Výsledky vyhledávání - Michael Chong

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  1. 1
    Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease

    Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease Autor Sébastien Thériault, Ricky Lali, Michael Chong, James L. Velianou, Madhu K. Natarajan, Guillaume Paré

    Vydáno 2018
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  2. 2
    Genetic Determinants of Vascular Dementia

    Genetic Determinants of Vascular Dementia Autor Nazia Pathan, Muskaan Kaur Kharod, Sajjha Nawab, Matteo Di Scipio, Guillaume Paré, Michael Chong

    Vydáno 2024
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  3. 3
    Effects of lifelong testosterone exposure on health and disease using Mendelian randomization

    Effects of lifelong testosterone exposure on health and disease using Mendelian randomization Autor Pedrum Mohammadi‐Shemirani, Michael Chong, Marie Pigeyre, Robert W. Morton, Hertzel C. Gerstein, Guillaume Paré

    Vydáno 2020
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  4. 4
    Blood CSF1 and CXCL12 as Causal Mediators of Coronary Artery Disease

    Blood CSF1 and CXCL12 as Causal Mediators of Coronary Artery Disease Autor Jennifer Sjaarda, Hertzel C. Gerstein, Michael Chong, Salim Yusuf, David Meyre, Sonia S. Anand, Sibylle Hess, Guillaume Paré

    Vydáno 2018
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  5. 5
    ACE and Type 2 Diabetes Risk: A Mendelian Randomization Study

    ACE and Type 2 Diabetes Risk: A Mendelian Randomization Study Autor Marie Pigeyre, Jennifer Sjaarda, Michael Chong, Sibylle Hess, Jackie Bosch, Salim Yusuf, Hertzel C. Gerstein, Guillaume Paré

    Vydáno 2020
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  6. 6
    Novel Drug Targets for Ischemic Stroke Identified Through Mendelian Randomization Analysis of the Blood Proteome

    Novel Drug Targets for Ischemic Stroke Identified Through Mendelian Randomization Analysis of the Blood Proteome Autor Michael Chong, Jennifer Sjaarda, Marie Pigeyre, Pedrum Mohammadi‐Shemirani, Ricky Lali, Ashkan Shoamanesh, Hertzel C. Gerstein, Guillaume Paré

    Vydáno 2019
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  7. 7
    A method to estimate the contribution of rare coding variants to complex trait heritability

    A method to estimate the contribution of rare coding variants to complex trait heritability Autor Nazia Pathan, Wei Q. Deng, Matteo Di Scipio, Mohammad Daud Khan, Shihong Mao, Robert W. Morton, Ricky Lali, Marie Pigeyre, Michael Chong, Guillaume Paré

    Vydáno 2024
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  8. 8
    Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis

    Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis Autor Sukrit Narula, Salim Yusuf, Michael Chong, Chinthanie Ramasundarahettige, Sumathy Rangarajan, Shrikant I. Bangdiwala, Martin van Eikels, Kirsten Leineweber, Annie M. Wu, Marie Pigeyre, Guillaume Paré

    Vydáno 2020
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  9. 9
    Elevated Lipoprotein(a) and Risk of Atrial Fibrillation

    Elevated Lipoprotein(a) and Risk of Atrial Fibrillation Autor Pedrum Mohammadi‐Shemirani, Michael Chong, Sukrit Narula, Nicolas Perrot, David Conen, Jason D. Roberts, Sébastien Thériault, Yohan Bossé, Matthew B. Lanktree, Marie Pigeyre, Guillaume Paré

    Vydáno 2022
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  10. 10
    Surrogate Adiposity Markers and Mortality

    Surrogate Adiposity Markers and Mortality Autor Irfan Khan, Michael Chong, Ann Le, Pedrum Mohammadi‐Shemirani, Robert W. Morton, Christina Brinza, Michel Kiflen, Sukrit Narula, Loubna Akhabir, Shihong Mao, Katherine M. Morrison, Marie Pigeyre, Guillaume Paré

    Vydáno 2023
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  11. 11
    A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulation

    A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulat... Autor Matthew B. Lanktree, Nicolas Perrot, Andrew Smyth, Michael Chong, Sukrit Narula, Meera Shanmuganathan, Zachary Kroezen, Philip Britz‐McKibbin, Mario Berger, Joan C. Krepinsky, Marie Pigeyre, Salim Yusuf, Guillaume Paré

    Vydáno 2023
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  12. 12
    Protein alterations in patients with delirium after cardiac surgery: An exploratory case-control sub-study of the VISION Cardiac Surgery Biobank

    Protein alterations in patients with delirium after cardiac surgery: An exploratory case-control sub-study of the VISION Cardiac Surgery Biobank Autor Jessica Spence, P.J. Devereaux, Shaheena Bashir, Katheryn Brady, Tao Sun, Matthew T.V. Chan, Chew Yin Wang, André Lamy, Richard Whitlock, William F. McIntyre, Emilie P. Belley‐Côté, Guillaume Paré, Michael Chong

    Vydáno 2025
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  13. 13
    GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia

    GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia Autor Michael Chong, Pedrum Mohammadi‐Shemirani, Nicolas Perrot, Walter Nelson, Robert W. Morton, Sukrit Narula, Ricky Lali, Irfan Khan, Mohammad Daud Khan, Conor Judge, Tafadzwa Machipisa, Nathan Cawte, Martin O’Donnell, Marie Pigeyre, Loubna Akhabir, Guillaume Paré

    Vydáno 2022
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  14. 14
    Cerebrovascular Disease Knowledge Portal

    Cerebrovascular Disease Knowledge Portal Autor Katherine Crawford, Cristina Gallego-Fábrega, Christina Kourkoulis, Laura Miyares, Sandro Marini, Jason Flannick, Noël P. Burtt, Marcin von Grotthuss, Benjamin Alexander, Maria C. Costanzo, Neil Vaishnav, Rainer Malik, Jennifer L. Hall, Michael Chong, Jonathan Rosand, Guido J. Falcone

    Vydáno 2018
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  15. 15
    Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease

    Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease Autor Caitlyn Vlasschaert, Amy J. M. McNaughton, Michael Chong, Elina K. Cook, Wilma M. Hopman, Bryan Kestenbaum, Cassianne Robinson‐Cohen, Jocelyn S. Garland, Sarah Moran, Guillaume Paré, Catherine M. Clase, Mila Tang, Adeera Levin, Rachel M. Holden, Michael J. Rauh, Matthew B. Lanktree

    Vydáno 2022
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  16. 16
    Identification of Cadherin 2 ( <i>CDH2</i> ) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy

    Identification of Cadherin 2 ( <i>CDH2</i> ) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy Autor Bongani M. Mayosi, Maryam Fish, Gasnat Shaboodien, Elisa Mastantuono, Sarah Kraus, Thomas Wieland, Maria‐Christina Kotta, Ashley Chin, Nakita Laing, Ntobeko Ntusi, Michael Chong, Christopher Horsfall, Simon N. Pimstone, Davide Gentilini, Gianfranco Parati, Tim-Matthias Strom, Thomas Meitinger, Guillaume Paré, Peter J. Schwartz, Lia Crotti

    Vydáno 2017
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  17. 17
    Moyamoya Disease Susceptibility Variant <i>RNF213</i> p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis

    Moyamoya Disease Susceptibility Variant <i>RNF213</i> p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis Autor Shuhei Okazaki, Takaaki Morimoto, Yoichiro Kamatani, Teppei Kamimura, Hatasu Kobayashi, Kouji H. Harada, Tsutomu Tomita, Aya Higashiyama, Jun Takahashi, Jyoji Nakagawara, Masatoshi Koga, Ḱazunori Toyoda, Kazuo Washida, Satoshi Saitô, Atsushi Takahashi, Makoto Hirata, Koichi Matsuda, Hideki Mochizuki, Michael Chong, Guillaume Paré, Martin O’Donnell, Tetsuro Ago, Jun Hata, Toshiharu Ninomiya, Martin Dichgans, Stéphanie Debette, Michiaki Kubo, Akio Koizumi, Masafumi Ihara

    Vydáno 2019
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  18. 18
    Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

    Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke Autor Keith L. Keene, Hyacinth I. Hyacinth, Joshua C. Bis, Steven J. Kittner, Braxton D. Mitchell, Yu-Ching Cheng, Guillaume Paré, Michael Chong, Martin O’Donnell, James F. Meschia, Wei‐Min Chen, Michèle M. Sale, Stephen S. Rich, Mike A. Nalls, Alan B. Zonderman, Michele K. Evans, James G. Wilson, Adolfo Correa, Hugh S. Markus, Matthew Traylor, Cathryn M. Lewis, Cara L. Carty, Alexander P. Reiner, Jeff Haessler, Carl D. Langefeld, Rebecca F. Gottesman, Thomas H. Mosley, Daniel Woo, Kristine Yaffe, YongMei Liu, W.T. Longstreth, Bruce M. Psaty, Charles Kooperberg, Leslie A. Lange, Ralph L. Sacco, Tatjana Rundek, Jin‐Moo Lee, Carlos Cruchaga, Karen L. Furie, Donna K. Arnett, Oscar Benavente, Raji P. Grewal, Leema Reddy Peddareddygari, Martin Dichgans, Rainer Malik, Bradford B. Worrall, Myriam Fornage

    Vydáno 2020
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  19. 19
    Body mass index is negatively associated with telomere length: a collaborative cross-sectional meta-analysis of 87 observational studies

    Body mass index is negatively associated with telomere length: a collaborative cross-sectional meta-analysis of 87 observational studies Autor Marij Gielen, Geja J. Hageman, Evangelia E. Antoniou, Katarina Nordfjäll, Massimo Mangino, Muthuswamy Balasubramanyam, Tim De Meyer, Audrey E. Hendricks, Erik J. Giltay, Steven C. Hunt, Jennifer A. Nettleton, Klelia D. Salpea, Vanessa Diaz, Ramin Farzaneh‐Far, Gil Atzmon, Sarah E. Harris, Lifang Hou, David Gilley, Iiris Hovatta, Jeremy D. Kark, Hisham Nassar, David J. Kurz, Karen A. Mather, Peter Willeit, Yun‐Ling Zheng, Sofia Pavanello, Ellen W. Demerath, Line Rode, Daniel Bunout, Andrew Steptoe, Lisa A. Boardman, Amelia Martí, Belinda L. Needham, Wei Zheng, Rosalind Ramsey‐Goldman, Andrew J. Pellatt, Jaakko Kaprio, Jonathan N. Hofmann, Christian Gieger, Giuseppe Paolisso, Jacob Hjelmborg, Kari G. Rabe, Teresa E. Seeman, Jason Wong, Pim van der Harst, Linda Broer, Florian Kronenberg, Barbara Kollerits, Timo Strandberg, Dan T. A. Eisenberg, Catherine Duggan, Josine E. Verhoeven, Roxanne Schaakxs, Raffaela Zannolli, Rosana M. R. dos Reis, Fadi J. Charchar, Maciej Tomaszewski, Ute Mons, Ilja Demuth, Andrea Elena Iglesias Molli, Guo Cheng, Dmytro Krasnienkov, Bianca D’Antono, Marek Kasielski, Barry J. McDonnell, Richard P. Ebstein, Kristina Sundquist, Guillaume Paré, Michael Chong, Maurice P. Zeegers

    Vydáno 2018
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  20. 20
    Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

    Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas Autor Odessica N. Hughes, Amy R. Bentley, Charles E. Breeze, François Aguet, Xiaoguang Xu, Girish N. Nadkarni, Quan Sun, Bridget M. Lin, Thomas Gilliland, Mariah Meyer, Jiawen Du, Laura M. Raffield, Holly Kramer, Robert W. Morton, Mateus H. Gouveia, Elizabeth G. Atkinson, Adán Valladares‐Salgado, Niels Wacher-Rodarte, Nicole Dueker, Xiuqing Guo, Yang Hai, Adebowale Adeyemo, Lyle G. Best, Jianwen Cai, Guanjie Chen, Michael Chong, Ayo P. Doumatey, James Eales, Mark O. Goodarzi, Eli Ipp, Marguerite R. Irvin, Min-Zhi Jiang, Alana Jones, Charles Kooperberg, José Eduardo Krieger, Ethan M. Lange, Matthew B. Lanktree, James P. Lash, Paulo A. Lotufo, Ruth J. F. Loos, Ha My T. Vy, Jesús Peralta‐Romero, Lihong Qi, Leslie J. Raffel, Stephen S. Rich, Erik J. Rodriquez, Eduardo Tarazona‐Santos, Kent D. Taylor, Jason G. Umans, Jia Wen, Bessie A. Young, Zhi Yu, Ying Zhang, Yii‐Der Ida Chen, Tatjana Rundek, Jerome I. Rotter, Miguel Cruz, Myriam Fornage, Maria Fernanda Lima‐Costa, Alexandre C. Pereira, Guillaume Paré, Pradeep Natarajan, Shelley A. Cole, April P. Carson, Leslie A. Lange, Yun Li, Eliseo J. Pérez‐Stable, Ron Do, Fadi J. Charchar, Maciej Tomaszewski, Josyf C. Mychaleckyj, Charles N. Rotimi, Andrew P. Morris, Nora Franceschini

    Vydáno 2023
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