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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Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous ThromboembolismJournal of the American College of Cardiology, 2012-08, Vol.60 (8), p.722-729 [Peer Reviewed Journal]American College of Cardiology Foundation ;2012 American College of Cardiology Foundation ;2015 INIST-CNRS ;Copyright © 2012 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Aug 21, 2012 ;ISSN: 0735-1097 ;ISSN: 1558-3597 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2012.01.078 ;PMID: 22898070 ;CODEN: JACCDIFull text available |
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Material Type: Article
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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillationNature genetics, 2017-06, Vol.49 (6), p.946-952 [Peer Reviewed Journal]COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2017 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3843 ;PMID: 28416818Full text available |
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Material Type: Article
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Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic RiskAmerican journal of respiratory and critical care medicine, 2015-09, Vol.192 (6), p.727-736 [Peer Reviewed Journal]Copyright American Thoracic Society Sep 15, 2015 ;Copyright © 2015 by the American Thoracic Society 2015 ;ISSN: 1073-449X ;ISSN: 1535-4970 ;EISSN: 1535-4970 ;DOI: 10.1164/rccm.201503-0418OC ;PMID: 26051272Full text available |
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Material Type: Article
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Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysisPLoS genetics, 2012-06, Vol.8 (6), p.e1002765-e1002765 [Peer Reviewed Journal]COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Kiryluk 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: Kiryluk K, Li Y, Sanna-Cherchi S, Rohanizadegan M, Suzuki H, et al. (2012) Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis. PLoS Genet 8(6): e1002765. doi:10.1371/journal.pgen.1002765 ;Kiryluk et al. 2012 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002765 ;PMID: 22737082Full text available |
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Material Type: Article
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Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African AmericansHuman molecular genetics, 2018-11, Vol.27 (21), p.3813-3824 [Peer Reviewed Journal]The Author(s) 2018. Published by Oxford University Press. 2018 ;ISSN: 0964-6906 ;ISSN: 1460-2083 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddy280 ;PMID: 30085094Full text available |
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Material Type: Article
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Genome-wide association and functional follow-up reveals new loci for kidney functionPLoS genetics, 2012-03, Vol.8 (3), p.e1002584-e1002584 [Peer Reviewed Journal]COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Pattaro 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: Pattaro C, Köttgen A, Teumer A, Garnaas M, Böger CA, et al. (2012) Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function. PLoS Genet 8(3): e1002584. doi:10.1371/journal.pgen.1002584 ;Pattaro et al. 2012 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002584 ;PMID: 22479191Full text available |
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Material Type: Article
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Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibilityPLoS genetics, 2011-05, Vol.7 (5), p.e1002079 [Peer Reviewed Journal]COPYRIGHT 2011 Public Library of Science ;COPYRIGHT 2011 Public Library of Science ;This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. 2011 ;2011 Public Library of Science. 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: Citation: Zhao J, Wu H, Khosravi M, Cui H, Qian X, et al. (2011) Association of Genetic Variants in Complement Factor H and Factor H-Related Genes with Systemic Lupus Erythematosus Susceptibility. PLoS Genet 7(5): e1002079. doi:10.1371/journal.pgen.1002079 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002079 ;PMID: 21637784Full text available |
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Material Type: Article
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MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosusPLoS genetics, 2013-02, Vol.9 (2), p.e1003336-e1003336 [Peer Reviewed Journal]COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Deng 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: Deng Y, Zhao J, Sakurai D, Kaufman KM, Edberg JC, et al. (2013) MicroRNA-3148 Modulates Allelic Expression of Toll-Like Receptor 7 Variant Associated with Systemic Lupus Erythematosus. PLoS Genet 9(2): e1003336. doi:10.1371/journal.pgen.1003336 ;2013 Deng et al 2013 Deng et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003336 ;PMID: 23468661Full text available |
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Material Type: Article
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Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody productionPLoS genetics, 2013-02, Vol.9 (2), p.e1003222-e1003222 [Peer Reviewed Journal]COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Molineros 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: Molineros JE, Maiti AK, Sun C, Looger LL, Han S, et al. (2013) Admixture Mapping in Lupus Identifies Multiple Functional Variants within IFIH1 Associated with Apoptosis, Inflammation, and Autoantibody Production. PLoS Genet 9(2): e1003222. doi:10.1371/journal.pgen.1003222 ;2013 Molineros et al 2013 Molineros et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003222 ;PMID: 23441136Full text available |
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Material Type: Article
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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with HeightAmerican journal of human genetics, 2011-01, Vol.88 (1), p.6-18 [Peer Reviewed Journal]2011 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright Cell Press Jan 7, 2011 ;2011 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2011 The American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2010.11.007 ;PMID: 21194676 ;CODEN: AJHGAGFull text available |
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Material Type: Article
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Molecular underpinnings of clinical disparity patterns in African American vs. Caucasian American multiple myeloma patientsBlood cancer journal (New York), 2019-02, Vol.9 (2), p.15-15, Article 15 [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. ;The Author(s) 2019 ;ISSN: 2044-5385 ;EISSN: 2044-5385 ;DOI: 10.1038/s41408-019-0177-9 ;PMID: 30718460Full text available |
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12 |
Material Type: Article
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Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosusAnnals of the rheumatic diseases, 2011-10, Vol.70 (10), p.1752-1757 [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 ;2015 INIST-CNRS ;Copyright: 2011 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: 0003-4967 ;ISSN: 1468-2060 ;EISSN: 1468-2060 ;DOI: 10.1136/ard.2011.154104 ;PMID: 21719445 ;CODEN: ARDIAOFull text available |
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Material Type: Article
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An evolutionary genomic approach to identify genes involved in human birth timingPLoS genetics, 2011-04, Vol.7 (4), p.e1001365-e1001365 [Peer Reviewed Journal]COPYRIGHT 2011 Public Library of Science ;COPYRIGHT 2011 Public Library of Science ;Plunkett et al. 2011 ;2011 Plunkett 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: Plunkett J, Doniger S, Orabona G, Morgan T, Haataja R, et al. (2011) An Evolutionary Genomic Approach to Identify Genes Involved in Human Birth Timing. PLoS Genet 7(4): e1001365. doi:10.1371/journal.pgen.1001365 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1001365 ;PMID: 21533219Full text available |
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Material Type: Article
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Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart FailurePLoS genetics, 2016-05, Vol.12 (5), p.e1006034-e1006034 [Peer Reviewed Journal]COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Public Library of Science. 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: Smith JG, Felix JF, Morrison AC, Kalogeropoulos A, Trompet S, Wilk JB, et al. (2016) Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. PLoS Genet 12(5): e1006034. doi:10.1371/journal.pgen.1006034 ;2016 Public Library of Science. 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: Smith JG, Felix JF, Morrison AC, Kalogeropoulos A, Trompet S, Wilk JB, et al. (2016) Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. PLoS Genet 12(5): e1006034. doi:10.1371/journal.pgen.1006034 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1006034 ;PMID: 27149122Full text available |
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Material Type: Article
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Identification of a Systemic Lupus Erythematosus Susceptibility Locus at 11p13 between PDHX and CD44 in a Multiethnic StudyAmerican journal of human genetics, 2011-01, Vol.88 (1), p.83-91 [Peer Reviewed Journal]2011 The American Society of Human Genetics ;Copyright Cell Press Jan 7, 2011 ;2011 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2011 The American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2010.11.014 ;PMID: 21194677Full text available |
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Material Type: Article
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Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokePloS one, 2018-11, Vol.13 (11), p.e0206554-e0206554 [Peer Reviewed Journal]COPYRIGHT 2018 Public Library of Science ;This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication: https://creativecommons.org/publicdomain/zero/1.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;info:eu-repo/semantics/openAccess ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0206554 ;PMID: 30383853Full text available |
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Material Type: Article
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Genome-wide association studies of the PR interval in African AmericansPLoS genetics, 2011-02, Vol.7 (2), p.e1001304-e1001304 [Peer Reviewed Journal]COPYRIGHT 2011 Public Library of Science ;COPYRIGHT 2011 Public Library of Science ;This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. 2011 ;2011 Public Library of Science. 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: Citation: Smith JG, Magnani JW, Palmer C, Meng YA, Soliman EZ, et al. (2011) Genome-Wide Association Studies of the PR Interval in African Americans. PLoS Genet 7(2): e1001304. doi:10.1371/journal.pgen.1001304 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1001304 ;PMID: 21347284Full text available |
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Material Type: Article
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GWA study data mining and independent replication identify cardiomyopathy-associated 5 ( ) as a risk gene for schizophreniaMolecular psychiatry, 2011-11, Vol.16 (11), p.1117-1129 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;Macmillan Publishers Limited 2011. ;Copyright Nature Publishing Group Nov 2011 ;2010 Macmillan Publishers Limited All rights reserved 2010 ;ISSN: 1359-4184 ;ISSN: 1476-5578 ;EISSN: 1476-5578 ;DOI: 10.1038/mp.2010.96 ;PMID: 20838396Full text available |
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Material Type: Article
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DNA Repair Pathways and Their Association With Lethal Prostate Cancer in African American and European American MenJNCI cancer spectrum, 2022-02, Vol.6 (1) [Peer Reviewed Journal]The Author(s) 2022. Published by Oxford University Press. ;The Author(s) 2022. Published by Oxford University Press. 2022 ;ISSN: 2515-5091 ;EISSN: 2515-5091 ;DOI: 10.1093/jncics/pkab097 ;PMID: 35079693Full text available |
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Material Type: Article
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Role of MYH9 and APOL1 in African and non-African populations with lupus nephritisGenes and immunity, 2012-04, Vol.13 (3), p.232-238 [Peer Reviewed Journal]COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2012 ;Macmillan Publishers Limited 2012. ;ISSN: 1466-4879 ;ISSN: 1476-5470 ;EISSN: 1476-5470 ;DOI: 10.1038/gene.2011.82 ;PMID: 22189356Full text available |