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1
NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants
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NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants

Genome 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: 31640730

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2
The GenomeAsia 100K Project enables genetic discoveries across Asia
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The GenomeAsia 100K Project enables genetic discoveries across Asia

Nature (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: 31802016

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3
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
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Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries

Nature 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: 33627673

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4
Genetic dating indicates that the Asian–Papuan admixture through Eastern Indonesia corresponds to the Austronesian expansion
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Genetic dating indicates that the Asian–Papuan admixture through Eastern Indonesia corresponds to the Austronesian expansion

Proceedings 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: 22396590

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5
Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians
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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 Asians

Diabetologia, 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: 22109280

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6
Investigation of Genetic Variation Underlying Central Obesity amongst South Asians
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Investigation of Genetic Variation Underlying Central Obesity amongst South Asians

PloS 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: 27195708

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7
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4
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Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4

Diabetologia, 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: 23532257

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8
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
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Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population

Nature 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: 30718926

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9
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
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Article
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Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease

The 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: 25390462

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10
Patterns of African and Asian admixture in the Afrikaner population of South Africa
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Patterns of African and Asian admixture in the Afrikaner population of South Africa

BMC 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: 32089133

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11
Genetic association between TNF-α G-308A and osteoarthritis in Asians: A case-control study and meta-analysis
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Article
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Genetic association between TNF-α G-308A and osteoarthritis in Asians: A case-control study and meta-analysis

PloS 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: 34735544

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12
Comparison of effects of UGT1A16 and UGT1A128 on irinotecan-induced adverse reactions in the Japanese population: analysis of the Biobank Japan Project
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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 Project

Journal 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: 31586129

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13
HIBAG--HLA genotype imputation with attribute bagging
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Article
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HIBAG--HLA genotype imputation with attribute bagging

The 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: 23712092

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14
The ChinaMAP reference panel for the accurate genotype imputation in Chinese populations
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The ChinaMAP reference panel for the accurate genotype imputation in Chinese populations

Cell 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: 34489580

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15
Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease
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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 disease

Nature 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: 29083407

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16
Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study
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Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study

Rheumatology (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: 28407095

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17
Intronic LINE-1 insertion in SLCO1B3 as a highly prevalent cause of rotor syndrome in East Asian population
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Article
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Intronic LINE-1 insertion in SLCO1B3 as a highly prevalent cause of rotor syndrome in East Asian population

Journal 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: 34354231

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18
NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population
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NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population

Cell 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: 34788621

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19
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study
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Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study

The 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: LANCAO

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20
Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese population
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Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese population

Nature 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: 30692682

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