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Material Type: Article
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Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scoresNature genetics, 2022-04, Vol.54 (4), p.450-458 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Apr 2022 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01036-9 ;PMID: 35393596Full text available |
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Material Type: Article
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Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and DissectionJournal of the American College of Cardiology, 2018-08, Vol.72 (6), p.605-615 [Peer Reviewed Journal]2018 American College of Cardiology Foundation ;Copyright © 2018 American College of Cardiology Foundation. All rights reserved. ;Copyright Elsevier Limited Aug 7, 2018 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2018.04.089 ;PMID: 30071989Full text available |
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3 |
Material Type: Article
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Genetic analysis of right heart structure and function in 40,000 peopleNature genetics, 2022-06, Vol.54 (6), p.792-803 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Jun 2022 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01090-3 ;PMID: 35697867Full text available |
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4 |
Material Type: Article
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Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLsNature communications, 2021-06, Vol.12 (1), p.3394-3394, Article 3394 [Peer Reviewed Journal]The Author(s) 2021. 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) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-23134-8 ;PMID: 34099641Full text available |
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5 |
Material Type: Article
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Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individualsCommunications biology, 2023-02, Vol.6 (1), p.143-143, Article 143 [Peer Reviewed Journal]2023. The Author(s). ;The Author(s) 2023. 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) 2023 ;ISSN: 2399-3642 ;EISSN: 2399-3642 ;DOI: 10.1038/s42003-023-04491-0 ;PMID: 36737517Full text available |
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6 |
Material Type: Article
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Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variantsNature genetics, 2023-12, Vol.55 (12), p.2065-2074 [Peer Reviewed Journal]2023. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Dec 2023 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-023-01534-4 ;PMID: 37945903Full text available |
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7 |
Material Type: Article
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Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesisNature medicine, 2021-07, Vol.27 (7), p.1239-1249 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to Springer Nature America, Inc. ;COPYRIGHT 2021 Nature Publishing Group ;The Author(s), under exclusive licence to Springer Nature America, Inc. 2021. ;ISSN: 1078-8956 ;ISSN: 1546-170X ;EISSN: 1546-170X ;DOI: 10.1038/s41591-021-01411-9 ;PMID: 34239136Full text available |
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8 |
Material Type: Article
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Genetics of hereditary large vessel diseasesJournal of human genetics, 2016-01, Vol.61 (1), p.21-26 [Peer Reviewed Journal]Copyright Nature Publishing Group Jan 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.119 ;PMID: 26446364Full text available |
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9 |
Material Type: Article
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Developmental stage-specific biphasic roles of Wnt/β-catenin signaling in cardiomyogenesis and hematopoiesisProceedings of the National Academy of Sciences - PNAS, 2006-12, Vol.103 (52), p.19812-19817 [Peer Reviewed Journal]Copyright 2006 The National Academy of Sciences of the United States of America ;2006 by The National Academy of Sciences of the USA 2006 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.0605768103 ;PMID: 17170140Full text available |
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10 |
Material Type: Article
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Mobile element variation contributes to population-specific genome diversification, gene regulation and disease riskNature genetics, 2023-06, Vol.55 (6), p.939-951 [Peer Reviewed Journal]2023. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Jun 2023 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-023-01390-2 ;PMID: 37169872Full text available |
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11 |
Material Type: Article
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Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic componentAnnals of the rheumatic diseases, 2022-09, Vol.81 (9), p.1301-1312 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: 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. ;Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. 2022 ;ISSN: 0003-4967 ;EISSN: 1468-2060 ;DOI: 10.1136/annrheumdis-2022-222460 ;PMID: 35753705Full text available |
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12 |
Material Type: Article
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Discovery of novel biomarkers for atherosclerotic aortic aneurysm through proteomics-based assessment of disease progressionScientific reports, 2020-04, Vol.10 (1), p.6429-6429, Article 6429 [Peer Reviewed Journal]The Author(s) 2020. 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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-63229-8 ;PMID: 32286426Full text available |
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13 |
Material Type: Article
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Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesisNature communications, 2023-06, Vol.14 (1), p.3671-3671, Article 3671 [Peer Reviewed Journal]2023. The Author(s). ;The Author(s) 2023. 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) 2023 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-023-39136-7 ;PMID: 37340002Full text available |
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14 |
Material Type: Article
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Nongenetic method for purifying stem cell-derived cardiomyocytesNature methods, 2010-01, Vol.7 (1), p.61-66 [Peer Reviewed Journal]COPYRIGHT 2010 Nature Publishing Group ;Copyright Nature Publishing Group Jan 2010 ;ISSN: 1548-7091 ;EISSN: 1548-7105 ;DOI: 10.1038/nmeth.1403 ;PMID: 19946277Full text available |
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15 |
Material Type: Article
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Vestigial-like 2 contributes to normal muscle fiber type distribution in miceScientific reports, 2017-08, Vol.7 (1), p.7168-12, Article 7168 [Peer Reviewed Journal]2017. 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) 2017 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-017-07149-0 ;PMID: 28769032Full text available |
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16 |
Material Type: Article
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Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association StudiesCirculation (New York, N.Y.), 2023-04, Vol.147 (14), p.1097-1109 [Peer Reviewed Journal]2023 The Authors. 2023 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/circulationaha.122.062349 ;PMID: 36802911Full text available |
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17 |
Material Type: Article
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ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer RiskClinical cancer research, 2023-08, Vol.29 (16), p.OF1-3050 [Peer Reviewed Journal]2023 The Authors; Published by the American Association for Cancer Research. ;2023 The Authors; Published by the American Association for Cancer Research 2023 American Association for Cancer Research ;ISSN: 1078-0432 ;EISSN: 1557-3265 ;DOI: 10.1158/1078-0432.CCR-23-0212 ;PMID: 37449874Full text available |
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18 |
Material Type: Article
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Assessing the Accuracy of Variant Detection in Cost-Effective Gene Panel Testing by Next-Generation SequencingThe Journal of molecular diagnostics : JMD, 2018-09, Vol.20 (5), p.572-582 [Peer Reviewed Journal]2018 American Society for Investigative Pathology and the Association for Molecular Pathology ;Copyright © 2018 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. All rights reserved. ;ISSN: 1525-1578 ;EISSN: 1943-7811 ;DOI: 10.1016/j.jmoldx.2018.04.004 ;PMID: 29953964Full text available |
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19 |
Material Type: Article
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Association of protein tyrosine phosphatase 1B gene polymorphism with the effects of weight reduction therapy on bodyweight and glycolipid profiles in obese patientsJournal of diabetes investigation, 2021-08, Vol.12 (8), p.1462-1470 [Peer Reviewed Journal]2021 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd ;2021 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd. ;2021. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2040-1116 ;EISSN: 2040-1124 ;DOI: 10.1111/jdi.13492 ;PMID: 33400373Full text available |
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20 |
Material Type: Article
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Hereditary hemorrhagic telangiectasia in Japanese patientsJournal of human genetics, 2014-01, Vol.59 (1), p.37-41 [Peer Reviewed Journal]ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2013.113 ;PMID: 24196379Full text available |