Publications

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Poulsen, J. B., Lescai, F., Grove, J., Bækvad-Hansen, M., Christiansen, M., Hagen, C. M., Maller, J., Stevens, C., Li, S., Li, Q., Sun, J., Wang, J., Nordentoft, M., Werge, T. M., Mortensen, P. B., Børglum, A. D., Daly, M., Hougaard, D. M., Bybjerg-Grauholm, J. & Hollegaard, M. V. (2016). High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA. PLoS One, 11(4), e0153253. Article e0153253. https://doi.org/10.1371/journal.pone.0153253
Qi, Y., Ooi, H. S., Wu, J., Chen, J., Zhang, X., Tan, S., Yu, Q., Li, Y.-Y., Kang, Y., Li, H., Xiong, Z., Zhu, T., Liu, B., Shao, Z. & Zhao, X. (2016). MALAT1 long ncRNA promotes gastric cancer metastasis by suppressing PCDH10. OncoTargets and Therapy, 7(11), 12693-12703. https://doi.org/10.18632/oncotarget.7281
Rasmussen, M., Vestergaard, E. M., Graakjaer, J., Petkov, Y., Bache, I., Fagerberg, C., Kibaek, M., Svaneby, D., Petersen, O. B., Brasch-Andersen, C. & Sunde, L. (2016). 17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature. American Journal of Medical Genetics - Part A, 170(11), 2934-2942. https://doi.org/10.1002/ajmg.a.37848
Rasmussen, M., Sunde, L., Nielsen, M. L., Ramsing, M., Petersen, A., Hjortshøj, T. D., Olsen, T. E., Tabor, A., Hertz, J. MI., Johnsen, I., Sperling, L., Petersen, O. B., Jensen, U. B., Petersen, M. B. & Lidballe, D. L. (2016). Fetal Kidney Anomalies: Next Generation Sequencing.
Rasmussen, M., Sunde, L., Nielsen, M. L., Ramsing, M., Petersen, A., Hjortshøj, T. D., Olsen, T. E., Tabor, A., Hertz, J. M., Johnsen, I., Sperling, L. S., Petersen, O. B., Jensen, U. B., Petersen, M. B. & Lildballe, D. L. (2016). Fetal Kidney Anomalies: Next Generation Sequencing. Abstract from European Society of Human Genetics Conference 2016, Barcelona, Spain.
Robinson, E. B., St Pourcain, B., Anttila, V., Kosmicki, J. A., Bulik-Sullivan, B., Grove, J., Maller, J., Samocha, K. E., Sanders, S. J., Ripke, S., Martin, J., Hollegaard, M. V., Werge, T., Hougaard, D. M., Neale, B. M., Evans, D. M., Skuse, D., Mortensen, P. B., Børglum, A. D. ... Als, T. D. (2016). Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population. Nature Genetics, 48(5), 552–555. https://doi.org/10.1038/ng.3529
Røder, M. E., Storgaard, H., Rungby, J., Knop, F. K. & Vilsbøll, T. (2016). Sodium-glucose cotransporter 2 (SGLT-2) inhibitors for patients with Type 2 diabetes. Ugeskrift for Læger, 178(38).