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American Journal Of Human Genetics
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasetsAmerican journal of human genetics, 2023-04, Vol.110 (4), p.575-591 [Peer Reviewed Journal]2023 American Society of Human Genetics ;Copyright © 2023 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2023 American Society of Human Genetics. 2023 American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2023.03.007 ;PMID: 37028392Full text available |
| 2 |
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15 years of GWAS discovery: Realizing the promiseAmerican journal of human genetics, 2023-02, Vol.110 (2), p.179-194 [Peer Reviewed Journal]2022 American Society of Human Genetics ;Copyright © 2022 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2022 American Society of Human Genetics. 2022 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2022.12.011 ;PMID: 36634672Full text available |
| 3 |
Material Type: Article
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Leveraging Polygenic Functional Enrichment to Improve GWAS PowerAmerican journal of human genetics, 2019-01, Vol.104 (1), p.65-75 [Peer Reviewed Journal]2018 American Society of Human Genetics ;Copyright © 2018 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2018 American Society of Human Genetics. 2018 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2018.11.008 ;PMID: 30595370Full text available |
| 4 |
Material Type: Article
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipidsAmerican journal of human genetics, 2022-08, Vol.109 (8), p.1366-1387 [Peer Reviewed Journal]2022 American Society of Human Genetics ;Copyright © 2022 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2022 American Society of Human Genetics. 2022 American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2022.06.012 ;PMID: 35931049Full text available |
| 5 |
Material Type: Article
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Fast two-stage phasing of large-scale sequence dataAmerican journal of human genetics, 2021-10, Vol.108 (10), p.1880-1890 [Peer Reviewed Journal]2021 American Society of Human Genetics ;Copyright © 2021 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2021 American Society of Human Genetics. 2021 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2021.08.005 ;PMID: 34478634Full text available |
| 6 |
Material Type: Article
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Extreme Polygenicity of Complex Traits Is Explained by Negative SelectionAmerican journal of human genetics, 2019-09, Vol.105 (3), p.456-476 [Peer Reviewed Journal]2019 American Society of Human Genetics ;Copyright © 2019 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2019 American Society of Human Genetics. 2019 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2019.07.003 ;PMID: 31402091Full text available |
| 7 |
Material Type: Article
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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk ScoresAmerican journal of human genetics, 2015-10, Vol.97 (4), p.576-592 [Peer Reviewed Journal]2015 The American Society of Human Genetics ;Copyright © 2015 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Oct 1, 2015 ;2015 by The American Society of Human Genetics. All rights reserved. 2015 The American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2015.09.001 ;PMID: 26430803Full text available |
| 8 |
Material Type: Article
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Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human TraitsAmerican journal of human genetics, 2014-04, Vol.94 (4), p.559-573 [Peer Reviewed Journal]2014 The American Society of Human Genetics ;Copyright © 2014 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Apr 3, 2014 ;2014 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2014 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2014.03.004 ;PMID: 24702953Full text available |
| 9 |
Material Type: Article
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Genetic Consequences of the Transatlantic Slave Trade in the AmericasAmerican journal of human genetics, 2020-08, Vol.107 (2), p.265-277 [Peer Reviewed Journal]2020 The Authors ;Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved. ;2020 The Authors 2020 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2020.06.012 ;PMID: 32707084Full text available |
| 10 |
Material Type: Article
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Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer SubtypesAmerican journal of human genetics, 2019-01, Vol.104 (1), p.21-34 [Peer Reviewed Journal]2018 The Authors ;Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved. ;2018 The Authors 2018 ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2018.11.002 ;PMID: 30554720Full text available |
| 11 |
Material Type: Article
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Meta-analysis of Correlated Traits via Summary Statistics from GWASs with an Application in HypertensionAmerican journal of human genetics, 2015-01, Vol.96 (1), p.21-36 [Peer Reviewed Journal]2015 The American Society of Human Genetics ;Copyright © 2015 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Jan 8, 2015 ;2015 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2015 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2014.11.011 ;PMID: 25500260Full text available |
| 12 |
Material Type: Article
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Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNAAmerican journal of human genetics, 2016-01, Vol.98 (1), p.58-74 [Peer Reviewed Journal]2016 The American Society of Human Genetics ;Copyright © 2016 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Jan 7, 2016 ;2016 by The American Society of Human Genetics. All rights reserved. 2016 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2015.11.023 ;PMID: 26749308Full text available |
| 13 |
Material Type: Article
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Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent LociAmerican journal of human genetics, 2020-03, Vol.106 (3), p.327-337 [Peer Reviewed Journal]2020 American Society of Human Genetics ;Copyright © 2020 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2020 American Society of Human Genetics. 2020 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2020.01.017 ;PMID: 32059762Full text available |
| 14 |
Material Type: Article
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Testing in Microbiome-Profiling Studies with MiRKAT, the Microbiome Regression-Based Kernel Association TestAmerican journal of human genetics, 2015-05, Vol.96 (5), p.797-807 [Peer Reviewed Journal]2015 The American Society of Human Genetics ;Copyright © 2015 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press May 7, 2015 ;2015 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2015 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2015.04.003 ;PMID: 25957468Full text available |
| 15 |
Material Type: Article
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Actionable, Pathogenic Incidental Findings in 1,000 Participants’ ExomesAmerican journal of human genetics, 2013-10, Vol.93 (4), p.631-640 [Peer Reviewed Journal]2013 The American Society of Human Genetics ;Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Oct 3, 2013 ;2013 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2013 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2013.08.006 ;PMID: 24055113Full text available |
| 16 |
Material Type: Article
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Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General PopulationAmerican journal of human genetics, 2019-11, Vol.105 (5), p.921-932 [Peer Reviewed Journal]2019 The Authors ;Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved. ;2019 The Authors 2019 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2019.09.016 ;PMID: 31607426Full text available |
| 17 |
Material Type: Article
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Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male InfertilityAmerican journal of human genetics, 2016-08, Vol.99 (2), p.489-500 [Peer Reviewed Journal]2016 American Society of Human Genetics ;Copyright © 2016 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Aug 4, 2016 ;Distributed under a Creative Commons Attribution 4.0 International License ;2016 American Society of Human Genetics. 2016 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2016.06.022 ;PMID: 27486783Full text available |
| 18 |
Material Type: Article
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Haplotype Estimation Using Sequencing ReadsAmerican journal of human genetics, 2013-10, Vol.93 (4), p.687-696 [Peer Reviewed Journal]2013 The American Society of Human Genetics ;Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Oct 3, 2013 ;2013 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2013 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2013.09.002 ;PMID: 24094745Full text available |
| 19 |
Material Type: Article
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The omnigenic model and polygenic prediction of complex traitsAmerican journal of human genetics, 2021-09, Vol.108 (9), p.1558-1563 [Peer Reviewed Journal]2021 American Society of Human Genetics ;Copyright © 2021 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2021 American Society of Human Genetics. 2021 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2021.07.003 ;PMID: 34331855Full text available |
| 20 |
Material Type: Article
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Introgression of Neandertal- and Denisovan-like Haplotypes Contributes to Adaptive Variation in Human Toll-like ReceptorsAmerican journal of human genetics, 2016-01, Vol.98 (1), p.22-33 [Peer Reviewed Journal]2016 The Authors ;Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Jan 7, 2016 ;2016 The Authors 2016 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2015.11.015 ;PMID: 26748514Full text available |
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