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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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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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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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5 |
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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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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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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8 |
Material Type: Article
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Polymorphisms of the Vitamin D Receptor Gene and Sex-Differential Associations with Lipid Profiles in Chinese Han AdultsBiomedical 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: 35197176Full text available |
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9 |
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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10 |
Material Type: Article
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Modelling of atorvastatin pharmacokinetics and the identification of the effect of a BCRP polymorphism in the Japanese populationPharmacogenetics and genomics, 2017-01, Vol.27 (1), p.27 [Peer Reviewed Journal]EISSN: 1744-6880 ;DOI: 10.1097/FPC.0000000000000252 ;PMID: 27787353Digital Resources/Online E-Resources |
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11 |
Material Type: Article
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Association of CETP Gene Variants With Risk for Vascular and Nonvascular Diseases Among Chinese AdultsJAMA cardiology, 2018-01, Vol.3 (1), p.34 [Peer Reviewed Journal]EISSN: 2380-6591 ;DOI: 10.1001/jamacardio.2017.4177 ;PMID: 29141072Digital Resources/Online E-Resources |
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12 |
Material Type: Article
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Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activityNature communications, 2019-01, Vol.10 (1), p.376-11, Article 376 [Peer Reviewed Journal]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. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-08008-w ;PMID: 30670697Full text available |
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13 |
Material Type: Article
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Genetic association analysis of ATG16L1 rs2241880, rs6758317 and ATG16L2 rs11235604 polymorphisms with rheumatoid arthritis in a Chinese populationInternational immunopharmacology, 2021-04, Vol.93, p.107378 [Peer Reviewed Journal]Copyright © 2021 Elsevier B.V. All rights reserved. ;EISSN: 1878-1705 ;DOI: 10.1016/j.intimp.2021.107378 ;PMID: 33529915Digital Resources/Online E-Resources |
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14 |
Material Type: Article
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Vitamin D and cause-specific vascular disease and mortality: a Mendelian randomisation study involving 99,012 Chinese and 106,911 European adultsBMC medicine, 2019-08, Vol.17 (1), p.160-12, Article 160 [Peer Reviewed Journal]COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;2019. 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). 2019 ;ISSN: 1741-7015 ;EISSN: 1741-7015 ;DOI: 10.1186/s12916-019-1401-y ;PMID: 31466528Full text available |
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15 |
Material Type: Article
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Isoniazid Population Pharmacokinetics and Dose Recommendation for Korean Patients With Tuberculosis Based on Target Attainment AnalysisJournal of clinical pharmacology, 2021-12, Vol.61 (12), p.1567 [Peer Reviewed Journal]2021, The American College of Clinical Pharmacology. ;EISSN: 1552-4604 ;DOI: 10.1002/jcph.1931 ;PMID: 34157153Digital Resources/Online E-Resources |
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16 |
Material Type: Article
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Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopiaNature communications, 2015-03, Vol.6 (1), p.6689-6689, Article 6689 [Peer Reviewed Journal]Copyright Nature Publishing Group Mar 2015 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms7689 ;PMID: 25823570Full text available |
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17 |
Material Type: Article
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HLA-B13 :01 Is a Predictive Marker of Dapsone-Induced Severe Cutaneous Adverse Reactions in Thai PatientsFrontiers in immunology, 2021-05, Vol.12, p.661135-661135 [Peer Reviewed Journal]Copyright © 2021 Satapornpong, Pratoomwun, Rerknimitr, Klaewsongkram, Nakkam, Rungrotmongkol, Konyoung, Saksit, Mahakkanukrauh, Amornpinyo, Khunarkornsiri, Tempark, Wantavornprasert, Jinda, Koomdee, Jantararoungtong, Rerkpattanapipat, Wang, Naisbitt, Tassaneeyakul, Ariyachaipanich, Roonghiranwat, Pirmohamed, Chung and Sukasem. ;Copyright © 2021 Satapornpong, Pratoomwun, Rerknimitr, Klaewsongkram, Nakkam, Rungrotmongkol, Konyoung, Saksit, Mahakkanukrauh, Amornpinyo, Khunarkornsiri, Tempark, Wantavornprasert, Jinda, Koomdee, Jantararoungtong, Rerkpattanapipat, Wang, Naisbitt, Tassaneeyakul, Ariyachaipanich, Roonghiranwat, Pirmohamed, Chung and Sukasem 2021 Satapornpong, Pratoomwun, Rerknimitr, Klaewsongkram, Nakkam, Rungrotmongkol, Konyoung, Saksit, Mahakkanukrauh, Amornpinyo, Khunarkornsiri, Tempark, Wantavornprasert, Jinda, Koomdee, Jantararoungtong, Rerkpattanapipat, Wang, Naisbitt, Tassaneeyakul, Ariyachaipanich, Roonghiranwat, Pirmohamed, Chung and Sukasem ;ISSN: 1664-3224 ;EISSN: 1664-3224 ;DOI: 10.3389/fimmu.2021.661135 ;PMID: 34017337Full text available |
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18 |
Material Type: Article
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Polymorphisms in NLRP1 Gene Are Associated with Type 1 DiabetesJournal of diabetes research, 2019, Vol.2019, p.7405120-9 [Peer Reviewed Journal]Copyright © 2019 Xiaoxiao Sun et al. ;Copyright © 2019 Xiaoxiao Sun et al. 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. ;Copyright © 2019 Xiaoxiao Sun et al. 2019 ;ISSN: 2314-6745 ;EISSN: 2314-6753 ;DOI: 10.1155/2019/7405120 ;PMID: 31396539Full text available |
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19 |
Material Type: Article
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Physiologically based pharmacokinetic modeling of candesartan related to CYP2C9 genetic polymorphism in adult and pediatric patientsArchives of pharmacal research, 2021-12, Vol.44 (12), p.1109 [Peer Reviewed Journal]2021. The Pharmaceutical Society of Korea. ;ISSN: 0253-6269 ;EISSN: 1976-3786 ;DOI: 10.1007/s12272-021-01363-1 ;PMID: 34817825Digital Resources/Online E-Resources |
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20 |
Material Type: Article
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A GWAS Finds Variants at 2p21 Associated with Self-Reported Sensitive Skin in the Han Chinese PopulationJournal of investigative dermatology, 2022-01, Vol.142 (1), p.243-247.e9 [Peer Reviewed Journal]2021 The Authors ;ISSN: 0022-202X ;EISSN: 1523-1747 ;DOI: 10.1016/j.jid.2021.04.021 ;PMID: 34023362Full text available |