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

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (189) 189
humans (184) 184
life sciences & biomedicine (153) 153
female (113) 113
male (111) 111
genetics & heredity (87) 87
genome-wide association study (87) 87
medicin och hälsovetenskap (87) 87
middle aged (86) 86
genetics (80) 80
polymorphism, single nucleotide (77) 77
genomes (73) 73
risk factors (70) 70
medical and health sciences (61) 61
genetic aspects (60) 60
adult (55) 55
blood pressure (53) 53
epidemiology (50) 50
aged (49) 49
research (49) 49
cardiovascular system & cardiology (48) 48
genomics (48) 48
genotype (46) 46
genetic predisposition to disease (44) 44
studies (44) 44
hypertension (42) 42
european continental ancestry group - genetics (40) 40
cohort studies (39) 39
genetic variation (39) 39
blood pressure - genetics (38) 38
genes (38) 38
phenotype (38) 38
cardiovascular disease (37) 37
multidisciplinary sciences (37) 37
science & technology - other topics (37) 37
medical genetics (36) 36
medicinsk genetik (35) 35
atherosclerosis (32) 32
hypertension - genetics (32) 32
basic medicine (31) 31
cardiac & cardiovascular systems (31) 31
clinical medicine (31) 31
gene frequency (31) 31
medicinska och farmaceutiska grundvetenskaper (31) 31
cardiovascular diseases (30) 30
genetic loci (29) 29
genome-wide association studies (29) 29
klinisk medicin (29) 29
african americans - genetics (28) 28
health aspects (28) 28
loci (28) 28
alleles (27) 27
coronary heart disease (26) 26
genetic research (26) 26
meta-analysis (26) 26
science (26) 26
analysis (25) 25
abridged index medicus (24) 24
medicine (24) 24
gene expression (23) 23
coronary artery disease (22) 22
peripheral vascular disease (22) 22
genetic association studies (21) 21
heart (21) 21
medical research (21) 21
polymorphism, single nucleotide - genetics (21) 21
public health (21) 21
cardiac and cardiovascular systems (20) 20
diabetes (20) 20
kardiologi (20) 20
lipids (20) 20
consortia (19) 19
genome, human (19) 19
heart diseases (19) 19
aged, 80 and over (18) 18
biochemistry & molecular biology (18) 18
research article (18) 18
single-nucleotide polymorphism (18) 18
usage (18) 18
african americans (17) 17
medicine and health sciences (17) 17
physiological aspects (17) 17
population (17) 17
risk (17) 17
single nucleotide polymorphisms (17) 17
adolescent (16) 16
case-control studies (16) 16
genetic predisposition to disease - genetics (16) 16
african continental ancestry group - genetics (15) 15
biology and life sciences (15) 15
genetic variance (15) 15
cholesterol (14) 14
gene loci (14) 14
young adult (14) 14
dna sequencing (13) 13
exome (13) 13
heart failure (13) 13
incidence (13) 13
metabolism (13) 13
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of the American College of Cardiology, ISSN 0735-1097, 06/2016, Volume 67, Issue 22, pp. 2578 - 2589
Journal Article
by Peloso, Gina M and Auer, Paul L and Bis, Joshua C and Voorman, Arend and Morrison, Alanna C and Stitziel, Nathan O and Brody, Jennifer A and Khetarpal, Sumeet A and Crosby, Jacy R and Fornage, Myriam and Isaacs, Aaron and Jakobsdottir, Johanna and Feitosa, Mary F and Davies, Gail and Huffman, Jennifer E and Manichaikul, Ani and Davis, Brian and Lohman, Kurt and Joon, Aron Y and Smith, Albert V and Grove, Megan L and Zanoni, Paolo and Redon, Valeska and Demissie, Serkalem and Lawson, Kim and Peters, Ulrike and Carlson, Christopher and Jackson, Rebecca D and Ryckman, Kelli K and Mackey, Rachel H and Robinson, Jennifer G and Siscovick, David S and Schreiner, Pamela J and Mychaleckyj, Josyf C and Pankow, James S and Hofman, Albert and Uitterlinden, Andre G and Harris, Tamara B and Taylor, Kent D and Stafford, Jeanette M and Reynolds, Lindsay M and Marioni, Riccardo E and Dehghan, Abbas and Franco, Oscar H and Patel, Aniruddh P and Lu, Yingchang and Hindy, George and Gottesman, Omri and Bottinger, Erwin P and Melander, Olle and Orho-Melander, Marju and Loos, Ruth J.F and Duga, Stefano and Merlini, Piera Angelica and Farrall, Martin and Goel, Anuj and Asselta, Rosanna and Girelli, Domenico and Martinelli, Nicola and Shah, Svati H and Kraus, William E and Li, Mingyao and Rader, Daniel J and Reilly, Muredach P and McPherson, Ruth and Watkins, Hugh and Ardissino, Diego and Zhang, Qunyuan and Wang, Judy and Tsai, Michael Y and Taylor, Herman A and Correa, Adolfo and Griswold, Michael E and Lange, Leslie A and Starr, John M and Rudan, Igor and Eiriksdottir, Gudny and Launer, Lenore J and Ordovas, Jose M and Levy, Daniel and Chen, Y.-D. Ida and Reiner, Alexander P and Hayward, Caroline and Polasek, Ozren and Deary, Ian J and Borecki, Ingrid B and Liu, Yongmei and Gudnason, Vilmundur and Wilson, James G and van Duijn, Cornelia M and Kooperberg, Charles and Rich, Stephen S and Psaty, Bruce M and Rotter, Jerome I and O’Donnell, Christopher J and Rice, Kenneth and Boerwinkle, Eric and Kathiresan, Sekar and Cupples, L. Adrienne and NHLBI GO Exome Sequencing Project
American journal of human genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 223 - 232
Journal Article
Human genetics, ISSN 1432-1203, 12/2017, Volume 137, Issue 1, pp. 85 - 94
Journal Article
by Nikpay, Majid and Goel, Anuj and Won, Hong-Hee and Hall, Leanne M and Willenborg, Christina and Kanoni, Stavroula and Saleheen, Danish and Kyriakou, Theodosios and Nelson, Christopher P and CHopewell, Jemma and Webb, Thomas R and Zeng, Lingyao and Dehghan, Abbas and Alver, Maris and MArmasu, Sebastian and Auro, Kirsi and Bjonnes, Andrew and Chasman, Daniel I and Chen, Shufeng and Ford, Ian and Franceschini, Nora and Gieger, Christian and Grace, Christopher and Gustafsson, Stefan and Huang, Jie and Hwang, Shih-Jen and Kim, Yun Kyoung and Kleber, Marcus E and Lau, King Wai and Lu, Xiangfeng and Lu, Yingchang and Lyytikäinen, Leo-Pekka and Mihailov, Evelin and Morrison, Alanna C and Pervjakova, Natalia and Qu, Liming and Rose, Lynda M and Salfati, Elias and Saxena, Richa and Scholz, Markus and Smith, Albert V and Tikkanen, Emmi and Uitterlinden, Andre and Yang, Xueli and Zhang, Weihua and Zhao, Wei and De Andrade, Mariza and De Vries, Paul S and Van Zuydam, Natalie R and Anand, Sonia S and Bertram, Lars and Beutner, Frank and Dedoussis, George and Frossard, Philippe and Gauguier, Dominique and Goodall, Alison H and Gottesman, Omri and Haber, Marc and Han, Bok-Ghee and Huang, Jianfeng and Jalilzadeh, Shapour and Kessler, Thorsten and König, Inke R and Lannfelt, Lars and Lieb, Wolfgang and Lind, Lars and MLindgren, Cecilia and Lokki, Marja-Liisa and Magnusson, Patrik K and Mallick, Nadeem H and Mehra, Narinder and Meitinger, Thomas and Memon, Fazal-Uur-Rehman and Morris, Andrew P and Nieminen, Markku S and Pedersen, Nancy L and Peters, Annette and Rallidis, Loukianos S and Rasheed, Asif and Samuel, Maria and Shah, Svati H and Sinisalo, Juha and EStirrups, Kathleen and Trompet, Stella and Wang, Laiyuan and Zaman, Khan S and Ardissino, Diego and Boerwinkle, Eric and Borecki, Ingrid B and Bottinger, Erwin P and Buring, Julie E and Chambers, John C and Collins, Rory and Cupples, Ladrienne and Danesh, John and Demuth, Ilja and Elosua, Roberto and Epstein, Stephen E and Esko, Tõnu and Feitosa, Mary F and ... and the CARDIoGRAMplusC4D Consortium and CARDIoGRAMplusC4D Consortium
Nature genetics, ISSN 1546-1718, 09/2015, Volume 47, Issue 10, pp. 1121 - 1130
Journal Article
Nature genetics, ISSN 1546-1718, 12/2009, Volume 42, Issue 1, pp. 45 - 52
Journal Article
by Liu, Chunyu and Kraja, Aldi T and Smith, Jennifer A and Brody, Jennifer A and Franceschini, Nora and Bis, Joshua C and Rice, Kenneth and Morrison, Alanna C and Lu, Yingchang and Weiss, Stefan and Guo, Xiuqing and Palmas, Walter and Martin, Lisa W and Chen, Yii-Der Ida and Surendran, Praveen and Drenos, Fotios and Cook, James P and Auer, Paul L and Chu, Audrey Y and Giri, Ayush and Zhao, Wei and Jakobsdottir, Johanna and Lin, Li-An and Stafford, Jeanette M and Amin, Najaf and Mei, Hao and Yao, Jie and Voorman, Arend and Larson, Martin G and Grove, Megan L and Smith, Albert V and Hwang, Shih-Jen and Chen, Han and Huan, Tianxiao and Kosova, Gulum and Stitziel, Nathan O and Kathiresan, Sekar and Samani, Nilesh and Schunkert, Heribert and Deloukas, Panos and Li, Man and Fuchsberger, Christian and Pattaro, Cristian and Gorski, Mathias and Kooperberg, Charles and Papanicolaou, George J and Rossouw, Jacques E and Faul, Jessica D and Kardia, Sharon L R and Bouchard, Claude and Raffel, Leslie J and Uitterlinden, André G and Franco, Oscar H and Vasan, Ramachandran S and O'Donnell, Christopher J and Taylor, Kent D and Liu, Kiang and Bottinger, Erwin P and Gottesman, Omri and Daw, E Warwick and Giulianini, Franco and Ganesh, Santhi and Salfati, Elias and Harris, Tamara B and Launer, Lenore J and Dörr, Marcus and Felix, Stephan B and Rettig, Rainer and Völzke, Henry and Kim, Eric and Lee, Wen-Jane and Lee, I-Te and Sheu, Wayne H-H and Tsosie, Krystal S and Edwards, Digna R Velez and Liu, Yongmei and Correa, Adolfo and Weir, David R and Völker, Uwe and Ridker, Paul M and Boerwinkle, Eric and Gudnason, Vilmundur and Reiner, Alexander P and van Duijn, Cornelia M and Borecki, Ingrid B and Edwards, Todd L and Chakravarti, Aravinda and Rotter, Jerome I and Psaty, Bruce M and Loos, Ruth J F and Fornage, Myriam and Ehret, Georg B and Newton-Cheh, Christopher and Levy, Daniel and Chasman, Daniel I and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia and CHD Exome+ Consortium and ExomeBP Consortium and GoT2DGenes Consortium and T2D-GENES Consortium and CKDGen Consortium and Myocardial Infarction Genetics CAR and GOT2Dgenes Consortium and CHD Exome Consortium and T2D-Genes Consortium
Nature genetics, ISSN 1546-1718, 09/2016, Volume 48, Issue 10, pp. 1162 - 1170
Journal Article