Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Ha My T. Vy"'
Autor:
Michael G. Levin, Noah L. Tsao, Pankhuri Singhal, Chang Liu, Ha My T. Vy, Ishan Paranjpe, Joshua D. 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 Burke, Nosheen Reza, Brian Charest, Regeneron Genetics Center, Renae L. Judy, Megan J. Puckelwartz, Hakon Hakonarson, Atlas Khan, Leah C. Kottyan, Iftikhar 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, Zoltan Arany, Thomas P. Cappola, Kenneth B. Margulies, Krishna G. Aragam, Christopher M. Haggerty, Jacob Joseph, Yan V. Sun, Benjamin F. Voight, Scott M. Damrauer
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-15 (2022)
Heart failure is a major cause of cardiovascular morbidity and mortality. Here, the authors report results of a genome-wide association study meta-analysis, characterizing the role of common genetic variants in heart failure, finding overlap with com
Externí odkaz:
https://doaj.org/article/2a5c23e2c7b142b5961a518b4d904c75
Autor:
Joshua K. Park, Ben O. Petrazzini, Aparna Saha, Akhil Vaid, Ha My T. Vy, Carla Márquez‐Luna, Lili Chan, Girish N. Nadkarni, Ron Do
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 8 (2023)
Externí odkaz:
https://doaj.org/article/c65c964459ff45d98476627f426b2e71
Autor:
Kristin Meliambro, Xuezhu Li, Fadi Salem, Zhengzi Yi, Zeguo Sun, Lili Chan, Miriam Chung, Jorge Chancay, Ha My T. Vy, Girish Nadkarni, Jenny S. Wong, Jia Fu, Kyung Lee, Weijia Zhang, John C. He, Kirk N. Campbell
Publikováno v:
Kidney Medicine, Vol 3, Iss 4, Pp 653-658 (2021)
Recent case reports suggest that coronavirus disease 2019 (COVID-19) is associated with collapsing glomerulopathy in African Americans with apolipoprotein L1 gene (APOL1) risk alleles; however, it is unclear whether disease pathogenesis is similar to
Externí odkaz:
https://doaj.org/article/16a9a594ddad44c7b2f31898eee1b372
Autor:
Ha My T, Vy, Bridget M, Lin, Faris F, Gulamali, Charles, Kooperberg, Mariaelisa, Graff, Jenny, Wong, Kirk N, Campbell, Tara C, Matise, Josef, Coresh, Fridtjof, Thomas, Alexander P, Reiner, Rami, Nassir, Peter F, Schnatz, Tanya, Johns, Steven, Buyske, Christopher, Haiman, Richard, Cooper, Ruth J F, Loos, Carol R, Horowitz, Orlando M, Gutierrez, Ron, Do, Nora, Franceschini, Girish N, Nadkarni
Publikováno v:
Clinical journal of the American Society of Nephrology : CJASN.
Autor:
Florian, Thibord, Derek, Klarin, Jennifer A, Brody, Ming-Huei, Chen, Michael G, Levin, Daniel I, Chasman, Ellen L, Goode, Kristian, Hveem, Maris, Teder-Laving, Angel, Martinez-Perez, Dylan, Aïssi, Delphine, Daian-Bacq, Kaoru, Ito, Pradeep, Natarajan, Pamela L, Lutsey, Girish N, Nadkarni, Paul S, de Vries, Gabriel, Cuellar-Partida, Brooke N, Wolford, Jack W, Pattee, Charles, Kooperberg, Sigrid K, Braekkan, Ruifang, Li-Gao, Noemie, Saut, Corriene, Sept, Marine, Germain, Renae L, Judy, Kerri L, Wiggins, Darae, Ko, Christopher J, O'Donnell, Kent D, Taylor, Franco, Giulianini, Mariza, De Andrade, Therese H, Nøst, Anne, Boland, Jean-Philippe, Empana, Satoshi, Koyama, Thomas, Gilliland, Ron, Do, Jennifer E, Huffman, Xin, Wang, Wei, Zhou, Jose, 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 R, Clapham, Ruth J F, Loos, Cristen J, Willer, Maria, Sabater-Lleal, James S, Pankow, Alexander P, Reiner, Vania 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
Publikováno v:
Circulation
Circulation, 2022, 146 (16), ⟨10.1161/CIRCULATIONAHA.122.059675⟩
CIRCULATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Circulation, 2022, 146 (16), ⟨10.1161/CIRCULATIONAHA.122.059675⟩
CIRCULATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Background: Venous thromboembolism (VTE) is a life-threatening vascular event with environmental and genetic determinants. Recent VTE genome-wide association studies (GWAS) meta-analyses involved nearly 30 000 VTE cases and identified up to 40 geneti
Autor:
Ha My T. Vy, Bridget M. Lin, Faris F. Gulamali, Charles Kooperberg, Mariaelisa Graff, Jenny Wong, Kirk N. Campbell, Tara C. Matise, Josef Coresh, Fridtjof Thomas, Alexander P. Reiner, Rami Nassir, Peter F. Schnatz, Tanya Johns, Steven Buyske, Christopher Haiman, Richard Cooper, Ruth J.F. Loos, Carol R. Horowitz, Orlando M. Gutierrez, Ron Do, Nora Franceschini, Girish N. Nadkarni
Publikováno v:
Clinical Journal of the American Society of Nephrology. 17:1522-1525
Autor:
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 M. Urbut, Kathryn J. Gray, Ben M. Brumpton, Snehal Patil, Sebastian Zöllner, Mariah C. Antopia, Richa Saxena, Girish N. Nadkarni, Ron Do, Qi Yan, Itsik Pe’er, Shefali Setia Verma, Rajat M. Gupta, David M. Haas, Hilary C. Martin, David A. van Heel, Triin Laisk, Pradeep Natarajan
Publikováno v:
Nature Medicine.
Autor:
Hongbo Liu, Tomohito Doke, Dong Guo, Xin Sheng, Ziyuan Ma, Joseph Park, Ha My T. Vy, Girish N. Nadkarni, Amin Abedini, Zhen Miao, Matthew Palmer, Benjamin F. Voight, Hongzhe Li, Christopher D. Brown, Marylyn D. Ritchie, Yan Shu, Katalin Susztak
Publikováno v:
Nature Genetics. 54:950-962
More than 800 million people suffer from kidney disease, yet the mechanism of kidney dysfunction is poorly understood. In the present study, we define the genetic association with kidney function in 1.5 million individuals and identify 878 (126 new)
Autor:
Jenny Wong, Kristin Meliambro, John Cijiang He, Zhengzi Yi, Lili Chan, Ha My T. Vy, Fadi Salem, Zeguo Sun, Miriam Chung, Girish N. Nadkarni, Kyung Lee, Jia Fu, Weijia Zhang, Xuezhu Li, Jorge Chancay, Kirk N. Campbell
Publikováno v:
Kidney Medicine, Vol 3, Iss 4, Pp 653-658 (2021)
Kidney Medicine
Kidney Medicine
Recent case reports suggest that coronavirus disease 2019 (COVID-19) is associated with collapsing glomerulopathy in African Americans with apolipoprotein L1 gene (APOL1) risk alleles; however, it is unclear whether disease pathogenesis is similar to
Autor:
Hong-Hee Won, Shantanu Bafna, Louis R. Pasquale, Girish N. Nadkarni, Ghislain Rocheleau, Ha My T. Vy, Kumardeep Chaudhary, Ruth J. F. Loos, Judy H. Cho, Iain S. Forrest, Ron Do, Soyeon Kim
Publikováno v:
Hum Mutat
Biobanks with exomes linked to electronic health records (EHRs) enable the study of genetic pleiotropy between rare variants and seemingly disparate diseases. We performed robust clinical phenotyping of rare, putatively deleterious variants (loss-of-