Ngā hua rapu - Flannick, Jason

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

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

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

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

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

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