Torthaí cuardaigh - Ha My T. Vy
- 1 - 9 toradh as 9 á dtaispeáint
-
1
A Composite-Likelihood Method for Detecting Incomplete Selective Sweep from Population Genomic Data de réir Ha My T. Vy, Yuseob Kim
Foilsithe / Cruthaithe 2015Artigo -
2
Population-Based Penetrance of Deleterious Clinical Variants de réir 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
Foilsithe / Cruthaithe 2022Artigo -
3
Genetically Downregulated Interleukin-6 Signaling Is Associated With a Favorable Cardiometabolic Profile de réir 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
Foilsithe / Cruthaithe 2021Carta -
4
Kidney disease genetic risk variants alter lysosomal beta-mannosidase ( <i>MANBA</i> ) expression and disease severity de réir 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
Foilsithe / Cruthaithe 2021Artigo -
5
Polygenic prediction of preeclampsia and gestational hypertension de réir 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
Foilsithe / Cruthaithe 2023Revisão -
6
Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program de réir 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
Foilsithe / Cruthaithe 2023Artigo -
7
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure de réir 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
Foilsithe / Cruthaithe 2022Revisão -
8
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas de réir 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
Foilsithe / Cruthaithe 2023Revisão -
9
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors de réir 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
Foilsithe / Cruthaithe 2022Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Genotype
Medicine
Single-nucleotide polymorphism
Bioinformatics
Genome-wide association study
Internal medicine
Genetic association
Disease
Genetic variants
Mendelian randomization
Population
1000 Genomes Project
Allele
Candidate gene
Computational biology
Endocrinology
Environmental health
Evolutionary biology
Expression quantitative trait loci
Kidney disease
Phenotype
Allele frequency
Aneurysm
Aorta
Aortic aneurysm
Aortic dissection
Aristolochic acid