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 (251) 251
humans (223) 223
life sciences & biomedicine (214) 214
female (160) 160
male (142) 142
genome-wide association study (111) 111
middle aged (109) 109
genetics (94) 94
genetics & heredity (93) 93
polymorphism, single nucleotide (93) 93
risk factors (88) 88
adult (84) 84
genomes (83) 83
aged (75) 75
genetic aspects (74) 74
genomics (62) 62
research (62) 62
epidemiology (60) 60
genotype (57) 57
studies (57) 57
phenotype (51) 51
medical and health sciences (47) 47
medicin och hälsovetenskap (47) 47
genetic predisposition to disease (44) 44
european continental ancestry group - genetics (42) 42
genome-wide association studies (41) 41
health aspects (41) 41
african americans (39) 39
meta-analysis (39) 39
adolescent (37) 37
cardiovascular system & cardiology (37) 37
blood pressure (36) 36
cohort studies (36) 36
gene frequency (36) 36
genetic variation (36) 36
multidisciplinary sciences (36) 36
science & technology - other topics (36) 36
genes (35) 35
medicine (35) 35
alleles (34) 34
cardiovascular disease (34) 34
medical research (34) 34
genetic loci (33) 33
science (33) 33
african americans - genetics (32) 32
analysis (32) 32
young adult (31) 31
urology & nephrology (30) 30
gene expression (29) 29
hypertension (29) 29
loci (29) 29
quantitative trait loci (29) 29
research article (29) 29
blood pressure - genetics (28) 28
medical genetics (27) 27
polymorphism, single nucleotide - genetics (27) 27
aged, 80 and over (26) 26
atherosclerosis (26) 26
public health (26) 26
body mass index (24) 24
cardiac & cardiovascular systems (24) 24
medicinsk genetik (24) 24
single-nucleotide polymorphism (24) 24
abridged index medicus (23) 23
physiological aspects (23) 23
single nucleotide polymorphisms (23) 23
basic medicine (22) 22
diabetes (22) 22
medicinska och farmaceutiska grundvetenskaper (22) 22
prospective studies (22) 22
womens health (22) 22
cardiovascular diseases (21) 21
clinical medicine (21) 21
human genetics (21) 21
hypertension - genetics (21) 21
klinisk medicin (21) 21
population (21) 21
biochemistry & molecular biology (20) 20
genetic association studies (20) 20
genetic research (20) 20
exome (19) 19
health risk assessment (19) 19
indians, north american - genetics (19) 19
peripheral vascular disease (19) 19
age factors (18) 18
animals (18) 18
cholesterol (18) 18
coronary heart disease (18) 18
lipids (18) 18
proteins (18) 18
united states - epidemiology (18) 18
diabetes mellitus, type 2 - genetics (17) 17
gene loci (17) 17
heart (17) 17
medicine and health sciences (17) 17
mortality (17) 17
smoking (17) 17
biology and life sciences (16) 16
chromosome mapping (16) 16
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


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
Hypertension (Dallas, Tex. 1979), ISSN 0194-911X, 09/2020, Volume 76, Issue Suppl_1
Introduction: The global deletion of collectrin encoded by the TMEM27 gene leads to endothelial dysfunction, salt sensitivity and hypertension. To translate... 
Journal Article
Kidney international, ISSN 0085-2538, 07/2020, Volume 98, Issue 1, pp. 35 - 41
Journal Article
Molecular neurobiology, ISSN 0893-7648, 12/2017, Volume 54, Issue 10, pp. 8021 - 8032
Journal Article
Circulation (New York, N.Y.), ISSN 0009-7322, 03/2019, Volume 139, Issue Suppl_1
Journal Article
by Howson, Joanna M M and Zhao, Wei and Barnes, Daniel R and Ho, Weang-Kee and Young, Robin and Paul, Dirk S and Waite, Lindsay L and Freitag, Daniel F and Fauman, Eric B and Salfati, Elias L and Sun, Benjamin B and Eicher, John D and Johnson, Andrew D and Sheu, Wayne H H and Nielsen, Sune F and Lin, Wei-Yu and Surendran, Praveen and Malarstig, Anders and Wilk, Jemma B and Tybjærg-Hansen, Anne and Rasmussen, Katrine L and Kamstrup, Pia R and Deloukas, Panos and Erdmann, Jeanette and Kathiresan, Sekar and Samani, Nilesh J and Schunkert, Heribert and Watkins, Hugh and Do, Ron and Rader, Daniel J and Johnson, Julie A and Hazen, Stanley L and Quyyumi, Arshed A and Spertus, John A and Pepine, Carl J and Franceschini, Nora and Justice, Anne and Reiner, Alex P and Buyske, Steven and Hindorff, Lucia A and Carty, Cara L and North, Kari E and Kooperberg, Charles and Boerwinkle, Eric and Young, Kristin and Graff, Mariaelisa and Peters, Ulrike and Absher, Devin and Hsiung, Chao A and Lee, Wen-Jane and Taylor, Kent D and Chen, Ying-Hsiang and Lee, I-Te and Guo, Xiuqing and Chung, Ren-Hua and Hung, Yi-Jen and Rotter, Jerome I and Juang, Jyh-Ming J and Quertermous, Thomas and Wang, Tzung-Dau and Rasheed, Asif and Frossard, Philippe and Alam, Dewan S and Majumder, Abdulla al Shafi and Di Angelantonio, Emanuele and Chowdhury, Rajiv and Chen, Yii-Der Ida and Nordestgaard, Børge G and Assimes, Themistocles L and Danesh, John and Butterworth, Adam S and Saleheen, Danish and EPIC-CVD and CARDIoGRAMplusC4D
Nature genetics, ISSN 1061-4036, 05/2017, Volume 49, Issue 7, pp. 1113 - 1119
Journal Article
by Elks, Cathy and Perry, John and Sulem, Patrick and Chasman, Daniel and Franceschini, Nora and He, Chunyan and Lunetta, Kathryn and Visser, Jenny and Byrne, Enda and Cousminer, Diana and Gudbjartsson, Daniel and Esko, Tõnu and Feenstra, Bjarke and Hottenga, Jouke Jan and Koller, Daniel and Kutalik, Zoltán and Lin, Peng and Mangino, Massimo and Marongiu, Mara and McArdle, Patrick and Smith, Albert Vernon and Stolk, Lisette and Wingerden, Sophie and Zhao, Jing Hua and Albrecht, Eva and Corre, Tanguy and Ingelsson, Erik and Hayward, Caroline and Magnusson, Patrik and Ulivi, Shelia and Warrington, Nicole and Zgaga, Lina and Alavere, Helene and Amin, Najaf and Aspelund, Thor and Bandinelli, Stefania and Barroso, Inês and Berenson, Gerald and Bergmann, Sven and Blackburn, Hannah and Boerwinkle, Eric and Buring, Julie and Busonero, F and Campbell, Harry and Chanock, Stephen and Chen, Wei and Cornelis, Marilyn and Couper, David and Coviello, Anea and Adamo, Pio and Faire, Ulf and Geus, Eco and Deloukas, Panagiotis and Döring, Angela and Easton, Douglas and Eiriksdottir, Gudny and Emilsson, Valur and Eriksson, Johan and Ferrucci, Luigi and Folsom, Aaron and Foroud, Tatiana and Garcia, Melissa and Gasparini, Paolo and Geller, Frank and Gieger, Christian and Gudnason, Vilmundur and Hall, Alistair and Hankinson, Susan and Ferreli, Liana and Heath, Anew and Hernandez, Dena and Hofman, Albert and Hu, Frank and Illig, Thomas and Järvelin, M.R and Johnson, Anew and Karasik, David and Khaw, Kay-Tee and Kiel, Douglas and Kilpelänen, Tuomas and Kolcic, Ivana and Kraft, Peter and Launer, Lenore and Laven, Joop and Li, Shengxu and Liu, Jianjun and Levy, Daniel and Martin, Nicholas and Melbye, Mads and Mooser, Vincent and Murray, Jeffrey and Nalls, Michael and Navarro, Pau and Nelis, Mari and Ness, Anew and Northstone, Kate and Oostra, Ben and Peacock, Munro and Palmer, Cameron and Palotie, Aarno and ... and GIANT Consortium and The GIANT Consortium
Nature genetics, ISSN 1061-4036, 12/2010, Volume 42, Issue 12, pp. 1077 - 1085
Journal Article