نتائج البحث - Flannick, Jason
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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 حسب Udler, Miriam, Flannick, Jason, Mercader, Josep, Fuchsberger, Christian, Mahajan, Anubha, Consortium, for the AMP-T2D
منشور في 2019نص -
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Simulation of Finnish Population History, Guided by Empirical Genetic Data, to Assess Power of Rare-Variant Tests in Finland حسب Wang, Sophie R., Agarwala, Vineeta, Flannick, Jason, Chiang, Charleston W.K., Altshuler, David, Hirschhorn, Joel N.
منشور في 2014نص -
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Genetic and Computational Identification of a Conserved Bacterial Metabolic Module حسب Boutte, Cara C., Srinivasan, Balaji S., Flannick, Jason A., Novak, Antal F., Martens, Andrew T., Batzoglou, Serafim, Viollier, Patrick H., Crosson, Sean
منشور في 2008نص -
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Targeted 'Next-Generation' sequencing in anophthalmia and microphthalmia patients confirms SOX2, OTX2 and FOXE3 mutations حسب Lopez Jimenez, Nelson, Flannick, Jason, Yahyavi, Mani, Li, Jiang, Bardakjian, Tanya, Tonkin, Leath, Schneider, Adele, Sherr, Elliott H, Slavotinek, Anne M
منشور في 2011نص -
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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes حسب Majithia, Amit R., Flannick, Jason, Shahinian, Peter, Guo, Michael, Bray, Mark-Anthony, Fontanillas, Pierre, Gabriel, Stacey B., Rosen, Evan D., Altshuler, David
منشور في 2014نص -
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Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population حسب Najmi, Laeya Abdoli, Aukrust, Ingvild, Flannick, Jason, Molnes, Janne, Burtt, Noel, Molven, Anders, Groop, Leif, Altshuler, David, Johansson, Stefan, Bjørkhaug, Lise, Njølstad, Pål Rasmus
منشور في 2017نص -
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The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community حسب 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
منشور في 2020نص -
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A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis حسب 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.
منشور في 2022نص -
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The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease حسب 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.
منشور في 2015نص -
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Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes حسب 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
منشور في 2021نص