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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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Material Type: Article
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Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetesNature communications, 2016-01, Vol.7 (1), p.10531-10531, Article 10531 [Peer Reviewed Journal]Copyright Nature Publishing Group Jan 2016 ;Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2016 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms10531 ;PMID: 26818947Full text available |
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3 |
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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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 |
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5 |
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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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 |
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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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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 |
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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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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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13 |
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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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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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 |
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16 |
Material Type: Article
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Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery DiseaseComputational and mathematical methods in medicine, 2021-08, Vol.2021, p.7036592-11 [Peer Reviewed Journal]Copyright © 2021 Yang Hu et al. ;Copyright © 2021 Yang Hu et al. 2021 ;ISSN: 1748-670X ;EISSN: 1748-6718 ;DOI: 10.1155/2021/7036592 ;PMID: 34447459Full text available |
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17 |
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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18 |
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 |
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19 |
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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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 |