Identification and functional validation of rare coding variants in genes linked to monogenic obesity von Köroğlu, Çiğdem, Traurig, Michael, Muller, Yunhua L., Day, Samantha E., Piaggi, Paolo, Wiedrich, Kim, Vazquez, Laura, Hanson, Robert L., Van Hout, Cristopher V., Alkelai, Anna, Shuldiner, Alan R., Bogardus, Clifton, Baier, Leslie J.

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A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes von Hanson, Robert L, Muller, Yunhua L, Kobes, Sayuko, Guo, Tingwei, Bian, Li, Ossowski, Victoria, Wiedrich, Kim, Sutherland, Jeffrey, Wiedrich, Christopher, Mahkee, Darin, Huang, Ke, Abdussamad, Maryam, Traurig, Michael, Weil, E Jennifer, Nelson, Robert G, Bennett, Peter H, Knowler, William C, Bogardus, Clifton, Baier, Leslie J

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Exome Sequencing of 21 Bardet‐Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians von Day, Samantha E., Muller, Yunhua L., Koroglu, Cigdem, Kobes, Sayuko, Wiedrich, Kim, Mahkee, Darin, Kim, Hye In, Van Hout, Cris, Gosalia, Nehal, Ye, Bin, Shuldiner, Alan R., Knowler, William C., Hanson, Robert L., Bogardus, Clifton, Baier, Leslie J.

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Identification of genetic variation that determines human trehalase activity and its association with type 2 diabetes von Muller, Yunhua L., Hanson, Robert L., Knowler, William C., Fleming, Jamie, Goswami, Jayita, Huang, Ke, Traurig, Michael, Sutherland, Jeff, Wiedrich, Chris, Wiedrich, Kim, Mahkee, Darin, Ossowski, Vicky, Kobes, Sayuko, Bogardus, Clifton, Baier, Leslie J.

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Variants in ASK1 Are Associated With Skeletal Muscle ASK1 Expression, In Vivo Insulin Resistance, and Type 2 Diabetes in Pima Indians von LI BIAN, HANSON, Robert L, BOGARDUS, Clifton, OSSOWSKI, Victoria, WIEDRICH, Kim, MASON, Clinton C, TRAURIG, Michael, MULLER, Yunhua L, KOBES, Sayuko, KNOWLER, William C, BAIER, Leslie J

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