Peer-reviewed publications

Peer-reviewed publications

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Xue, J., Thomas, L., Dominguez Rieg, J. A., Fenton, R. A. & Rieg, T. (2022). NHE3 in the thick ascending limb is required for sustained but not acute furosemide-induced urinary acidification. American journal of physiology. Renal physiology, 323(2), F141-F155. https://doi.org/10.1152/ajprenal.00013.2022
Khanbabaei, H., Ebrahimi, S., García-Rodríguez, J. L., Ghasemi, Z., Pourghadamyari, H., Mohammadi, M. & Kristensen, L. S. (2022). Non-coding RNAs and epithelial mesenchymal transition in cancer: molecular mechanisms and clinical implications. Journal of Experimental and Clinical Cancer Research, 41(1), Article 278. https://doi.org/10.1186/s13046-022-02488-x
Nielsen, T. A., Andersen, C. U., Vorum, H., Riahi, S., Sega, R., Drewes, A. M., Karmisholt, J., Jakobsen, P. E., Brock, B. & Brock, C. (2022). Palpebral Fissure Response to Phenylephrine Indicates Autonomic Dysfunction in Patients with Type 1 Diabetes and Polyneuropathy. Investigative Ophthalmology & Visual Science, 63(9), Article 21. https://doi.org/10.1167/iovs.63.9.21
Sadik, A., Dardani, C., Pagoni, P., Havdahl, A., Stergiakouli, E., Khandaker, G. M., Sullivan, S. A., Zammit, S., Jones, H. J., Davey Smith, G., Dalman, C., Karlsson, H., Gardner, R. M., Rai, D. & The iPSYCH Autism Spectrum Disorder Working Group (2022). Parental inflammatory bowel disease and autism in children. Nature Medicine, 28(7), 1406-1411. https://doi.org/10.1038/s41591-022-01845-9
Rossi, M., Altea-Manzano, P., Demicco, M., Doglioni, G., Bornes, L., Fukano, M., Vandekeere, A., Cuadros, A. M., Fernández-García, J., Riera-Domingo, C., Jauset, C., Planque, M., Alkan, H. F., Nittner, D., Zuo, D., Broadfield, L. A., Parik, S., Pane, A. A., Rizzollo, F. ... Fendt, S. M. (2022). PHGDH heterogeneity potentiates cancer cell dissemination and metastasis. Nature, 605(7911), 747-753. https://doi.org/10.1038/s41586-022-04758-2
Polyansky, A., Shatz, O., Fraiberg, M., Shimoni, E., Dadosh, T., Mari, M., Reggiori, F. M., Qin, C., Han, X. & Elazar, Z. (2022). Phospholipid imbalance impairs autophagosome completion. The EMBO Journal, 41(23), Article e110771. https://doi.org/10.15252/embj.2022110771
Piga, M., Chessa, E., Morand, E. F., Ugarte-Gil, M. F., Tektonidou, M., van Vollenhoven, R., Petri, M., Arnaud, L. & PISCOS Investigator Group (2022). Physician Global Assessment International Standardisation COnsensus in Systemic Lupus Erythematosus: the PISCOS study. The Lancet Rheumatology, 4(6), e441-e449. https://doi.org/10.1016/S2665-9913(22)00107-2
Frøbert, A. M., Gregersen, S., Brohus, M., Welinder, K. G., Kindberg, J., Fröbert, O. & Overgaard, M. T. (2022). Plasma proteomics data from hibernating and active Scandinavian brown bears. Data in Brief, 41, Article 107959. https://doi.org/10.1016/j.dib.2022.107959
Porpiglia, E. & Blau, H. M. (2022). Plasticity of muscle stem cells in homeostasis and aging. Current Opinion in Genetics & Development, 77, Article 101999. https://doi.org/10.1016/j.gde.2022.101999
McDonough, A. A. & Fenton, R. A. (2022). Potassium homeostasis: sensors, mediators, and targets. Pflügers Archiv - European Journal of Physiology, 474(8), 853-867. https://doi.org/10.1007/s00424-022-02718-3
Tomar, N., Uldbjerg, C. S., Bech, B. H., Burgner, D. P., Pedersen, L. H. & Miller, J. E. (2022). Prenatal antibiotic exposure and birth weight. Pediatric obesity, 17(2), Article e12831. https://doi.org/10.1111/ijpo.12831
Nordenskjöld, A. M., Johansson, N., Sunnefeldt, E., Athlin, S. & Fröbert, O. (2022). Prevalence and prognostic implications of myocardial injury in patients with influenza. European Heart Journal Open, 2(5), Article oeac051. https://doi.org/10.1093/ehjopen/oeac051
Zaheer, Y., Vorup-Jensen, T., Webster, T. J., Ahmed, M., Khan, W. & Ihsan, A. (2022). Protein based nanomedicine: Promising therapeuticmodalities against inflammatory disorders. Nano Select, 3(4), 733-750. https://doi.org/10.1002/nano.202100214
Reimer, L., Gram, H., Jensen, N. M., Betzer, C., Yang, L., Jin, L., Shi, M., Boudeffa, D., Fusco, G., De Simone, A., Kirik, D., Lashuel, H. A., Zhang, J. & Jensen, P. H. (2022). Protein kinase R dependent phosphorylation of α-synuclein regulates its membrane binding and aggregation. PNAS Nexus, 1(5), Article pgac259. https://doi.org/10.1093/pnasnexus/pgac259
Lissel Isaksson, G., Bodilsen Nielsen, M., Hinrichs, G. R., Krogstrup, N. V., Zachar, R., Stubmark, H., Svenningsen, P., Madsen, K., Bistrup, C., Jespersen, B., Birn, H., Palarasah, Y. & Jensen, B. L. (2022). Proteinuria is accompanied by intratubular complement activation and apical membrane deposition of C3dg and C5b-9 in kidney transplant recipients. American Journal of Physiology: Renal Physiology, 322(2), F150-F163. https://doi.org/10.1152/ajprenal.00300.2021
Cehofski, L. J., Kruse, A., Alsing, A. N., Sejergaard, B. F., Ellegaard Nielsen, J., Schlosser, A., Sorensen, G. L., Grauslund, J., Honoré, B. & Vorum, H. (2022). Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion. Molecules, 27(11), Article 3360. https://doi.org/10.3390/molecules27113360
Antaki, D., Guevara, J., Maihofer, A. X., Klein, M., Gujral, M., Grove, J., Carey, C. E., Hong, O., Arranz, M. J., Hervas, A., Corsello, C., Vaux, K. K., Muotri, A. R., Iakoucheva, L. M., Courchesne, E., Pierce, K., Gleeson, J. G., Robinson, E. B., Nievergelt, C. M. & Sebat, J. (2022). Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. Nature Genetics, 54(8), Article 1259. https://doi.org/10.1038/s41588-022-01145-5
Henriksen, M. L., Nielsen, C., Pedersen, D., Andersen, G. R., Thiel, S., Palarasah, Y. & Hansen, S. W. K. (2022). Quantification of the pro-form of human complement component factor D (adipsin). Journal of Immunological Methods, 507, Article 113295. https://doi.org/10.1016/j.jim.2022.113295
Tani, C., Elefante, E., Arnaud, L., Barreira, S. C., Bulina, I., Cavagna, L., Costedoat-Chalumeau, N., Doria, A., Fonseca, J. E., Franceschini, F., Fredi, M., Iaccarino, L., Limper, M., Majnik, J., Nagy, G., Pamfil, C., Rednic, S., Reynolds, J. A., Tektonidou, M. G. ... Mosca, M. (2022). Rare clinical manifestations in systemic lupus erythematosus: a review on frequency and clinical presentation. Clinical and Experimental Rheumatology, 40(5), S93-S102. https://doi.org/10.55563/clinexprheumatol/jrz47c
Singh, T., Poterba, T., Curtis, D., Akil, H., Al Eissa, M., Barchas, J. D., Bass, N., Bigdeli, T. B., Breen, G., Bromet, E. J., Buckley, P. F., Bunney, W. E., Bybjerg-Grauholm, J., Byerley, W. F., Chapman, S. B., Chen, W. J., Churchhouse, C., Craddock, N., Cusick, C. M. ... Daly, M. J. (2022). Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature, 604(7906), 509-516. https://doi.org/10.1038/s41586-022-04556-w
Bjornsdottir, G., Stefánsdóttir, L., Thorleifsson, G., Sulem, P., Norland, K., Ferkingstad, E., Oddsson, A., Zink, F., Lund, S. H., Nawaz, M. S., Bragi Walters, G., Skuladottir, A. T., Gudjonsson, S. A., Einarsson, G., Halldorsson, G. H., Bjarnadottir, V., Sveinbjornsson, G., Helgadottir, A., Styrkársdóttir, U. ... Nyegaard, M. (2022). Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature Communications, 13, Article 634. https://doi.org/10.1038/s41467-022-28167-1