Որոնման արդյունքները - Flannick, Jason
- Ցուցադրվում են 1 - 20 արդյունքները 60
- Գնացեք Հաջորդ էջ
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OR05-1 Genetic Discovery and Translational Decision Support from Exome Sequencing of 45,231 Type 2 Diabetes Cases and Controls from Five Ancestries Udler, Miriam, Flannick, Jason, Mercader, Josep, Fuchsberger, Christian, Mahajan, Anubha, Consortium, for the AMP-T2D
Հրապարակվել է 2019Տեքստ -
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Simulation of Finnish Population History, Guided by Empirical Genetic Data, to Assess Power of Rare-Variant Tests in Finland Wang, Sophie R., Agarwala, Vineeta, Flannick, Jason, Chiang, Charleston W.K., Altshuler, David, Hirschhorn, Joel N.
Հրապարակվել է 2014Տեքստ -
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Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation Flannick, Jason, Korn, Joshua M., Fontanillas, Pierre, Grant, George B., Banks, Eric, Depristo, Mark A., Altshuler, David
Հրապարակվել է 2012Տեքստ -
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Genetic and Computational Identification of a Conserved Bacterial Metabolic Module Boutte, Cara C., Srinivasan, Balaji S., Flannick, Jason A., Novak, Antal F., Martens, Andrew T., Batzoglou, Serafim, Viollier, Patrick H., Crosson, Sean
Հրապարակվել է 2008Տեքստ -
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Targeted 'Next-Generation' sequencing in anophthalmia and microphthalmia patients confirms SOX2, OTX2 and FOXE3 mutations Lopez Jimenez, Nelson, Flannick, Jason, Yahyavi, Mani, Li, Jiang, Bardakjian, Tanya, Tonkin, Leath, Schneider, Adele, Sherr, Elliott H, Slavotinek, Anne M
Հրապարակվել է 2011Տեքստ -
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Evaluating human genetic support for hypothesized metabolic disease genes Dornbos, Peter, Singh, Preeti, Jang, Dong-Keun, Mahajan, Anubha, Biddinger, Sudha B., Rotter, Jerome I., McCarthy, Mark I., Flannick, Jason
Հրապարակվել է 2022Տեքստ -
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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes Majithia, Amit R., Flannick, Jason, Shahinian, Peter, Guo, Michael, Bray, Mark-Anthony, Fontanillas, Pierre, Gabriel, Stacey B., Rosen, Evan D., Altshuler, David
Հրապարակվել է 2014Տեքստ -
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Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population Najmi, Laeya Abdoli, Aukrust, Ingvild, Flannick, Jason, Molnes, Janne, Burtt, Noel, Molven, Anders, Groop, Leif, Altshuler, David, Johansson, Stefan, Bjørkhaug, Lise, Njølstad, Pål Rasmus
Հրապարակվել է 2017Տեքստ -
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The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community Kiel, Douglas P., Kemp, John P., Rivadeneira, Fernando, Westendorf, Jennifer J., Karasik, David, Duncan, Emma, Imai, Yuuki, Müller, Ralph, Flannick, Jason, Bonewald, Lynda, Burtt, Noel
Հրապարակվել է 2020Տեքստ -
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A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis McNulty, Michelle T., Fermin, Damian, Eichinger, Felix, Jang, Dongkeun, Kretzler, Matthias, Burtt, Noel, Pollak, Martin R., Flannick, Jason, Weins, Astrid, Friedman, David J., Sampson, Matthew G.
Հրապարակվել է 2022Տեքստ -
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The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease Moutsianas, Loukas, Agarwala, Vineeta, Fuchsberger, Christian, Flannick, Jason, Rivas, Manuel A., Gaulton, Kyle J., Albers, Patrick K., McVean, Gil, Boehnke, Michael, Altshuler, David, McCarthy, Mark I.
Հրապարակվել է 2015Տեքստ -
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Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes Santoro, Nicola, Chen, Ling, Todd, Jennifer, Divers, Jasmin, Shah, Amy S, Gidding, Samuel S, Burke, Brian, Haymond, Morey, Lange, Leslie, Marcovina, Santica, Flannick, Jason, Caprio, Sonia, Florez, Jose C, Srinivasan, Shylaja
Հրապարակվել է 2021Տեքստ