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1
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores
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Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores

Nature 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: 35393596

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2
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection
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Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection

Journal 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: 30071989

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3
Genetic analysis of right heart structure and function in 40,000 people
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Genetic analysis of right heart structure and function in 40,000 people

Nature 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: 35697867

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4
Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs
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Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs

Nature 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: 34099641

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5
Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals
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Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals

Communications 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: 36737517

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6
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
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Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

Nature 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: 37945903

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7
Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
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Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis

Nature 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: 34239136

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8
Genetics of hereditary large vessel diseases
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Article
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Genetics of hereditary large vessel diseases

Journal 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: 26446364

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9
Developmental stage-specific biphasic roles of Wnt/β-catenin signaling in cardiomyogenesis and hematopoiesis
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Developmental stage-specific biphasic roles of Wnt/β-catenin signaling in cardiomyogenesis and hematopoiesis

Proceedings 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: 17170140

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10
Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk
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Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk

Nature 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: 37169872

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11
Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component
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Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component

Annals 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: 35753705

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12
Discovery of novel biomarkers for atherosclerotic aortic aneurysm through proteomics-based assessment of disease progression
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Discovery of novel biomarkers for atherosclerotic aortic aneurysm through proteomics-based assessment of disease progression

Scientific 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: 32286426

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13
Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
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Article
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Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis

Nature 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: 37340002

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14
Nongenetic method for purifying stem cell-derived cardiomyocytes
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Article
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Nongenetic method for purifying stem cell-derived cardiomyocytes

Nature 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: 19946277

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15
Vestigial-like 2 contributes to normal muscle fiber type distribution in mice
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Article
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Vestigial-like 2 contributes to normal muscle fiber type distribution in mice

Scientific 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: 28769032

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16
Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Studies
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Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Studies

Circulation (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: 36802911

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17
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk
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Article
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ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

Clinical 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: 37449874

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18
Assessing the Accuracy of Variant Detection in Cost-Effective Gene Panel Testing by Next-Generation Sequencing
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Assessing the Accuracy of Variant Detection in Cost-Effective Gene Panel Testing by Next-Generation Sequencing

The 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: 29953964

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19
Association of protein tyrosine phosphatase 1B gene polymorphism with the effects of weight reduction therapy on bodyweight and glycolipid profiles in obese patients
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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 patients

Journal 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: 33400373

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20
Hereditary hemorrhagic telangiectasia in Japanese patients
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Article
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Hereditary hemorrhagic telangiectasia in Japanese patients

Journal 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: 24196379

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