Search Results - Moses, E.

Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children by Song, Y., Higgins, H., Guo, J., Harrison, K., Schultz, E., Hales, B., Moses, E., Goldblatt, J., Pachter, N., Zhang, Guicheng

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Genome wide association and pathway analysis of segment-specific carotid intima-media thickness phenotypes: The San Antonio Family Heart Study by Melton, Phillip, Curran, J., Carless, M., Johnson, M., Dyer, T., MacCluer, J., Moses, E., Goering, H., Blangero, J., Almasy, L.

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Assessment of Cognition and Personality as Potential Endophenotypes in the Western Australian Family Study of Schizophrenia. by McCarthy, N., Badcock, J., Clark, M., Knowles, E., Cadby, G., Melton, Phillip, Morgan, V., Blangero, J., Moses, E., Glahn, D., Jablensky, A.

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Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes by Melton, Phillip, Johnson, M., Gokhale-Agashe, D., Rea, A., Ariff, A., Cadby, G., Peralta, J., Mcnab, T., Allcock, R., Abraham, L., Blangero, J., Brennecke, S., Moses, E.

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A genome-wide association study for malignant mesothelioma risk by Cadby, G., Mukherjee, S., Musk, A., Reid, A., Garlepp, Michael, Dick I., Robinson, C., Hui, J., Fiorito, G., Guarrera, S., Beilby, J., Melton, P., Moses, E., Ugolini, D., Mirabelli, D., Bonassi, S., Magnani, C., Dianzani, I., Matullo, G., Robinson, B., Creaney, J., Palmer, L.

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