Results 1 - 20 of 10,074 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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SLE risk variant regulates IRF8 expressionNature reviews. Rheumatology, 2022-06, Vol.18 (6), p.306-306 [Peer Reviewed Journal]Springer Nature Limited 2022. ;ISSN: 1759-4790 ;EISSN: 1759-4804 ;DOI: 10.1038/s41584-022-00791-7 ;PMID: 35538211Full text available |
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Genetic variant rs7820258 regulates the expression of indoleamine 2,3-dioxygenase 1 in brain regions/Reply to Han et al.: On track for an IDO1-based personalized therapy in autoimmunityProceedings of the National Academy of Sciences - PNAS, 2020-09, Vol.117 (39), p.24035 [Peer Reviewed Journal]Copyright National Academy of Sciences Sep 29, 2020 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.2007022117Full text available |
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Orthogonal Estimates of Variances for Additive, Dominance, and Epistatic Effects in PopulationsGenetics (Austin), 2017-07, Vol.206 (3), p.1297-1307 [Peer Reviewed Journal]Copyright © 2017 by the Genetics Society of America. ;Copyright Genetics Society of America Jul 2017 ;Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2017 by the Genetics Society of America 2017 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.116.199406 ;PMID: 28522540Full text available |
| 4 |
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Brain mechanisms of insomnia: new perspectives on causes and consequencesPhysiological reviews, 2021-07, Vol.101 (3), p.995-1046 [Peer Reviewed Journal]Copyright American Physiological Society Jul 2021 ;ISSN: 0031-9333 ;EISSN: 1522-1210 ;DOI: 10.1152/physrev.00046.2019Full text available |
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Quantifying the effect of reference genome choiceNature reviews. Genetics, 2021-08, Vol.22 (8), p.481-481 [Peer Reviewed Journal]COPYRIGHT 2021 Nature Publishing Group ;Springer Nature Limited 2021. ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-021-00392-2Full text available |
| 6 |
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Correction: Genetic variants influence on the placenta regulatory landscapePLoS genetics, 2019-04, Vol.15 (4), p.e1008118-e1008118 [Peer Reviewed Journal]COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Delahaye 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 Delahaye et al 2019 Delahaye et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008118 ;PMID: 30978184Full text available |
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Benefits and limitations of genome-wide association studiesNature reviews. Genetics, 2019-08, Vol.20 (8), p.467-484 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Springer Nature Limited 2019. ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-019-0127-1 ;PMID: 31068683Full text available |
| 8 |
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The effect of APOE and other common genetic variants on the onset of Alzheimer's disease and dementia: a community-based cohort studyLancet neurology, 2018-05, Vol.17 (5), p.434-444 [Peer Reviewed Journal]2018 Elsevier Ltd ;Copyright © 2018 Elsevier Ltd. All rights reserved. ;Copyright Elsevier Limited May 2018 ;ISSN: 1474-4422 ;EISSN: 1474-4465 ;DOI: 10.1016/S1474-4422(18)30053-X ;PMID: 29555425Full text available |
| 9 |
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Diabetes in China: Epidemiology and Genetic Risk Factors and Their Clinical Utility in Personalized MedicationDiabetes (New York, N.Y.), 2018-01, Vol.67 (1), p.3-11 [Peer Reviewed Journal]2017 by the American Diabetes Association. ;Copyright American Diabetes Association Jan 1, 2018 ;ISSN: 0012-1797 ;EISSN: 1939-327X ;DOI: 10.2337/dbi17-0013 ;PMID: 29263166Full text available |
| 10 |
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Disease variant prediction with deep generative models of evolutionary dataNature (London), 2021-11, Vol.599 (7883), p.91-95 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to Springer Nature Limited. ;Copyright Nature Publishing Group Nov 4, 2021 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-021-04043-8 ;PMID: 34707284Full text available |
| 11 |
Material Type: Article
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The human genetic epidemiology of COVID-19Nature reviews. Genetics, 2022-09, Vol.23 (9), p.533-546 [Peer Reviewed Journal]2022. Springer Nature Limited. ;Springer Nature Limited 2022. ;Springer Nature Limited 2022 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-022-00478-5 ;PMID: 35501396Full text available |
| 12 |
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A universal SNP and small-indel variant caller using deep neural networksNature biotechnology, 2018-11, Vol.36 (10), p.983-987 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2018 ;ISSN: 1087-0156 ;EISSN: 1546-1696 ;DOI: 10.1038/nbt.4235 ;PMID: 30247488Full text available |
| 13 |
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From genome-wide associations to candidate causal variants by statistical fine-mappingNature reviews. Genetics, 2018-08, Vol.19 (8), p.491-504 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Aug 2018 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-018-0016-z ;PMID: 29844615Full text available |
| 14 |
Material Type: Article
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Challenges in the diagnosis of Parkinson's diseaseLancet neurology, 2021-05, Vol.20 (5), p.385-397 [Peer Reviewed Journal]2021 Elsevier Ltd ;Copyright © 2021 Elsevier Ltd. All rights reserved. ;COPYRIGHT 2021 Elsevier B.V. ;2021. Elsevier Ltd ;ISSN: 1474-4422 ;EISSN: 1474-4465 ;DOI: 10.1016/S1474-4422(21)00030-2 ;PMID: 33894193Full text available |
| 15 |
Material Type: Article
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Autoimmunity and organ damage in systemic lupus erythematosusNature immunology, 2020-06, Vol.21 (6), p.605-614 [Peer Reviewed Journal]COPYRIGHT 2020 Nature Publishing Group ;Springer Nature America, Inc. 2020. ;ISSN: 1529-2908 ;EISSN: 1529-2916 ;DOI: 10.1038/s41590-020-0677-6 ;PMID: 32367037Full text available |
| 16 |
Material Type: Article
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Pan-cancer whole-genome analyses of metastatic solid tumoursNature (London), 2019-11, Vol.575 (7781), p.210-216 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Nov 7, 2019 ;The Author(s) 2019 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-019-1689-y ;PMID: 31645765Full text available |
| 17 |
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Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort studyThe Lancet (British edition), 2019-02, Vol.393 (10173), p.758-767 [Peer Reviewed Journal]2019 Elsevier Ltd ;Copyright © 2019 Elsevier Ltd. All rights reserved. ;2019. Elsevier Ltd ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(18)32042-7 ;PMID: 30712878Full text available |
| 18 |
Material Type: Article
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Mendelian Randomization: Concepts and ScopeCold Spring Harbor perspectives in biology, 2022-01, Vol.12 (1), p.a040501 [Peer Reviewed Journal]Copyright © 2022 Cold Spring Harbor Laboratory Press; all rights reserved. ;Copyright Cold Spring Harbor Laboratory Press Jan 2022 ;2022 ;ISSN: 2157-1422 ;EISSN: 2157-1422 ;EISSN: 1943-0264 ;DOI: 10.1101/cshperspect.a040501 ;PMID: 34426474Full text available |
| 19 |
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The genetic architecture of Parkinson's diseaseLancet neurology, 2020-02, Vol.19 (2), p.170-178 [Peer Reviewed Journal]2020 Elsevier Ltd ;Copyright © 2020 Elsevier Ltd. All rights reserved. ;2020. Elsevier Ltd ;ISSN: 1474-4422 ;EISSN: 1474-4465 ;DOI: 10.1016/S1474-4422(19)30287-X ;PMID: 31521533Full text available |
| 20 |
Material Type: Article
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PANTHER: Making genome‐scale phylogenetics accessible to allProtein science, 2022-01, Vol.31 (1), p.8-22 [Peer Reviewed Journal]2021 The Protein Society. ;2022 The Protein Society ;ISSN: 0961-8368 ;EISSN: 1469-896X ;DOI: 10.1002/pro.4218 ;PMID: 34717010Full text available |
Results 1 - 20 of 10,074 for All Library Resources
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- Genetic Variance (9,805)
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