Aarhus Universitets segl

80 PURE

Text element

Personliste

Publikationsliste

Publikationsliste

Sortér efter: Dato | Forfatter | Titel

Manikandan, V., Reinert, L., Paludan, S. R., Grove, J., Nielsen, P. F. R., Hougaard, D. M., Nordentoft, M., Werge, T., Børglum, A., Mortensen, P. B. & Demontis, D. (2016). Gene-environmental interactions between genetic variants in antiviral response genes and prenatal maternal infections in schizophrenia. Poster-session præsenteret på American Society of Human Genetics 2016, Vancouver, Canada.
Olesen, M. S., Starnawska, A., Agerholm, I., Forman, A., Overgaard, M. T. & Nyegaard, M. (2016). Gene Expression analysis of the endometrium after endometrial biopsy in fertile women. Poster-session præsenteret på The 3rd Biomarker meeting: Personalized Reproductive Medicine, Valencia, Spanien.
Lassen, K. G., McKenzie, C. I., Mari, M., Murano, T., Begun, J., Baxt, L. A., Goel, G., Villablanca, E. J., Kuo, S.-Y., Huang, H., Macia, L., Bhan, A. K., Batten, M., Daly, M. J., Reggiori, F., Mackay, C. R. & Xavier, R. J. (2016). Genetic Coding Variant in GPR65 Alters Lysosomal pH and Links Lysosomal Dysfunction with Colitis Risk. Immunity, 44(6), 1392-405. https://doi.org/10.1016/j.immuni.2016.05.007
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
Bøttger, P., Pedersen, S. G., Gesslein, B., Illarionova, N., Isaksen, T. J., Heuck, A., Clausen, B. H., Füchtbauer, E.-M., Gramsbergen, J. B., Gunnarson, E., Aperia, A., Lauritzen, M., Lambertsen, K. L., Nissen, P. & Lykke-Hartmann, K. (2016). Glutamate-system defects behind psychiatric manifestations in a familial hemiplegic migraine type 2 disease-mutation mouse model. Scientific Reports, 6(22047), Artikel 22047. https://doi.org/10.1038/srep22047
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. Artikel e0153253. https://doi.org/10.1371/journal.pone.0153253
Simunovic, M., Evergren, E., Golushko, I., Prévost, C., Renard, H. F., Johannes, L., McMahon, H. T., Lorman, V., Voth, G. A. & Bassereau, P. (2016). How curvature-generating proteins build scaffolds on membrane nanotubes. Proceedings of the National Academy of Sciences of the United States of America, 113(40), 11226-11231. https://doi.org/10.1073/pnas.1606943113
Kragh-Hansen, U. (2016). Human Serum Albumin: A Multifunctional Protein. I M. Otagiri & V. T. Giam Chuang (red.), Albumin in Medicine: Pathological and Clinical Applications (s. 1-24). Springer. https://doi.org/10.1007/978-981-10-2116-9_1
Jiang, B., Wu, Q., Deng, N., Chen, Y., Zhang, L., Liang, Z. & Zhang, Y. (2016). Hydrophilic GO/Fe 3 O 4 /Au/PEG nanocomposites for highly selective enrichment of glycopeptides. Nanoscale, 8(9), 4894-4897. https://doi.org/10.1039/c5nr08126b
Bennedbæk, M., Rossing, M., Rasmussen, Å. K., Gerdes, A.-M., Skytte, A.-B., Jensen, U. B., Nielsen, F. C. & Hansen, T. V. O. (2016). Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. Familial Cancer, 14(13), 13. Artikel 13. https://doi.org/10.1186/s13053-016-0053-6
Couch, F. J., Kuchenbaecker, K. B., Michailidou, K., Mendoza-Fandino, G. A., Nord, S., Lilyquist, J., Olswold, C., Hallberg, E., Agata, S., Ahsan, H., Aittomäki, K., Ambrosone, C., Andrulis, I. L., Anton-Culver, H., Arndt, V., Arun, B. K., Arver, B., Barile, M., Barkardottir, R. B. ... Antoniou, A. C. (2016). Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Nature Communications, 7, Artikel 11375. https://doi.org/10.1038/ncomms11375
on behalf of HEBON, on behalf of KConFab, AOCS Investigators, on behalf of EMBRACE & behalf of GEMO Study Collaborators (2016). Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Breast Cancer Research, 18(1), Artikel 64. https://doi.org/10.1186/s13058-016-0718-0
van der Sluis, R. M., Kumar, N. A., Evans, V. A., Harman, A. N., Mota, T., Tannakoon, S., Hertzog, P., Lewin, S. R. & Cameron, P. U. (2016). IFNα activates latent HIV-1 in non-proliferating latently infected T-cells. Poster-session præsenteret på 2016 Towards an HIV Cure Symposium, Durban, Sydafrika.
Kugadas, A., Christiansen, S. H., Sankaranarayanan, S., Surana, N. K., Gauguet, S., Kunz, R., Fichorova, R., Vorup-Jensen, T. & Gadjeva, M. (2016). IMPACT OF MICROBIOTA ON RESISTANCE TO OCULAR PSEUDOMONAS AERUGINOSA–INDUCED KERATITIS. PLoS Pathogens, 12(9), Artikel e1005855. https://doi.org/10.1371/journal.ppat.1005855