NCA Publications

New NCA Publications

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Wen, J. G., Chang, Q. L., Lou, A. F., Li, Z. Z., Lu, S., Wang, Y., Wang, Y. L., Hu, J. H., Mao, S. P., Zhang, Y., Xue, R., Ren, C., Xing, L., Zhang, G. X., Zhang, S., Djurhuus, J. C. & Frøkiaer, J. (2011). Melamine-Related Urinary Stones in 195 Infants and Young Children: Clinical Features within 2 Years of Follow-Up. Urologia Internationalis. https://doi.org/10.1159/000330795
Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J. I., Okbay, A., Bybjerg-Grauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S. J., Bishop, S., Mortensen, P. B. ... iPSYCH-Broad Autism Group (2017). Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nature Genetics, 49(7), 978-985. https://doi.org/10.1038/ng.3863
Weiner, D. J., Ling, E., Erdin, S., Tai, D. J. C., Yadav, R., Grove, J., Fu, J. M., Nadig, A., Carey, C. E., Baya, N., Bybjerg-Grauholm, J., iPSYCH Consortium, ASD Working Group of the Psychiatric Genomics Consortium, ADHD Working Group of the Psychiatric Genomics Consortium, Berretta, S., Macosko, E. Z., Sebat, J., O'Connor, L. J., Hougaard, D. M. ... Robinson, E. B. (2022). Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nature Genetics, 54(11), 1630-1639. https://doi.org/10.1038/s41588-022-01203-y
Weigand, K., Laursen, M., Swarts, H. G. P., Engwerda, A. H. J., Prufert, C., Sandrock, J., Nissen, P., Fedosova, N., Russel, F. G. M. & Koenderink, J. B. (2014). Na(+),K(+)-ATPase Isoform Selectivity for Digitalis-Like Compounds Is Determined by Two Amino Acids in the First Extracellular Loop. Chemical Research in Toxicology, 27(12), 2082-2092. https://doi.org/10.1021/tx500290k
Wei, Y., Backlund, L., Wegener, G., Mathe, A. A. & Lavebratt, C. (2015). Telomerase dysregulation in the hippocampus of a rat model of depression. Normalization by lithium. International Journal of Neuropsychopharmacology. https://doi.org/10.1093/ijnp/pyv002
Wei, Y. B., Liu, J. J., Villaescusa, J. C., Åberg, E., Brené, S., Wegener, G., Mathé, A. A. & Lavebratt, C. (2016). Elevation of Il6 is associated with disturbed let-7 biogenesis in a genetic model of depression. Translational Psychiatry, 6(8), e869. https://doi.org/10.1038/tp.2016.136
Wei, Y. B., Melas, P. A., Villaescusa, J. C., Liu, J. J., Xu, N., Christiansen, S. H., Elbrønd-Bek, H., Woldbye, D. P. D., Wegener, G., Mathé, A. A. & Lavebratt, C. (2016). MicroRNA 101b is downregulated in the prefrontal cortex of a genetic model of depression and targets the glutamate transporter SLC1A1 (EAAT3) in vitro. International Journal of Neuropsychopharmacology, 19(12). https://doi.org/10.1093/ijnp/pyw069