Risultati della ricerca - Carla Márquez‐Luna
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Multi-ethnic polygenic risk scores improve risk prediction in diverse populations di Carla Márquez‐Luna, Po‐Ru Loh, Alkes L. Price
Pubblicazione 2016Pré-impressão -
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Multiethnic polygenic risk scores improve risk prediction in diverse populations di Carla Márquez‐Luna, Po‐Ru Loh, Alkes L. Price
Pubblicazione 2017Artigo -
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Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association di Jack W. O’Sullivan, Sridharan Raghavan, Carla Márquez‐Luna, Jasmine A. Luzum, Scott M. Damrauer, Euan A. Ashley, Christopher J. O’Donnell, Cristen J. Willer, Pradeep Natarajan
Pubblicazione 2022Revisão -
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Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts di Iain S. Forrest, Ben Omega Petrazzini, Áine Duffy, Joshua K. Park, Carla Márquez‐Luna, Daniel M. Jordan, Ghislain Rocheleau, Judy H. Cho, Robert S. Rosenson, Jagat Narula, Girish N. Nadkarni, Ron Do
Pubblicazione 2022Artigo -
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Functionally informed fine-mapping and polygenic localization of complex trait heritability di Omer Weissbrod, Farhad Hormozdiari, Christian Benner, Ran Cui, Jacob C. Ulirsch, Steven Gazal, Armin Schoech, Bryce van de Geijn, Yakir Reshef, Carla Márquez‐Luna, Luke J. O’Connor, Matti Pirinen, Hilary K. Finucane, Alkes L. Price
Pubblicazione 2020Artigo -
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Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets di Carla Márquez‐Luna, Steven Gazal, Po‐Ru Loh, Samuel S. Kim, Nicholas A. Furlotte, Adam Auton, Michelle Agee, Babak Alipanahi, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, David A. Hinds, Jey C. McCreight, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, Matthew H. McIntyre, Joanna L. Mountain, Elizabeth S. Noblin, Carrie A. M. Northover, Steven J. Pitts, J. Fah Sathirapongsasuti, Olga V. Sazonova, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Vladimir Vacic, Catherine H. Wilson, Alkes L. Price
Pubblicazione 2021Revisão -
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Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico di A. L. Williams Amy, S. B R Jacobs Suzanne, Hortensia Moreno-Macías, Alicia Huerta-Chagoya, Claire Churchhouse, Carla Márquez‐Luna, María José Gómez-Vázquez, N. P. Burtt Noël, Carlos A. Aguilar‐Salinas, Clicerio González‐Villalpando, José C. Florez, Lorena Orozco, Teresa Tusié‐Luna, David Altshuler, Stephan Ripke, Alisa K. Manning, Humberto Garcia‐Ortíz, Benjamin M. Neale, David Reich, Daniel O. Stram, Juan Carlos Fernández-López, Sandra Romero‐Hidalgo, Nick Patterson, Christopher A Haiman, Irma Aguilar-Delfín, Angélica Martínez‐Hernández, Federico Centeno-Cruz, Elvia Mendoza‐Caamal, M. Revilla, Sergio Islas‐Andrade, Emilio J. Córdova, Martha Eunice Rodríguez-Arellano, Xavier Soberón, Jobinse Jose, M. A. González-Villalpando María Elena, Brian E. Henderson, Kristine R. Monroe, Lynne R. Wilkens, Laurence N. Kolonel, Loı̈c Le Marchand, Laura Riba, Ma Luisa, Rosario Rodríguez-Guillén, Ivette Cruz‐Bautista, M. Rodríguez‐Torres, Liliana Muñóz-Hernández, Tamara Sáenz, Donají Gómez, Ulices Alvirde, Robert C. Onofrio, Wendy Brodeur, Diane Gage, Jacquelyn Murphy, Jennifer Franklin, Scott Mahan, Kristin Ardlie, Andrew Crenshaw, Wendy Winckler, Kay Prüfer, M.V. Shunkov, Susanna Sawyer, Udo Stenzel, Janet Kelso, Monkol Lek, Sriram Sankararaman, Daniel G. MacArthur, А. П. Деревянко, Svante Pääbo, Suzanne B.R. Jacobs, Shuba Gopal, James A. Grammatikos, Ian C. P. Smith, Kevin Bullock, Amy Deik, Amanda L. Souza, Kerry A. Pierce, Clary B. Clish, Timothy R. Fennell, Yossi Farjoun, Stacey Gabriel, Myron D. Gross, Mark A. Pereira, Mark Seielstad, Woon‐Puay Koh, E. Shyong Tai, Jason Flannick, Pierre Fontanillas, Andrew P. Morris, Tanya M. Teslovich, Gil Atzmon, John Blangero, Donald W. Bowden, John C. Chambers, Yoon Shin Cho, Ravindranath Duggirala, Benjamin Gläser, Craig L. Hanis, Jaspal S. Kooner, Markku Laakso, Jong‐Young Lee
Pubblicazione 2013Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Gene
Genetics
Computer science
Biobank
Genotype
Medicine
Single-nucleotide polymorphism
Bioinformatics
Environmental health
Machine learning
Mathematics
Population
Statistics
Artificial intelligence
Genome-wide association study
Heritability
Internal medicine
Programming language
Quantitative trait locus
Trait
Bayesian probability
Chemistry
Chromatography
Cohort
Computational biology
Confidence interval
Data mining
Demography
Genetic architecture