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1
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Nature 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: 29808027

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2
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
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Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

Nature 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: 26818947

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3
HIBAG--HLA genotype imputation with attribute bagging
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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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4
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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5
Genetic variants underlying differences in facial morphology in East Asian and European populations
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Genetic variants underlying differences in facial morphology in East Asian and European populations

Nature 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: 35393595

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6
Limb development genes underlie variation in human fingerprint patterns
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Limb development genes underlie variation in human fingerprint patterns

Cell, 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: 34995520

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7
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

Nature 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: NGENEC

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8
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
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Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci

Nature 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: NGENEC

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9
Meta-analysis identifies multiple loci associated with kidney function―related traits in east Asian populations
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Meta-analysis identifies multiple loci associated with kidney function―related traits in east Asian populations

Nature 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: NGENEC

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10
Genetic variants of calcium and vitamin D metabolism in kidney stone disease
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Genetic variants of calcium and vitamin D metabolism in kidney stone disease

Nature 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: 31729369

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11
Genetic Origins and Sex-Biased Admixture of the Huis
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Genetic Origins and Sex-Biased Admixture of the Huis

Molecular 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: 34021754

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12
Large-scale gene-centric analysis identifies novel variants for coronary artery disease
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Large-scale gene-centric analysis identifies novel variants for coronary artery disease

PLoS 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: 21966275

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13
Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations
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Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations

Hereditas, 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: 29636655

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14
Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People
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Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People

Molecular 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: 33170928

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15
SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians
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SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians

PloS 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: 23565137

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16
Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease
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Article
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Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease

Computational 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: 34447459

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17
Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes
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Article
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Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes

Human 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: 33607655

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18
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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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 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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19
The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent
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Article
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The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent

PLoS 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: 24244186

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20
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
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Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

American 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: AJHGAG

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