Results 1 - 20 of 17,811 for All Library Resources
Sorted by:
Sorted by:
RelevanceOr hit Enter to replace sort method
- Relevance
- Date-newest
- Date-oldest
- Popularity
- Author
- Title
Show only
- Peer-reviewed Journals (16,801)
Refined by:
subject:
Risk Factors
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Article
|
|
Identification of common genetic risk variants for autism spectrum disorderNature genetics, 2019-03, Vol.51 (3), p.431-444 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2019 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0344-8 ;PMID: 30804558Full text available |
| 2 |
Material Type: Article
|
|
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translationNature genetics, 2022-05, Vol.54 (5), p.560-572 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group May 2022 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01058-3 ;PMID: 35551307Full text available |
| 3 |
Material Type: Article
|
|
Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association StudiesThe American journal of psychiatry, 2019-03, Vol.176 (3), p.217-227 [Peer Reviewed Journal]Copyright © 2019 by the American Psychiatric Association 2019 ;Copyright American Psychiatric Association Mar 2019 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-953X ;EISSN: 1535-7228 ;DOI: 10.1176/appi.ajp.2018.18070857 ;PMID: 30818990Full text available |
| 4 |
Material Type: Article
|
|
Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial)Circulation (New York, N.Y.), 2016-03, Vol.133 (12), p.1181-1188 [Peer Reviewed Journal]2016 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2016 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.115.020109 ;PMID: 26915630Full text available |
| 5 |
Material Type: Article
|
|
The Missing Diversity in Human Genetic StudiesCell, 2019-03, Vol.177 (1), p.26-31 [Peer Reviewed Journal]2019 ;Copyright © 2019. Published by Elsevier Inc. ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2019.02.048 ;PMID: 30901543Full text available |
| 6 |
Material Type: Article
|
|
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutationsNature genetics, 2018-09, Vol.50 (9), p.1219-1224 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0183-z ;PMID: 30104762Full text available |
| 7 |
Material Type: Article
|
|
Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseasesNature genetics, 2020-10, Vol.52 (10), p.1122-1131 [Peer Reviewed Journal]COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2020 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-0682-6 ;PMID: 32895551Full text available |
| 8 |
Material Type: Article
|
|
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's diseaseNature genetics, 2021-09, Vol.53 (9), p.1276-1282 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to Springer Nature America, Inc. ;COPYRIGHT 2021 Nature Publishing Group ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00921-z ;PMID: 34493870Full text available |
| 9 |
Material Type: Article
|
|
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressionNature genetics, 2018-05, Vol.50 (5), p.668-681 [Peer Reviewed Journal]Copyright Nature Publishing Group May 2018 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0090-3 ;PMID: 29700475Full text available |
| 10 |
Material Type: Article
|
|
Variation in FTO contributes to childhood obesity and severe adult obesityNature genetics, 2007-06, Vol.39 (6), p.724-726 [Peer Reviewed Journal]COPYRIGHT 2007 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2007 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng2048 ;PMID: 17496892Full text available |
| 11 |
Material Type: Article
|
|
Gene expression elucidates functional impact of polygenic risk for schizophreniaNature neuroscience, 2016-11, Vol.19 (11), p.1442-1453 [Peer Reviewed Journal]COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2016 ;ISSN: 1097-6256 ;ISSN: 1546-1726 ;EISSN: 1546-1726 ;DOI: 10.1038/nn.4399 ;PMID: 27668389 ;CODEN: NANEFNFull text available |
| 12 |
Material Type: Article
|
|
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scoresNature genetics, 2022-04, Vol.54 (4), p.450-458 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Apr 2022 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01036-9 ;PMID: 35393596Full text available |
| 13 |
Material Type: Article
|
|
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderNature neuroscience, 2017-04, Vol.20 (4), p.602-611 [Peer Reviewed Journal]COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2017 ;ISSN: 1097-6256 ;EISSN: 1546-1726 ;DOI: 10.1038/nn.4524 ;PMID: 28263302 ;CODEN: NANEFNFull text available |
| 14 |
Material Type: Article
|
|
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analysesNature genetics, 2016-06, Vol.48 (6), p.624-633 [Peer Reviewed Journal]COPYRIGHT 2016 Nature Publishing Group ;COPYRIGHT 2016 Nature Publishing Group ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3552 ;PMID: 27089181Full text available |
| 15 |
Material Type: Article
|
|
Genome-wide association study identifies 30 loci associated with bipolar disorderNature genetics, 2019-05, Vol.51 (5), p.793-803 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group May 2019 ;info:eu-repo/semantics/openAccess ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0397-8 ;PMID: 31043756Full text available |
| 16 |
Material Type: Article
|
|
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseNature genetics, 2014-09, Vol.46 (9), p.989-993 [Peer Reviewed Journal]COPYRIGHT 2014 Nature Publishing Group ;COPYRIGHT 2014 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2014 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3043 ;PMID: 25064009Full text available |
| 17 |
Material Type: Article
|
|
Genetic polymorphisms in DNA repair genes XRCC1 and 3 are associated with increased risk of breast cancer in Bangladeshi populationBreast cancer research and treatment, 2020-08, Vol.182 (3), p.739-750 [Peer Reviewed Journal]Springer Science+Business Media, LLC, part of Springer Nature 2020 ;Springer Science+Business Media, LLC, part of Springer Nature 2020. ;ISSN: 0167-6806 ;EISSN: 1573-7217 ;DOI: 10.1007/s10549-020-05738-8 ;PMID: 32562117Full text available |
| 18 |
Material Type: Article
|
|
Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically characterised cohortJournal of hepatology, 2020-09, Vol.73 (3), p.505-515 [Peer Reviewed Journal]Attribution - NonCommercial - NoDerivatives ;ISSN: 0168-8278 ;ISSN: 1600-0641 ;EISSN: 1600-0641 ;DOI: 10.1016/j.jhep.2020.04.003 ;PMID: 32298765Digital Resources/Online E-Resources |
| 19 |
Material Type: Article
|
|
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populationsCell, 2021-09, Vol.184 (18), p.4784-4818.e17 [Peer Reviewed Journal]2021 The Authors ;Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved. ;info:eu-repo/semantics/openAccess ;2021 The Authors 2021 ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2021.07.038 ;PMID: 34450027Full text available |
| 20 |
Material Type: Article
|
|
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetesProceedings of the National Academy of Sciences - PNAS, 2014-09, Vol.111 (36), p.13127-13132 [Peer Reviewed Journal]copyright © 1993–2008 National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Sep 9, 2014 ;ISSN: 0027-8424 ;ISSN: 1091-6490 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1410428111 ;PMID: 25157153Full text available |
Results 1 - 20 of 17,811 for All Library Resources
Sorted by:
Sorted by:
RelevanceOr hit Enter to replace sort method
- Relevance
- Date-newest
- Date-oldest
- Popularity
- Author
- Title
Personalize your results
Refine Search Results
Expand My Results
Show only
- Peer-reviewed Journals (16,801)
Refine My Results
Creation Date
- Before 2003 (106)
- 2003 To 2007 (1,267)
- 2008 To 2012 (5,524)
- 2013 To 2018 (7,630)
- After 2018 (3,285)
-
More options
New Records
- New From Last Week (11)
- New From Last Month (72)
- New From Last 3 Month (176)
-
More options
Subject
- Humans (17,612)
- Science & Technology (16,681)
- Life Sciences & Biomedicine (14,544)
- Polymorphism, Single Nucleotide (13,170)
- Female (12,114)
- Male (10,679)
- Genetic Predisposition To Disease (8,899)
- Middle Aged (8,720)
- Case-Control Studies (6,979)
- Genotype (6,766)
- Adult (6,668)
- Aged (5,875)
- Genetic Aspects (5,601)
- Polymorphism, Single Nucleotide - Genetics (4,553)
- Polymorphism (4,368)
- Alleles (4,175)
- Genetics & Heredity (3,878)
- Single-Nucleotide Polymorphism (3,823)
- Gene Frequency (3,679)
-
More options
Databases
- MEDLINE (17,491)
- ProQuest Central (11,766)
- GFMER Free Medical Journals (9,423)
- PubMed Central (8,048)
- DOAJ Directory of Open Access Journals (7,338)
- ROAD: Directory of Open Access Scholarly Resources (6,264)
- HighWire Press (Free Journals) (2,302)
- Springer Nature OA/Free Journals (2,217)
- Public Library of Science (PLoS) (1,981)
- Nature Free (1,716)
- SWEPUB Freely available online (883)
- ProQuest One Psychology (858)
- Wiley Online Library Open Access (772)
- SAGE Open Access Journals (459)
- Journals@Ovid Open Access Journal Collection Rolling (408)
- IngentaConnect Free/Open Access Journals (358)
- Free E- Journals (348)
- Mary Ann Liebert Online - Open Access (320)
- Cambridge University Library IR - DSpace@Cambridge (210)
- Hyper Article en Ligne (HAL) (Open Access) (182)
-
More options
Language
Journal Title
- Bmc Medical Genetics (429)
- Cancer Epidemiology, Biomarkers & Prevention (276)
- Genes And Immunity (253)
- Genetics And Molecular Research (248)
- Molecular Biology Reports (373)
- Molecular Psychiatry (274)
- Nature Genetics (547)
- Plos One (1,651)
- Scientific Reports (340)
- Tumor Biology (346)
-
More options
|
||||
 |
INSPIRE LIBRARY - TON DUC THANG UNIVERSITY |  |
(84-028) 37 755 057 | Feedback |
| 19 Nguyen Huu Tho St. Dist.7, HCM |  |
thuvien@tdtu.edu.vn | ||