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Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized DataGenetic epidemiology, 2013-11, Vol.37 (7), p.658-665 [Tạp chí có phản biện]2013 The Authors. * published by Wiley Periodicals, Inc. ;2013 WILEY PERIODICALS, INC. ;2013 The Authors. * published by Wiley Periodicals, Inc. 2013 ;ISSN: 0741-0395 ;EISSN: 1098-2272 ;DOI: 10.1002/gepi.21758 ;PMID: 24114802Tài liệu số/Tài liệu điện tử |
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Pleiotropic Effects of Statins on the Cardiovascular SystemCirculation research, 2017-01, Vol.120 (1), p.229-243 [Tạp chí có phản biện]2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Jan 6, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.116.308537 ;PMID: 28057795Tài liệu số/Tài liệu điện tử |
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Exome Sequencing, ANGPTL3 Mutations, and Familial Combined HypolipidemiaThe New England journal of medicine, 2010-12, Vol.363 (23), p.2220-2227 [Tạp chí có phản biện]Copyright © 2010 Massachusetts Medical Society. All rights reserved. ;2015 INIST-CNRS ;Copyright © 2010 Massachusetts Medical Society. 2010 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1002926 ;PMID: 20942659 ;CODEN: NEJMAGTài liệu số/Tài liệu điện tử |
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Association of small, dense LDL-cholesterol concentration and lipoprotein particle characteristics with coronary heart disease: A systematic review and meta-analysisPloS one, 2020-11, Vol.15 (11), p.e0241993-e0241993 [Tạp chí có phản biện]COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Liou, Kaptoge. 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. ;2020 Liou, Kaptoge 2020 Liou, Kaptoge ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0241993 ;PMID: 33166340Tài liệu số/Tài liệu điện tử |
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Addressing dyslipidemic risk beyond LDL-cholesterolThe Journal of clinical investigation, 2022-01, Vol.132 (1), p.1-10 [Tạp chí có phản biện]COPYRIGHT 2022 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation Jan 2022 ;2022 Tall et al. 2022 Tall et al. ;ISSN: 1558-8238 ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/JCI148559 ;PMID: 34981790Tài liệu số/Tài liệu điện tử |
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Variation in PCSK9 and HMGCR and Risk of Cardiovascular Disease and DiabetesThe New England journal of medicine, 2016-12, Vol.375 (22), p.2144-2153 [Tạp chí có phản biện]Copyright © 2016 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1604304 ;PMID: 27959767Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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Two Phase 3 Trials of Inclisiran in Patients with Elevated LDL CholesterolThe New England journal of medicine, 2020-04, Vol.382 (16), p.1507-1519 [Tạp chí có phản biện]Copyright © 2020 Massachusetts Medical Society. All rights reserved. ;Copyright © 2020 Massachusetts Medical Society. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1912387 ;PMID: 32187462Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countriesClinical chemistry (Baltimore, Md.), 2015-01, Vol.61 (1), p.231-238 [Tạp chí có phản biện]2014 American Association for Clinical Chemistry. ;COPYRIGHT 2015 American Association for Clinical Chemistry, Inc. ;Copyright American Association for Clinical Chemistry Jan 2015 ;ISSN: 0009-9147 ;EISSN: 1530-8561 ;DOI: 10.1373/clinchem.2014.231365 ;PMID: 25414277Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL CholesterolThe New England journal of medicine, 2017-04, Vol.376 (15), p.1430-1440 [Tạp chí có phản biện]Copyright © 2017 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1615758 ;PMID: 28306389Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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A robust and efficient method for Mendelian randomization with hundreds of genetic variantsNature communications, 2020-01, Vol.11 (1), p.376-376, Article 376 [Tạp chí có phản biện]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) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-14156-4 ;PMID: 31953392Tài liệu số/Tài liệu điện tử |