X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (35120) 35120
Book Review (5198) 5198
Publication (4001) 4001
Newsletter (864) 864
Book Chapter (211) 211
Conference Proceeding (114) 114
Book / eBook (49) 49
Dissertation (30) 30
Newspaper Article (15) 15
Magazine Article (13) 13
Data Set (11) 11
Reference (11) 11
Government Document (3) 3
Trade Publication Article (3) 3
Presentation (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (29744) 29744
humans (24964) 24964
female (14248) 14248
susceptibility (13645) 13645
male (13336) 13336
genetic aspects (11749) 11749
genetic predisposition to disease (10023) 10023
disease susceptibility (9881) 9881
middle aged (8023) 8023
risk factors (7864) 7864
adult (7828) 7828
genotype (7704) 7704
genetics & heredity (7527) 7527
research (7331) 7331
genes (7312) 7312
polymorphism, single nucleotide (7120) 7120
genetics (6788) 6788
animals (6616) 6616
genome-wide association (5760) 5760
analysis (5659) 5659
case-control studies (5583) 5583
alleles (5529) 5529
aged (5101) 5101
risk (4956) 4956
association (4878) 4878
genetic research (4746) 4746
polymorphism (4622) 4622
immunology (4442) 4442
genomics (4281) 4281
disease (3931) 3931
health aspects (3851) 3851
gene frequency (3797) 3797
genomes (3768) 3768
mice (3689) 3689
cancer (3632) 3632
genome-wide association study (3583) 3583
research article (3572) 3572
haplotypes (3542) 3542
expression (3528) 3528
population (3514) 3514
oncology (3452) 3452
single nucleotide polymorphisms (3296) 3296
mutation (3258) 3258
article (3236) 3236
susceptibility locus (3222) 3222
susceptibility loci (3207) 3207
biochemistry & molecular biology (3111) 3111
gene expression (3088) 3088
studies (3071) 3071
phenotype (2898) 2898
polymorphism, genetic (2897) 2897
adolescent (2879) 2879
medicine (2820) 2820
gene (2678) 2678
multidisciplinary sciences (2609) 2609
genetic predisposition to disease - genetics (2578) 2578
single-nucleotide polymorphism (2524) 2524
neurosciences (2502) 2502
linkage disequilibrium (2500) 2500
genetic variation (2482) 2482
polymorphism, single nucleotide - genetics (2473) 2473
variants (2406) 2406
child (2381) 2381
epidemiology (2367) 2367
genetic susceptibility (2315) 2315
medical research (2290) 2290
physiological aspects (2278) 2278
polymorphisms (2277) 2277
cell biology (2260) 2260
chromosome mapping (2184) 2184
abridged index medicus (2003) 2003
proteins (1998) 1998
science (1998) 1998
genetic polymorphisms (1959) 1959
identification (1946) 1946
linkage (1938) 1938
development and progression (1935) 1935
genetic association studies (1921) 1921
young adult (1908) 1908
polymerase chain reaction (1903) 1903
genetic linkage (1895) 1895
locus (1822) 1822
biology (1821) 1821
asian continental ancestry group - genetics (1780) 1780
psychiatry (1757) 1757
aged, 80 and over (1733) 1733
endocrinology & metabolism (1700) 1700
loci (1672) 1672
microbiology (1669) 1669
genetic markers (1623) 1623
schizophrenia (1620) 1620
chromosomes (1589) 1589
metaanalysis (1500) 1500
quantitative trait loci (1484) 1484
medicine, experimental (1483) 1483
human genetics (1477) 1477
infectious diseases (1469) 1469
diabetes (1455) 1455
odds ratio (1415) 1415
mutations (1411) 1411
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (28) 28
Collection Dvlpm't (Acquisitions) - Vendor file (11) 11
Collection Dvlpm't (Acquisitions) - Closed Orders (5) 5
UofT at Mississauga - Stacks (5) 5
UTL at Downsview - May be requested (3) 3
Online Resources - Online (2) 2
Robarts - Stacks (2) 2
UofT at Scarborough - Stacks (2) 2
Gerstein Science - Circulation Desk (1) 1
Gerstein Science - Reference (1) 1
Law (Bora Laskin) - Stacks (1) 1
Physics - Stacks (1) 1
Scarborough Hospital - General (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Trinity College (John W Graham) - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (35989) 35989
French (75) 75
German (56) 56
Spanish (46) 46
Russian (19) 19
Chinese (12) 12
Polish (10) 10
Japanese (8) 8
Portuguese (6) 6
Korean (4) 4
Turkish (4) 4
Italian (3) 3
Czech (2) 2
Dutch (2) 2
Swedish (2) 2
Croatian (1) 1
Hebrew (1) 1
Persian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The New England Journal of Medicine, ISSN 0028-4793, 09/2007, Volume 357, Issue 12, pp. 1199 - 1209
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2008, Volume 40, Issue 12, pp. 1404 - 1406
Journal Article
Nature Genetics, ISSN 1061-4036, 2009, Volume 41, Issue 2, pp. 221 - 227
Journal Article
Journal Article
Journal Article
by Williams, Frances M K and Carter, Angela M and Hysi, Pirro G and Surdulescu, Gabriela and Hodgkiss, Dylan and Soranzo, Nicole and Traylor, Matthew and Bevan, Steve and Dichgans, Martin and Rothwell, Peter M W and Sudlow, Cathie and Farrall, Martin and Silander, Kaisa and Kaunisto, Mari and Wagner, Peter and Saarela, Olli and Kuulasmaa, Kari and Virtamo, Jarmo and Salomaa, Veikko and Amouyel, Philippe and Arveiler, Dominique and Ferrieres, Jean and Wiklund, Per-Gunnar and Ikram, M Arfan and Hofman, Albert and Boncoraglio, Giorgio B and Parati, Eugenio A and Helgadottir, Anna and Gretarsdottir, Solveig and Thorsteinsdottir, Unnur and Thorleifsson, Gudmar and Stefansson, Kari and Seshadri, Sudha and DeStefano, Anita and Gschwendtner, Andreas and Psaty, Bruce and Longstreth, Will and Mitchell, Braxton D and Cheng, Yu-Ching and Clarke, Robert and Ferrario, Marco and Bis, Joshua C and Levi, Christopher and Attia, John and Holliday, Elizabeth G and Scott, Rodney J and Fornage, Myriam and Sharma, Pankaj and Furie, Karen L and Rosand, Jonathan and Nalls, Mike and Meschia, James and Mosely, Thomas H and Evans, Alun and Palotie, Aarno and Markus, Hugh S and Grant, Peter J and Spector, Tim D and EuroCLOT Investigators, Investigators and Wellcome Trust Case Control Consortium 2, Trust Case Control Consortium 2 and MOnica Risk, Genetics, Archiving and Monograph, Risk, Genetics, Archiving and Monograph and MetaStroke, MetaStroke and International Stroke Genetics Consortium, Stroke Genetics Consortium and EuroCLOT Investigators and Wellcome Trust Case Control Consor and Int Stroke Genetics Consortium and MOnica Risk, Genetics, Archiving and Monograph and MetaStroke and International Stroke Genetics Consortium and Wellcome Trust Case Control Consortium 2 and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
Annals of neurology, ISSN 0364-5134, 2013, Volume 73, Issue 1, pp. 16 - 31
Objective: End-stage coagulation and the structure/function of fibrin are implicated in the pathogenesis of ischemic stroke. We explored whether genetic... 
HEALTHY FAMILIES | RISK-FACTORS | BLOOD-GROUPS | PLASMA-LEVELS | SUSCEPTIBILITY | NEUROSCIENCES | CORONARY-ARTERY-DISEASE | HERITABILITY | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | ATRIAL-FIBRILLATION | FACTOR-VII | Humans | Middle Aged | Stroke - diagnosis