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Results 21 - 40 of 10,392  for All Library Resources

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21
The biological and clinical significance of emerging SARS-CoV-2 variants
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The biological and clinical significance of emerging SARS-CoV-2 variants

Nature reviews. Genetics, 2021-12, Vol.22 (12), p.757-773 [Peer Reviewed Journal]

2021. Springer Nature Limited. ;COPYRIGHT 2021 Nature Publishing Group ;Springer Nature Limited 2021. ;Springer Nature Limited 2021 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-021-00408-x ;PMID: 34535792

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22
Mendelian randomization accounting for correlated and uncorrelated pleiotropic effects using genome-wide summary statistics
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Mendelian randomization accounting for correlated and uncorrelated pleiotropic effects using genome-wide summary statistics

Nature genetics, 2020-07, Vol.52 (7), p.740-747 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2020 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-0631-4 ;PMID: 32451458

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23
Activity-by-contact model of enhancer-promoter regulation from thousands of CRISPR perturbations
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Activity-by-contact model of enhancer-promoter regulation from thousands of CRISPR perturbations

Nature genetics, 2019-12, Vol.51 (12), p.1664-1669 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2019 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0538-0 ;PMID: 31784727

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24
Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay
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Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay

PLoS genetics, 2019-06, Vol.15 (6), p.e1008230-e1008230 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Duverger 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. ;2019 Duverger et al 2019 Duverger et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008230 ;PMID: 31233495

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25
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Nature genetics, 2021-09, Vol.53 (9), p.1300-1310 [Peer Reviewed Journal]

2021. The Author(s), under exclusive licence to Springer Nature America, Inc. ;COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2021 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00913-z ;PMID: 34475573

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26
Partitioning of genetic variation across the genome using multimarker methods in a wild bird population
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Partitioning of genetic variation across the genome using multimarker methods in a wild bird population

Molecular ecology, 2013-08, Vol.22 (15), p.3963-3980 [Peer Reviewed Journal]

2013 John Wiley & Sons Ltd ;2014 INIST-CNRS ;2013 John Wiley & Sons Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0962-1083 ;EISSN: 1365-294X ;DOI: 10.1111/mec.12375 ;PMID: 23848161

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27
A super pan-genomic landscape of rice
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A super pan-genomic landscape of rice

Cell research, 2022-10, Vol.32 (10), p.878-896 [Peer Reviewed Journal]

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: 1748-7838 ;ISSN: 1001-0602 ;EISSN: 1748-7838 ;DOI: 10.1038/s41422-022-00685-z ;PMID: 35821092

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28
Next-generation characterization of the Cancer Cell Line Encyclopedia
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Next-generation characterization of the Cancer Cell Line Encyclopedia

Nature (London), 2019-05, Vol.569 (7757), p.503-508 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group May 23, 2019 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-019-1186-3 ;PMID: 31068700

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29
Graph pangenome captures missing heritability and empowers tomato breeding
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Graph pangenome captures missing heritability and empowers tomato breeding

Nature (London), 2022-06, Vol.606 (7914), p.527-534 [Peer Reviewed Journal]

2022. The Author(s). ;Copyright Nature Publishing Group Jun 16, 2022 ;The Author(s) 2022 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-022-04808-9 ;PMID: 35676474

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30
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
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Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Nature genetics, 2019-03, Vol.51 (3), p.414-430 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2019 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0358-2 ;PMID: 30820047

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31
Effective gene expression prediction from sequence by integrating long-range interactions
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Effective gene expression prediction from sequence by integrating long-range interactions

Nature methods, 2021-10, Vol.18 (10), p.1196-1203 [Peer Reviewed Journal]

2021. The Author(s). ;COPYRIGHT 2021 Nature Publishing Group ;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: 1548-7091 ;EISSN: 1548-7105 ;DOI: 10.1038/s41592-021-01252-x ;PMID: 34608324

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32
Identification of common genetic risk variants for autism spectrum disorder
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Identification of common genetic risk variants for autism spectrum disorder

Nature 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: 30804558

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33
1108-P: Care Cascade Engagement and Characteristics of Diabetes Awareness in Adult Samoans in 2010 and 2018
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Article
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1108-P: Care Cascade Engagement and Characteristics of Diabetes Awareness in Adult Samoans in 2010 and 2018

Diabetes (New York, N.Y.), 2021-06, Vol.70 (Supplement_1) [Peer Reviewed Journal]

Copyright American Diabetes Association Jun 1, 2021 ;ISSN: 0012-1797 ;EISSN: 1939-327X ;DOI: 10.2337/db21-1108-P

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34
Presence of Genetic Variants Among Young Men With Severe COVID-19
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Article
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Presence of Genetic Variants Among Young Men With Severe COVID-19

JAMA, 2020-08, Vol.324 (7), p.663 [Peer Reviewed Journal]

2020. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://jamanetwork.com/journals/jama/pages/coronavirus-alert . ;DOI: 10.1001/jama.2020.13719

Digital Resources/Online E-Resources

35
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
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Article
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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Nature genetics, 2019-01, Vol.51 (1), p.63-75 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Jan 2019 ;info:eu-repo/semantics/openAccess ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0269-7 ;PMID: 30478444

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36
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
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Article
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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature 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: 30643251

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37
Addendum: A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications
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Addendum: A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications

Nature communications, 2018-07, Vol.9 (1), p.2861-1, Article 2861 [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/s41467-018-05088-6 ;PMID: 30030451

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38
ClinGen — The Clinical Genome Resource
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Article
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ClinGen — The Clinical Genome Resource

The New England journal of medicine, 2015-06, Vol.372 (23), p.2235-2242 [Peer Reviewed Journal]

Copyright © 2015 Massachusetts Medical Society. All rights reserved. ;Copyright © 2015 Massachusetts Medical Society. 2015 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMsr1406261 ;PMID: 26014595

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39
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
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Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics

Nature communications, 2018-05, Vol.9 (1), p.1825-20, Article 1825 [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. ;info:eu-repo/semantics/openAccess © The Author(s) 2018. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. http://creativecommons.org/licenses/by/4.0/ ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-03621-1 ;PMID: 29739930

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40
The mutational constraint spectrum quantified from variation in 141,456 humans
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The mutational constraint spectrum quantified from variation in 141,456 humans

Nature (London), 2020-05, Vol.581 (7809), p.434-443 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group May 28, 2020 ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2020 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-020-2308-7 ;PMID: 32461654

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