X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (503) 503
Newspaper Article (54) 54
Magazine Article (8) 8
Book / eBook (5) 5
Book Chapter (5) 5
Publication (3) 3
Web Resource (3) 3
Patent (1) 1
Trade Publication Article (1) 1
Video Recording (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (270) 270
female (181) 181
male (176) 176
ophthalmology (172) 172
middle aged (116) 116
aged (114) 114
glaucoma (99) 99
adult (96) 96
eye diseases (76) 76
aged, 80 and over (70) 70
genetics & heredity (70) 70
adolescent (66) 66
open-angle glaucoma (66) 66
polymorphism, single nucleotide (66) 66
prevalence (64) 64
genome-wide association study (63) 63
genetics (62) 62
risk factors (58) 58
genetic aspects (55) 55
young adult (54) 54
genomes (53) 53
genetic structures (52) 52
genome-wide association (52) 52
mutation (52) 52
analysis (50) 50
genotype (50) 50
glaucoma, open-angle - genetics (50) 50
genetic predisposition to disease (48) 48
sense organs (47) 47
research (42) 42
genes (40) 40
gene expression (38) 38
australia (37) 37
case-control studies (37) 37
age (36) 36
child (36) 36
multidisciplinary sciences (36) 36
phenotype (36) 36
research article (36) 36
gene (35) 35
population (35) 35
medical research (33) 33
macular degeneration (31) 31
mutations (31) 31
heritability (30) 30
pedigree (30) 30
studies (30) 30
biochemistry & molecular biology (29) 29
cohort studies (29) 29
european continental ancestry group - genetics (29) 29
eye (29) 29
genomics (29) 29
retina (29) 29
disease (28) 28
identification (28) 28
intraocular-pressure (27) 27
myopia (27) 27
animals (26) 26
association (26) 26
epidemiology (26) 26
intraocular pressure (26) 26
eye proteins - genetics (24) 24
medicine (24) 24
abridged index medicus (23) 23
cross-sectional studies (23) 23
risk (23) 23
alleles (22) 22
blindness (22) 22
biology (21) 21
diabetic retinopathy (21) 21
expression (21) 21
glaucoma - genetics (21) 21
risk-factors (21) 21
surveys and questionnaires (21) 21
common variants (20) 20
health aspects (20) 20
science (20) 20
child, preschool (19) 19
genetic variation (19) 19
metaanalysis (19) 19
polymorphism, single nucleotide - genetics (19) 19
variants (19) 19
cornea (18) 18
gene frequency (18) 18
genetic research (18) 18
haplotypes (18) 18
loci (18) 18
optic nerve (18) 18
children (17) 17
optic disk - pathology (17) 17
proteins (17) 17
susceptibility (17) 17
twins (17) 17
cell biology (16) 16
glycoproteins - genetics (16) 16
mice (16) 16
care and treatment (15) 15
single-nucleotide polymorphism (15) 15
stem cells (15) 15
central corneal thickness (14) 14
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
UTL at Downsview - May be requested (2) 2
UofT at Mississauga - Stacks (2) 2
UofT at Scarborough - Stacks (2) 2
Chemistry (A D Allen) - Stacks (1) 1
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Media Commons - Audio Visual (1) 1
Online Resources - Online (1) 1
Robarts - Reference (1) 1
Robarts - Stacks (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Lu, Yi and Vitart, Veronique and Burdon, Kathryn P and Khor, Chiea Chuen and Bykhovskaya, Yelena and Mirshahi, Alireza and Hewitt, Alex W and Koehn, Demelza and Hysi, Pirro G and Ramdas, Wishal D and Zeller, Tanja and Vithana, Eranga N and Cornes, Belinda K and Tay, Wan-Ting and Tai, E Shyong and Cheng, Ching-Yu and Liu, Jianjun and Foo, Jia-Nee and Saw, Seang Mei and Thorleifsson, Gudmar and Stefansson, Kari and Dimasi, David P and Mills, Richard A and Mountain, Jenny and Ang, Wei and Hoehn, René and Verhoeven, Virginie J M and Grus, Franz and Wolfs, Roger and Castagne, Raphaële and Lackner, Karl J and Springelkamp, Henriët and Yang, Jian and Jonasson, Fridbert and Leung, Dexter Y L and Chen, Li J and Tham, Clement C Y and Rudan, Igor and Vatavuk, Zoran and Hayward, Caroline and Gibson, Jane and Cree, Angela J and MacLeod, Alex and Ennis, Sarah and Polasek, Ozren and Campbell, Harry and Wilson, James F and Viswanathan, Ananth C and Fleck, Brian and Li, Xiaohui and Siscovick, David and Taylor, Kent D and Rotter, Jerome I and Yazar, Seyhan and Ulmer, Megan and Li, Jun and Yaspan, Brian L and Ozel, Ayse B and Richards, Julia E and Moroi, Sayoko E and Haines, Jonathan L and Kang, Jae H and Pasquale, Louis R and Allingham, R Rand and Ashley-Koch, Allison and Mitchell, Paul and Wang, Jie Jin and Wright, Alan F and Pennell, Craig and Spector, Timothy D and Young, Terri L and Klaver, Caroline C W and Martin, Nicholas G and Montgomery, Grant W and Anderson, Michael G and Aung, Tin and Willoughby, Colin E and Wiggs, Janey L and Pang, Chi P and Thorsteinsdottir, Unnur and Lotery, Andrew J and Hammond, Christopher J and van Duijn, Cornelia M and Hauser, Michael A and Rabinowitz, Yaron S and Pfeiffer, Norbert and Mackey, David A and Craig, Jamie E and Macgregor, Stuart and Wong, Tien Y and NEIGHBOR Consortium
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 2, pp. 155 - 163
Journal Article
PLoS genetics, ISSN 1553-7390, 2012, Volume 8, Issue 5, p. e1002611
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 1, p. e53830
Journal Article
by Fritsche, Lars G and Igl, Wilmar and Bailey, Jessica N Cooke and Grassmann, Felix and Sengupta, Sebanti and Bragg-Gresham, Jennifer L and Burdon, Kathryn P and Hebbring, Scott J and Wen, Cindy and Gorski, Mathias and Kim, Ivana K and Cho, David and Zack, Donald and Souied, Eric and Scholl, Hendrik P N and Bala, Elisa and Lee, Kristine E and Hunter, David J and Sardell, Rebecca J and Mitchell, Paul and Merriam, Joanna E and Cipriani, Valentina and Hoffman, Joshua D and Schick, Tina and Lechanteur, Yara T E and Guymer, Robyn H and Johnson, Matthew P and Jiang, Yingda and Stanton, Chloe M and Buitendijk, Gabriëlle H S and Zhan, Xiaowei and Kwong, Alan M and Boleda, Alexis and Brooks, Matthew and Gieser, Linn and Ratnapriya, Rinki and Branham, Kari E and Foerster, Johanna R and Heckenlively, John R and Othman, Mohammad I and Vote, Brendan J and Liang, Helena Hai and Souzeau, Emmanuelle and McAllister, Ian L and Isaacs, Timothy and Hall, Janette and Lake, Stewart and Mackey, David A and Constable, Ian J and Craig, Jamie E and Kitchner, Terrie E and Yang, Zhenglin and Su, Zhiguang and Luo, Hongrong and Chen, Daniel and Ouyang, Hong and Flagg, Ken and Lin, Danni and Mao, Guanping and Ferreyra, Henry and Stark, Klaus and von Strachwitz, Claudia N and Wolf, Armin and Brandl, Caroline and Rudolph, Guenther and Olden, Matthias and Morrison, Margaux A and Morgan, Denise J and Schu, Matthew and Ahn, Jeeyun and Silvestri, Giuliana and Tsironi, Evangelia E and Park, Kyu Hyung and Farrer, Lindsay A and Orlin, Anton and Brucker, Alexander and Li, Mingyao and Curcio, Christine A and Mohand-Saïd, Saddek and Sahel, José-Alain and Audo, Isabelle and Benchaboune, Mustapha and Cree, Angela J and Rennie, Christina A and Goverdhan, Srinivas V and Grunin, Michelle and Hagbi-Levi, Shira and Campochiaro, Peter and Katsanis, Nicholas and Holz, Frank G and Blond, Frédéric and Blanché, Hélène and Deleuze, Jean-François and Igo, Robert P and Truitt, Barbara and Peachey, Neal S and Meuer, Stacy M and Myers, Chelsea E and Moore, Emily L and Klein, Ronald and ...
Nature genetics, ISSN 1546-1718, 2015, Volume 48, Issue 2, pp. 134 - 143
Journal Article
by Hysi, Pirro G and Cheng, Ching-Yu and Springelkamp, Henriët and Macgregor, Stuart and Bailey, Jessica N Cooke and Wojciechowski, Robert and Vitart, Veronique and Nag, Abhishek and Hewitt, Alex W and Höhn, René and Venturini, Cristina and Mirshahi, Alireza and Ramdas, Wishal D and Thorleifsson, Gudmar and Vithana, Eranga and Khor, Chiea-Chuen and Stefansson, Arni B and Liao, Jiemin and Haines, Jonathan L and Amin, Najaf and Wang, Ya Xing and Wild, Philipp S and Ozel, Ayse B and Li, Jun Z and Fleck, Brian W and Zeller, Tanja and Staffieri, Sandra E and Teo, Yik-Ying and Cuellar-Partida, Gabriel and Luo, Xiaoyan and Allingham, R Rand and Richards, Julia E and Senft, Andrea and Karssen, Lennart C and Zheng, Yingfeng and Bellenguez, Céline and Xu, Liang and Iglesias, Adriana I and Wilson, James F and Kang, Jae H and van Leeuwen, Elisabeth M and Jonsson, Vesteinn and Thorsteinsdottir, Unnur and Despriet, Dominiek D G and Ennis, Sarah and Moroi, Sayoko E and Martin, Nicholas G and Jansonius, Nomdo M and Yazar, Seyhan and Tai, E-Shyong and Amouyel, Philippe and Kirwan, James and van Koolwijk, Leonieke M E and Hauser, Michael A and Jonasson, Fridbert and Leo, Paul and Loomis, Stephanie J and Fogarty, Rhys and Rivadeneira, Fernando and Kearns, Lisa and Lackner, Karl J and de Jong, Paulus T V M and Simpson, Claire L and Pennell, Craig E and Oostra, Ben A and Uitterlinden, André G and Saw, Seang-Mei and Lotery, Andrew J and Bailey-Wilson, Joan E and Hofman, Albert and Vingerling, Johannes R and Maubaret, Cécilia and Pfeiffer, Norbert and Wolfs, Roger C W and Lemij, Hans G and Young, Terri L and Pasquale, Louis R and Delcourt, Cécile and Spector, Timothy D and Klaver, Caroline C W and Small, Kerrin S and Burdon, Kathryn P and Stefansson, Kari and Wong, Tien-Yin and Viswanathan, Ananth and Mackey, David A and Craig, Jamie E and Wiggs, Janey L and van Duijn, Cornelia M and Hammond, Christopher J and Aung, Tin and NEIGHBORHOOD Consortium and Wellcome Trust Case Control Consortium 2 and BMES GWAS Group and BMES GWAS Grp and Wellcome Trust Case Control Conso
Nature genetics, ISSN 1546-1718, 2014, Volume 46, Issue 10, pp. 1126 - 1130
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 6, p. e65804
..., Global BPGen Consortium, Guo Li 2, Nicholas L. Smith 3,20,37, Kerri L. Wiggins 2,15, Jane Z. Kuo 7, Kent D. Taylor 7, Alex W. Hewitt 9, Nicholas G. Martin 8, Grant W... 
FASTING GLUCOSE | VESSEL DIAMETERS | MICROVASCULAR ABNORMALITIES | MULTIDISCIPLINARY SCIENCES | VASCULAR CALIBER | PREVALENCE | HYPERTENSION | ATHEROSCLEROSIS RISK | BLOOD-PRESSURE | GENOME-WIDE ASSOCIATION | AGE | European Continental Ancestry Group - genetics | Genome-Wide Association Study | MEF2 Transcription Factors - genetics | Microcirculation - genetics | Retinal Vessels - metabolism | Humans | Middle Aged | Genetic Loci - genetics | Genotype | Male | Arterioles - metabolism | Aged, 80 and over | Female | Aged | Models, Genetic | Chromosomes, Human, Pair 5 - genetics | Hypertension | Medical research | Genes | Genomics | Research | Coronary heart disease | Epidemiology | Stroke (Disease) | Consortia | Atherosclerosis | Medicine, Experimental | Genetic research | Genetic aspects | Myocardial infarction | Biometrics | MEF2c gene | Demography | Laboratories | Arterioles | Retina | Genomes | Vascular diseases | Aging | Heart diseases | Public health | Cerebral infarction | Stroke | Internal medicine | Research & development--R&D | Coronary artery | Flow resistance | Chromosome 5 | Genetic diversity | Coronary artery disease | Loci | Ethnic factors | Quantitative genetics | Medicine | Hospitals | Arteriosclerosis | Digitization | Infarction | Photographs | Gene loci | Microvasculature | Diabetes | Research & development | R&D
Journal Article