Results 1 - 20 of 3,895 for All Library Resources
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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Associations of TNFα-308G/A and TNFα-238G/A Polymorphisms with Ischemic Stroke in East Asians and Non-East Asians: A Meta-AnalysisGenetic testing and molecular biomarkers, 2017-01, Vol.21 (1), p.10-16 [Peer Reviewed Journal]ISSN: 1945-0265 ;EISSN: 1945-0257 ;DOI: 10.1089/gtmb.2015.0265 ;PMID: 27809599Full text available |
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Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneityNature communications, 2017-02, Vol.8 (1), p.14364-14364, Article 14364 [Peer Reviewed Journal]Copyright Nature Publishing Group Feb 2017 ;Copyright © 2017, The Author(s) 2017 The Author(s) ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms14364 ;PMID: 28232668Full text available |
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Adult Moyamoya Disease: A Burden of Intracranial Stenosis in East Asians?PloS one, 2015-06, Vol.10 (6), p.e0130663-e0130663 [Peer Reviewed Journal]COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Bang 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. ;2015 Bang et al 2015 Bang et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0130663 ;PMID: 26125557Full text available |
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Genome-wide association study identifies eight new risk loci for polycystic ovary syndromeNature genetics, 2012-09, Vol.44 (9), p.1020-1025 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2012 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.2384 ;PMID: 22885925 ;CODEN: NGENECFull text available |
| 5 |
Material Type: Article
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Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populationsEuropean journal of human genetics : EJHG, 2013-09, Vol.21 (9), p.994-999 [Peer Reviewed Journal]Copyright Nature Publishing Group Sep 2013 ;Copyright © 2013 Macmillan Publishers Limited 2013 Macmillan Publishers Limited ;ISSN: 1018-4813 ;ISSN: 1476-5438 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2012.277 ;PMID: 23249952Full text available |
| 6 |
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Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populationsGut, 2014-01, Vol.63 (1), p.80-87 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2014 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 0017-5749 ;EISSN: 1468-3288 ;DOI: 10.1136/gutjnl-2013-305193 ;PMID: 23850713 ;CODEN: GUTTAKFull text available |
| 7 |
Material Type: Article
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Genetic and Clinical Predictors for Breast Cancer Risk Assessment and Stratification Among Chinese WomenJNCI : Journal of the National Cancer Institute, 2010-07, Vol.102 (13), p.972-981 [Peer Reviewed Journal]2015 INIST-CNRS ;Copyright Oxford Publishing Limited(England) Jul 7, 2010 ;The Author 2010. Published by Oxford University Press. 2010 ;ISSN: 0027-8874 ;EISSN: 1460-2105 ;DOI: 10.1093/jnci/djq170 ;PMID: 20484103 ;CODEN: JNCIEQFull text available |
| 8 |
Material Type: Article
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A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathyNature genetics, 2012-02, Vol.44 (2), p.178-182 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2012 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.1047 ;PMID: 22197929 ;CODEN: NGENECFull text available |
| 9 |
Material Type: Article
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HLA‐B alleles associated with severe cutaneous reactions to antiepileptic drugs in Han ChineseEpilepsia (Copenhagen), 2013-07, Vol.54 (7), p.1307-1314 [Peer Reviewed Journal]Wiley Periodicals, Inc. © 2013 International League Against Epilepsy ;Wiley Periodicals, Inc. © 2013 International League Against Epilepsy. ;Copyright © 2013 International League Against Epilepsy ;ISSN: 0013-9580 ;EISSN: 1528-1167 ;DOI: 10.1111/epi.12217 ;PMID: 23692434 ;CODEN: EPILAKFull text available |
| 10 |
Material Type: Article
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Comparative genetic architectures of schizophrenia in East Asian and European populationsNature genetics, 2019-12, Vol.51 (12), p.1670-1678 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2019 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0512-x ;PMID: 31740837Full text available |
| 11 |
Material Type: Article
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Genome-wide association study of morbid obesity in Han ChineseBMC genetics, 2019-12, Vol.20 (1), p.97-97, Article 97 [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: 1471-2156 ;EISSN: 1471-2156 ;DOI: 10.1186/s12863-019-0797-x ;PMID: 31852448Full text available |
| 12 |
Material Type: Article
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Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controlsNature communications, 2018-10, Vol.9 (1), p.4083-7, Article 4083 [Peer Reviewed Journal]2018. 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) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-06581-8 ;PMID: 30287823Full text available |
| 13 |
Material Type: Article
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A functional polymorphism in the 5′ UTR of GDF5 is associated with susceptibility to osteoarthritisNature genetics, 2007-04, Vol.39 (4), p.529-533 [Peer Reviewed Journal]2007 INIST-CNRS ;COPYRIGHT 2007 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2007 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/2005 ;PMID: 17384641 ;CODEN: NGENECFull text available |
| 14 |
Material Type: Article
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5HTTLPR polymorphism and postpartum depression risk: A meta-analysisMedicine (Baltimore), 2020-09, Vol.99 (39), p.e22319-e22319 [Peer Reviewed Journal]Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000022319 ;PMID: 32991440Full text available |
| 15 |
Material Type: Article
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Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteriaPLoS genetics, 2018-12, Vol.14 (12), p.e1007813-e1007813 [Peer Reviewed Journal]COPYRIGHT 2018 Public Library of Science ;COPYRIGHT 2018 Public Library of Science ;2018 Day 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. ;2018 Day et al 2018 Day et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1007813 ;PMID: 30566500Full text available |
| 16 |
Material Type: Article
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Genetic association of the cytochrome c oxidase-related genes with Alzheimer's disease in Han ChineseNeuropsychopharmacology (New York, N.Y.), 2018-10, Vol.43 (11), p.2264-2276 [Peer Reviewed Journal]Copyright Nature Publishing Group Oct 2018 ;American College of Neuropsychopharmacology 2018 ;ISSN: 0893-133X ;EISSN: 1740-634X ;DOI: 10.1038/s41386-018-0144-3 ;PMID: 30054583Full text available |
| 17 |
Material Type: Article
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Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian CohortsHuman mutation, 2016-07, Vol.37 (7), p.669-678 [Peer Reviewed Journal]2016 WILEY PERIODICALS, INC. ;Copyright © 2016 Wiley Periodicals, Inc. ;ISSN: 1059-7794 ;EISSN: 1098-1004 ;DOI: 10.1002/humu.22996 ;PMID: 27068483Full text available |
| 18 |
Material Type: Article
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Association of genetic variants for susceptibility to obesity with type 2 diabetes in Japanese individualsDiabetologia, 2011-06, Vol.54 (6), p.1350-1359 [Peer Reviewed Journal]Springer-Verlag 2011 ;2015 INIST-CNRS ;ISSN: 0012-186X ;EISSN: 1432-0428 ;DOI: 10.1007/s00125-011-2086-8 ;PMID: 21369819Full text available |
| 19 |
Material Type: Article
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Identification of a Genetic Variant Common to Moyamoya Disease and Intracranial Major Artery Stenosis/OcclusionStroke (1970), 2012-12, Vol.43 (12), p.3371-3374 [Peer Reviewed Journal]2014 INIST-CNRS ;ISSN: 0039-2499 ;EISSN: 1524-4628 ;DOI: 10.1161/strokeaha.112.663864 ;PMID: 23010677 ;CODEN: SJCCA7Full text available |
| 20 |
Material Type: Article
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Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of GlycemiaThe journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.3854-3864 [Peer Reviewed Journal]The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020 ;Copyright © Oxford University Press 2015 ;The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. ;The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com ;ISSN: 0021-972X ;EISSN: 1945-7197 ;DOI: 10.1210/clinem/dgaa658 ;PMID: 32936915Full text available |
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