X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (679) 679
Publication (99) 99
Newspaper Article (52) 52
Patent (28) 28
Book Review (21) 21
Book / eBook (16) 16
Magazine Article (12) 12
Book Chapter (7) 7
Conference Proceeding (7) 7
Reference (5) 5
Report (5) 5
Paper (2) 2
Web Resource (2) 2
Dissertation (1) 1
Government Document (1) 1
Journal / eJournal (1) 1
Streaming Audio (1) 1
Video Recording (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (257) 257
female (190) 190
index medicus (183) 183
male (178) 178
adult (137) 137
middle aged (135) 135
article (95) 95
risk factors (95) 95
aged (89) 89
higher education (88) 88
research (82) 82
genetics (80) 80
genome-wide association study (72) 72
genetics & heredity (64) 64
polymorphism, single nucleotide (62) 62
college students (59) 59
medical and health sciences (52) 52
medicin och hälsovetenskap (52) 52
genotype (51) 51
genetic aspects (50) 50
risk (49) 49
adolescent (45) 45
united states (43) 43
phenotype (42) 42
genetic predisposition to disease (41) 41
health aspects (41) 41
college faculty (40) 40
genome-wide association (40) 40
aged, 80 and over (39) 39
clinical neurology (38) 38
endocrinology & metabolism (38) 38
genetic variation (35) 35
genomes (35) 35
stroke (35) 35
education & educational research (34) 34
association (33) 33
cohort studies (33) 33
metaanalysis (32) 32
peripheral vascular disease (32) 32
atherosclerosis (30) 30
abridged index medicus (29) 29
disease (29) 29
heritability (29) 29
meta-analysis (29) 29
population (29) 29
young adult (29) 29
clinical medicine (28) 28
epidemiology (28) 28
european continental ancestry group - genetics (28) 28
public, environmental & occupational health (28) 28
stroke - genetics (28) 28
education (27) 27
klinisk medicin (27) 27
universities (26) 26
african americans (25) 25
neurosciences (25) 25
polymorphism, single nucleotide - genetics (25) 25
academic persistence (24) 24
medical genetics (24) 24
medicine (24) 24
mortality (24) 24
neurology (24) 24
obesity (24) 24
scholarship (24) 24
studies (24) 24
basic medicine (23) 23
cardiac & cardiovascular systems (23) 23
diagnosis (23) 23
expression (23) 23
prevalence (23) 23
surgery (23) 23
animals (22) 22
case-control studies (22) 22
prevention (22) 22
variants (22) 22
body mass index (21) 21
genomics (21) 21
medicinska och farmaceutiska grundvetenskaper (21) 21
analysis (20) 20
blood pressure (20) 20
cardiovascular diseases (20) 20
colleges & universities (20) 20
college instruction (19) 19
colleges (19) 19
diabetes (19) 19
gene frequency (19) 19
genes (19) 19
loci (19) 19
medicinsk genetik (19) 19
mice (19) 19
multidisciplinary sciences (19) 19
osteoporosis (19) 19
brain ischemia - genetics (18) 18
diabetes mellitus, type 2 - genetics (18) 18
earth drilling (18) 18
earth drilling, e.g. deep drilling (18) 18
fixed constructions (18) 18
mining (18) 18
obtaining oil, gas, water, soluble or meltable materials or aslurry of minerals from wells (18) 18
pedigree (18) 18
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
OISE - Stacks (6) 6
Robarts - Stacks (4) 4
UofT at Scarborough - Stacks (3) 3
Online Resources - Online (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Gerstein Science - Stacks (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Trinity College (John W Graham) - Stacks (1) 1
UofT at Mississauga - Stacks (1) 1
UofT at Scarborough - Periodical Stacks (1) 1
Victoria University Emmanuel College - 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 Traylor, Matthew, MSc and Farrall, Martin, FRCPath and Holliday, Elizabeth G, PhD and Sudlow, Cathie, FRCP and Hopewell, Jemma C, PhD and Cheng, Yu-Ching, PhD and Fornage, Myriam, PhD and Ikram, M Arfan, MD and Malik, Rainer, PhD and Bevan, Steve, PhD and Thorsteinsdottir, Unnur, PhD and Nalls, Mike A, PhD and Longstreth, WT, MD and Wiggins, Kerri L, MS and Yadav, Sunaina, MSc and Parati, Eugenio A, MD and DeStefano, Anita L, PhD and Worrall, Bradford B, MD and Kittner, Steven J, MD and Khan, Muhammad Saleem, MSc and Reiner, Alex P, MD and Helgadottir, Anna, MD and Achterberg, Sefanja, PhD and Fernandez-Cadenas, Israel, PhD and Abboud, Sherine, MD and Schmidt, Reinhold, MD and Walters, Matthew, MD and Chen, Wei-Min, PhD and Ringelstein, E Bernd, MD and O'Donnell, Martin, MD and Ho, Weang Kee, PhD and Pera, Joanna, MD and Lemmens, Robin, MD and Norrving, Bo, MD and Higgins, Peter, MRCP and Benn, Marianne, MD and Sale, Michele, PhD and Kuhlenbäumer, Gregor, MD and Doney, Alexander S F, PhD and Vicente, Astrid M, PhD and Delavaran, Hossein, MD and Algra, Ale, MD and Davies, Gail, PhD and Oliveira, Sofia A, PhD and Palmer, Colin N A, PhD and Deary, Ian, PhD and Schmidt, Helena, MD and Pandolfo, Massimo, MD and Montaner, Joan, MD and Carty, Cara, PhD and de Bakker, Paul I W, PhD and Kostulas, Konstantinos, MD and Ferro, Jose M, MD and van Zuydam, Natalie R, MSc and Valdimarsson, Einar, MD and Nordestgaard, Børge G, MD and Lindgren, Arne, MD and Thijs, Vincent, MD and Slowik, Agnieszka, MD and Saleheen, Danish, MD and Paré, Guillaume, MD and Berger, Klaus, MD and Thorleifsson, Gudmar, PhD and Hofman, Albert, MD and Mosley, Thomas H, PhD and Mitchell, Braxton D, PhD and Furie, Karen, MD and Clarke, Robert, FRCP and Levi, Christopher, MD and Seshadri, Sudha, MD and Gschwendtner, Andreas, MD and Boncoraglio, Giorgio B, MD and Sharma, Pankaj, PhD and Bis, Joshua C, PhD and Gretarsdottir, Solveig, PhD and Psaty, Bruce M and Rothwell, Peter M, FMedSci and Rosand, Jonathan, MD and Meschia, James F, MD and Stefansson, Kari, MD and Dichgans, Martin, MD and Markus, Hugh S, Dr and The Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and on behalf of the International Stroke Genetics Consortium and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2)
The Lancet Neurology, ISSN 1474-4422, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
by Estrada Gil, Karol and Styrkarsdottir, Unnur and Evangelou, Evangelos and Hsu, Yi-Hsiang and Duncan, Emma and Ntzani, Evangelia and Oei, Ling and Albagha, Omar M and Amin, Najaf and Kemp, John and Koller, Daniel and Li, Guo and Liu, Ching-Ti and Minster, Ryan and Moayyeri, Alireza and Vandenput, Liesbeth and Willner, Dana and Xiao, Su-Mei and Yerges-Armstrong, Laura and Zheng, Hou-Feng and Alonso, Nerea and Eriksson, Joel and Kammerer, Candace and Kaptoge, Stephen and Leo, Paul and Thorleifsson, Gudmar and Wilson, Scott and Wilson, James and Aalto, Ville and Alen, Theo and Aragaki, Aaron and Aspelund, Thor and Center, Jacqueline and Dailiana, Zoe and Duggan, C and Garcia, Melissa and Garcia-Giralt, Natàlia and Giroux, Sylvie and Hallmans, Göran and Hocking, Lynne and Husted, Lise Bjerre and Jameson, Karen and Khusainova, Rita and Kim, Ghi Su and Kooperberg, Charles and Koromila, Theodora and Kruk, Marcin and Laaksonen, Marika and LaCroix, Anea and Lee, Seung and Leung, Ping and Lewis, Joshua and Masi, Laura and Mencej-Beac, Simona and Nguyen, Tuan and Nogues, Xavier and Patel, Millan and Prezelj, Janez and Rose, Lynda and Scollen, Serena and Siggeirsdottir, Kristin and Smith, Davey and Svensson, Olle and Trompet, Stella and Trummer, Olivia and Schoor, Natasja and Woo, Margaret M and Zhu, Kun and Balcells, Susana and Brandi, M.L and Buckley, Brendan M and Cheng, Sulin and Christiansen, C and Cooper, Charles and Dedoussis, George and Ford, Ian and Frost, Morten and Goltzman, David and González-Macías, Jesús and Kähönen, Mika and Karlsson, Magnus and Khusnutdinova, Elza and Koh, Jung-Min and Kollia, Panagoula and Langdahl, Bente and Leslie, William and Lips, Paul and Ljunggren, Östen and Lorenc, Roman and Marc, Janja and Mellström, Dan and Obermayer-Pietsch, Barbara and Olmos, David and Pettersson-Kymmer, Ulrika and Reid, David and Riancho, José and Ridker, Paul and Rousseau, Francois and Lagboom, P Eline and Tang, Nelson L and ... and Medicinska fakulteten and Umeå universitet and Institutionen för folkhälsa och klinisk medicin and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk farmakologi and Näringsforskning and Institutionen för kirurgisk och perioperativ vetenskap
Nature Genetics, ISSN 1061-4036, 05/2012, Volume 44, Issue 5, pp. 491 - 501
textabstractBone mineral density (BMD) is the most widely used predictor of fracture risk. We performed the largest meta-analysis to date on lumbar spine and... 
WOMEN | GENE | VARIANTS | DISEASE | GENETICS & HEREDITY | OSTEOPOROTIC FRACTURES | LRP5 | PATTERNS | EXPRESSION | BURDEN | HIP | Glycoproteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Low Density Lipoprotein Receptor-Related Protein-5 - genetics | Extracellular Matrix Proteins - genetics | Humans | Risk Factors | Computational Biology | Intercellular Signaling Peptides and Proteins - genetics | European Continental Ancestry Group | Genotype | Male | Bone Density - genetics | Gene Expression Profiling | Phosphoproteins - genetics | Fractures, Bone - genetics | Mitochondrial Membrane Transport Proteins - genetics | Polymorphism, Single Nucleotide - genetics | Female | Femur Neck - physiopathology | Osteoporosis - genetics | Spectrin - genetics | Quantitative Trait Loci | Lumbar Vertebrae - physiopathology | Quantitative trait loci | Measurement | Fractures | Bones | Genetic aspects | Identification and classification | Density | Risk factors | Medical research | Osteoporosis | Genomics | Bone density | Gene loci | Vèrtebres lumbars | Gens | Femur | Genes | Bone densitometry | Densitometria òssia | Fèmur | Lumbar vertebrae | Basic Medicine | Medical Genetics | Medicinsk genetik | ortopedi | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | genetik | Genetics | Orthopaedics
Journal Article
2000, 1st ed., Vanderbilt issues in higher education, ISBN 9780826513083, vi, 288
Book
American journal of human genetics, ISSN 0002-9297, 2012, Volume 91, Issue 5, pp. 823 - 838
Journal Article
by Porcu, Eleonora and Medici, Marco and Pistis, Giorgio and Volpato, C.B and Wilson, Scott and Cappola, Anne and Bos, Steffan and Deelen, Joris and Heijer, Martin and Freathy, Rachel and Lahti, Jari and Liu, Chunyu and Lopez, Lorna and Nolte, Ilja and O´Connell, J.R and Tanaka, Toshiko and Trompet, Stella and Arnold, Alice and Bandinelli, Stefania and Beekman, Marian and Böhringer, Stefan and Brown, Stephen and Buckley, Brendan M and Camaschella, Clara and Craen, Anton and Davies, Gail and Visser, Marieke and Ford, Ian and Forsen, Tom and Frayling, Timothy and Fugazzola, Laura and Gögele, Martin and Hattersley, Anew and Hermus, Ad and Hofman, Albert and Houwing-Duistermaat, Jeanine and Jensen, Richard and Kajantie, Eero and Kloppenburg, Margreet and Lim, Ee Mun and Masciullo, Corrado and Mariotti, Stefano and Minelli, Cosetta and Mitchell, Braxton and Nagaraja, Ramaiah and Netea-Maier, Romana and Palotie, Aarno and Persani, Luca and Piras, Maria Grazia and Psaty, Bruce and Räikkönen, Katri and Richards, Brent and Rivadeneira Ramirez, Fernando and Sala, Cinzia and Sabra, Mona and Sattar, Naveed and Shields, Beverley and Soranzo, Nicole and Starr, John and Stott, David. J and Sweep, Fred and Usala, G and Klauw, Melanie and Heemst, Diana and Mol-van Mullem, Alies and Vermeulen, Sita and Walsh, John and Westendorp, Rudi and Widen, Elisabeth and Zhai, Guangju and Cucca, Francesco and Deary, Ian and Visser, Wil Edward and Eriksson, Johan and Ferrucci, Luigi and Fox, Craig and Jukema, Jan Wouter and Kiemeney, Bart and Pramstaller, Peter Paul and Schlessinger, D and Shuldiner, Alan and Slagboom, Eline and Uitterlinden, Ané and Vaidya, Bijay and Visser, Theo and Wolffenbuttel, Bruce and Meulenbelt, Ingrid and Rotter, Jerome and Spector, Timothy and Hicks, Anew and Toniolo, Daniela and Sanna, Serena and Peeters, Robin and Naitza, Silvia
PL o S Genetics (Online), ISSN 1553-7390, 02/2013, Volume 9, Issue 2, p. e1003266
Journal Article
Nature, ISSN 0028-0836, 07/2012, Volume 487, Issue 7406, p. 165
Journal Article
Nature Communications, ISSN 2041-1723, 07/2017, Volume 8, Issue 1, p. 16015
Journal Article
by Pulit, Sara L and McArdle, Patrick F and Wong, Quenna and Malik, Rainer and Gwinn, Katrina and Achterberg, Sefanja and Algra, Ale and Amouyel, Philippe and Anderson, Christopher D and Arnett, Donna K and Arsava, Ethem Murat and Attia, John and Ay, Hakan and Bartz, Traci M and Battey, Thomas and Benavente, Oscar R and Bevan, Steve and Biffi, Alessandro and Bis, Joshua C and Blanton, Susan H and Boncoraglio, Giorgio B and Brown, Robert D and Burgess, Annette I and Carrera, Caty and Chapman Smith, Sherita N and Chasman, Daniel I and Chauhan, Ganesh and Chen, Wei-Min and Cheng, Yu-Ching and Chong, Michael and Cloonan, Lisa K and Cole, John W and Cotlarciuc, Ioana and Cruchaga, Carlos and Cuadrado-Godia, Elisa and Dave, Tushar and Dawson, Jesse and Debette, Stéphanie and Delavaran, Hossein and Dell, Cameron A and Dichgans, Martin and Doheny, Kimberly F and Dong, Chuanhui and Duggan, David J and Engström, Gunnar and Evans, Michele K and Pallejà, Xavier Estivill and Faul, Jessica D and Fernández-Cadenas, Israel and Fornage, Myriam and Frossard, Philippe M and Furie, Karen and Gamble, Dale M and Gieger, Christian and Giese, Anne-Katrin and Giralt-Steinhauer, Eva and González, Hector M and Goris, An and Gretarsdottir, Solveig and Grewal, Raji P and Grittner, Ulrike and Gustafsson, Stefan and Han, Buhm and Hankey, Graeme J and Heitsch, Laura and Higgins, Peter and Hochberg, Marc C and Holliday, Elizabeth and Hopewell, Jemma C and Horenstein, Richard B and Howard, George and Ikram, M Arfan and Ilinca, Andreea and Ingelsson, Erik and Irvin, Marguerite R and Jackson, Rebecca D and Jern, Christina and Conde, Jordi Jiménez and Johnson, Julie A and Jood, Katarina and Kahn, Muhammad S and Kaplan, Robert and Kappelle, L Jaap and Kardia, Sharon L R and Keene, Keith L and Kissela, Brett M and Kleindorfer, Dawn O and Koblar, Simon and Labovitz, Daniel and Launer, Lenore J and Laurie, Cathy C and Laurie, Cecelia A and Lee, Cue Hyunkyu and Lee, Jin-Moo and Lehm, Manuel and Lemmens, Robin and Levi, Christopher and Leys, Didier and Lindgren, Arne and Longstreth, W T and ... and International Stroke Genetics Consortium (ISGC) and NINDS Stroke Genetics Network (SiGN) and NINDS Stroke Genetics Network SiGN and ISGC and Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering and Institute of Neuroscience and Physiology and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Pathology and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy and Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation and Institutionen för biomedicin, avdelningen för patologi and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 2, pp. 174 - 184
Journal Article