Results 21 - 40 of 660 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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| 21 |
Material Type: Article
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HIBAG--HLA genotype imputation with attribute baggingThe pharmacogenomics journal, 2014-04, Vol.14 (2), p.192-200 [Peer Reviewed Journal]COPYRIGHT 2014 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2014 ;Copyright © 2014 Macmillan Publishers Limited 2014 Macmillan Publishers Limited ;ISSN: 1470-269X ;EISSN: 1473-1150 ;DOI: 10.1038/tpj.2013.18 ;PMID: 23712092Full text available |
| 22 |
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The ChinaMAP reference panel for the accurate genotype imputation in Chinese populationsCell research, 2021-12, Vol.31 (12), p.1308-1310 [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: 1001-0602 ;EISSN: 1748-7838 ;DOI: 10.1038/s41422-021-00564-z ;PMID: 34489580Full text available |
| 23 |
Material Type: Article
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Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery diseaseNature genetics, 2017-12, Vol.49 (12), p.1722-1730 [Peer Reviewed Journal]COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2017 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3978 ;PMID: 29083407Full text available |
| 24 |
Material Type: Article
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Estimating yields of prenatal carrier screening and implications for design of expanded carrier screening panelsGenetics in medicine, 2019-09, Vol.21 (9), p.1940-1947 [Peer Reviewed Journal]2019 The Author(s) ;2019© American College of Medical Genetics and Genomics 2019 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0472-7 ;PMID: 30846881Full text available |
| 25 |
Material Type: Article
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Prevalence of BRCA1/BRCA2 pathogenic variation in Chinese Han populationJournal of medical genetics, 2021-08, Vol.58 (8), p.565-569 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2020-106970 ;PMID: 32467295Full text available |
| 26 |
Material Type: Article
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Apportioning archaic variants among modern populationsPhilosophical transactions of the Royal Society of London. Series B. Biological sciences, 2022-06, Vol.377 (1852), p.20200411-20200411 [Peer Reviewed Journal]2022 The Authors. 2022 ;ISSN: 0962-8436 ;EISSN: 1471-2970 ;DOI: 10.1098/rstb.2020.0411 ;PMID: 35430882Full text available |
| 27 |
Material Type: Article
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NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese populationCell reports (Cambridge), 2021-11, Vol.37 (7), p.110017-110017, Article 110017 [Peer Reviewed Journal]2021 The Authors ;Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved. ;ISSN: 2211-1247 ;EISSN: 2211-1247 ;DOI: 10.1016/j.celrep.2021.110017 ;PMID: 34788621Full text available |
| 28 |
Material Type: Article
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Interferon-induced transmembrane protein-3 genetic variant rs12252-C is associated with severe influenza in Chinese individualsNature communications, 2013-01, Vol.4 (1), p.1418-1418, Article 1418 [Peer Reviewed Journal]Copyright Nature Publishing Group Jan 2013 ;The Author(s) 2013 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms2433 ;PMID: 23361009Full text available |
| 29 |
Material Type: Article
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Genetic variants underlying differences in facial morphology in East Asian and European populationsNature genetics, 2022-04, Vol.54 (4), p.403-411 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Apr 2022 ;Attribution ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01038-7 ;PMID: 35393595Full text available |
| 30 |
Material Type: Article
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Limb development genes underlie variation in human fingerprint patternsCell, 2022-01, Vol.185 (1), p.95-112.e18 [Peer Reviewed Journal]2022 ;Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved. ;2021 The Authors 2021 ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2021.12.008 ;PMID: 34995520Full text available |
| 31 |
Material Type: Article
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Molecular Features and Functional Implications of Germline Variants in Triple-Negative Breast CancerJNCI : Journal of the National Cancer Institute, 2021-07, Vol.113 (7), p.884-892 [Peer Reviewed Journal]The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com. ;The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com ;ISSN: 0027-8874 ;EISSN: 1460-2105 ;DOI: 10.1093/jnci/djaa175 ;PMID: 33151324Full text available |
| 32 |
Material Type: Article
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Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese populationNature genetics, 2019-03, Vol.51 (3), p.470-480 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2019 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0336-0 ;PMID: 30692682Full text available |
| 33 |
Material Type: Article
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Frequent alterations in cytoskeleton remodelling genes in primary and metastatic lung adenocarcinomasNature communications, 2015-12, Vol.6 (1), p.10131-10131, Article 10131 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2015 ;Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2015 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms10131 ;PMID: 26647728Full text available |
| 34 |
Material Type: Article
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High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigationsThorax, 2018-02, Vol.73 (2), p.157-166 [Peer Reviewed Journal]Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;Copyright: 2018 © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;ISSN: 0040-6376 ;EISSN: 1468-3296 ;DOI: 10.1136/thoraxjnl-2017-209999 ;PMID: 28790179Full text available |
| 35 |
Material Type: Article
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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery diseaseNature genetics, 2011-04, Vol.43 (4), p.339-344 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2011 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.782 ;PMID: 21378988 ;CODEN: NGENECFull text available |
| 36 |
Material Type: Article
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Ethnic-specific BRCA1/2 variation within Asia population: evidence from over 78 000 cancer and 40 000 non-cancer cases of Indian, Chinese, Korean and Japanese populationsJournal of medical genetics, 2021-11, Vol.58 (11), p.752-759 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2020-107299 ;PMID: 32963034Full text available |
| 37 |
Material Type: Article
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Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility lociNature genetics, 2011-10, Vol.43 (10), p.984-989 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2011 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.921 ;PMID: 21874001 ;CODEN: NGENECFull text available |
| 38 |
Material Type: Article
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Rare Pathogenic Variants in IL36RN Underlie a Spectrum of Psoriasis-Associated Pustular PhenotypesJournal of investigative dermatology, 2013-05, Vol.133 (5), p.1366-1369 [Peer Reviewed Journal]2013 The Society for Investigative Dermatology, Inc ;Copyright Nature Publishing Group May 2013 ;ISSN: 0022-202X ;EISSN: 1523-1747 ;DOI: 10.1038/jid.2012.490 ;PMID: 23303454Full text available |
| 39 |
Material Type: Article
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Meta-analysis identifies multiple loci associated with kidney function―related traits in east Asian populationsNature genetics, 2012-08, Vol.44 (8), p.904-909 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.2352 ;PMID: 22797727 ;CODEN: NGENECFull text available |
| 40 |
Material Type: Article
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Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patientsBlood, 2014-10, Vol.124 (16), p.2544-2553 [Peer Reviewed Journal]2014 American Society of Hematology ;2014 by The American Society of Hematology. ;2014 by The American Society of Hematology 2014 ;ISSN: 0006-4971 ;ISSN: 1528-0020 ;EISSN: 1528-0020 ;DOI: 10.1182/blood-2013-12-546309 ;PMID: 25171927Full text available |
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