Sequencing of Lp-PLA2-encoding PLA2G7 gene in 2000 Europeans reveals several rare loss-of-function mutations von Song, K, Nelson, M R, Aponte, J, Manas, E S, Bacanu, S-A, Yuan, X, Kong, X, Cardon, L, Mooser, V E, Whittaker, J C, Waterworth, D M

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Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism von Xu, C-F, Reck, B H, Xue, Z, Huang, L, Baker, K L, Chen, M, Chen, E P, Ellens, H E, Mooser, V E, Cardon, L R, Spraggs, C F, Pandite, L

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Concomitant use of pazopanib and simvastatin increases the risk of transaminase elevations in patients with cancer von Xu, C.F., Xue, Z., Bing, N., King, K.S., McCann, L.A., de Souza, P.L., Goodman, V.L., Spraggs, C.F., Mooser, V.E., Pandite, L.N.

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HLA-DRB107:01-DQA102:01 and UGT1A128 allele carriage in hepatic serious adverse event cases identified during lapatinib clinical trials von Spraggs, C. F., Budde, L. R., Briley, L. P., Cox, C., Rappold, E., Aktan, G., Williams, L. S., Mooser, V. E., Cardon, L. R.

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Pharmacogenetic investigation of lapatinib-associated diarrhea in metastatic breast cancer clinical trials von Briley, L. P., Chiano, M., King, K., Casey, M., Preston, A. J., Sapunar, F., Mooser, V. E., Cardon, L. R., Spraggs, C. F.

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Association of genetic markers in angiogenesis- or exposure-related genes with overall survival in pazopanib (P) treated patients (Pts) with advanced renal cell carcinoma von Xu, C., Ball, H. A., Bing, N., Sternberg, C. N., Xue, Z., McCann, L., King, K., Spraggs, C. F., Mooser, V. E., Pandite, L. N.

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Association of the hemochromatosis (HFE) gene with pazopanib-induced transaminase elevations in renal cell carcinoma von Xu, C., Reck, B. H., Goodman, V. L., Xue, Z., Huang, L., Spraggs, C. F., Mooser, V. E., Cardon, L. R., Pandite, L.

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Association of germ-line SNPs with overall survival (OS) in pazopanib-treated patients (Pts) with advanced renal cell carcinoma (RCC) von Xu, C., Bing, N., Ball, H. A., Sternberg, C. N., Davis, I. D., Xue, Z., McCann, L., King, K., Whittaker, J. C., Spraggs, C. F., Mooser, V. E., Pandite, L. N.

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Genetic evaluation of fatigue in pazopanib-treated patients (pts) with advanced renal cell carcinoma (RCC) von Glass, S. M., Huang, L., King, K., Ragone, L. J., Ball, H. A., De Souza, P. L., Wagstaff, J., Spraggs, C. F., Mooser, V. E., Pandite, L. N., Xu, C.

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Association of germ-line genetic markers in IL8, HIF1A, VEGFA, and VEGFR2 with treatment response to pazopanib in renal cell carcinoma von Ball, H. A., Xu, C., Sternberg, C. N., Bing, N., Rajagopalan, D., Spraggs, C. F., Mooser, V. E., Amado, R. G., Cardon, L. R., Pandite, L.

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Relationship of HLA-DQA10201 and lapatinib-induced hepatotoxicity in women with advanced breast cancer von Spraggs, C. F., Budde, L. R., Briley, L. P., Bing, N., Preston, A. J., Mooser, V. E., Cardon, L. R., Stein, S. H.

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Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGTIAI polymorphism von XU, C.-F, RECK, B. H, SPRAGGS, C. F, PANDITE, L, XUE, Z, HUANG, L, BAKER, K. L, CHEN, M, CHEN, E. P, ELLENS, H. E, MOOSER, V. E, CARTON, L. R

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An 18-kDa Translocator Protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28 von Owen, DR, Yeo, AJ, Gunn, RN, Song, K, Wadsworth, G, Lewis, A, Rhodes, C, Pulford, DJ, Bennacef, I, Parker, CA, StJean, PL, Cardon, LR, Mooser, VE, Matthews, PM, Rabiner, EA, Rubio, JP

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Concomitant use of pazopanib and simvastatin increases the risk of transaminase elevations in patients with cancer von Xu, C F, Xue, Z, Bing, N, King, K S, McCann, L A, de Souza, P L, Goodman, V L, Spraggs, C F, Mooser, V E, Pandite, L N

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Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals von Dastani, Z, Perry, JRB, Yuan, X, Scott, RA, Heid, IM, Lyytikainen, L-P, Fuchsberger, C, Tanaka, T, Morris, AP, Small, K, Isaacs, A, Beekman, M, Coassin, S, Lohman, K, Kanoni, S, Pankow, JS, Uh, H-W, Wu, Y, Bidulescu, A, Rasmussen-Torvik, LJ, Greenwood, CMT, Ladouceur, M, Manning, AK, Liu, C-T, Kooner, J, Mooser, VE, Vollenweider, P, Kapur, KA, Chambers, J, Wareham, NJ, Langenberg, C, Frants, R, Willems-vanDijk, K, Oostra, BA, Willems, SM, Lamina, C, Winkler, TW, Psaty, BM, Tracy, RP, Brody, J, Chen, I, Viikari, J, Kahonen, M, Pramstaller, PP, Evans, DM, St Pourcain, B, Sattar, N, Wood, AR, Bandinelli, S, Carlson, OD, Egan, JM, Bohringer, S, Van Heemst, D, Kedenko, L, Kristiansson, K, Loo, B-M, Harris, T, Garcia, M, Kanaya, A, Haun, M, Klopp, N, Wichmann, H-E, Deloukas, P, Couper, DJ, Duncan, BB, Kloppenburg, M, Adair, LS, Borja, JB, Wilson, JG, Musani, S, Johnson, T, Semple, R, Teslovich, TM, Allison, MA, Redline, S, Buxbaum, SG, Mohlke, KL, Meulenbelt, I, Ballantyne, CM, Dedoussis, GV, Hu, FB, Paulweber, B, Spector, TD, Ferrucci, L, Jula, A, Perola, M, Raitakari, O, Salomaa, V, Eriksson, JG, Frayling, TM, Lehtimaki, T, Smith, GD, Siscovick, DS, Kronenberg, F, Van Duijn, C, Loos, RJF, Waterworth, DM, Meigs, JB, Dupuis, J, Richards, JB

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Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways von Soranzo, N, Sanna, S, Langenberg, C, Prokopenko, I, Stolerman, E, Sandhu, MS, Devaney, JM, Reilly, MP, Ricketts, SL, Stewart, AF, Arking, D, Balkau, B, Böhm, B, Bonnefond, A, Bonnycastle, LL, Bornstein, SR, Burnett-Miller, MS, Campbell, H, Cao, A, Chambers, J, Clark, R, Collins, FS, Deloukas, P, Egan, JM, Ferrucci, L, Forouhi, N, Fox, CS, Franzosi, MG, Goel, A, Grallert, H, Hadley, D, Hamsten, A, Hayward, C, Heath, S, Herder, C, Homuth, G, Hottenga, JJ, Hunter-Merrill, R, Illig, T, Jackson, AU, Kleber, M, Knouff, CW, Kooner, J, Köttgen, A, Kovacs, P, Kühnel, B, Lathrop, M, Loos, RJ, Mägi, R, Magnusson, PK, Mangino, M, McArdle, WL, McPherson, R, Meitinger, T, Melander, O, Mohlke, KL, Morken, MA, Nathan, DM, Oexle, K, Olla, N, Pankow, JS, Pedersen, NL, Peltonen, L, Perola, M, Polasek, O, Porcu, E, Rathmann, W, Rocheleau, G, Roden, M, Rudan, I, Salomaa, V, Schlessinger, D, Seedorf, U, Selvin, E, Serrano-Ríos, M, Shrader, P, Siscovick, D, Song, K, Spector, TD, Stefansson, K, Strawbridge, R, Stumvoll, M, Tanaka, T, Teumer, A, Thorsteinsdottir, U, Tönjes, A, Wallaschofski, H, Watkins, H, Wild, SH, Willemsen, G, Williams, GH, Wright, AF, Epstein, SE, Hakonarson, HH, Roberts, R, Fleming, MD, Sladek, R, Froguel, P, McCarthy, MI, Uda, M

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Sequencing of Lp-PLA2-encoding PLA2G7 gene in 2000 Europeans reveals several rare loss-of-function mutations von Song, K, Nelson, MR, Aponte, J, Manas, ES, Bacanu, S-A, Yuan, X, Kong, X, Cardon, L, Mooser, VE, Whittaker, JC, Waterworth, DM

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Direct limits on the interaction of antiprotons with axion-like dark matter von Smorra, C., Stadnik, Y. V., Blessing, P. E., Bohman, M., Borchert, M. J., Devlin, J. A., Erlewein, S., Harrington, J. A., Higuchi, T., Mooser, A., Schneider, G., Wiesinger, M., Wursten, E., Blaum, K., Matsuda, Y., Ospelkaus, C., Quint, W., Walz, J., Yamazaki, Y., Budker, D., Ulmer, S.

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Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts von Muglia, P, Tozzi, F, Galwey, N W, Francks, C, Upmanyu, R, Kong, X Q, Antoniades, A, Domenici, E, Perry, J, Rothen, S, Vandeleur, C L, Mooser, V, Waeber, G, Vollenweider, P, Preisig, M, Lucae, S, Müller-Myhsok, B, Holsboer, F, Middleton, L T, Roses, A D

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Sympathetic cooling of a trapped proton mediated by an LC circuit von Bohman, M., Grunhofer, V., Smorra, C., Wiesinger, M., Will, C., Borchert, M. J., Devlin, J. A., Erlewein, S., Fleck, M., Gavranovic, S., Harrington, J., Latacz, B., Mooser, A., Popper, D., Wursten, E., Blaum, K., Matsuda, Y., Ospelkaus, C., Quint, W., Walz, J., Ulmer, S.

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