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21
Polymorphisms of the Vitamin D Receptor Gene and Sex-Differential Associations with Lipid Profiles in Chinese Han Adults
Polymorphisms of the Vitamin D Receptor Gene and Sex-Differential Associations with Lipid Profiles in Chinese Han Adults
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Polymorphisms of the Vitamin D Receptor Gene and Sex-Differential Associations with Lipid Profiles in Chinese Han Adults

Biomedical and environmental sciences, 2022-02, Vol.35 (2), p.115-125 [Peer Reviewed Journal]

2022 The Editorial Board of Biomedical and Environmental Sciences ;Copyright © 2022 The Editorial Board of Biomedical and Environmental Sciences. Published by China CDC. All rights reserved. ;Copyright © Wanfang Data Co. Ltd. All Rights Reserved. ;ISSN: 0895-3988 ;EISSN: 2214-0190 ;DOI: 10.3967/bes2022.016 ;PMID: 35197176

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22
Genetic Origins and Sex-Biased Admixture of the Huis
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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23
Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error
Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error
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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

American 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: 24144296

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24
Clinical Predictors and Long-term Impact of Acute Kidney Injury on Progression of Diabetic Kidney Disease in Chinese Patients With Type 2 Diabetes
Clinical Predictors and Long-term Impact of Acute Kidney Injury on Progression of Diabetic Kidney Disease in Chinese Patients With Type 2 Diabetes
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Clinical Predictors and Long-term Impact of Acute Kidney Injury on Progression of Diabetic Kidney Disease in Chinese Patients With Type 2 Diabetes

Diabetes (New York, N.Y.), 2022-03, Vol.71 (3), p.520-529 [Peer Reviewed Journal]

2022 by the American Diabetes Association. ;2022 by the American Diabetes Association 2022 ;ISSN: 0012-1797 ;EISSN: 1939-327X ;DOI: 10.2337/db21-0694 ;PMID: 35043149

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25
Large-scale gene-centric analysis identifies novel variants for coronary artery disease
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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26
Interleukin-1 Beta Gene Polymorphism rs16944 May Associate with Increased Susceptibility to Extremity Chronic Osteomyelitis in Chinese Han Population
Interleukin-1 Beta Gene Polymorphism rs16944 May Associate with Increased Susceptibility to Extremity Chronic Osteomyelitis in Chinese Han Population
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Interleukin-1 Beta Gene Polymorphism rs16944 May Associate with Increased Susceptibility to Extremity Chronic Osteomyelitis in Chinese Han Population

BioMed research international, 2019-01, Vol.2019, p.7483537-9 [Peer Reviewed Journal]

Copyright © 2019 Zi-long Yao et al. ;Copyright © 2019 Zi-long Yao et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 ;Copyright © 2019 Zi-long Yao et al. 2019 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2019/7483537 ;PMID: 30949508

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27
Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People
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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28
Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India
Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India
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Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India

Diabetes (New York, N.Y.), 2013-05, Vol.62 (5), p.1746-1755 [Peer Reviewed Journal]

2014 INIST-CNRS ;COPYRIGHT 2013 American Diabetes Association ;COPYRIGHT 2013 American Diabetes Association ;Copyright American Diabetes Association May 2013 ;2013 by the American Diabetes Association. 2013 ;ISSN: 0012-1797 ;EISSN: 1939-327X ;DOI: 10.2337/db12-1077 ;PMID: 23300278 ;CODEN: DIAEAZ

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29
Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease
Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease
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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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30
Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes
Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes
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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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31
Genome-Wide Association Study for Type 2 Diabetes in Indians Identifies a New Susceptibility Locus at 2q21
Genome-Wide Association Study for Type 2 Diabetes in Indians Identifies a New Susceptibility Locus at 2q21
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Genome-Wide Association Study for Type 2 Diabetes in Indians Identifies a New Susceptibility Locus at 2q21

Diabetes (New York, N.Y.), 2013-03, Vol.62 (3), p.977-986 [Peer Reviewed Journal]

2014 INIST-CNRS ;COPYRIGHT 2013 American Diabetes Association ;COPYRIGHT 2013 American Diabetes Association ;Copyright American Diabetes Association Mar 2013 ;2013 by the American Diabetes Association. 2013 ;ISSN: 0012-1797 ;EISSN: 1939-327X ;DOI: 10.2337/db12-0406 ;PMID: 23209189 ;CODEN: DIAEAZ

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32
Genetic Polymorphisms of IL1B, IL6, and TNFα in a Chinese Han Population with Pulmonary Tuberculosis
Genetic Polymorphisms of IL1B, IL6, and TNFα in a Chinese Han Population with Pulmonary Tuberculosis
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Genetic Polymorphisms of IL1B, IL6, and TNFα in a Chinese Han Population with Pulmonary Tuberculosis

BioMed research international, 2018-01, Vol.2018, p.3010898-10 [Peer Reviewed Journal]

Copyright © 2018 Shouquan Wu et al. ;Copyright © 2018 Shouquan Wu et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright © 2018 Shouquan Wu et al. 2018 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2018/3010898 ;PMID: 29888256

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33
Association of EPAS1 and PPARA Gene Polymorphisms with High-Altitude Headache in Chinese Han Population
Association of EPAS1 and PPARA Gene Polymorphisms with High-Altitude Headache in Chinese Han Population
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Association of EPAS1 and PPARA Gene Polymorphisms with High-Altitude Headache in Chinese Han Population

BioMed research international, 2020, Vol.2020, p.1593068-11 [Peer Reviewed Journal]

Copyright © 2020 Yang Shen et al. ;Copyright © 2020 Yang Shen et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 ;Copyright © 2020 Yang Shen et al. 2020 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2020/1593068 ;PMID: 32185192

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34
The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent
The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent
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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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35
Association of CYP2C192 and associated haplotypes with lower norendoxifen concentrations in tamoxifen‐treated Asian breast cancer patients
Association of CYP2C192 and associated haplotypes with lower norendoxifen concentrations in tamoxifen‐treated Asian breast cancer patients
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Association of CYP2C192 and associated haplotypes with lower norendoxifen concentrations in tamoxifen‐treated Asian breast cancer patients

British journal of clinical pharmacology, 2016-06, Vol.81 (6), p.1142-1152 [Peer Reviewed Journal]

2016 The British Pharmacological Society ;ISSN: 0306-5251 ;EISSN: 1365-2125 ;DOI: 10.1111/bcp.12886 ;PMID: 26799162

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36
The Decisive Case-Control Study Elaborates the Null Association between ADAMTS5 rs226794 and Osteoarthritis in Asians: A Case-Control Study and Meta-Analysis
The Decisive Case-Control Study Elaborates the Null Association between ADAMTS5 rs226794 and Osteoarthritis in Asians: A Case-Control Study and Meta-Analysis
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The Decisive Case-Control Study Elaborates the Null Association between ADAMTS5 rs226794 and Osteoarthritis in Asians: A Case-Control Study and Meta-Analysis

Genes, 2021-11, Vol.12 (12), p.1916 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes12121916 ;PMID: 34946864

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37
Polymorphisms of SLC11A1(NRAMP1) rs17235409 associated with and susceptibility to spinal tuberculosis in a southern Han Chinese population
Polymorphisms of SLC11A1(NRAMP1) rs17235409 associated with and susceptibility to spinal tuberculosis in a southern Han Chinese population
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Polymorphisms of SLC11A1(NRAMP1) rs17235409 associated with and susceptibility to spinal tuberculosis in a southern Han Chinese population

Infection, genetics and evolution, 2022-03, Vol.98, p.105202-105202, Article 105202 [Peer Reviewed Journal]

2022 The Authors ;Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved. ;ISSN: 1567-1348 ;EISSN: 1567-7257 ;DOI: 10.1016/j.meegid.2021.105202 ;PMID: 34990850

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38
Decisive gene strategy on osteoporosis: a comprehensive whole-literature-based approach for conclusive candidate gene targets
Decisive gene strategy on osteoporosis: a comprehensive whole-literature-based approach for conclusive candidate gene targets
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Decisive gene strategy on osteoporosis: a comprehensive whole-literature-based approach for conclusive candidate gene targets

Aging (Albany, NY.), 2022-04, Vol.14 (8), p.3484-3528

Copyright: © 2022 Chen et al. ;ISSN: 1945-4589 ;EISSN: 1945-4589 ;DOI: 10.18632/aging.204026 ;PMID: 35452412

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39
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
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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40
Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian Populations
Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian Populations
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Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian Populations

Human 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: 33547791

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