Publications

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Hansen, S. N., Ehlers, N. S., Zhu, S., Thomsen, M. B. H., Nielsen, R. L., Liu, D., Wang, G., Hou, Y., Zhang, X., Xu, X., Bolund, L., Yang, H., Wang, J., Moreira, J., Ditzel, H. J., Brünner, N., Schrohl, A.-S., Stenvang, J. & Gupta, R. (2016). The stepwise evolution of the exome during acquisition of docetaxel resistance in breast cancer cells. BMC Genomics, 17(1), 442. Article 442. https://doi.org/10.1186/s12864-016-2749-4
Herold, C., Hooli, B. V., Mullin, K., Liu, T., Roehr, J. T., Mattheisen, M., Parrado, A. R., Bertram, L., Lange, C. & Tanzi, R. E. (2016). Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. Molecular Psychiatry, 21(11), 1608-1612. https://doi.org/10.1038/mp.2015.218
Hersom, M., Helms, H. C., Pretzer, N., Goldeman, C., Jensen, A. I., Severin, G., Nielsen, M. S., Holm, R. & Brodin, B. (2016). Transferrin receptor expression and role in transendothelial transport of transferrin in cultured brain endothelial monolayers. Molecular and Cellular Neuroscience, 76, 59-67. https://doi.org/10.1016/j.mcn.2016.08.009
Higuti, E., Cecchi, C. R., Oliveira, N. A. J., Lima, E. R., Vieira, D. P., Aagaard, L., Jensen, T. G., Jorge, A. A. L., Bartolini, P. & Peroni, C. N. (2016). Partial correction of the dwarf phenotype by non-viral transfer of the growth hormone gene in mice: Treatment age is critical. Growth Hormone and IGF Research, 26, 1-7. https://doi.org/10.1016/j.ghir.2015.12.001
Hill, M., Johnson, J.-A., Langlois, S., Lee, H., Winsor, S., Dineley, B., Horniachek, M., Lalatta, F., Ronzoni, L., Barrett, A. N., Advani, H. V., Choolani, M., Rabinowitz, R., Pajkrt, E., van Schendel, R. V., Henneman, L., Rommers, W., Bilardo, C. M., Rendeiro, P. ... Chitty, L. S. (2016). Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals. European Journal of Human Genetics, 24(7), 968-975. https://doi.org/10.1038/ejhg.2015.249
Hou, L., Heilbronner, U., Degenhardt, F., Adli, M., Akiyama, K., Akula, N., Ardau, R., Arias, B., Backlund, L., Banzato, C. E. M., Benabarre, A., Bengesser, S., Bhattacharjee, A. K., Biernacka, J. M., Birner, A., Brichant-Petitjean, C., Bui, E. T., Cervantes, P., Chen, G.-B. ... Schulze, T. G. (2016). Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. The Lancet, 387(10023), 1085-1093. https://doi.org/10.1016/S0140-6736(16)00143-4