Pharmacogenomics, ancestry and clinical decision making for global populations von Ramos, E, Doumatey, A, Elkahloun, A G, Shriner, D, Huang, H, Chen, G, Zhou, J, McLeod, H, Adeyemo, A, Rotimi, C N

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Breast cancer and metabolic syndrome linked through the plasminogen activator inhibitor-1 cycle von Beaulieu, L.M, Whitley, B.R, Wiesner, T.F, Rehault, S.M, Palmieri, D, Elkahloun, A.G, Church, F.C

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Identification of a larger than 3 Mb deletion including JAG1 in an Alagille syndrome patient with a translocation t(3;20)(q13.3;p12.2) von Oda, T., Elkahloun, A.G., Meltzer, P.S., Okajima, K., Sugiyama, K., Wada, Y., Chandrasekharappa, S.C.

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Isolation of a Cosmid Sublibrary for a Region of Chromosome 12 Frequently Amplified in Human Cancers Using a Complex Chromosome Microdissection Probe von Elkahloun, Abdel G., Meltzer, Paul S., Guan, Xin-Yuan, McNinch, Jennifer S., Trent, Jeffrey M., de Jong, Pieter J.

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Frequent truncating mutations of STAG2 in bladder cancer von Solomon, D.A., Kim, J.S., Bondaruk, J., Shariat, S.F., Wang, Z.F., Elkahloun, A.G., Ozawa, T., Gerard, J., Zhuang, D.Z., Zhang, S.Z., Navai, N., Siefker-Radtke, A., Phillips, J.J., Robinson, B.D., Rubin, M.A., Volkmer, B., Hautmann, R., Kufer, R., Hogendoorn, P.C.W., Netto, G., Theodorescu, D., James, C.D., Czerniak, B., Miettinen, M., Waldman, T.

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