UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Search Filters
Format Format
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
science & technology (38) 38
humans (33) 33
life sciences & biomedicine (25) 25
genomes (16) 16
genome-wide association study (15) 15
genetic variation (14) 14
genetics (14) 14
genetics & heredity (14) 14
science & technology - other topics (14) 14
genotype (13) 13
multidisciplinary sciences (13) 13
research (13) 13
medicin och hälsovetenskap (12) 12
polymorphism, single nucleotide (12) 12
genetic aspects (11) 11
genetic predisposition to disease (11) 11
medical and health sciences (11) 11
alleles (10) 10
klinisk medicin (10) 10
clinical medicine (9) 9
female (9) 9
gene frequency (9) 9
genomics (9) 9
male (9) 9
diabetes mellitus, type 2 - genetics (8) 8
endocrinology and diabetes (8) 8
endokrinologi och diabetes (8) 8
genes (8) 8
risk factors (8) 8
algorithms (7) 7
biochemistry & molecular biology (7) 7
diabetes (7) 7
polymorphism, single nucleotide - genetics (7) 7
population genetics (7) 7
quality control (7) 7
studies (7) 7
biotechnology & applied microbiology (6) 6
disease (6) 6
european continental ancestry group - genetics (6) 6
gene expression (6) 6
genetic predisposition to disease - genetics (6) 6
genotype & phenotype (6) 6
health aspects (6) 6
models, genetic (6) 6
mutation (6) 6
adult (5) 5
biochemical research methods (5) 5
biomedical research (5) 5
case-control studies (5) 5
genetic research (5) 5
genome-wide association study - methods (5) 5
histocompatibility antigens (5) 5
hla histocompatibility antigens (5) 5
medical genetics (5) 5
medical research (5) 5
medicinsk genetik (5) 5
middle aged (5) 5
multiple sclerosis (5) 5
phenotype (5) 5
software (5) 5
abridged index medicus (4) 4
aged (4) 4
autoimmune diseases (4) 4
computer science (4) 4
deoxyribonucleic acid--dna (4) 4
disease susceptibility (4) 4
european continental ancestry group (4) 4
genetic diversity (4) 4
genome-wide association studies (4) 4
genomics - methods (4) 4
haplotypes (4) 4
hla antigens - genetics (4) 4
human genome (4) 4
inflammatory bowel disease (4) 4
mathematical & computational biology (4) 4
mathematics (4) 4
medicinska och farmaceutiska grundvetenskaper (4) 4
multiple sclerosis - genetics (4) 4
physiological aspects (4) 4
risk assessment (4) 4
sequence analysis, dna (4) 4
single nucleotide polymorphisms (4) 4
statistical methods (4) 4
statistics (4) 4
technology (4) 4
aged, 80 and over (3) 3
basic medicine (3) 3
chromosome mapping (3) 3
computational biology (3) 3
computer science, interdisciplinary applications (3) 3
development and progression (3) 3
diabetes mellitus (3) 3
diseases (3) 3
epidemiology (3) 3
evolution, molecular (3) 3
exome - genetics (3) 3
experiments (3) 3
finland (3) 3
genetic loci (3) 3
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

Nature genetics, ISSN 1546-1718, 01/2017, Volume 49, Issue 2, pp. 256 - 261
Journal Article
by Altshuler, David M and Gibbs, Richard A and Peltonen, Leena and Schaffner, Stephen F and Yu, Fuli and Dermitzakis, Emmanouil and Bonnen, Penelope E and De Bakker, Paul I. W and Deloukas, Panos and Gabriel, Stacey B and Gwilliam, Rhian and Hunt, Sarah and Inouye, Michael and Jia, Xiaoming and Aarno Palotie, Palotie and Parkin, Melissa and Whittaker, Pamela and Chang, Kyle and Hawes, Alicia and Lewis, Lora R and Ren, Yanru and Wheeler, David and Muzny, Donna Marie and Barnes, Chris and Darvishi, Katayoon and Hurles, Matthew and Korn, Joshua M and Kristiansson, Kati and Lee, Charles and McCarroll, Steven A and Nemesh, James and Keinan, Alon and Montgomery, Stephen B and Samuela Pollack, Pollack and Price, Alkes L and Soranzo, Nicole and Gonzaga-Jauregui, Claudia and Anttila, Verneri and Brodeur, Wendy and Daly, Mark J and Leslie, Stephen and McVean, Gil and Moutsianas, Loukas and Nguyen, Huy and Zhang, Qingrun and Ghori, Mohammed J. R and McGinnis, Ralph and McLaren, William and Pollack, Samuela and Takeuchi, Fumihiko and Grossman, Sharon R and Shlyakhter, Ilya and Hostetter, Elizabeth B and Sabeti, Pardis C and Adebamowo, Clement A and Foster, Morris W and Gordon, Deborah R and Licinio, Julio and Manca, Maria Cristina and Marshall, Patricia A and Matsuda, Ichiro and Ngare, Duncan and Wang, Vivian Ota and Reddy, Deepa and Rotimi, Charles N and Royal, Charmaine D and Sharp, Richard R and Zeng, Changqing and Brooks, D.B and McEwen, Jean E and The International HapMap 3 Consortium and Int HapMap 3 Consortium and International HapMap 3 Consortium
Nature (London), ISSN 1476-4687, 09/2010, Volume 467, Issue 7311, pp. 52 - 58
Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Population Groups - genetics | Polymorphism, Single Nucleotide | Genome, Human | Human Genome Project | Humans | DNA Copy Number Variations | Human genome | Genetic variation | Research | Genetics | Algorithms | Genetic testing | Genomics | Quality control | Index Medicus
Journal Article
by Strange, Amy and Capon, Francesca and Spencer, Chris C.A and Knight, Jo and Weale, Michael E and Allen, Michael H and Barton, Ane and Band, Gavin and Bellenguez, Céline and Bergboer, Judith G.M and BlackweL, Jenefer M and Bramon, Elvira and Bumpstead, Suzanah J and Casas, Juan P and Cork, Michael J and Corvin, Aiden and Deloukas, Panos and Dilthey, Alexander and Duncanson, Audrey and Edkins, Sarah and EstiviL, Xavier and Fitzgerald, Oliver and FrEman, Colin and Giardina, Emiliano and Gray, Ema and Hofer, Angelika and Hüffmeier, Ulrike and Hunt, Sarah E and Irvine, Alan D and Jankowski, Janusz and Kirby, Brian and Langford, Cordelia and Lascorz, Jesés and Leman, Joyce and Leslie, Stephen and MaLbris, Lotus and Markus, Hugh S and Mathew, Christopher G and McLean, W H Irwin and McManus, Ros and MöSner, Rotraut and Moutsianas, Loukas and Naluai, Asa T and Nestle, Frank O and NoveLi, Giuseppe and Onoufriadis, Alexandros and Palmer, Colin N.A and Perricone, Carlo and Pirinen, Mati and Plomin, Robert and PoTer, Simon C and Pujol, Ramon M and Rautanen, Ana and Riveira-Munoz, Eva and Ryan, Anthony W and Salmhofer, Wolfgang and SamuelSon, Lena and Sawcer, Stephen J and Schalkwijk, Jost and Smith, Catherine H and Ståhle, Mona and Su, Zhan and Tazi-Ahnini, Rachid and Traupe, Heiko and Viswanathan, Ananth C and Warren, Richard B and Weger, Wolfgang and Wolk, Katarina and WOd, Nicholas and Worthington, Jane and Young, Helen S and Zeeuwen, Patrick L J.M and Hayday, Adrian and Burden, A David and Griffiths, Christopher E.M and Kere, Juha and Reis, André and McVean, Gilean and Evans, David M and Brown, Mathew A and Barker, Jonathan N and Peltonen, Lena and Donely, Peter and Trembath, Richard C
Nature genetics, ISSN 1061-4036, 11/2010, Volume 42, Issue 11, pp. 985 - 990
Journal Article
by Beecham, Ashley H and Patsopoulos, Nikolaos A and Xifara, Dionysia K and Davis, Mary F and Kemppinen, Anu and Cotsapas, Chris and Shah, Tejas S and Spencer, Chris and Booth, David and Goris, An and Oturai, Annette and Saarela, Janna and Fontaine, Bertrand and Hemmer, Bernhard and Martin, Claes and Zipp, Frauke and D'Alfonso, Sandra and Martinelli-Boneschi, Filippo and Taylor, Bruce and Harbo, Hanne F and Kockum, Ingrid and Hillert, Jan and Olsson, Tomas and Ban, Maria and Oksenberg, Jorge R and Hintzen, Rogier and Barcellos, Lisa F and Agliardi, Cristina and Alfredsson, Lars and Alizadeh, Mehdi and Anderson, Carl and Andrews, Robert and Søndergaard, Helle Bach and Baker, Amie and Band, Gavin and Baranzini, Sergio E and Barizzone, Nadia and Barrett, Jeffrey and Bellenguez, Céline and Bergamaschi, Laura and Bernardinelli, Luisa and Berthele, Achim and Biberacher, Viola and Binder, Thomas M.C and Blackburn, Hannah and Bomfim, Izaura L and Brambilla, Paola and Broadley, Simon and Brochet, Bruno and Brundin, Lou and Buck, Dorothea and Butzkueven, Helmut and Caillier, Stacy J and Camu, William and Carpentier, Wassila and Cavalla, Paola and Celius, Elisabeth G and Coman, Irène and Comi, Giancarlo and Corrado, Lucia and Cosemans, Leentje and Cournu-Rebeix, Isabelle and Cree, Bruce A.C and Cusi, Daniele and Damotte, Vincent and Defer, Gilles and Delgado, Silvia R and Deloukas, Panos and Di Sapio, Alessia and Dilthey, Alexander T and Donnelly, Peter and Dubois, Bénédicte and Duddy, Martin and Edkins, Sarah and Elovaara, Irina and Esposito, Federica and Evangelou, Nikos and Fiddes, Barnaby and Field, Judith and Franke, Andre and Freeman, Colin and Frohlich, Irene Y and Galimberti, Daniela and Gieger, Christian and Gourraud, Pierre-Antoine and Graetz, Christiane and Graham, Andrew and Grummel, Verena and Guaschino, Clara and Hadjixenofontos, Athena and Hakonarson, Hakon and Halfpenny, Christopher and Hall, Gillian and Hall, Per and Hamsten, Anders and Harley, James and Harrower, Timothy and Hawkins, Clive and Hellenthal, Garrett and Hillier, Charles and ... and International Multiple Sclerosis Genetics Consortium (IMSGC) and Wellcome Trust Case Control Consor and Int IBD Genetics Consortium IIBDGC and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International IBD Genetics Consortium (IIBDGC) and Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation
Nature genetics, ISSN 1546-1718, 09/2013, Volume 45, Issue 11, pp. 1353 - 1360
Journal Article
by Evans, David M and Spencer, Chris C A and Pointon, Jennifer J and Su, Zhan and Harvey, David and Kochan, Grazyna and Oppermann, Udo and Dilthey, Alexander and Pirinen, Matti and Stone, Millicent A and Appleton, Louise and Moutsianas, Loukas and Leslie, Stephen and Wordsworth, Tom and Kenna, Tony J and Karaderi, Tugce and Thomas, Gethin P and Ward, Michael M and Weisman, Michael H and Farrar, Claire and Bradbury, Linda A and Danoy, Patrick and Inman, Robert D and Maksymowych, Walter and Gladman, Dafna and Rahman, Proton and Morgan, Ann and Marzo-Ortega, Helena and Bowness, Paul and Gaffney, Karl and Gaston, J S Hill and Smith, Malcolm and Bruges-Armas, Jacome and Couto, Ana-Rita and Sorrentino, Rosa and Paladini, Fabiana and Ferreira, Manuel A and Xu, Huji and Liu, Yu and Jiang, Lei and Lopez-Larrea, Carlos and Díaz-Peña, Roberto and López-Vázquez, Antonio and Zayats, Tetyana and Band, Gavin and Bellenguez, Céline and Blackburn, Hannah and Blackwell, Jenefer M and Bramon, Elvira and Bumpstead, Suzannah J and Casas, Juan P and Corvin, Aiden and Craddock, Nicholas and Deloukas, Panos and Dronov, Serge and Duncanson, Audrey and Edkins, Sarah and Freeman, Colin and Gillman, Matthew and Gray, Emma and Gwilliam, Rhian and Hammond, Naomi and Hunt, Sarah E and Jankowski, Janusz and Jayakumar, Alagurevathi and Langford, Cordelia and Liddle, Jennifer and Markus, Hugh S and Mathew, Christopher G and McCann, Owen T and McCarthy, Mark I and Palmer, Colin N A and Peltonen, Leena and Plomin, Robert and Potter, Simon C and Rautanen, Anna and Ravindrarajah, Radhi and Ricketts, Michelle and Samani, Nilesh and Sawcer, Stephen J and Strange, Amy and Trembath, Richard C and Viswanathan, Ananth C and Waller, Matthew and Weston, Paul and Whittaker, Pamela and Widaa, Sara and Wood, Nicholas W and McVean, Gilean and Reveille, John D and Wordsworth, B Paul and Brown, Matthew A and Donnelly, Peter and The Australo-Anglo-American Spondyloarthritis Consortium (TASC) and the Wellcome Trust Case Control Consortium 2 (WTCCC2) and Spondyloarthritis Research Consortium of Canada (SPARCC) and Australo-Anglo-Amer Spondyloarthri and Wellcome Trust Case Control Consor and Spondyloarthrit Res Consortium Can and Wellcome Trust Case Control Consortium 2 (WTCCC2) and Australo-Anglo-American Spondyloarthritis Consortium (TASC)
Nature genetics, ISSN 1546-1718, 07/2011, Volume 43, Issue 8, pp. 761 - 767
Journal Article