Results 1 - 20 of 83 for All Library Resources
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Efficient multiple-trait association and estimation of genetic correlation using the matrix-variate linear mixed modelGenetics (Austin), 2015-05, Vol.200 (1), p.59-68 [Peer Reviewed Journal]Copyright © 2015 by the Genetics Society of America. ;Copyright Genetics Society of America May 2015 ;Copyright © 2015 by the Genetics Society of America 2015 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.114.171447 ;PMID: 25724382 ;CODEN: GENTAEFull text available |
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Epigenome-Wide Association of Liver Methylation Patterns and Complex Metabolic Traits in MiceCell metabolism, 2015-06, Vol.21 (6), p.905-917 [Peer Reviewed Journal]2015 Elsevier Inc. ;Copyright © 2015 Elsevier Inc. All rights reserved. ;2015 Published by Elsevier Inc. 2015 ;ISSN: 1550-4131 ;EISSN: 1932-7420 ;DOI: 10.1016/j.cmet.2015.04.025 ;PMID: 26039453Full text available |
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DeepNull models non-linear covariate effects to improve phenotypic prediction and association powerNature communications, 2022-01, Vol.13 (1), p.241-241, Article 241 [Peer Reviewed Journal]2022. The Author(s). ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-27930-0 ;PMID: 35017556Full text available |
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Disease risk scores for skin cancersNature communications, 2021-01, Vol.12 (1), p.160-13, Article 160 [Peer Reviewed Journal]The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-20246-5 ;PMID: 33420020Full text available |
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An atlas of genetic influences on osteoporosis in humans and miceNature genetics, 2019-02, Vol.51 (2), p.258-266 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2019 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0302-x ;PMID: 30598549Full text available |
| 6 |
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Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathwaysNature genetics, 2019-03, Vol.51 (3), p.394-403 [Peer Reviewed Journal]Copyright Nature Publishing Group Mar 2019 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0333-3 ;PMID: 30804565Full text available |
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Multi-trait analysis of genome-wide association summary statistics using MTAGNature genetics, 2018-02, Vol.50 (2), p.229-237 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2018 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-017-0009-4 ;PMID: 29292387Full text available |
| 8 |
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Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disordersNature neuroscience, 2018-12, Vol.21 (12), p.1656-1669 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2018 ;ISSN: 1097-6256 ;ISSN: 1546-1726 ;EISSN: 1546-1726 ;DOI: 10.1038/s41593-018-0275-1 ;PMID: 30482948Full text available |
| 9 |
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Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathwaysNature genetics, 2018-07, Vol.50 (7), p.920-927 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2018 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0151-7 ;PMID: 29942085Full text available |
| 10 |
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Gene expression imputation identifies candidate genes and susceptibility loci associated with cutaneous squamous cell carcinomaNature communications, 2018-10, Vol.9 (1), p.4264-9, Article 4264 [Peer Reviewed Journal]2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-06149-6 ;PMID: 30323283Full text available |
| 11 |
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Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathwaysNature communications, 2018-04, Vol.9 (1), p.1470-10, Article 1470 [Peer Reviewed Journal]2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-03819-3 ;PMID: 29662059Full text available |
| 12 |
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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol useNature genetics, 2019-02, Vol.51 (2), p.237-244 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2019 ;info:eu-repo/semantics/openAccess ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0307-5 ;PMID: 30643251Full text available |
| 13 |
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Quantifying the uncertainty in heritabilityJournal of human genetics, 2014-05, Vol.59 (5), p.269-275 [Peer Reviewed Journal]The Author(s) 2014. This work is published under https://creativecommons.org/licenses/by-nc-nd/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2014 The Japan Society of Human Genetics 2014 The Japan Society of Human Genetics ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2014.15 ;PMID: 24670270Full text available |
| 14 |
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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosisNature communications, 2019-10, Vol.10 (1), p.4857-11, Article 4857 [Peer Reviewed Journal]2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019. corrected publication 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019, corrected publication 2022 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-12536-4 ;PMID: 31649266Full text available |
| 15 |
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Genetic analyses identify widespread sex-differential participation biasNature genetics, 2021-05, Vol.53 (5), p.663-671 [Peer Reviewed Journal]COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group May 2021 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00846-7 ;PMID: 33888908Full text available |
| 16 |
Material Type: Article
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Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's diseaseNature genetics, 2020-05, Vol.52 (5), p.482-493 [Peer Reviewed Journal]COPYRIGHT 2020 Nature Publishing Group ;COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group May 2020 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-0610-9 ;PMID: 32341526Full text available |
| 17 |
Material Type: Article
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Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysisLancet neurology, 2017-11, Vol.16 (11), p.898-907 [Peer Reviewed Journal]2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license ;Copyright © 2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved. ;Copyright Elsevier Limited Nov 1, 2017 ;Distributed under a Creative Commons Attribution 4.0 International License ;2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license 2017 ;ISSN: 1474-4422 ;EISSN: 1474-4465 ;DOI: 10.1016/S1474-4422(17)30327-7 ;PMID: 29029846Full text available |
| 18 |
Material Type: Article
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Genetic determinants of daytime napping and effects on cardiometabolic healthNature communications, 2021-02, Vol.12 (1), p.900-900, Article 900 [Peer Reviewed Journal]The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-20585-3 ;PMID: 33568662Full text available |
| 19 |
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 |
| 20 |
Material Type: Article
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Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathwaysNature genetics, 2022-08, Vol.54 (8), p.1125-1132 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Aug 2022 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01124-w ;PMID: 35835914Full text available |
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