Peer-reviewed publikationer

Peer-reviewed publications

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Doğanli, C., Oxvig, C. & Lykke-Hartmann, K. (2013). Zebrafish as a novel model to assess Na⁺/K⁺-ATPase-related neurological disorders. Neuroscience & Biobehavioral Reviews, 37(10 Part2), 2774–2787. https://doi.org/10.1016/j.neubiorev.2013.09.013

Hellsten, L., Ahlqvist, V. H., Nielsen, A. M., Brandén, G., Ekström, A. M. & Kosidou, K. (2025). Youth Uptake of Digital Sexual and Reproductive Health Services Across Sociodemographic Groups (2018-2022): A Total Population Study from Stockholm, Sweden. Mayo Clinic Proceedings: Digital Health, 3(3), Artikel 100251. https://doi.org/10.1016/j.mcpdig.2025.100251

Bonde, J. P., Kold Jensen, T., Brixen Larsen, S., Abell, A., Scheike, T., Hjøllund, N. H. I., Kolstad, H., Ernst, E., Giwercman, A., Skakkebaek, N. E., Keiding, N. & Olsen, J. (1998). Year of birth and sperm count in 10 Danish occupational studies. Scandinavian Journal of Work, Environment & Health, 24(5), 407-13.

Bor, P., Hindkjaer, J., Kølvraa, S. & Ingerslev, H. J. (2002). Y-chromosome microdeletions and cytogenetic findings in unselected ICSI candidates at a Danish fertility clinic. Journal of Assisted Reproduction and Genetics, 19(5), 224-31.

La Rosa, L. R., Perrone, L., Nielsen, M. S., Calissano, P., Andersen, O. M. & Matrone, C. (2015). Y682G Mutation of Amyloid Precursor Protein Promotes Endo-Lysosomal Dysfunction by Disrupting APP-SorLA Interaction. Frontiers in Cellular Neuroscience, 9, 109. https://doi.org/10.3389/fncel.2015.00109

Juraeva, D., Treutlein, J., Scholz, H., Frank, J., Degenhardt, F., Cichon, S., Ridinger, M., Mattheisen, M., Witt, S. H., Lang, M., Sommer, W. H., Hoffmann, P., Herms, S., Wodarz, N., Soyka, M., Zill, P., Maier, W., Jünger, E., Gaebel, W. ... Rietschel, M. (2015). XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set Based Analysis and Follow-up Studies in Drosophila and Humans. Neuropsychopharmacology, 40, 361–371. https://doi.org/10.1038/npp.2014.178

Vorup-Jensen, T., Hjort, T., Abraham-Peskir, J. V., Guttmann, P., Jensenius, J. C., Uggerhøj, E. & Medenwaldt, R. (1999). X-ray microscopy of human spermatozoa shows change of mitochondrial morphology after capacitation. Human Reproduction, 14(4), 880-4.

Dahl, H. H., Hansen, L. L., Brown, R. M., Danks, D. M., Rogers, J. G. & Brown, G. K. (1992). X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation. Journal of Inherited Metabolic Disease, 15(6), 835-47.

Christensen, B. A. O., Koudahl, V., Honoré, B., Overgaard, J., Damsgaard, T. E. & Vorum, H. (2014). Wound Healing – A Proteomic Analysis of the Effect of Erythropoietin on Granulation Tissue Isolated from ePTFE Implants. Archives of Clinical and Experimental Surgery, 3(1), 26-33. https://doi.org/10.5455/aces.20130319090616

Rahmioglu, N., Fassbender, A., Vitonis, A. F., Tworoger, S. S., Hummelshoj, L., D'Hooghe, T. M., Adamson, G. D., Giudice, L. C., Becker, C. M., Zondervan, K. T., Missmer, S. A., Adamson, G. D., Allaire, C., Anchan, R., Becker, C. M., Bedaiwy, M. A., Buck Louis, G. M., Calhaz-Jorge, C., Chwalisz, K. ... Zondervan, K. T. (2014). World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonization Project: III. Fluid biospecimen collection, processing, and storage in endometriosis research: Fertility and Sterility. Fertility and Sterility, 102(5), 1233-1243. https://doi.org/10.1016/j.fertnstert.2014.07.1208

Vitonis, A. F., Vincent, K., Rahmioglu, N., Fassbender, A., Buck Louis, G. M., Hummelshoj, L., Giudice, L. C., Stratton, P., Adamson, G. D., Becker, C. M., Zondervan, K. T., Missmer, S. A., Adamson, G. D., Allaire, C., Anchan, R., Becker, C. M., Bedaiwy, M. A., Buck Louis, G. M., Calhaz-Jorge, C. ... Zondervan, K. T. (2014). World Endometriosis Research Foundation Endometriosis Phenome and biobanking harmonization project: II. Clinical and covariate phenotype data collection in endometriosis research: Fertility and Sterility. Fertility and Sterility, 102(5), 1223-1232. https://doi.org/10.1016/j.fertnstert.2014.07.1244

Fassbender, A., Rahmioglu, N., Vitonis, A. F., Viganò, P., Giudice, L. C., D’Hooghe, T. M., Hummelshoj, L., Adamson, G. D., Becker, C. M., Missmer, S. A., Zondervan, K. T., Adamson, G. D., Allaire, C., Anchan, R., Becker, C. M., Bedaiwy, M. A., Buck Louis, G. M., Calhaz-Jorge, C., Chwalisz, K. ... Zondervan, K. T. (2014). World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonisation Project: IV. Tissue collection, processing, and storage in endometriosis research: Fertility and Sterility. Fertility and Sterility, 102(5), 1244-1253. https://doi.org/10.1016/j.fertnstert.2014.07.1209

Becker, C. M., Laufer, M. R., Stratton, P., Hummelshoj, L., Missmer, S. A., Zondervan, K. T., Adamson, G. D., Adamson, G. D., Allaire, C., Anchan, R., Becker, C. M., Bedaiwy, M. A., Buck Louis, G. M., Calhaz-Jorge, C., Chwalisz, K., D'Hooghe, T. M., Fassbender, A., Faustmann, T., Fazleabas, A. T. ... Zondervan, K. T. (2014). World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonisation Project: I. Surgical phenotype data collection in endometriosis research: Fertility and Sterility. Fertility and Sterility, 102(5), 1213-1222. https://doi.org/10.1016/j.fertnstert.2014.07.709

Moses, M., Tiego, J., Demontis, D., Bragi Walters, G., Stefansson, H., Stefansson, K., Børglum, A. D., Arnatkeviciute, A. & Bellgrove, M. A. (2022). Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample. Molecular Psychiatry, 27(12), 5028-5037. https://doi.org/10.1038/s41380-022-01775-5

Vidarsson, G., Overbeeke, N., Stemerding, AM., van den Dobbelsteen, G., van Ulsen, P., van der Ley, P., Kilian, M. & van de Winkel, JGJ. (2005). Working mechanism of immunoglobulin A1 (IgA1) protease: cleavage of IgA1 antibody to Neisseria meningitidis PorA requires de novo synthesis of IgA1 Protease. Infection and Immunity, 73, 6721-26.

Vidarsson, G., Overbeeke, N., Stemerding, A. M., van den Dobbelsteen, G., van Ulsen, P., van der Ley, P., Kilian, M. & van de Winkel, J. G. (2005). Working mechanism of immunoglobulin A1 (IgA1) protease: cleavage of IgA1 antibody to Neisseria meningitidis PorA requires de novo synthesis of IgA1 protease. Infection and Immunity, 73, 6721-6726.

Fenton, R. A. (2024). Working Less Is the Key to Greater Scientific Productivity. Physiologist, 2024, 40-41.

Kaiser, K., Gyllborg, D., Procházka, J., Salašová, A., Kompaníková, P., Molina, F. L., Laguna-Goya, R., Radaszkiewicz, T., Harnoš, J., Procházková, M., Potěšil, D., Barker, R. A., Casado, Á. G., Zdráhal, Z., Sedláček, R., Arenas, E., Villaescusa, J. C. & Bryja, V. (2019). WNT5A is transported via lipoprotein particles in the cerebrospinal fluid to regulate hindbrain morphogenesis. Nature Communications, 10(1), Artikel 1498. https://doi.org/10.1038/s41467-019-09298-4

Saha, B., Leite-Dellova, D. C. A., Demko, J., Sørensen, M. V., Takagi, E., Gleason, C. E., Shabbir, W. & Pearce, D. (2022). WNK1 is a chloride-stimulated scaffold that regulates mTORC2 activity and ion transport. Journal of Cell Science, 135(23), Artikel jcs260313. https://doi.org/10.1242/jcs.260313

Orlowski, D., Elfving, B., Müller, H. K., Wegener, G. & Bjarkam, C. R. (2012). Wistar rats subjected to chronic restraint stress display increased hippocampal spine density paralleled by increased expression levels of synaptic scaffolding proteins. Stress: The International Journal on the Biology of Stress , 15(5), 514-523. https://doi.org/10.3109/10253890.2011.643516

Nyvold, C. G., Stentoft, J., Braendstrup, K., Melsvik, D., Moestrup, S. K., Juhl-Christensen, C., Hasle, H. & Hokland, P. (2006). Wilms' tumor 1 mutation accumulated during therapy in acute myeloid leukemia: Biological and clinical implications. Leukemia, 20(11), 2051-4. https://doi.org/10.1038/sj.leu.2404389

Nielsen, S. B., Macchi, F., Raccosta, S., Langkilde, A. E., Giehm, L., Kyrsting, A., Svane, A. S. P., Manno, M., Christiansen, G., Nielsen, N. C., Oddershede, L., Vestergaard, B. & Otzen, D. (2013). Wildtype and A30P Mutant Alpha-Synuclein Form Different Fibril Structures. PLoS One, 8(7), Artikel e67713. https://doi.org/10.1371/journal.pone.0067713

Søborg, D. A., Hendriksen, N. B., Kilian, M. & Kroer, N. (2013). Widespread occurrence of bacterial human virulence determinants in soil and freshwater environments. Applied and Environmental Microbiology, 79(18), 5488-97. https://doi.org/10.1128/AEM.01633-13

Ubhi, K., Rockenstein, E., Kragh, C., Inglis, C., Spencer, B., Michael, S., Mante, M., Adame, A., Galasko, D. & Masliah, E. (2013). Widespread microRNA dysregulation in multiple system atrophy - disease-related alteration in miR-96. The European journal of neuroscience. https://doi.org/10.1111/ejn.12444

Jensen, P. L., Dueholm, M. S., Larsen, P., Petersen, S. V., Enghild, J. J., Christiansen, G., Højrup, P., Nielsen, P. H. & Otzen, D. (2009). Widespread abundance of Functional Bacterial Amyloid in Mycolata and other Gram positive Bacteria. Applied and Environmental Microbiology, 75, 4101-4110.

Jordal, P. B., Dueholm, M. S., Larsen, P., Petersen, S. V., Enghild, J. J., Christiansen, G., Højrup, P., Nielsen, P. H. & Otzen, D. E. (2009). Widespread abundance of functional bacterial amyloid in mycolata and other gram-positive bacteria. Applied and Environmental Microbiology, 75(12), 4101-10. https://doi.org/10.1128/AEM.02107-08

Findsen, A., Pedersen, T. H., Petersen, A. G., Nielsen, O. B. & Overgaard, J. (2014). Why do insects enter and recover from chill coma? Low temperature and high extracellular potassium compromises muscle function in Locusta migratoria. Journal of Experimental Biology, 217(8), 1297-1306. https://doi.org/10.1242/jeb.098442

Lexner, M. O., Bardow, A., Hertz, J. M., Almer, L., Nauntofte, B. & Kreiborg, S. (2007). Whole saliva in X-linked hypohidrotic ectodermal dysplasia. International Journal of Paediatric Dentistry (Print), 17(3), 155-62. https://doi.org/10.1111/j.1365-263X.2006.00812.x

Vogel, I., Andreasen, L., Balslev-Harder, M., Becher, N., Ernst, A., Gadsbøll, K., Hjortshøj, T. D., Hvidbjerg, M. S., Larsen, M., Lou, S., Bay Lund, I. C., Pedersen, L. H., Sønderberg Roos, L. K., Sperling, L., Sunde, L., Tørring, P. M., Vedel, C. & Petersen, O. B. (2025). Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare. Prenatal Diagnosis. Advance online publication. https://doi.org/10.1002/pd.6780

Zheng, H.-F., Forgetta, V., Hsu, Y.-H., Estrada, K., Rosello-Diez, A., Leo, P. J., Dahia, C. L., Park-Min, K. H., Tobias, J. H., Kooperberg, C., Kleinman, A., Styrkarsdottir, U., Liu, C.-T., Uggla, C., Evans, D. S., Nielson, C. M., Walter, K., Pettersson-Kymmer, U., McCarthy, S. ... AOGC Consortium (2015). Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Nature, 526(7571), 112-7. https://doi.org/10.1038/nature14878

Kim, S. W., Lee, H., Song, D. Y., Lee, G. H., Ji, J., Park, J. W., Han, J. H., Lee, J. W., Byun, H. J., Son, J. H., Kim, Y. R., Lee, Y., Kim, J., Jung, A., Lee, J., Kim, E., Kim, S. H., Lee, J. H., Satterstrom, F. K. ... An, J. Y. (2024). Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism. Genome Medicine, 16(1), Artikel 114. https://doi.org/10.1186/s13073-024-01385-6

Qin, H., Samuels, J. F., Wang, Y., Zhu, Y., Grados, M. A., Riddle, M. A., Greenberg, B. D., Knowles, J. A., Fyer, A. J., McCracken, J. T., Murphy, D. L., Rasmussen, S. A., Cullen, B. A., Piacentini, J., Geller, D., Stewart, S. E., Pauls, D., Bienvenu, O. J., Goes, F. S. ... Shugart, Y. Y. (2015). Whole-genome association analysis of treatment response in obsessive-compulsive disorder. Molecular Psychiatry. https://doi.org/10.1038/mp.2015.32

Demontis, D., Lescai, F., Børglum, A., Glerup, S., Østergaard, S. D., Mors, O., Li, Q., Liang, J., Jiang, H., Li, Y., Wang, J., Lesch, K.-P., Reif, A., Buitelaar, J. K. & Franke, B. (2016). Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 55(6), 521-3. https://doi.org/10.1016/j.jaac.2016.03.009

Heinz, J. L., Swagemakers, S. M. A., von Hofsten, J., Helleberg, M., Thomsen, M. M., De Keukeleere, K., de Boer, J. H., Ilginis, T., Verjans, G. M. G. M., van Hagen, P. M., van der Spek, P. J. & Mogensen, T. H. (2023). Whole exome sequencing of patients with varicella-zoster virus and herpes simplex virus induced acute retinal necrosis reveals rare disease-associated genetic variants. Frontiers in Molecular Neuroscience, 16, Artikel 1253040. https://doi.org/10.3389/fnmol.2023.1253040

Hait, A. S., Thomsen, M. M., Larsen, S. M., Helleberg, M., Mardahl, M., Barfod, T. S., Christiansen, M., Brandt, C. & Mogensen, T. H. (2021). Whole-Exome Sequencing of Patients With Recurrent HSV-2 Lymphocytic Mollaret Meningitis. The Journal of Infectious Diseases, 223(10), 1776-1786. https://doi.org/10.1093/infdis/jiaa589

Lescai, F., Als, T. D., Li, Q., Nyegaard, M., Andorsdottir, G., Biskopstø, M., Hedemand, A., Fiorentino, A., O'Brien, N. L., Jarram, A., Liang, T. J., Grove, J., Pallesen, J., Eickhardt, E., Mattheisen, M., Bolund, L., Demontis, D., Wang, A. G., McQuillin, A. ... Børglum, A. D. (2017). Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder. Translational Psychiatry, 7(2), e1034. Artikel 3. https://doi.org/10.1038/tp.2017.3

Nissen, S. K., Christiansen, M., Helleberg, M., Kjær, K., Jørgensen, S. E., Gerstoft, J., Katzenstein, T. L., Benfield, T., Kronborg, G., Larsen, C. S., Laursen, A., Pedersen, G., Jakobsen, M. R., Tolstrup, M. & Mogensen, T. H. (2018). Whole Exome Sequencing of HIV-1 long-term non-progressors identifies rare variants in genes encoding innate immune sensors and signaling molecules. Scientific Reports, 8(1), 15253. Artikel 15253. https://doi.org/10.1038/s41598-018-33481-0

Gregersen, N., Lescai, F., Liang, J., Li, Q., Als, T. D., Buttenschøn, H. N., Hedemand, A., Biskopstø, M., Wang, J., Wang, A., Børglum, A., Mors, O. & Demontis, D. (2016). Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 171(8), 1013-1022. https://doi.org/10.1002/ajmg.b.32464

Andersen, C. L., Nielsen, H. M., Kristensen, L. S., Søgaard, A., Vikeså, J., Jønson, L., Nielsen, F. C., Hasselbalch, H., Bjerrum, O. W., Punj, V. & Grønbæk, K. (2015). Whole-exome sequencing and genome-wide methylation analyses identify novel disease associated mutations and methylation patterns in idiopathic hypereosinophilic syndrome. OncoTarget, 6(38), 40588-97. https://doi.org/10.18632/oncotarget.5845

Andreasen, M. & Hablitz, J. (1992). Whole-cell patch clamp studies of paired pulse potentiation in the dentate gyrus. Poster-session præsenteret på ASBMB/Biophysical Society meeting, Houston, USA.

Dollerup, M. R., Alstrup, A. K. O., Gormsen, L. C., Nielsen, E. N., Falborg, L., Vendelbo, M., Luong, T. V. & Simonsen, M. I. T. (2022). Whole body biodistribution and myocardial kinetics of the ketone PET radiotracer 3-[11C]OHB: A pilot study in domestic pigs. Poster-session præsenteret på The World Molecular Imaging Congress 2022, Miami, USA.

Nielsen, B., Hokland, P., Ellegaard, J., Hasselbalch, H. & Hokland, M. (1989). Whole blood assay for NK activity in splenectomized and non-splenectomized hairy cell leukemia patients during IFN-alpha-2b treatment. Leukemia Research, 13(6), 451-6.

Jensen, P. H., Schlossmacher, M. G. & Stefanis, L. (2023). Who Ever Said It Would Be Easy? Reflecting on Two Clinical Trials Targeting α-Synuclein. Movement disorders : official journal of the Movement Disorder Society, 38(3), 378-384. https://doi.org/10.1002/mds.29318

McMahon, L., Maher, G. J., Joyce, C., Niemann, I., Fisher, R. & Sunde, L. (2024). When to Consult a Geneticist Specialising in Gestational Trophoblastic Disease. Gynecologic and Obstetric Investigation, 89(3), 198-213. https://doi.org/10.1159/000531218

Sip, K. E., Carmel, D., Marchant, J. L., Li, J., Petrovic, P., Roepstorff, A., McGregor, W. B. & Frith, C. D. (2013). When Pinocchio's nose does not grow: belief regarding lie-detectability modulates production of deception. Frontiers in Human Neuroscience, 7, 1-11. Artikel 16. https://doi.org/10.3389/fnhum.2013.00016

Sedgwick, P. M., Hammer, A., Kesmodel, U. S. & Pedersen, L. H. (2022). When controversies in null hypothesis significance testing prove to be controversial. Acta Obstetricia et Gynecologica Scandinavica, 101(11), 1339-1339. https://doi.org/10.1111/aogs.14456

West, M. J. (2013). What to report: information to be included in the publication of a stereological study. Cold Spring Harbor Protocols, 2013(9). https://doi.org/10.1101/pdb.top071894

Bonnefond, A., Saulnier, P.-J., Stathopoulou, M. G., Grarup, N., Ndiaye, N. C., Roussel, R., Nezhad, M. A., Dechaume, A., Lantieri, O., Hercberg, S., Lauritzen, T., Balkau, B., El-Sayed Moustafa, J. S., Hansen, T., Pedersen, O., Froguel, P., Charpentier, G., Marre, M., Hadjadj, S. & Visvikis-Siest, S. (2013). What is the contribution of two genetic variants regulating VEGF levels to type 2 diabetes risk and to microvascular complications? PLoS One, 8(2), Artikel e55921. https://doi.org/10.1371/journal.pone.0055921

Støvring, H., Ekstrøm, C. T., Schneider, J. W. & Strøm, C. (2025). What is actually the emerging evidence about non-specific vaccine effects in randomized trials from the Bandim Health Project? Vaccine, 68, Artikel 127937. https://doi.org/10.1016/j.vaccine.2025.127937

Moroni, L., Tabury, K., Stenuit, H., Grimm, D., Baatout, S. & Mironov, V. (2022). What can biofabrication do for space and what can space do for biofabrication? Trends in Biotechnology, 40(4), 398-411. https://doi.org/10.1016/j.tibtech.2021.08.008

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