Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Article
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Using electronic patient records to discover disease correlations and stratify patient cohortsPLoS computational biology, 2011-08, Vol.7 (8), p.e1002141-e1002141 [Peer Reviewed Journal]Roque et al. 2011 ;2011 Roque 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: Roque FS, Jensen PB, Schmock H, Dalgaard M, Andreatta M, et al. (2011) Using Electronic Patient Records to Discover Disease Correlations and Stratify Patient Cohorts. PLoS Comput Biol 7(8): e1002141. doi:10.1371/journal.pcbi.1002141 ;ISSN: 1553-7358 ;ISSN: 1553-734X ;EISSN: 1553-7358 ;DOI: 10.1371/journal.pcbi.1002141 ;PMID: 21901084Full text available |
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Material Type: Article
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Methods of integrating data to uncover genotype-phenotype interactionsNature reviews. Genetics, 2015-02, Vol.16 (2), p.85-97 [Peer Reviewed Journal]COPYRIGHT 2015 Nature Publishing Group ;COPYRIGHT 2015 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2015 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/nrg3868 ;PMID: 25582081Full text available |
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Material Type: Article
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From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS DiscoveriesFrontiers in genetics, 2021-09, Vol.12, p.713230-713230 [Peer Reviewed Journal]Copyright © 2021 Li and Ritchie. 2021 Li and Ritchie ;ISSN: 1664-8021 ;EISSN: 1664-8021 ;DOI: 10.3389/fgene.2021.713230 ;PMID: 34659337Full text available |
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Material Type: Article
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Electronic health records and polygenic risk scores for predicting disease riskNature reviews. Genetics, 2020-08, Vol.21 (8), p.493-502 [Peer Reviewed Journal]COPYRIGHT 2020 Nature Publishing Group ;Springer Nature Limited 2020. ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-020-0224-1 ;PMID: 32235907Full text available |
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Material Type: Article
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The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS eraHuman genetics, 2012-10, Vol.131 (10), p.1615-1626 [Peer Reviewed Journal]The Author(s) 2012 ;COPYRIGHT 2012 Springer ;Springer-Verlag 2012 ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-012-1221-z ;PMID: 22923055Full text available |
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Material Type: Article
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Defining the role of common variation in the genomic and biological architecture of adult human heightNature genetics, 2014-11, Vol.46 (11), p.1173-1186 [Peer Reviewed Journal]COPYRIGHT 2014 Nature Publishing Group ;COPYRIGHT 2014 Nature Publishing Group ;Wageningen University & Research ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3097 ;PMID: 25282103Full text available |
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Material Type: Book
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Pacific Symposium on Biocomputing 2023: Kohala Coast, Hawaii, USA, 3 – 7 January 2023ISBN: 9789811270604 ;ISBN: 9811270600 ;DOI: 10.1142/13257Digital Resources/Online E-Resources |
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Material Type: Article
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A first update on mapping the human genetic architecture of COVID-19Nature (London), 2022-08, Vol.608 (7921), p.E1-E10 [Peer Reviewed Journal]Copyright Nature Publishing Group Aug 4, 2022 ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-022-04826-7 ;PMID: 35922517Full text available |
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Material Type: Article
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The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studiesBMC genomics, 2011-01, Vol.4 (1), p.13-13, Article 13 [Peer Reviewed Journal]COPYRIGHT 2011 BioMed Central Ltd. ;COPYRIGHT 2011 BioMed Central Ltd. ;2011 McCarty et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2011 McCarty et al; licensee BioMed Central Ltd. 2011 McCarty et al; licensee BioMed Central Ltd. ;ISSN: 1755-8794 ;ISSN: 1471-2164 ;EISSN: 1755-8794 ;EISSN: 1471-2164 ;DOI: 10.1186/1755-8794-4-13 ;PMID: 21269473Full text available |
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10 |
Material Type: Article
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Genetics of height and risk of atrial fibrillation: A Mendelian randomization studyPLoS medicine, 2020-10, Vol.17 (10), p.e1003288-e1003288 [Peer Reviewed Journal]COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Levin 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. ;2020 Levin et al 2020 Levin et al ;ISSN: 1549-1676 ;ISSN: 1549-1277 ;EISSN: 1549-1676 ;DOI: 10.1371/journal.pmed.1003288 ;PMID: 33031386Full text available |
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Material Type: Article
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PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associationsBioinformatics, 2010-05, Vol.26 (9), p.1205-1210 [Peer Reviewed Journal]The Author(s) 2010. Published by Oxford University Press. 2010 ;ISSN: 1367-4803 ;EISSN: 1460-2059 ;EISSN: 1367-4811 ;DOI: 10.1093/bioinformatics/btq126 ;PMID: 20335276Full text available |
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12 |
Material Type: Article
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Inactivating Variants in ANGPTL4 and Risk of Coronary Artery DiseaseThe New England journal of medicine, 2016-03, Vol.374 (12), p.1123-1133 [Peer Reviewed Journal]Copyright © 2016 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1510926 ;PMID: 26933753Full text available |
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Material Type: Article
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Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE studyPLoS biology, 2013-09, Vol.11 (9), p.e1001661-e1001661 [Peer Reviewed Journal]2013 ;2013 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: Citation: Carlson CS, Matise TC, North KE, Haiman CA, Fesinmeyer MD, et al. (2013) Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study. PLoS Biol 11(9): e1001661. doi:10.1371/journal.pbio.1001661 ;ISSN: 1545-7885 ;ISSN: 1544-9173 ;EISSN: 1545-7885 ;DOI: 10.1371/journal.pbio.1001661 ;PMID: 24068893Full text available |
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Material Type: Article
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Disrupting upstream translation in mRNAs is associated with human diseaseNature communications, 2021-03, Vol.12 (1), p.1515-14, Article 1515 [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/s41467-021-21812-1 ;PMID: 33750777Full text available |
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Material Type: Article
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The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and futureGenetics in medicine, 2013-10, Vol.15 (10), p.761-771 [Peer Reviewed Journal]2013 The Author(s) ;The Author(s) 2013. This work is published under http://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 © 2013 American College of Medical Genetics and Genomics 2013 American College of Medical Genetics and Genomics ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2013.72 ;PMID: 23743551Full text available |
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16 |
Material Type: Article
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Harmonizing Clinical Sequencing and Interpretation for the eMERGE III NetworkAmerican journal of human genetics, 2019-09, Vol.105 (3), p.588-605 [Peer Reviewed Journal]2019 American Society of Human Genetics ;Copyright © 2019 American Society of Human Genetics. 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.2019.07.018 ;PMID: 31447099Full text available |
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Material Type: Article
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Using Biological Knowledge to Uncover the Mystery in the Search for Epistasis in Genome‐Wide Association StudiesAnnals of human genetics, 2011-01, Vol.75 (1), p.172-182 [Peer Reviewed Journal]2010 The Author Annals of Human Genetics © 2010 Blackwell Publishing Ltd/University College London ;2010 The Author Annals of Human Genetics © 2010 Blackwell Publishing Ltd/University College London. ;ISSN: 0003-4800 ;EISSN: 1469-1809 ;DOI: 10.1111/j.1469-1809.2010.00630.x ;PMID: 21158748Full text available |
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Material Type: Article
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Genetic Determinants of Response to Warfarin during Initial AnticoagulationThe New England journal of medicine, 2008-03, Vol.358 (10), p.999-1008 [Peer Reviewed Journal]Copyright © 2008 Massachusetts Medical Society. All rights reserved. ;2008 INIST-CNRS ;Copyright 2008 Massachusetts Medical Society. ;Copyright © 2008 Massachusetts Medical Society. 2008 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa0708078 ;PMID: 18322281 ;CODEN: NEJMAGFull text available |
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Material Type: Article
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Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approachBMC bioinformatics, 2022-10, Vol.23 (1), p.420-420, Article 420 [Peer Reviewed Journal]2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;2022. 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) 2022 ;ISSN: 1471-2105 ;EISSN: 1471-2105 ;DOI: 10.1186/s12859-022-04977-4 ;PMID: 36229773Full text available |
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Material Type: Article
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Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetesPLoS genetics, 2014-08, Vol.10 (8), p.e1004517-e1004517 [Peer Reviewed Journal]COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 ;2014 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: Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, et al. (2014) Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes. PLoS Genet 10(8): e1004517. doi:10.1371/journal.pgen.1004517 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1004517 ;PMID: 25102180Full text available |