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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Colocalization of GWAS and eQTL Signals Detects Target GenesAmerican journal of human genetics, 2016-12, Vol.99 (6), p.1245-1260 [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 Dec 1, 2016 ;2016 American Society of Human Genetics. 2016 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2016.10.003 ;PMID: 27866706Full text available |
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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variationNature genetics, 2018-07, Vol.50 (7), p.956-967 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2018 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0154-4 ;PMID: 29955180Full text available |
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Exploiting the GTEx resources to decipher the mechanisms at GWAS lociGenome Biology, 2021-01, Vol.22 (1), p.49-49, Article 49 [Peer Reviewed Journal]2021. This work is licensed 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: 1474-760X ;ISSN: 1474-7596 ;EISSN: 1474-760X ;DOI: 10.1186/s13059-020-02252-4 ;PMID: 33499903Full text available |
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The Lin28/let-7 Axis Regulates Glucose MetabolismCell, 2011-09, Vol.147 (1), p.81-94 [Peer Reviewed Journal]2011 Elsevier Inc. ;Copyright © 2011 Elsevier Inc. All rights reserved. ;2011 Elsevier Inc. All rights reserved. 2011 ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2011.08.033 ;PMID: 21962509Full text available |
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Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the MicrovasculatureCirculation (New York, N.Y.), 2022-01, Vol.145 (2), p.134-150 [Peer Reviewed Journal]2021 The Authors. 2021 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.121.057709 ;PMID: 34743558Full text available |
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Machine Learning-Derived Baseline Visual Field Patterns Predict Future Glaucoma Onset in the Ocular Hypertension Treatment StudyInvestigative ophthalmology & visual science, 2024-02, Vol.65 (2), p.35-35 [Peer Reviewed Journal]Copyright 2024 The Authors 2024 ;ISSN: 0146-0404 ;EISSN: 1552-5783 ;DOI: 10.1167/iovs.65.2.35 ;PMID: 38393715Full text available |
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TIE1 and TEK signalling, intraocular pressure, and primary open-angle glaucoma: a Mendelian randomization studyJournal of translational medicine, 2023-11, Vol.21 (1), p.847-847, Article 847 [Peer Reviewed Journal]2023. Crown. ;COPYRIGHT 2023 BioMed Central Ltd. ;2023. This work is licensed 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. ;ISSN: 1479-5876 ;EISSN: 1479-5876 ;DOI: 10.1186/s12967-023-04737-9 ;PMID: 37996923Full text available |
| 8 |
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Widespread Allelic Heterogeneity in Complex TraitsAmerican journal of human genetics, 2017-05, Vol.100 (5), p.789-802 [Peer Reviewed Journal]2017 ;Copyright © 2017. Published by Elsevier Inc. ;2017. 2017 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2017.04.005 ;PMID: 28475861Full text available |
| 9 |
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Transcriptomic analysis of the ocular posterior segment completes a cell atlas of the human eyeProceedings of the National Academy of Sciences - PNAS, 2023-08, Vol.120 (34), p.e2306153120-e2306153120 [Peer Reviewed Journal]Copyright National Academy of Sciences Aug 22, 2023 ;Copyright © 2023 the Author(s). Published by PNAS. 2023 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.2306153120 ;PMID: 37566633Full text available |
| 10 |
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QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degenerationNature communications, 2024-03, Vol.15 (1), p.1972-1972 [Peer Reviewed Journal]2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024. 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. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-46063-8 ;PMID: 38438351Full text available |
| 11 |
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Interaction of background genetic risk, psychotropic medications, and primary angle closure glaucoma in the UK BiobankPloS one, 2022-06, Vol.17 (6), p.e0270530 [Peer Reviewed Journal]COPYRIGHT 2022 Public Library of Science ;2022 Sekimitsu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 Sekimitsu et al 2022 Sekimitsu et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0270530 ;PMID: 35763501Full text available |
| 12 |
Material Type: Article
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Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseasesScientific reports, 2015-10, Vol.5 (1), p.15145-15145, Article 15145 [Peer Reviewed Journal]Copyright Nature Publishing Group Oct 2015 ;info:eu-repo/semantics/openAccess © Nature Publishing Group. http://www.nature.com/articles/srep15145/nThis work is licensed under a Creative Commons Attribution 4.0 International License. http://creativecommons.org/licenses/by/4.0/ ;Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep15145 ;PMID: 26477495Full text available |
| 13 |
Material Type: Article
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Sharing and Specificity of Co-expression Networks across 35 Human TissuesPLoS computational biology, 2015-05, Vol.11 (5), p.e1004220-e1004220 [Peer Reviewed Journal]COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Pierson et al 2015 Pierson et al ;2015 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Pierson E, the GTEx Consortium, Koller D, Battle A, Mostafavi S (2015) Sharing and Specificity of Co-expression Networks across 35 Human Tissues. PLoS Comput Biol 11(5): e1004220. doi:10.1371/journal.pcbi.1004220 ;ISSN: 1553-7358 ;ISSN: 1553-734X ;EISSN: 1553-7358 ;DOI: 10.1371/journal.pcbi.1004220 ;PMID: 25970446Full text available |
| 14 |
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Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart developmentProceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (35), p.14035-14040 [Peer Reviewed Journal]copyright © 1993-2008 National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Aug 28, 2012 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1210730109 ;PMID: 22904188Full text available |
| 15 |
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Systems Genetics Analysis of Genome-Wide Association Study Reveals Novel Associations Between Key Biological Processes and Coronary Artery DiseaseArteriosclerosis, thrombosis, and vascular biology, 2015-07, Vol.35 (7), p.1712-1722 [Peer Reviewed Journal]2015 American Heart Association, Inc. ;ISSN: 1079-5642 ;EISSN: 1524-4636 ;DOI: 10.1161/ATVBAHA.115.305513 ;PMID: 25977570Full text available |
| 16 |
Material Type: Article
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Predicting molecular mechanisms of hereditary diseases by using their tissue‐selective manifestationMolecular systems biology, 2023-08, Vol.19 (8), p.e11407-n/a [Peer Reviewed Journal]2023 The Authors. Published under the terms of the CC BY 4.0 license. ;2023. 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. ;ISSN: 1744-4292 ;EISSN: 1744-4292 ;DOI: 10.15252/msb.202211407 ;PMID: 37232043Full text available |
| 17 |
Material Type: Article
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ForestPMPlot: A Flexible Tool for Visualizing Heterogeneity Between Studies in Meta-analysisG3 : genes - genomes - genetics, 2016-07, Vol.6 (7), p.1793-1798 [Peer Reviewed Journal]Copyright © 2016 Kang et al. ;Copyright © 2016 Kang 2016 ;ISSN: 2160-1836 ;EISSN: 2160-1836 ;DOI: 10.1534/g3.116.029439 ;PMID: 27194809Full text available |
| 18 |
Material Type: Article
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Identification of novel type 2 diabetes candidate genes involved in the crosstalk between the mitochondrial and the insulin signaling systemsPLoS genetics, 2012-12, Vol.8 (12), p.e1003046-e1003046 [Peer Reviewed Journal]COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Mercader et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Mercader JM, Puiggros M, Segrè AV, Planet E, Sorianello E, et al. (2012) Identification of Novel Type 2 Diabetes Candidate Genes Involved in the Crosstalk between the Mitochondrial and the Insulin Signaling Systems. PLoS Genet 8(12): e1003046. doi:10.1371/journal.pgen.1003046 ;cc-by (c) Mercader, Josep M. et al., 2012 info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/3.0/es ;2012 Mercader et al 2012 Mercader et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003046 ;PMID: 23236286Full text available |
| 19 |
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Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traitsPLoS genetics, 2010-08, Vol.6 (8), p.e1001058 [Peer Reviewed Journal]COPYRIGHT 2010 Public Library of Science ;COPYRIGHT 2010 Public Library of Science ;Segrè et al. 2010 ;2010 Segrè et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Segrè AV, DIAGRAM Consortium, MAGIC investigators, Groop L, Mootha VK, et al. (2010) Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits. PLoS Genet 6(8): e1001058. doi:10.1371/journal.pgen.1001058 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1001058 ;PMID: 20714348Full text available |
| 20 |
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Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseasesScientific reports, 2016-01, Vol.6, p.19384-19384 [Peer Reviewed Journal]Copyright Nature Publishing Group Jan 2016 ;Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;EISSN: 2045-2322 ;DOI: 10.1038/srep19384 ;PMID: 26795431Full text available |
Results 1 - 20 of 55 for All Library Resources
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