Results 1 - 20 of 173 for All Library Resources
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Genotype
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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The GenomeAsia 100K Project enables genetic discoveries across AsiaNature (London), 2019-12, Vol.576 (7785), p.106-111 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;The Author(s) 2019 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-019-1793-z ;PMID: 31802016Full text available |
| 2 |
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Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese populationNature genetics, 2019-03, Vol.51 (3), p.379-386 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2019 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0332-4 ;PMID: 30718926Full text available |
| 3 |
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Inactivating Mutations in NPC1L1 and Protection from Coronary Heart DiseaseThe New England journal of medicine, 2014-11, Vol.371 (22), p.2072-2082 [Peer Reviewed Journal]Copyright © 2014 Massachusetts Medical Society. All rights reserved. ;Copyright © 2014 Massachusetts Medical Society 2014 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1405386 ;PMID: 25390462Full text available |
| 4 |
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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 |
| 5 |
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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 |
| 6 |
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 |
| 7 |
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 |
| 8 |
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 |
| 9 |
Material Type: Article
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Genetic variants of calcium and vitamin D metabolism in kidney stone diseaseNature communications, 2019-11, Vol.10 (1), p.5175-10, Article 5175 [Peer Reviewed Journal]2019. 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) 2019. corrected publication 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) 2019, corrected publication 2022 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-13145-x ;PMID: 31729369Full text available |
| 10 |
Material Type: Article
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Genome sequencing of 320 Chinese children with epilepsy: a clinical and molecular studyBrain (London, England : 1878), 2021-12, Vol.144 (12), p.3623-3634 [Peer Reviewed Journal]The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. ;The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. 2021 ;ISSN: 0006-8950 ;EISSN: 1460-2156 ;DOI: 10.1093/brain/awab233 ;PMID: 34145886Full text available |
| 11 |
Material Type: Article
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Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activityNature communications, 2019-01, Vol.10 (1), p.376-11, Article 376 [Peer Reviewed Journal]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. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-08008-w ;PMID: 30670697Full text available |
| 12 |
Material Type: Article
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SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and CaucasiansPloS one, 2013-04, Vol.8 (4), p.e58618-e58618 [Peer Reviewed Journal]COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Miyashita et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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. ;2013 Miyashita et al 2013 Miyashita et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0058618 ;PMID: 23565137Full text available |
| 13 |
Material Type: Article
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NOTCH2NLC-related disorders: the widening spectrum and genotype–phenotype correlationJournal of medical genetics, 2022-01, Vol.59 (1), p.1-9 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2021-107883 ;PMID: 34675123Full text available |
| 14 |
Material Type: Article
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Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetesHuman molecular genetics, 2021-05, Vol.30 (8), p.716-726 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2021 ;The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddab044 ;PMID: 33607655Full text available |
| 15 |
Material Type: Article
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Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South AsiansDiabetologia, 2012-04, Vol.55 (4), p.981-995 [Peer Reviewed Journal]The Author(s) 2011 ;2015 INIST-CNRS ;Springer-Verlag 2012 ;ISSN: 0012-186X ;EISSN: 1432-0428 ;DOI: 10.1007/s00125-011-2370-7 ;PMID: 22109280Full text available |
| 16 |
Material Type: Article
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Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual DisabilityAmerican journal of human genetics, 2012-05, Vol.90 (5), p.856-863 [Peer Reviewed Journal]2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press May 4, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.03.023 ;PMID: 22541562 ;CODEN: AJHGAGFull text available |
| 17 |
Material Type: Article
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Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian PopulationsHuman molecular genetics, 2021-05, Vol.30 (7), p.603-618 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2021 ;The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddab038 ;PMID: 33547791Full text available |
| 18 |
Material Type: Article
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MTHFR 1298A>C Substitution is a Strong Candidate for Analysis in Recurrent Pregnancy Loss: Evidence from 14,289 SubjectsReproductive sciences (Thousand Oaks, Calif.), 2022-04, Vol.29 (4), p.1039-1053 [Peer Reviewed Journal]Society for Reproductive Investigation 2021 ;2021. Society for Reproductive Investigation. ;ISSN: 1933-7191 ;EISSN: 1933-7205 ;DOI: 10.1007/s43032-021-00530-5 ;PMID: 33742421Full text available |
| 19 |
Material Type: Article
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Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopiaNature communications, 2015-03, Vol.6 (1), p.6689-6689, Article 6689 [Peer Reviewed Journal]Copyright Nature Publishing Group Mar 2015 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms7689 ;PMID: 25823570Full text available |
| 20 |
Material Type: Article
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A cross-tissue transcriptome-wide association study identifies novel susceptibility genes for lung cancer in Chinese populationsHuman molecular genetics, 2021-08, Vol.30 (17), p.1666-1676 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2021 ;The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddab119 ;PMID: 33909040Full text available |
Results 1 - 20 of 173 for All Library Resources
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- Polymorphism, Single Nucleotide (77)
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- Genetic Predisposition To Disease (65)
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- Gene Frequency (64)
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