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Material Type: Article
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NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variantsGenome medicine, 2019-10, Vol.11 (1), p.64-64, Article 64 [Peer Reviewed Journal]COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;The Author(s). 2019 ;ISSN: 1756-994X ;EISSN: 1756-994X ;DOI: 10.1186/s13073-019-0677-z ;PMID: 31640730Full text available |
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Material Type: Article
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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive errorNature genetics, 2018-06, Vol.50 (6), p.834-848 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2018 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0127-7 ;PMID: 29808027Full text available |
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3 |
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 |
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4 |
Material Type: Article
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Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populationsHereditas, 2018-04, Vol.155 (1), p.19-19, Article 19 [Peer Reviewed Journal]The Author(s) 2018 ;ISSN: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-018-0057-5 ;PMID: 29636655Full text available |
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5 |
Material Type: Article
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Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern AsiansPLoS genetics, 2019-04, Vol.15 (4), p.e1008092 [Peer Reviewed Journal]COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Molineros 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 Molineros et al 2019 Molineros et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008092 ;PMID: 31022184Full text available |
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6 |
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 |
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7 |
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 |
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8 |
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 |
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9 |
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 |
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10 |
Material Type: Article
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FTO genetic variants, dietary intake and body mass index: insights from 177,330 individualsHuman molecular genetics, 2014-12, Vol.23 (25), p.6961-6972 [Peer Reviewed Journal]The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2014 ;ISSN: 0964-6906 ;ISSN: 1460-2083 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddu411 ;PMID: 25104851Full text available |
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11 |
Material Type: Article
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Genetic Origins and Sex-Biased Admixture of the HuisMolecular biology and evolution, 2021-09, Vol.38 (9), p.3804-3819 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2021 ;The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. ;COPYRIGHT 2021 Oxford University Press ;ISSN: 1537-1719 ;ISSN: 0737-4038 ;EISSN: 1537-1719 ;DOI: 10.1093/molbev/msab158 ;PMID: 34021754Full text available |
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12 |
Material Type: Article
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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive ErrorAmerican journal of human genetics, 2013-08, Vol.93 (2), p.264-277 [Peer Reviewed Journal]2013 The American Society of Human Genetics ;Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Aug 8, 2013 ;2013 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2013 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2013.06.016 ;PMID: 24144296Full text available |
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13 |
Material Type: Article
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Large-scale gene-centric analysis identifies novel variants for coronary artery diseasePLoS genetics, 2011-09, Vol.7 (9), p.e1002260-e1002260 [Peer Reviewed Journal]COPYRIGHT 2011 Public Library of Science ;COPYRIGHT 2011 Public Library of Science ;Butterworth et al. 2011 ;2011 Butterworth 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: The IBC 50K CAD Consortium (2011) Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease. PLoS Genet 7(9): e1002260. doi:10.1371/journal.pgen.1002260 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002260 ;PMID: 21966275Full text available |
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14 |
Material Type: Article
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Detecting Genetic Ancestry and Adaptation in the Taiwanese Han PeopleMolecular biology and evolution, 2021-10, Vol.38 (10), p.4149-4165 [Peer Reviewed Journal]The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2020 ;The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. ;COPYRIGHT 2021 Oxford University Press ;ISSN: 1537-1719 ;ISSN: 0737-4038 ;EISSN: 1537-1719 ;DOI: 10.1093/molbev/msaa276 ;PMID: 33170928Full text available |
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15 |
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 |
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16 |
Material Type: Article
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The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descentPLoS genetics, 2013-11, Vol.9 (11), p.e1003912-e1003912 [Peer Reviewed Journal]COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Basu Mallick et al 2013 Basu Mallick et al ;2013 Basu Mallick 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: Basu Mallick C, Iliescu FM, Möls M, Hill S, Tamang R, et al. (2013) The Light Skin Allele of SLC24A5 in South Asians and Europeans Shares Identity by Descent. PLoS Genet 9(11): e1003912. doi:10.1371/journal.pgen.1003912 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003912 ;PMID: 24244186Full text available |
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17 |
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 |
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18 |
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 |
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19 |
Material Type: Article
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Dysfunction of VIPR2 leads to myopia in humans and miceJournal of medical genetics, 2022-01, Vol.59 (1), p.88-100 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;Author(s) (or their employer(s)) 2020. 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-2020-107220 ;PMID: 33318135Full text available |
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20 |
Material Type: Article
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Resolving the ancestry of Austronesian-speaking populationsHuman genetics, 2016-03, Vol.135 (3), p.309-326 [Peer Reviewed Journal]The Author(s) 2016 ;COPYRIGHT 2016 Springer ;Springer-Verlag Berlin Heidelberg 2016 ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-015-1620-z ;PMID: 26781090Full text available |