Patel, Sanjay and Pistis, Giorgio and Porcu, E and Quaye, Lydia and Raitakari, Olli and Redline, Susan and Rimm, Eric B and Rotter, J.I and Smith, Albert and Spector, Timothy and Teumer, Alexander and Uitterlinden, Ané and Vohl, Marie-Claude and Widen, E and Willemsen, Gonneke and Young, Terri L and Zhang, X and Liu, Y and Blangero, John and Boomsma, Dorret and Gudnason, Vilmundur and Hu, F and Mangino, M and Martin, Nicholas and O'Connor, George and Stone, Katie L and Tanaka, T and Viikari, Jorma and Gharib, Sina and Punjabi, Naresh and Räikkönen, Katri and Völzke, Henry and Mignot, E and Tiemeier, Henning
Molecular psychiatry, ISSN 1359-4184, 01/2015, Volume 20, Issue 10, pp. 1232 - 1239
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Genetic Association Studies | Humans | Middle Aged | Self Report | African Americans - genetics | Male | Sleep - genetics | Dyssomnias - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Quantitative trait loci | Genome-wide association studies | Genetic aspects | Sleep | Health aspects | Identification and classification | Attention deficit hyperactivity disorder | Genomes | Metabolism | Loci | Chromosome 2 | Morbidity | Consortia | Genetic variance | Gene frequency | Alleles | Cardiovascular diseases | Chromosomes | Pax8 protein | Thyroid | Index Medicus | Genome-wide association study
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia
by Ulfarsson, M.O and Walters, G.B and Gustafsson, O and Steinberg, S and Silva, A and Doyle, O.M and Brammer, M and Gudbjartsson, D.F and Arnarsdottir, S and Jonsdottir, G.A and Gisladottir, R.S and Bjornsdottir, G and Helgason, H and Ellingsen, L.M and Halldorsson, J.G and Saemundsen, E and Stefansdottir, B and Jonsson, L and Eiriksdottir, V.K and Eiriksdottir, G.R and Johannesdottir, G.H and Unnsteinsdottir, U and Jonsdottir, B and Magnusdottir, B.B and Sulem, P and Thorsteinsdottir, U and Sigurdsson, E and Brandeis, D and Meyer-Lindenberg, A and Stefansson, H and Stefansson, K
Translational psychiatry, ISSN 2158-3188, 2017, Volume 7, Issue 4, pp. e1109 - e1109
Life Sciences & Biomedicine | Psychiatry | Science & Technology | Iceland - epidemiology | Humans | Middle Aged | Magnetic Resonance Imaging - methods | Male | Temporal Lobe - anatomy & histology | Developmental Disabilities - genetics | Functional Neuroimaging - methods | Functional Neuroimaging - standards | Temporal Lobe - diagnostic imaging | Intellectual Disability - genetics | Young Adult | Dyscalculia - genetics | Cognition - physiology | Adult | Female | Chromosome Deletion | Neuropsychological Tests - standards | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Dyslexia - genetics | Phenotype | Adolescent | Chromosome Aberrations | Heterozygote | Aged | Index Medicus | Original
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment
by Cornelius A. Rietveld and Sarah E. Medland and Jaime Derringer and Jian Yang and Tõnu Esko and Nicolas W. Martin and Harm-Jan Westra and Konstantin Shakhbazov and Abdel Abdellaoui and Arpana Agrawal and Eva Albrecht and Behrooz Z. Alizadeh and Najaf Amin and John Barnard and Sebastian E. Baumeister and Kelly S. Benke and Lawrence F. Bielak and Jeffrey A. Boatman and Patricia A. Boyle and Gail Davies and Christiaan de Leeuw and Niina Eklund and Daniel S. Evans and Rudolf Ferhmann and Krista Fischer and Christian Gieger and Håkon K. Gjessing and Sara Hägg and Jennifer R. Harris and Caroline Hayward and Christina Holzapfel and Carla A. Ibrahim-Verbaas and Erik Ingelsson and Bo Jacobsson and Peter K. Joshi and Astanand Jugessur and Marika Kaakinen and Stavroula Kanoni and Juha Karjalainen and Ivana Kolcic and Kati Kristiansson and Zoltán Kutalik and Jari Lahti and Sang H. Lee and Peng Lin and Penelope A. Lind and Yongmei Liu and Kurt Lohman and Marisa Loitfelder and George McMahon and Pedro Marques Vidal and Osorio Meirelles and Lili Milani and Ronny Myhre and Marja-Liisa Nuotio and Christopher J. Oldmeadow and Katja E. Petrovic and Wouter J. Peyrot and Ozren Polašek and Lydia Quaye and Eva Reinmaa and John P. Rice and Thais S. Rizzi and Helena Schmidt and Reinhold Schmidt and Albert V. Smith and Jennifer A. Smith and Toshiko Tanaka and Antonio Terracciano and Matthijs J. H. M. van der Loos and Veronique Vitart and Henry Völzke and Jürgen Wellmann and Lei Yu and Wei Zhao and Jüri Allik and John R. Attia and Stefania Bandinelli and François Bastardot and Jonathan Beauchamp and David A. Bennett and Klaus Berger and Laura J. Bierut and Dorret I. Boomsma and Ute Bültmann and Harry Campbell and Christopher F. Chabris and Lynn Cherkas and Mina K. Chung and Francesco Cueca and Mariza de Andrade and Philip L. De Jager and Jan-Emmanuel De Neve and Ian J. Deary and George V. Dedoussis and Panos Deloukas and Maria Dimitriou and Guðný Eiríksdóttir and Martin F. Elderson and Johan G. Eriksson and ... and LifeLines Cohort Study and The LifeLines Cohort Study and Institutionen för kliniska vetenskaper, Avdelningen för obstetrik och gynekologi and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Clinical Sciences, Department of Obstetrics and Gynecology and Sahlgrenska Academy
Science (American Association for the Advancement of Science), ISSN 0036-8075, 6/2013, Volume 340, Issue 6139, pp. 1467 - 1471
Medical research | Phenotypes | Psychology | REPORTS | Personality traits | Genetic research | Research facilities | Genetics | Epidemiology | Research universities | Educational attainment | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genome-Wide Association Study | Endophenotypes | Humans | Female | Male | Cognition | Educational Status | Polymorphism, Single Nucleotide | Genetic Loci | Multifactorial Inheritance | Academic achievement | Genetic aspects | Research | Single nucleotide polymorphisms | Genetic variation | Genomics | Science education | Index Medicus | Single Nucleotide | Medicinsk genetik | Medical Genetics | Psykiatri | Psychiatry | Polymorphism
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text GWAS for executive function and processing speed suggests involvement of the CADM2 gene
by Ibrahim-Verbaas, Carla and Bressler, Jan and Debette, Stéphanie and Schuur, Maaike and Smith, Albert and Bis, Joshua and Davies, Gail and Trompet, Stella and Smith, J.A and Björnsson, Asgeir and Chibnik, Lori and Liu, Y and Vitart, Veronique and Kirin, Mirna and Petrovic, Katja and Polasek, Ozren and Zgaga, Lina and Fawns-Ritchie, C and Hoffmann, Per and Karjalainen, Juha and Lahti, J and Llewellyn, D.J and Schmidt, Carsten O and Mather, R and Chouraki, Vincent and Sun, Q and Resnick, Susan and Rose, Lynda and Oldmeadow, Christopher and Stewart, M and Smith, B.H and Gudnason, Vilmundur and Yang, Qiong and Mirza, Saira and Jukema, J.W and DeJager, Philip L and Harris, Tamara and Liewald, David C and Amin, Najaf and Coker, Laura and Stegle, Oliver and Lopez, O.L and Schmidt, R and Teumer, Alexander and Ford, I and Karbalai, Nazanin and Becker, James and Jonsdottir, Maria K and Au, Rhoda and Fehrmann, Rudolf and Herms, Stefan and Nalls, Michael and Zhao, W and Turner, Stephen and Yaffe, K and Lohman, Kurt and Swieten, John and Kardia, Sharon L.r and Knopman, David and Meeks, William and Heiss, Gerardo and Holliday, Elizabeth and Schofield, P.W and Tanaka, Toshiko and Stott, David J and Wang, Jing and Ridker, Paul and Gow, A.J and Pattie, Alison and Starr, John and Hocking, L.J and Armstrong, Nicola and McLachlan, Stela and Shulman, J.M and Pilling, Luke and Eiriksdottir, Gudny and Scott, Rodney and Kochan, Nicole A and Palotie, Aarno and Hsieh, Yi-Chen and Eriksson, Johan G and Penman, Alan and Gottesman, Rebecca and Oostra, Ben and Yu, Lei and DeStefano, Anita and Beiser, Alexa and Garcia, M and Rotter, Jerome I and Nöthen, Markus M and Hofman, Albert and Slagboom, Eline and Westendorp, R.G.J and Buckley, Brendan M and Wolf, P.A and Uitterlinden, Ané and Psaty, Bruce and Grabe, Hans Jörgen and Bandinelli, Stefania and Chasman, Daniel and ... and Generation Scotland and on behalf of Generation Scotland
Molecular psychiatry, ISSN 1359-4184, 02/2016, Volume 21, Issue 2, pp. 189 - 197
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | gamma-Aminobutyric Acid | Cell Adhesion Molecules - genetics | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Cell Adhesion Molecules - physiology | Genetic Association Studies | Introns | Genomics | Humans | Middle Aged | Male | Executive Function - physiology | Neuropsychological Tests | Aged, 80 and over | Cognition - physiology | Female | Aged | Genetic Variation - genetics | Polymorphism, Single Nucleotide | Cohort Studies | GABA | Physiological aspects | Genetic aspects | Single nucleotide polymorphisms | Research | Diagnosis | Dementia | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data
by Wensley, Frances and Gao, Pei and Burgess, Stephen and Kaptoge, Stephen and Di Angelantonio, Emanuele and Shah, Tina and Engert, James C and Clarke, Robert and Davey-Smith, George and Nordestgaard, Børge G and Saleheen, Danish and Samani, Nilesh J and Sandhu, Manjinder and Anand, Sonia and Pepys, Mark B and Smeeth, Liam and Whittaker, John and Casas, Juan Pablo and Thompson, Simon G and Hingorani, Aroon D and Danesh, John and EAS and INTERHEART and CRPHANS and LOLIPOP and FRAMOFF and PROSPER and SPEED and NPHSII and GERMIFS and HVHS and CHAOS and ISIS and PENNCATH and ROTTERDAM and CCHS CGPS CIHDS and ELSA and C Reactive Prot Coronary Heart Dis and HPFS and HIFMECH and 4D and EPICNOR and BWHHS and GISSI-P and MALMO and ARIC and PROMIS and SHEEP and WOSCOPS and HEALTHABC and WHIOS and BHF-FHS and EPICNL and NHS and LURIC and PROCARDIS and AGES and UCP and BRHS and CHS and CAPS and HIMS and CUDAS CUPID and MONICAKORA and NSC and WHITEII and C Reactive Protein Coronary Heart Disease Genetics Collaboration (CCGC)
BMJ, ISSN 0959-8138, 2011, Volume 342, Issue 7794, pp. 425 - 425
RESEARCH | Disease risk | Coronary artery disease | Medical genetics | Predisposing factors | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Coronary Disease - blood | Prospective Studies | Gene Frequency | Humans | Middle Aged | Risk Factors | Male | C-Reactive Protein - genetics | C-Reactive Protein - metabolism | Coronary Disease - genetics | Mendelian Randomization Analysis | Polymorphism, Single Nucleotide - genetics | Female | Cardiovascular disease | Genetic markers | Causality | RecA protein | Meta-analysis | Index Medicus | Abridged Index Medicus | Medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
by Perry, John and Day, Felix and Elks, Cathy and Sulem, Patrick and Thompson, Deborah and Ferreira, Teresa and He, Chunyan and Chasman, Daniel and Esko, Tõnu and Thorleifsson, Gudmar and Albrecht, Eva and Ang, Wei and Corre, Tanguy and Cousminer, Diana and Feenstra, Bjarke and Franceschini, Nora and Ganna, Anea and Johnson, Anew and Kjellqvist, Sanela and Lunetta, Kathryn and Mcmahon, George and Nolte, Ilja and Paternoster, Lavinia and Porcu, Eleonora and Smith, Davey and Stolk, Lisette and Teumer, Alexander and Tsernikova, Natalia and Tikkanen, Emmi and Ulivi, Shelia and Wagner, Erin K and Amin, Najaf and Bierut, Laura and Byrne, Enda and Hottenga, Jouke Jan and Koller, Daniel and Mangino, Massimo and Pers, Tune and Yerges-Armstrong, Laura and Zhao, Jing Hua and Anulis, Irene and Anton-Culver, Hoda and Atsma, Femke and Bandinelli, Stefania and Beckmann, Matthias and Benítez, Javier and Blomqvist, Carl and Bojesen, Stig and Bolla, Manjeet and Bonnani, Bernardo and Brauch, Hiltrud and Brenner, Hermann and Buring, Julie and Chang-Claude, Jenny and Chanock, Stephen and Chen, Jinhui and Chenevix-Trench, Georgia and Collée, Margriet and Couch, Fergus and Couper, David and Coviello, Anea and Cox, Angela and Czene, Kamila and Adamo, Pio and Vivo, Immaculata and Demerath, Ellen and Dennis, Joe and Devilee, Peter and Dieffenbach, Aida Karina and Dunning, Alison and Eiriksdottir, Gudny and Hagen, Knut and Fasching, Peter and Ferrucci, Luigi and Flesch-Janys, Dieter and Flyger, Henrik and Foroud, Tatiana and Franke, Lude and Garcia, Melissa and García-Closas, Montserrat and Geller, Frank and Geus, Eco and Giles, Graham and Gudbjartsson, Daniel and Gudnason, Vilmundur and Guénel, Pascal and Guo, Suiqun and Hall, Per and Hamann, Ute and Haring, Robin and Hartman, Catharina and Heath, Anew and Hofman, Albert and Hooning, Maartje and Hopper, John and Hu, Frank and Hunter, David and Karasik, David and Kiel, Douglas P and Knight, Julia and ... and kConFabt LifeLines Cohort Study and InterAct Consortium and Australian Ovarian Canc Study and Early Growth Genetics EGG Consorti and GENICA Network and Australian Ovarian Cancer Study and kConFab and LifeLines Cohort Study and Early Growth Genetics (EGG) Consortium and The GENICA Network and The InterAct Consortium and The LifeLines Cohort Study
Nature (London), ISSN 0028-0836, 10/2014, Volume 514, Issue 7520, pp. 92 - 97
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Age Factors | Diabetes Mellitus, Type 2 - genetics | Humans | Genetic Loci - genetics | Parents | Male | Cardiovascular Diseases - genetics | Obesity - genetics | Europe - ethnology | Female | Ribonucleoproteins - genetics | Hypothalamo-Hypophyseal System - physiology | Child | Body Mass Index | Genome-Wide Association Study | Calcium-Binding Proteins | Membrane Proteins - genetics | Menarche - genetics | Intercellular Signaling Peptides and Proteins - genetics | Potassium Channels, Tandem Pore Domain - genetics | Ovary - physiology | Receptors, Retinoic Acid - metabolism | Genomic Imprinting - genetics | Proteins - genetics | Breast Neoplasms - genetics | Adolescent | Alleles | Polymorphism, Single Nucleotide - genetics | Quantitative Trait Loci - genetics | Receptors, GABA-B - metabolism | Allelomorphism | Menarche | Physiological aspects | Genome-wide association studies | Genetic aspects | Vitamin A | Puberty | Menstruation | Acids | Genomes | Mutation | Chromosomes | Girls | Age | Index Medicus | Medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights