X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2406) 2406
Patent (353) 353
Publication (162) 162
Book Chapter (63) 63
Conference Proceeding (60) 60
Book Review (47) 47
Book / eBook (44) 44
Magazine Article (37) 37
Dissertation (31) 31
Newspaper Article (15) 15
Trade Publication Article (14) 14
Web Resource (2) 2
Data Set (1) 1
Paper (1) 1
Poster (1) 1
Report (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (699) 699
female (400) 400
male (385) 385
middle aged (245) 245
adult (232) 232
rheumatology (227) 227
index medicus (210) 210
aged (195) 195
performing operations (162) 162
transporting (162) 162
alleles (160) 160
animals (155) 155
genotype (141) 141
genetic predisposition to disease (137) 137
physics (126) 126
immunology (119) 119
genetics & heredity (107) 107
arthritis, rheumatoid - genetics (106) 106
polymorphism, genetic (106) 106
gene frequency (105) 105
genetics (101) 101
association (99) 99
electricity (95) 95
polymorphism, single nucleotide (94) 94
analysis (88) 88
genetic aspects (87) 87
haplotypes (86) 86
susceptibility (86) 86
disease (83) 83
rheumatoid arthritis (80) 80
polymorphism (78) 78
adolescent (77) 77
hla-drb1 chains (77) 77
research (77) 77
risk factors (76) 76
conveying (74) 74
handling thin or filamentary material (74) 74
hla-dr antigens - genetics (74) 74
packing (74) 74
storing (74) 74
aged, 80 and over (73) 73
mechanical engineering (70) 70
blasting (69) 69
case-control studies (69) 69
genes (69) 69
heating (69) 69
lighting (69) 69
weapons (69) 69
medicine, general & internal (65) 65
child (63) 63
arthritis, rheumatoid - immunology (62) 62
hla (61) 61
general tagging of cross-sectional technologies spanning over several sections of the ipc (59) 59
general tagging of new technological developments (59) 59
technical subjects covered by former uspc cross-reference art collections [xracs] and digests (59) 59
cohort studies (57) 57
expression (55) 55
phenotype (54) 54
dogs (53) 53
major histocompatibility complex (53) 53
basic electric elements (52) 52
life sciences (49) 49
molecular sequence data (49) 49
rheumatoid-arthritis (49) 49
base sequence (48) 48
optics (45) 45
cell biology (44) 44
gathering or removal of domestic or like refuse (44) 44
risk (44) 44
semiconductor devices (44) 44
surgery (44) 44
arthritis (43) 43
electric solid state devices not otherwise provided for (43) 43
studies (43) 43
linkage disequilibrium (42) 42
population (42) 42
health aspects (41) 41
disease susceptibility (40) 40
gene (40) 40
genetic research (40) 40
genomes (40) 40
microstructural technology (40) 40
polymorphisms (40) 40
vehicles in general (40) 40
biochemistry & molecular biology (39) 39
human necessities (39) 39
epidemiology (38) 38
genome-wide association study (38) 38
united kingdom (38) 38
pathology (37) 37
physics, nuclear (36) 36
cancer (35) 35
child, preschool (35) 35
single nucleotide polymorphisms (35) 35
polymerase chain reaction (34) 34
1900-1999 (33) 33
chemistry (33) 33
european continental ancestry group - genetics (33) 33
genetic predisposition to disease - genetics (33) 33
materials science, multidisciplinary (33) 33
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (14) 14
UTL at Downsview - May be requested (7) 7
Earth Sciences (Noranda) - Stacks (4) 4
Gerstein Science - Stacks (3) 3
Thomas Fisher Rare Book - Rare Book (3) 3
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Online Resources - Online (2) 2
UofT at Mississauga - Stacks (2) 2
UofT at Scarborough - Stacks (2) 2
Victoria University E.J. Pratt - Stacks (2) 2
Earth Sciences (Noranda) - Missing (1) 1
Massey College (Robertson Davies) - Rare Book (1) 1
Royal Ontario Museum - Rare Oversize (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
UofT at Scarborough - Withdrawn (1) 1
Victoria University CRRS - Library use only (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1877) 1877
French (1263) 1263
German (79) 79
Spanish (11) 11
Portuguese (3) 3
Norwegian (2) 2
Italian (1) 1
Korean (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Okbay, Aysu and Beauchamp, Jonathan and Fontana, M.A and Lee, James J and Pers, Tune and Rietveld, C.A and Turley, Patrick and Chen, G.-B and Emilsson, Valur and Meddens, S.F.W and Oskarsson, S and Pickrell, J.K and Thom, K and Timshel, P and Vlaming, Ronald and Abdellaoui, Abdel and Ahluwalia, Tarunveer Singh and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, G and Brandsma, Johan and Pina Concas, M and Derringer, J and Furlotte, N.A and Galesloot, Tessel and Girotto, S and Gupta, R and Hall, Leanne M and Harris, Sarah and Hofer, E and Horikoshi, M and Huffman, Jennifer E and Kaasik, K and Kalafati, Ioanna-Panagiota and Karlsson, Robert and Kong, Augustine and Lahti, Jari and Lee, Sven and Deleeuw, C and Lind, Penelope and Lindgren, K.-O and Liu, T and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Mike and Most, Peter and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter and Qian, Y and Raitakari, Olli and Rueedi, R and Salvi, E and Schmidt, B and Schraut, K.E and Shi, J and Smith, Albert Vernon and Poot, Raymond and St Pourcain, Beate and Teumer, Alexander and Thorleifsson, Gudmar and Verweij, Niek and Vuckovic, gana and Wellmann, J and Westra, Harm-Jan and Yang, J and Zhao, W and Zhu, Z and Alizadeh, Behrooz and Amin, Najaf and Bakshi, A and Baumeister, Sebastian and Biino, G and Bønnelykke, Klaus and Boyle, Patricia and Campbell, Harry and Cappuccio, F.P and Davies, Gail and Neve, Jan-Emmanuel and Deloukas, Panagiotis and Demuth, Ilja and Ding, J and Eibich, P and Eisele, L and Eklund, Niina and Evans, David and Faul, Jessica D and Feitosa, Mary Furlan and Forstner, Aneas and Gandin, Ilaria and Gunnarsson, B and Halldorsson, Bjarni and Harris, Tamara and Holliday, Elizabeth and Heath, Anew C and Hocking, L.J and Homuth, Georg and Horan, Mike and ... and LifeLines Cohort Study and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 05/2016, Volume 533, Issue 7604, pp. 539 - 542
Journal Article
by Sawcer, Stephen and Hellenthal, Garrett and Pirinen, Matti and Spencer, Chris C.A and Patsopoulos, Nikolaos A and Moutsianas, Loukas and Dilthey, Alexander and Su, Zhan and Freeman, Colin and Hunt, Sarah E and Edkins, Sarah and Gray, Emma and Booth, David R and Potter, Simon C and Goris, An and Band, Gavin and Oturai, Annette Bang and Strange, Amy and Saarela, Janna and Bellenguez, Céline and Fontaine, Bertrand and Gillman, Matthew and Hemmer, Bernhard and Gwilliam, Rhian and Zipp, Frauke and Jayakumar, Alagurevathi and Martin, Roland and Leslie, Stephen and Hawkins, Stanley and Giannoulatou, Eleni and D'Alfonso, Sandra and Blackburn, Hannah and Boneschi, Filippo Martinelli and Liddle, Jennifer and Harbo, Hanne F and Perez, Marc L and Spurkland, Anne and Waller, Matthew J and Mycko, Marcin P and Ricketts, Michelle and Comabella, Manuel and Hammond, Naomi and Kockum, Ingrid and McCann, Owen T and Ban, Maria and Whittaker, Pamela and Kemppinen, Anu and Weston, Paul and Hawkins, Clive and Widaa, Sara and Zajicek, John and Dronov, Serge and Robertson, Neil and Bumpstead, Suzannah J and Barcellos, Lisa F and Ravindrarajah, Rathi and Abraham, Roby and Alfredsson, Lars and Ardlie, Kristin and Aubin, Cristin and Baker, Amie and Baker, Katharine and Baranzini, Sergio E and Bergamaschi, Laura and Bergamaschi, Roberto and Bernstein, Allan and Berthele, Achim and Boggild, Mike and Bradfield, Jonathan P and Brassat, David and Broadley, Simon A and Buck, Dorothea and Butzkueven, Helmut and Capra, Ruggero and Carroll, William M and Cavalla, Paola and Celius, Elisabeth G and Cepok, Sabine and Chiavacci, Rosetta and Clerget-Darpoux, Françoise and Clysters, Katleen and Comi, Giancarlo and Cossburn, Mark and Cournu-Rebeix, Isabelle and Cox, Mathew B and Cozen, Wendy and Cree, Bruce A.C and Cross, Anne H and Cusi, Daniele and Daly, Mark J and Davis, Emma and De Bakker, Paul I.W and Debouverie, Marc and D'Hooghe, Marie Beatrice and Dixon, Katherine and Dobosi, Rita and Dubois, Bénédicte and Ellinghaus, David and Elovaara, Irina and Esposito, Federica and ... and Wellcome Trust Case Control Consor and Int Multiple Sclerosis Genetics Co and Wellcome Trust Case Control Consortium 2 and International Multiple Sclerosis Genetics Consortium and The International Multiple Sclerosis Genetics Consortium & The Wellcome Trust Case Control Consortium 2 and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature, ISSN 0028-0836, 08/2011, Volume 476, Issue 7359, pp. 214 - 219
Journal Article
by Savage, Jeanne E and Jansen, Philip R and Stringer, Sven and Watanabe, Kyoko and Bryois, Julien and De Leeuw, Christiaan A and Nagel, Mats and Awasthi, Swapnil and Barr, Peter B and Coleman, Jonathan R. I and Grasby, Katrina L and Hammerschlag, Anke R and Kaminski, Jakob A and Karlsson, Robert and Krapohl, Eva and Lam, Max and Nygaard, Marianne and Reynolds, Chandra A and Trampush, Joey W and Young, Hannah and Zabaneh, Delilah and Hägg, Sara and Hansell, Narelle K and Karlsson, Ida K and Linnarsson, Sten and Montgomery, Grant W and Muñoz-Manchado, Ana B and Quinlan, Erin B and Schumann, Gunter and Skene, Nathan G and Webb, Bradley T and White, Tonya and Arking, Dan E and Avramopoulos, Dimitrios and Bilder, Robert M and Bitsios, Panos and Burdick, Katherine E and Cannon, Tyrone D and Chiba-Falek, Ornit and Christoforou, Andrea and Cirulli, Elizabeth T and Congdon, Eliza and Corvin, Aiden and Davies, Gail and Deary, Ian J and Derosse, Pamela and Dickinson, Dwight and Djurovic, Srdjan and Donohoe, Gary and Conley, Emily Drabant and Eriksson, Johan G and Espeseth, Thomas and Freimer, Nelson A and Giakoumaki, Stella and Giegling, Ina and Gill, Michael and Glahn, David C and Hariri, Ahmad R and Hatzimanolis, Alex and Keller, Matthew C and Knowles, Emma and Koltai, Deborah and Konte, Bettina and Lahti, Jari and Le Hellard, Stephanie and Lencz, Todd and Liewald, David C and London, Edythe and Lundervold, Astri J and Malhotra, Anil K and Melle, Ingrid and Morris, Derek and Need, Anna C and Ollier, William and Palotie, Aarno and Payton, Antony and Pendleton, Neil and Poldrack, Russell A and Räikkönen, Katri and Reinvang, Ivar and Roussos, Panos and Rujescu, Dan and Sabb, Fred W and Scult, Matthew A and Smeland, Olav B and Smyrnis, Nikolaos and Starr, John M and Steen, Vidar M and Stefanis, Nikos C and Straub, Richard E and Sundet, Kjetil and Tiemeier, Henning and Voineskos, Aristotle N and Weinberger, Daniel R and Widen, Elisabeth and Yu, Jin and Abecasis, Goncalo and Andreassen, Ole A and Breen, Gerome and Christiansen, Lene and ...
Nature Genetics, ISSN 1061-4036, 07/2018, Volume 50, Issue 7, pp. 912 - 919
Intelligence is highly heritable(1) and a major determinant of human health and well-being(2). Recent genome-wide meta-analyses have identified 24 genomic loci... 
GENERAL COGNITIVE FUNCTION | CONSORTIUM | TEST BATTERIES | GWAS | ANNOTATION | GENETICS & HEREDITY | RISK | LOCI | EDUCATIONAL-ATTAINMENT | TRAITS | HERITABILITY | Genetic Predisposition to Disease | Humans | Middle Aged | Adolescent | Female | Male | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Intelligence - genetics | Quantitative Trait Loci | Brain - physiology | Brain | Chromatin | Neurosciences | Intelligence | Synaptogenesis | Mental disorders | Genomics | Genes | Cognitive ability | Schizophrenia | Association analysis | Nervous system | Identification | Mapping | Genomes | Genetic effects | Annotations | Coding | Genetic analysis | Neostriatum | Alzheimer's disease | Bioinformatics | Neurodegenerative diseases | Neurons | Attention deficit hyperactivity disorder | Causation | Gene expression | Spiny neurons | Loci | Educational attainment | Meta-analysis | Quantitative trait loci | Neurological diseases | Studies | Pyramidal cells | Gene loci | Gene mapping | Alzheimers disease | Hippocampus | Medical and Health Sciences | Medicin och hälsovetenskap | Alzheimer disease | Article | nervous system development | genetic association | gene location | schizophrenia | Klinisk medicin | pleiotropy | gene mapping | genetic correlation | priority journal | human | Neurologi | corpus striatum | hippocampus | synapse | chromatin | heredity | genetic variability | intelligence | pyramidal nerve cell | gene locus | Mendelian randomization analysis | Clinical Medicine | Neurology | expression quantitative trait locus | medium spiny neuron | genome-wide association study | attention deficit disorder | exon | conserved sequence | gene expression
Journal Article
by Davies, Gail and Lam, Max and Harris, Sarah E and Trampush, Joey W and Luciano, Michelle and Hill, W. David and Hagenaars, Saskia P and Ritchie, Stuart J and Marioni, Riccardo E and Fawns-Ritchie, Chloe and Liewald, David C. M and Okely, Judith A and Ahola-Olli, Ari V and Barnes, Catriona L. K and Bertram, Lars and Bis, Joshua C and Burdick, Katherine E and Christoforou, Andrea and Derosse, Pamela and Djurovic, Srdjan and Espeseth, Thomas and Giakoumaki, Stella and Giddaluru, Sudheer and Gustavson, Daniel E and Hayward, Caroline and Hofer, Edith and Ikram, M. Arfan and Karlsson, Robert and Knowles, Emma and Lahti, Jari and Leber, Markus and Li, Shuo and Mather, Karen A and Melle, Ingrid and Morris, Derek and Oldmeadow, Christopher and Palviainen, Teemu and Payton, Antony and Pazoki, Raha and Petrovic, Katja and Reynolds, Chandra A and Sargurupremraj, Muralidharan and Scholz, Markus and Smith, Jennifer A and Smith, Albert V and Terzikhan, Natalie and Thalamuthu, Anbupalam and Trompet, Stella and Van Der Lee, Sven J and Ware, Erin B and Windham, B. Gwen and Wright, Margaret J and Yang, Jingyun and Yu, Jin and Ames, David and Amin, Najaf and Amouyel, Philippe and Andreassen, Ole A and Armstrong, Nicola J and Assareh, Amelia A and Attia, John R and Attix, Deborah and Avramopoulos, Dimitrios and Bennett, David A and Böhmer, Anne C and Boyle, Patricia A and Brodaty, Henry and Campbell, Harry and Cannon, Tyrone D and Cirulli, Elizabeth T and Congdon, Eliza and Conley, Emily Drabant and Corley, Janie and Cox, Simon R and Dale, Anders M and Dehghan, Abbas and Dick, Danielle and Dickinson, Dwight and Eriksson, Johan G and Evangelou, Evangelos and Faul, Jessica D and Ford, Ian and Freimer, Nelson A and Gao, He and Giegling, Ina and Gillespie, Nathan A and Gordon, Scott D and Gottesman, Rebecca F and Griswold, Michael E and Gudnason, Vilmundur and Harris, Tamara B and Hartmann, Annette M and Hatzimanolis, Alex and Heiss, Gerardo and Holliday, Elizabeth G and Joshi, Peter K and Kähönen, Mika and Kardia, Sharon L. R and Karlsson, Ida and Kleineidam, Luca and ...
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2098 - 16
General cognitive function is a prominent and relatively stable human trait that is associated with many important life outcomes. We combine cognitive and... 
COMMON VARIANTS | METAANALYSIS | REACTION-TIME | PROCESSING SPEED | MULTIDISCIPLINARY SCIENCES | INTELLIGENCE DIFFERENCES | SCHIZOPHRENIA | DCDC2 | DISCOVERY | GENOME-WIDE ASSOCIATION | REVEALS | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genetic Loci - genetics | Neurodegenerative Diseases - genetics | Neurodevelopmental Disorders - genetics | Reaction Time - genetics | Young Adult | Mental Disorders - genetics | Adolescent | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Hypertension | Brain | Cognitive ability | Genomes | Gene expression | Neurodevelopmental disorders | Loci | Consortia | Illnesses | Mathematical analysis | Reaction time | Heritability | Gene loci | Polygenic inheritance | brain cortex | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | osteoarthritis | Article | heart infarction | Klinisk medicin | lung cancer | identification method | longevity | grip strength | angina pectoris | genetic correlation | human | major depression | Neurologi | cognition | data set | aged | brain | gene locus | Clinical Medicine | Neurology | genome | vision | genetic analysis | controlled study | response time | adolescent | nervous system disorder | adult | hypertension | gene expression
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 01/2014, Volume 19, Issue 1, pp. 76 - 87
Journal Article