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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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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 |
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3 |
Material Type: Article
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Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestriesNature communications, 2021-02, Vol.12 (1), p.1258-1258, Article 1258 [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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-20851-4 ;PMID: 33627673Full text available |
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Material Type: Article
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Genetic dating indicates that the Asian–Papuan admixture through Eastern Indonesia corresponds to the Austronesian expansionProceedings of the National Academy of Sciences - PNAS, 2012-03, Vol.109 (12), p.4574-4579 [Peer Reviewed Journal]copyright © 1993-2008 National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Mar 20, 2012 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1118892109 ;PMID: 22396590Full text available |
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5 |
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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Material Type: Article
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Investigation of Genetic Variation Underlying Central Obesity amongst South AsiansPloS one, 2016-05, Vol.11 (5), p.e0155478-e0155478 [Peer Reviewed Journal]COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Scott 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. ;2016 Scott et al 2016 Scott et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0155478 ;PMID: 27195708Full text available |
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7 |
Material Type: Article
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Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4Diabetologia, 2013-06, Vol.56 (6), p.1291-1305 [Peer Reviewed Journal]The Author(s) 2013 ;2014 INIST-CNRS ;Springer-Verlag Berlin Heidelberg 2013 ;ISSN: 0012-186X ;EISSN: 1432-0428 ;DOI: 10.1007/s00125-013-2874-4 ;PMID: 23532257Full text available |
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8 |
Material Type: Article
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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 |
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9 |
Material Type: Article
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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 |
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10 |
Material Type: Article
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Patterns of African and Asian admixture in the Afrikaner population of South AfricaBMC biology, 2020-02, Vol.18 (1), p.16-16, Article 16 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed 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). 2020 ;ISSN: 1741-7007 ;EISSN: 1741-7007 ;DOI: 10.1186/s12915-020-0746-1 ;PMID: 32089133Full text available |
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11 |
Material Type: Article
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Genetic association between TNF-α G-308A and osteoarthritis in Asians: A case-control study and meta-analysisPloS one, 2021-11, Vol.16 (11), p.e0259561-e0259561 [Peer Reviewed Journal]2021 Wang 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. ;2021 Wang et al 2021 Wang et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0259561 ;PMID: 34735544Full text available |
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12 |
Material Type: Article
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Comparison of effects of UGT1A16 and UGT1A128 on irinotecan-induced adverse reactions in the Japanese population: analysis of the Biobank Japan ProjectJournal of human genetics, 2019-12, Vol.64 (12), p.1195-1202 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2019 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-019-0677-2 ;PMID: 31586129Full text available |
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13 |
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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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 |
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15 |
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 |
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16 |
Material Type: Article
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Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control studyRheumatology (Oxford, England), 2017-08, Vol.56 (8), p.1282-1292 [Peer Reviewed Journal]The Author 2017. Published by Oxford University Press on behalf of the British Society for Rheumatology. ;The Author 2017. Published by Oxford University Press on behalf of the British Society for Rheumatology. 2017 ;ISSN: 1462-0324 ;EISSN: 1462-0332 ;DOI: 10.1093/rheumatology/kex048 ;PMID: 28407095Full text available |
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17 |
Material Type: Article
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Intronic LINE-1 insertion in SLCO1B3 as a highly prevalent cause of rotor syndrome in East Asian populationJournal of human genetics, 2022-02, Vol.67 (2), p.71-77 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to The Japan Society of Human Genetics. ;The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-021-00967-1 ;PMID: 34354231Full text available |
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18 |
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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19 |
Material Type: Article
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Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association studyThe Lancet (British edition), 2013-08, Vol.382 (9894), p.790-796 [Peer Reviewed Journal]Elsevier Ltd ;2013 Elsevier Ltd ;2014 INIST-CNRS ;Copyright © 2013 Elsevier Ltd. All rights reserved. ;Copyright Elsevier Limited Aug 31, 2013 ;2013 Elsevier Ltd. All rights reserved. 2013 Elsevier Ltd ;ISSN: 0140-6736 ;ISSN: 1474-547X ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(13)60681-9 ;PMID: 23755828 ;CODEN: LANCAOFull text available |
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20 |
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 |