Rezultati - Flannick, Jason

The Contribution of Low-Frequency and Rare Coding Variation to Susceptibility to Type 2 Diabetes od Flannick, Jason

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Data driven T2D patient clusters predict metabolic surgery outcomes od Flannick, Jason

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Using multiple alignments to improve seeded local alignment algorithms od Flannick, Jason, Batzoglou, Serafim

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MON-186 An Evaluation of the Ability of Current Exome Sequence Datasets to Retrospectively Validate Drugs for T2D or Related Metabolic Traits od Gupta, Adit, Flannick, Jason

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A Novel Algorithm for Rare Disease Gene Prediction Based on Phenotypic Similarity od Fan, Yibo, Flannick, Jason

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Evaluating empirical bounds on complex disease genetic architecture od Agarwala, Vineeta, Flannick, Jason, Sunyaev, Shamil, Altshuler, David

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Automatic Parameter Learning for Multiple Local Network Alignment od Flannick, Jason, Novak, Antal, Do, Chuong B., Srinivasan, Balaji S., Batzoglou, Serafim

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Græmlin: General and robust alignment of multiple large interaction networks od Flannick, Jason, Novak, Antal, Srinivasan, Balaji S., McAdams, Harley H., Batzoglou, Serafim

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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 od Udler, Miriam, Flannick, Jason, Mercader, Josep, Fuchsberger, Christian, Mahajan, Anubha, Consortium, for the AMP-T2D

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Simulation of Finnish Population History, Guided by Empirical Genetic Data, to Assess Power of Rare-Variant Tests in Finland od Wang, Sophie R., Agarwala, Vineeta, Flannick, Jason, Chiang, Charleston W.K., Altshuler, David, Hirschhorn, Joel N.

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Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation od Flannick, Jason, Korn, Joshua M., Fontanillas, Pierre, Grant, George B., Banks, Eric, Depristo, Mark A., Altshuler, David

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Genetic and Computational Identification of a Conserved Bacterial Metabolic Module od Boutte, Cara C., Srinivasan, Balaji S., Flannick, Jason A., Novak, Antal F., Martens, Andrew T., Batzoglou, Serafim, Viollier, Patrick H., Crosson, Sean

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Targeted 'Next-Generation' sequencing in anophthalmia and microphthalmia patients confirms SOX2, OTX2 and FOXE3 mutations od Lopez Jimenez, Nelson, Flannick, Jason, Yahyavi, Mani, Li, Jiang, Bardakjian, Tanya, Tonkin, Leath, Schneider, Adele, Sherr, Elliott H, Slavotinek, Anne M

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Evaluating human genetic support for hypothesized metabolic disease genes od Dornbos, Peter, Singh, Preeti, Jang, Dong-Keun, Mahajan, Anubha, Biddinger, Sudha B., Rotter, Jerome I., McCarthy, Mark I., Flannick, Jason

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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes od Majithia, Amit R., Flannick, Jason, Shahinian, Peter, Guo, Michael, Bray, Mark-Anthony, Fontanillas, Pierre, Gabriel, Stacey B., Rosen, Evan D., Altshuler, David

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Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population od Najmi, Laeya Abdoli, Aukrust, Ingvild, Flannick, Jason, Molnes, Janne, Burtt, Noel, Molven, Anders, Groop, Leif, Altshuler, David, Johansson, Stefan, Bjørkhaug, Lise, Njølstad, Pål Rasmus

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The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community od 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

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A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis od 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.

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The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease od 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.

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Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes od 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

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