Результати пошуку - Ha My T. Vy

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  1. 1
    A Composite-Likelihood Method for Detecting Incomplete Selective Sweep from Population Genomic Data

    A Composite-Likelihood Method for Detecting Incomplete Selective Sweep from Population Genomic Data за авторством Ha My T. Vy, Yuseob Kim

    Опубліковано 2015
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  2. 2
    Population-Based Penetrance of Deleterious Clinical Variants

    Population-Based Penetrance of Deleterious Clinical Variants за авторством Iain S. Forrest, Kumardeep Chaudhary, Ha My T. Vy, Ben Omega Petrazzini, Shantanu Bafna, Daniel M. Jordan, Ghislain Rocheleau, Ruth J. F. Loos, Girish N. Nadkarni, Judy H. Cho, Ron Do

    Опубліковано 2022
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  3. 3
    Genetically Downregulated Interleukin-6 Signaling Is Associated With a Favorable Cardiometabolic Profile

    Genetically Downregulated Interleukin-6 Signaling Is Associated With a Favorable Cardiometabolic Profile за авторством Marios K. Georgakis, Rainer Malik, Xue Li, Dipender Gill, Michael G. Levin, Ha My T. Vy, Renae Judy, Marylyn D. Ritchie, Shefali S. Verma, Girish N. Nadkarni, Scott M. Damrauer, Evropi Τheodoratou, Martin Dichgans

    Опубліковано 2021
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    Carta
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  4. 4
    Kidney disease genetic risk variants alter lysosomal beta-mannosidase ( <i>MANBA</i> ) expression and disease severity

    Kidney disease genetic risk variants alter lysosomal beta-mannosidase ( <i>MANBA</i> ) expression and disease severity за авторством Xiangchen Gu, Hongliu Yang, Xin Sheng, Yi-An Ko, Chengxiang Qiu, Jihwan Park, Shizheng Huang, Rachel L. Kember, Renae Judy, Joseph Park, Scott M. Damrauer, Girish N. Nadkarni, Ruth J. F. Loos, Ha My T. Vy, Kumardeep Chaudhary, Erwin P. Böttinger, Ishan Paranjpe, Aparna Saha, Christopher D. Brown, Shreeram Akilesh, Adriana M. Hung, Matthew Palmer, Aris Baras, John D. Overton, Jeffrey G. Reid, Marylyn D. Ritchie, Daniel J. Rader, Katalin Suszták

    Опубліковано 2021
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  5. 5
    Polygenic prediction of preeclampsia and gestational hypertension

    Polygenic prediction of preeclampsia and gestational hypertension за авторством Michael C. Honigberg, Buu Truong, Raiyan R. Khan, Brenda Xiao, Laxmi Bhatta, Ha My T. Vy, Rafael F. Guerrero, Art Schuermans, Margaret Sunitha Selvaraj, Aniruddh P. Patel, Satoshi Koyama, So Mi Jemma Cho, Shamsudheen Karuthedath Vellarikkal, Mark Trinder, Sarah Urbut, Kathryn J. Gray, Ben Brumpton, Snehal Patil, Sebastian Zöllner, Mariah C. Antopia, Richa Saxena, Girish N. Nadkarni, Ron Do, Qi Yan, Itsik Pe’er, Shefali S. Verma, Rajat M. Gupta, David M. Haas, Hilary C. Martin, David A. van Heel, Triin Laisk, Pradeep Natarajan

    Опубліковано 2023
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  6. 6
    Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program

    Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program за авторством Derek Klarin, Poornima Devineni, Anoop K. Sendamarai, Anthony R. Angueira, Sarah E. Graham, Ying H. Shen, Michael G. Levin, James P. Pirruccello, Ida Surakka, Purushotham Karnam, Tanmoy Roychowdhury, Yanming Li, Minxian Wang, Krishna G. Aragam, Kaavya Paruchuri, Verena Zuber, Gabrielle Shakt, Noah L. Tsao, Renae Judy, Ha My T. Vy, Shefali S. Verma, Daniel J. Rader, Ron Do, Joseph E. Bavaria, Girish N. Nadkarni, Marylyn D. Ritchie, Stephen Burgess, Dongchuan Guo, Patrick T. Ellinor, Scott A. LeMaire, Dianna M. Milewicz, Cristen J. Willer, Pradeep Natarajan, Philip S. Tsao, Saiju Pyarajan, Scott M. Damrauer

    Опубліковано 2023
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  7. 7
    Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

    Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure за авторством Michael G. Levin, Noah L. Tsao, Pankhuri Singhal, Chang Liu, Ha My T. Vy, Ishan Paranjpe, Joshua Backman, Tiffany R. Bellomo, William P. Bone, Kiran J. Biddinger, Qin Hui, Ozan Dikilitas, Benjamin A. Satterfield, Yifan Yang, Michael P. Morley, Yuki Bradford, Megan F. Burke, Nosheen Reza, Brian Charest, Renae Judy, Megan J. Puckelwartz, Hákon Hákonarson, Atlas Khan, Leah C. Kottyan, Iftikhar J. Kullo, Yuan Luo, Elizabeth M. McNally, Laura J. Rasmussen‐Torvik, Sharlene M. Day, Ron Do, Lawrence S. Phillips, Patrick T. Ellinor, Girish N. Nadkarni, Marylyn D. Ritchie, Zoltàn Arany, Thomas P. Cappola, Kenneth B. Margulies, Krishna G. Aragam, Christopher M. Haggerty, Jacob Joseph, Yan V. Sun, Benjamin F. Voight, Scott M. Damrauer

    Опубліковано 2022
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  8. 8
    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 за авторством 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

    Опубліковано 2023
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  9. 9
    Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

    Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors за авторством Florian Thibord, Derek Klarin, Jennifer A. Brody, Ming‐Huei Chen, Michael G. Levin, Daniel I. Chasman, Ellen L. Goode, Kristian Hveem, Maris Teder‐Laving, Ángel Martínez-Pérez, Dylan Aïssi, Delphine Daian-Bacq, Kaoru Ito, Pradeep Natarajan, Pamela L. Lutsey, Girish N. Nadkarni, Paul S. de Vries, Gabriel Cuéllar-Partida, Brooke N. Wolford, Jack Pattee, Charles Kooperberg, Sigrid K. Brækkan, Ruifang Li‐Gao, Noémie Saut, Corriene Sept, Marine Germain, Renae Judy, Kerri L. Wiggins, Darae Ko, Christopher J. O’Donnell, Kent D. Taylor, Franco Giulianini, Mariza de Andrade, Therese Haugdahl Nøst, Anne Boland, Jean‐Philippe Empana, Satoshi Koyama, Thomas Gilliland, Ron Do, Jennifer E. Huffman, Xin Wang, Wei Zhou, José Manuel Soria, Juan Carlos Souto, Nathan Pankratz, Jeffery Haessler, Kristian Hindberg, Frits R. Rosendaal, Constance Turman, Robert Olaso, Rachel L. Kember, Traci M. Bartz, Julie A. Lynch, Susan R. Heckbert, Sebastian M. Armasu, Ben Brumpton, David M. Smadja, Xavier Jouven, Issei Komuro, Katharine Clapham, Ruth J. F. Loos, Cristen J. Willer, Maria Sabater‐Lleal, James S. Pankow, Alexander P. Reiner, Vânia M. Morelli, Paul M. Ridker, Astrid van Hylckama Vlieg, Jean-François Deleuze, Peter Kraft, Daniel J. Rader, Kyung Min Lee, Bruce M. Psaty, Anne Heidi Skogholt, Joseph Emmerich, Pierre Suchon, Stephen S. Rich, Ha My T. Vy, Weihong Tang, Rebecca D. Jackson, John‐Bjarne Hansen, Pierre‐Emmanuel Morange, Christopher Kabrhel, David‐Alexandre Trégouët, Scott M. Damrauer, Andrew D. Johnson, Nicholas L. Smith

    Опубліковано 2022
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