Canlyniadau Chwilio - Flannick, Jason

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

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

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Using multiple alignments to improve seeded local alignment algorithms gan 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 gan Gupta, Adit, Flannick, Jason

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

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

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Automatic Parameter Learning for Multiple Local Network Alignment gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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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