X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (872) 872
Newspaper Article (285) 285
Publication (100) 100
Patent (52) 52
Book Review (45) 45
Newsletter (24) 24
Book / eBook (14) 14
Magazine Article (14) 14
Book Chapter (12) 12
Conference Proceeding (12) 12
Web Resource (3) 3
Data Set (1) 1
Dissertation (1) 1
Streaming Video (1) 1
Video Recording (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (480) 480
index medicus (463) 463
female (305) 305
male (274) 274
endocrinology & metabolism (229) 229
diabetes (220) 220
genetic aspects (198) 198
research (193) 193
adult (190) 190
diabetes mellitus, type 2 - genetics (185) 185
mutation (164) 164
genetics (147) 147
type 2 diabetes (137) 137
abridged index medicus (136) 136
middle aged (117) 117
risk factors (110) 110
insulin (104) 104
genetics & heredity (103) 103
infant, newborn (102) 102
mellitus (100) 100
medical and health sciences (99) 99
medicin och hälsovetenskap (99) 99
genetic predisposition to disease (98) 98
polymorphism, single nucleotide (94) 94
article (81) 81
diagnosis (80) 80
genotype (80) 80
diabetes mellitus (78) 78
aged (75) 75
diabetes mellitus - genetics (75) 75
health aspects (74) 74
adolescent (73) 73
genome-wide association (72) 72
physiological aspects (71) 71
child (69) 69
genetic variation (67) 67
infant (65) 65
case-control studies (61) 61
genome-wide association study (61) 61
genes (59) 59
potassium channels, inwardly rectifying - genetics (59) 59
clinical medicine (58) 58
glucose (58) 58
genomes (57) 57
body mass index (56) 56
gene (55) 55
phenotype (55) 55
analysis (54) 54
mutations (54) 54
pedigree (54) 54
alleles (52) 52
obesity (51) 51
gene mutations (50) 50
klinisk medicin (50) 50
risk (50) 50
studies (50) 50
identification (49) 49
endokrinologi och diabetes (47) 47
transcription factors - genetics (47) 47
activating mutations (46) 46
endocrinology and diabetes (46) 46
medicine (46) 46
pregnancy (44) 44
young (44) 44
pediatrics (43) 43
medical research (42) 42
medicine, general & internal (42) 42
cohort studies (41) 41
association (40) 40
birth weight (40) 40
animals (39) 39
child, preschool (39) 39
hyperglycemia (39) 39
disease (38) 38
insulin resistance (38) 38
multidisciplinary sciences (38) 38
care and treatment (37) 37
children (37) 37
diabetes mellitus, type 1 - genetics (37) 37
united kingdom (37) 37
european continental ancestry group - genetics (36) 36
genetic testing (36) 36
internal medicine (36) 36
medical genetics (35) 35
population (35) 35
endocrine system (34) 34
genetic predisposition to disease - genetics (34) 34
infants (34) 34
gene frequency (33) 33
hypoglycemic agents - therapeutic use (33) 33
kir6.2 (33) 33
polymorphism, single nucleotide - genetics (33) 33
human necessities (32) 32
hygiene (32) 32
medical or veterinary science (32) 32
prevalence (32) 32
age (31) 31
expression (31) 31
biochemistry & molecular biology (30) 30
insulin - metabolism (30) 30
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (7) 7
UTL at Downsview - May be requested (6) 6
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Media Commons - Audio Visual (1) 1
Online Resources - Online (1) 1
UofT at Mississauga - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
Victoria University E.J. Pratt - Storage (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Lancet, ISSN 0140-6736, 2005, Volume 366, Issue 9493, pp. 1315 - 1323
Genetic association studies are central to efforts to identify and characterise genomic variants underlying susceptibility to multifactorial disease. However,... 
Genetic Variation | Genetic Predisposition to Disease - genetics | Gene Frequency | Humans | Genotype | Genetic Markers | Polymorphism, Genetic | Research | Genetic susceptibility | Genetic variation | Health aspects | Index Medicus | Abridged Index Medicus
Journal Article
by Locke, A.E and Kahali, B and Berndt, S.I and Justice, A.E and Pers, T.H and Day, F.R and Powell, C and Vedantam, S and Buchkovich, M.L and Yang, J and Croteau-Chonka, D.C and Esko, T and Fall, T and Ferreira, T and Gustafsson, S and Kutalik, Z and Luan, J and Magi, R and Randall, J.C and Winkler, T.W and Wood, A.R and Workalemahu, T and Faul, J.D and Smith, J.A and Zhao, J and Zhao, W and Chen, J and Fehrmann, R and Hedman, A.K and Karjalainen, J and Schmidt, E.M and Absher, D and Amin, N and Anderson, D and Beekman, M and Bolton, J.L and Bragg-Gresham, J.L and Buyske, S and Demirkan, A and Deng, G and Ehret, G.B and Feenstra, B and Feitosa, M.F and Fischer, K and Goel, A and Gong, J and Jackson, A.U and Kanoni, S and Kleber, M.E and Kristiansson, K and Lim, U and Lotay, V and Mangino, M and Leach, I. Mateo and Medina-Gomez, C and Medland, S.E and Nalls, M.A and Palmer, C.D and Pasko, D and Pechlivanis, S and Peters, M.J.W and Prokopenko, I and Shungin, D and Stancakova, A and Strawbridge, R.J and Sung, Y. Ju and Tanaka, T and Teumer, A and Trompet, S and Laan, S.W. van der and Setten, J. van and Vliet-Ostaptchouk, J.V. Van and Wang, Z and Yengo, L and Zhang, W and Isaacs, A and Albrecht, E and Arnlov, J and Arscott, G.M and Attwood, A.P and Bandinelli, S and Barrett, A and Bas, I.N and Bellis, C and Bennett, A.J and Berne, C and Blagieva, R and Bluher, M and Bohringer, S and Bonnycastle, L.L and Bottcher, Y and Boyd, H.A and Bruinenberg, M and Caspersen, I.H and Chen, Y.D and Clarke, R and Daw, E.W and Craen, A.J. de and Delgado, G and Dimitriou, M and ... and ADIPOGen Consortium and PAGE Consortium and LifeLines Cohort Study and MIGen Consortium and CARDIOGRAMplusC4D Consortium and MuTHER Consortium and ICBP and CKDGen Consortium and Int Endogene Consortium and GENIE Consortium and MAGIC Investigators and ReproGen Consortium and AGEN-BMI Working Grp and GLGC and International Endogene Consortium and AGEN-BMI Working Group and The PAGE Consortium and The International Endogene Consortium and The MAGIC Investigators and The ReproGen Consortium and The CKDGen Consortium and The ADIPOGen Consortium and The ICBP and The CARDIOGRAMplusC4D Consortium and The GLGC and The GENIE Consortium and The AGEN-BMI Working Group and The MIGen Consortium and The MuTHER Consortium and The LifeLines Cohort Study and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Medicinsk genetik och genomik and Geriatrik and Uppsala universitet and Klinisk diabetologi och metabolism and Institutionen för immunologi, genetik och patologi and Molekylär medicin and Kardiovaskulär epidemiologi and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature, ISSN 0028-0836, 2015, Volume 518, Issue 7538, pp. 197 - 206
Journal Article
by Wood, Anew R and Esko, Tonu and Yang, Jian and Vedantam, Sailaja and Pers, Tune H and Gustafsson, Stefan and Chu, Auey Y and Estrada, Karol and Luan, Jian'an and Kutalik, Zoltán and Amin, Najaf and Buchkovich, Martin L and Croteau-Chonka, Damien C and Day, Felix R and Duan, Yanan and Fall, Tove and Fehrmann, Rudolf and Ferreira, Teresa and Jackson, Anne U and Karjalainen, Juha and Lo, Ken Sin and Locke, Adam E and Mägi, Reedik and Mihailov, Evelin and Porcu, Eleonora and Randall, Joshua C and Scherag, Ané and Vinkhuyzen, Anna A. E and Westra, Harm-Jan and Winkler, Thomas W and Workalemahu, Tsegaselassie and Zhao, Jing Hua and Absher, Devin and Albrecht, Eva and Anderson, Denise and Baron, Jeffrey and Beekman, Marian and Demirkan, Ayse and Ehret, Georg B and Feenstra, Bjarke and Feitosa, Mary F and Fischer, Krista and Fraser, Ross M and Goel, Anuj and Gong, Jian and Justice, Anne E and Kanoni, Stavroula and Kleber, Marcus E and Kristiansson, Kati and Lim, Unhee and Lotay, Vaneet and Lui, Julian C and Mangino, Massimo and Mateo Leach, Irene and Medina-Gomez, Carolina and Nalls, Michael A and Nyholt, Dale R and Palmer, Cameron D and Pasko, Dorota and Pechlivanis, Sonali and Prokopenko, Inga and Ried, Janina S and Ripke, Stephan and Shungin, Dmitry and Stancáková, Alena and Strawbridge, Rona J and Sung, Yun Ju and Tanaka, Toshiko and Teumer, Alexander and Trompet, Stella and van der Laan, Sander W and van Setten, Jessica and van Vliet-Ostaptchouk, Jana V and Wang, Zhaoming and Yengo, Loïc and Zhang, Weihua and Afzal, Uzma and Arnlöv, Johan and Arscott, Gillian M and Bandinelli, Stefania and Barrett, Amy and Bellis, Claire and Bennett, Amanda J and Berne, Christian and Blüher, Matthias and Bolton, Jennifer L and Böttcher, Yvonne and Boyd, Heather A and Bruinenberg, Marcel and Buckley, Brendan M and Buyske, Steven and Caspersen, Ida H and Chines, Peter S and Clarke, Robert and Claudi-Boehm, Simone and Cooper, Matthew and Daw, E. Warwick and de Jong, Pim A and Deelen, Joris and Delgado, Graciela and ... and PAGE Consortium and MIGen Consortium and LifeLines Cohort Study and Elect Med Records & Genom eMERGE C and Electronic Medical Records and Genomics (eMEMERGEGE) Consortium and PAGEGE Consortium and The MIGen Consortium and The PAGE Consortium and The Electronic Medical Records and Genomics (eMERGE) Consortium and The LifeLines Cohort Study and Högskolan Dalarna and Akademin Utbildning, hälsa och samhälle and Medicinsk vetenskap
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 11, pp. 1173 - 1186
Journal Article
by Allen, H.L and Estrada Gil, Karol and Lettre, Guillaume and Berndt, Sonja and Rivadeneira Ramirez, Fernando and Willer, Cristen and Jackson, Anne and Vedantam, Sailaja and Raychaudhuri, Soumya and Ferreira, Teresa and Wood, Anew and Weyant, Robert and Segrè, Ayellet and Speliotes, Elizabeth and Wheeler, Eleanor and Soranzo, Nicole and Park, J.H and Yang, Joanna and Gudbjartsson, Daniel and Heard-Costa, Nancy and Randall, Joshua and Qi, Lu and Smith, Albert Vernon and Mägi, Reedik and Pastinen, Tomi and Liang, Liming and Heid, Iris and Luan, J and Thorleifsson, Gudmar and Winkler, Thomas and Goddard, Michael and Lo, K.S and Palmer, Cameron and Workalemahu, Tsegaselassie and Aulchenko, Yurii and Johansson, Åsa and Zillikens, Carola and Feitosa, Mary Furlan and Esko, Tõnu and Johnson, Toby and Ketkar, Shamika and Kraft, Peter and Mangino, Massimo and Prokopenko, Inga and Absher, Devin and Albrecht, Eva and Ernst, Florian and Glazer, Nicole and Hayward, Caroline and Hottenga, Jouke Jan and Jacobs, Kevin and Knowles, Joshua and Kutalik, Zoltán and Monda, Keri and Polasek, Ozren and Preuss, Michael and Rayner, Nigel William and Robertson, Neil and Steinthorsdottir, Valgerdur and Tyrer, Jonathan and Voight, Benjamin and Wiklund, Freik and Xu, Jianfeng and Zhao, Jing Hua and Nyholt, Dale and Pellikka, Niina and Perola, Markus and Perry, John and Surakka, Ida and Tammesoo, M.L and Altmaier, Elizabeth and Amin, Najaf and Aspelund, Thor and Bhangale, Tushar and Boucher, Gabrielle and Chasman, Daniel and Chen, Constance and Coin, Lachlan and Cooper, Matthew and Dixon, Anna and Gibson, Quince and Grundberg, Elin and Hao, Ke and Junttila, Juhani and Kaplan, Robert and Kettunen, Johannes and König, Inke and Kwan, Tony and Lawrence, Robert and Levinson, Douglas and Lorentzon, Mattias and McKnight, Barbara and Morris, Anew and Müller, Martina and Ngwa, J.S and Purcell, Shaun and Rafelt, Suzanne and Salem, Rany and Salvi, Erika and Sanna, Serena and ... and Procardis Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature: international weekly journal of science, ISSN 0028-0836, 10/2010, Volume 467, Issue 7317, pp. 832 - 838
Journal Article