Thorsted, A., Thygesen, P., Agersø, H.
, Laursen, T. & Kreilgaard, M. (2016).
Translational mixed-effects PKPD modelling of recombinant human growth hormone - from hypophysectomized rat to patients. British Journal of Pharmacology,
173(11), 1742-1755.
http://10.1111/bph.13473
Haahr, T., Ersbøll, A. S., Karlsen, M. A., Svare, J., Sneider, K., Hee, L., Weile, L. K.
, Ziobrowska-Bech, A., Østergaard, C., Jensen, J. S.
, Helmig, R. B. & Uldbjerg, N. (2016).
Treatment of bacterial vaginosis in pregnancy in order to reduce the risk of spontaneous preterm delivery – A clinical guideline. Poster session presented at European spontaneous preterm birth congress (ESPBC) 2016.
Haahr, T., Ersbøll, A. S., Karlsen, M. A., Svare, J.
, Sneider, K., Hee, L., Weile, L. K.
, Ziobrowska-Bech, A., Østergaard, C., Jensen, J. S.
, Helmig, R. B. & Uldbjerg, N. (2016).
Treatment of bacterial vaginosis in pregnancy in order to reduce the risk of spontaneous preterm delivery - a clinical recommendation.
Acta Obstetricia et Gynecologica Scandinavica,
95(8), 850-860.
https://doi.org/10.1111/aogs.12933
Carvacho, I., Ardestani, G., Lee, H. C., McGarvey, K., Fissore, R. A.
& Lykke-Hartmann, K. (2016).
TRPM7-like channels are functionally expressed in oocytes and modulate post-fertilization embryo development in mouse.
Scientific Reports,
6, Article 34236.
https://doi.org/10.1038/srep34236
Lee, H. C., Sook-Young, Y.
, Lykke-Hartmann, K., Fissore, R. A.
& Carvacho, I. (2016).
TRPV3 channels mediate Ca2+ influx induced by 2-APB in mouse eggs.
Cell Calcium,
59(1), 21-31. Article 26725171.
http://www.sciencedirect.com/science/article/pii/S0143416015001724
Nygaard, U., Hvid, M., Johansen, C., Buchner, M., Fölster-Holst, R.
, Deleuran, M. & Vestergaard, C. (2016).
TSLP, IL-31, IL-33 and sST2 are new biomarkers in endophenotypic profiling of adult and childhood atopic dermatitis.
Journal of the European Academy of Dermatology and Venereology. Supplement,
30(11), 1930-1938.
https://doi.org/10.1111/jdv.13679
Terryn, S., Tanaka, K., Lengelé, J.-P., Olinger, E., Dubois-Laforgue, D., Garbay, S., Kozyraki, R., Van Der Smissen, P.
, Christensen, E. I., Courtoy, P. J., Bellanné-Chantelot, C., Timsit, J., Pontoglio, M. & Devuyst, O. (2016).
Tubular proteinuria in patients with HNF1α mutations: HNF1α drives endocytosis in the proximal tubule.
Kidney International. Supplement,
89(5), 1075-89.
https://doi.org/10.1016/j.kint.2016.01.027
Aslan, D., Garde, C., Nygaard, M. K., Helbo, A. S., Dimopoulos, K., Hansen, J. W.
, Severinsen, M. T., Treppendahl, M. B., Sjø, L. D.
, Grønbæk, K. & Kristensen, L. S. (2016).
Tumor suppressor microRNAs are downregulated in myelodysplastic syndrome with spliceosome mutations.
OncoTarget,
7(9), 9951-63.
https://doi.org/10.18632/oncotarget.7127
Hilbers, F., Kopec, W.
, Isaksen, T. J., Holm, T. H., Lykke-Hartmann, K., Nissen, P., Khandelia, H.
& Poulsen, H. (2016).
Tuning of the Na,K-ATPase by the beta subunit. Scientific Reports,
6(20442), Article 20442.
https://doi.org/10.1038/srep20442
Nexø, B. A., Jensen, S. B., Nissen, K. K., Hansen, B. & Laska, M. J. (2016).
Two endogenous retroviral loci appear to contribute to Multiple Sclerosis.
BMC Neurology,
16(1), 57. Article 57.
https://doi.org/10.1186/s12883-016-0580-9
Rasmussen, M. R., Nielsen, K. L., Christensen, M. B. L. R., Nielsen, C. B., Svendsen, P., Dimke, H.
, Christensen, E. I., Johannsen, M. & Moestrup, S. K. (2016).
Untargeted Metabolomics Analysis of ABCC6-Deficient Mice Discloses an Altered Metabolic Liver Profile.
Journal of Proteome Research,
15(12), 4591-4600.
https://doi.org/10.1021/acs.jproteome.6b00669
Starup-Linde, J., Gejl, M., Borghammer, P., Knop, F. K.
, Gregersen, S., Rungby, J. & Vestergaard, P. (2016).
Vagotomy and subsequent development of diabetes - A nested case-control study.
Metabolism,
65(7), 954-60.
https://doi.org/10.1016/j.metabol.2016.04.002
Lhaneche, L., Domingues, A., Hannouche, D., Delepine, M., Zelenika, D., Boland, A., Ostertag, A., Cohen-Solal, M.
, Langdahl, B. L., Harsløf, T., de Vernejoul, M.-C., Geoffroy, V. & Jehan, F. (2016).
Variations of SOST mRNA expression in human bone are associated with DNA polymorphism and DNA methylation in the SOST gene.
Bone,
92, 107-115.
https://doi.org/10.1016/j.bone.2016.08.004
Oliván-Viguera, A., Valero, M. S.
, Pinilla, E., Amor, S., García-Villalón, Á. L., Coleman, N., Laría, C., Calvín-Tienza, V., García-Otín, Á.-L., Fernández-Fernández, J. M., Murillo, M. D., Gálvez, J. A., Díaz-de-Villegas, M. D., Badorrey, R.
, Simonsen, U., Rivera, L., Wulff, H. & Köhler, R. (2016).
Vascular reactivity profile of novel KC a 3.1-selective positive-gating modulators in the coronary vascular bed.
Basic & Clinical Pharmacology & Toxicology,
119(2), 184-92.
https://doi.org/10.1111/bcpt.12560
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
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
Wendelboe, M. H.
, Thomsen, J. S., Henriksen, K.
, Vegger, J. B. & Brüel, A. (2016).
Zoledronate prevents lactation induced bone loss and results in additional post-lactation bone mass in mice.
Bone,
87, 27-36.
https://doi.org/10.1016/j.bone.2016.03.012
Christiansen, J. R., Olesen, M. N., Otzen, D. E., Romero-Ramos, M. & Sanchez-Guajardo, V. (2016).
α-Synuclein vaccination modulates regulatory T cell activation and microglia in the absence of brain pathology.
Journal of Neuroinflammation,
13(1), Article 74.
https://doi.org/10.1186/s12974-016-0532-8
Gilbert, B., Ahmad, K., Roos, J., Lehmann, C., Chiba, T., Ulrich-Rückert, S., Smeenk, L., van Heeringen, S.
, Maier, T. J., Groner, B. & Steinhilber, D. (2015).
5-Lipoxygenase is a direct p53 target gene in humans.
BBA Gene Regulatory Mechanisms,
1849(8), 1003-16.
https://doi.org/10.1016/j.bbagrm.2015.06.004
Langdahl, B. L., Teglbjaerg, C. S., Ho, P.-R., Chapurlat, R., Czerwinski, E., Kendler, D. L., Reginster, J.-Y., Kivitz, A., Lewiecki, E. M., Miller, P. D., Bolognese, M. A., McClung, M. R., Bone, H. G., Ljunggren, Ö., Abrahamsen, B., Gruntmanis, U., Yang, Y.-C., Wagman, R. B., Mirza, F. ... Orwoll, E. (2015).
A 24-month Study Evaluating the Efficacy and Safety of Denosumab for the Treatment of Men With Low Bone Mineral Density: Results From the ADAMO Trial.
Journal of Clinical Endocrinology and Metabolism, jc20144079.
https://doi.org/10.1210/jc.2014-4079
Björkman, A.
, Qvist, P., Du, L., Bartish, M., Zaravinos, A., Georgiou, K.
, Børglum, A., Gatti, R. A., Törngren, T. & Pan-Hammerström, Q. (2015).
Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells.
Proceedings of the National Academy of Sciences (PNAS),
112(7), 2157-2162.
https://doi.org/10.1073/pnas.1418947112
Lisi, S.
, Madsen, P., Botta, R.
, Petersen, C. M., Nykjær, A., Latrofa, F., Vitti, P. & Marinò, M. (2015).
ABSENCE OF A THYROID PHENOTYPE IN SORTILIN-DEFICIENT MICE.
Endocrine Practice,
21(9), 981-985.
https://doi.org/10.4158/EP15697.OR
Vestergaard, L. D., Løfgren, B., Jessen, C. L.
, Petersen, C. B., Wolff, A.
, Nielsen, H. V. & Krarup, N. H. V. (2015).
A comparison of pediatric basic life support self-led and instructor-led training among nurses.
European Journal of Emergency Medicine.
https://doi.org/10.1097/MEJ.0000000000000294
Siupka, P., Hamming, O. T., Kang, L.
, Gad, H. H. & Hartmann, R. (2015).
A conserved sugar bridge connected to the WSXWS motif has an important role for transport of IL-21R to the plasma membrane.
Genes and Immunity,
16(6), 405-413.
https://doi.org/10.1038/gene.2015.22
Ornstrup, M. J., Kjær, T. N., Harsløf, T., Stødkilde-Jørgensen, H., Hougaard, D. M., Cohen, A.
, Pedersen, S. B. & Langdahl, B. L. (2015).
Adipose tissue, estradiol levels, and bone health in obese men with metabolic syndrome.
European Journal of Endocrinology,
172, 205-216 .
https://doi.org/10.1530/EJE-14-0792
Bjerg Christensen, A.
, Dige, A., Vad-Nielsen, J., Brinkmann, C. R., Bendix, M.
, Østergaard, L. J., Tolstrup, M., Søgaard, O. S., Rasmussen, T. A., Randel Nyengaard, J., Agnholt, J. & Denton, P. W. (2015).
Administration of Panobinostat Is Associated with Increased IL-17A mRNA in the Intestinal Epithelium of HIV-1 Patients.
Mediators of Inflammation,
2015, Article 120605.
https://doi.org/10.1155/2015/120605
Bro, S. P., Kjærsgaard, M. I. S., Parner, E. T., Sørensen, M. J., Olsen, J., Bech, B. H., Pedersen, L. H., Christensen, J. & Vestergaard, M. (2015).
Adverse pregnancy outcomes after exposure to methylphenidate or atomoxetine during pregnancy.
Clinical epidemiology,
2015:7, 139-47.
https://doi.org/10.2147/CLEP.S72906
Andreasen, M. F., Telving, R., Rosendal, I., Eg, M. B., Hasselstrøm, J. B. & Andersen, L. V. (2015).
A fatal poisoning involving 25C-NBOMe.
Forensic Science International.
https://doi.org/10.1016/j.forsciint.2015.03.012
Lutz, S. M., Cho, M. H., Young, K., Hersh, C. P., Castaldi, P. J., McDonald, M.-L., Regan, E.
, Mattheisen, M., DeMeo, D. L., Parker, M., Foreman, M., Make, B. J., Jensen, R. L., Casaburi, R., Lomas, D. A., Bhatt, S. P., Bakke, P., Gulsvik, A., Crapo, J. D. ... ECLIPSE Investigators (2015).
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
BMC Genetics,
16, 138.
https://doi.org/10.1186/s12863-015-0299-4
Thomsen, J. S., Jensen, M. V., Niklassen, A. S., Ebbesen, E. N.
& Brüel, A. (2015).
Age-related changes in vertebral and iliac crest 3D bone microstructure-differences and similarities.
Osteoporosis International,
26(1), 219-228.
https://doi.org/10.1007/s00198-014-2851-x
Mathiesen, J. S.
, Krag, K. S., Poulsen, P. L., Vestergaard, E. M., Christiansen, P. M. & Vestergaard, P. (2015).
Aggressive Medullary Thyroid Carcinoma in a 10-Year-Old Patient with Multiple Endocrine Neoplasia 2B due to the A883F Mutation.
Thyroid : official journal of the American Thyroid Association,
25(1), 139-40.
https://doi.org/10.1089/thy.2014.0177
Grønbæk, L., Vilstrup, H., Deleuran, B., Wiest, R., Krag, A.
& Jepsen, P. (2015).
Alcoholic Cirrhosis Increases Risk for Autoimmune Diseases: A Nationwide Registry-Based Cohort Study.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
https://doi.org/10.1016/j.cgh.2015.05.032
Kofod-Olsen, E., Jørgensen, S. E., Nissen, S. K., Westh, L.
, Møller, B. K., Østergaard, L., Larsen, C. S. & Mogensen, T. H. (2015).
Altered fraction of regulatory B and T cells is correlated with autoimmune phenomena and splenomegaly in patients with CVID.
Clinical Immunology,
162, 49-57.
https://doi.org/10.1016/j.clim.2015.11.003
Anraku, M., Shintomo, R., Taguchi, K.
, Kragh-Hansen, U., Kai, T., Maruyama, T. & Otagiri, M. (2015).
Amino acids of importance for the antioxidant activity of human serum albumin as revealed by recombinant mutants and genetic variants.
Life Sciences,
134, 36-41.
Rajkumar, A. P., Christensen, J. H., Mattheisen, M., Jacobsen, I., Bache, I.
, Pallesen, J., Grove, J., Qvist, P., Mcquillin, A., Gurling, H. M., Tümer, Z.
, Mors, O. & Børglum, A. D. (2015).
Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder.
Bipolar Disorders (English Edition, Online),
17(2), 205-211.
https://doi.org/10.1111/bdi.12239
Piesche, M., Ho, V. T., Kim, H., Nakazaki, Y., Nehil, M., Yaghi, N. K., Kolodin, D., Weiser, J., Altevogt, P., Kiefel, H., Alyea, E. P., Antin, J. H., Cutler, C., Koreth, J., Canning, C., Ritz, J., Soiffer, R. J. & Dranoff, G. (2015).
Angiogenic cytokines are antibody targets during graft-versus-leukemia reactions.
Clinical Cancer Research,
21(5), 1010-8.
https://doi.org/10.1158/1078-0432.CCR-14-1956
Iversen, M. B., Reinert, L. S., Thomsen, M. K., Bagdonaite, I.
, Nandakumar, R., Cheshenko, N.
, Prabakaran, T., Vakhrushev, S. Y., Krzyzowska, M.
, Kratholm, S. K., Ruiz-Perez, F.
, Petersen, S. V., Goriely, S.
, Bibby, B. M., Eriksson, K., Ruland, J., Thomsen, A. R., Herold, B. C., Wandall, H. H.
... Paludan, S. R. (2015).
An innate antiviral pathway acting before interferons at epithelial surfaces.
Nature Immunology.
https://doi.org/10.1038/ni.3319
Bundgaard Christiansen, G., Harbak, B., E. Hede, S., H. Gouliaev, A., Olsen, L., Frydenvang, K.
, Jensen, J. E., Sandholm Kastrup, J.
& Holm, M. M. (2015).
A novel dualistic profile of an allosteric AMPA receptor modulator identified through studies on recombinant receptors, mouse hippocampal synapses and crystal structures.
Neuroscience,
310, 709.
Habib, R., Ansar, M.
, Mattheisen, M., Shahid, M., Ali, G., Ahmad, W. & Betz, R. C. (2015).
A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31.
P L o S One,
10(6), Article 0129811.
https://doi.org/10.1371/journal.pone.0129811
Nyegaard, M., Rendtorff, N. D.
, Nielsen, M. S., Corydon, T. J., Demontis, D., Starnawska, A., Hedemand, A., Buniello, A., Niola, F., Overgaard, M. T., Leal, S. M., Ahmad, W.
, Wikman, F. P., Petersen, K. B., Crüger, D. G., Oostrik, J., Kremer, H., Tommerup, N., Frödin, M.
... Børglum, A. D. (2015).
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
P L o S Genetics,
11(7), e1005386.
https://doi.org/10.1371/journal.pgen.1005386
Pen, A. E., Nyegaard, M., Fang, M., Jiang, H.
, Christensen, R., Mølgaard, H., Andersen, H., Ulhøi, B. P., Østergaard, J. R., Væth, S., Sommerlund, M., de Brouwer, A. P. M., Zhang, X.
& Jensen, U. B. (2015).
A novel single nucleotide splice site mutation in FHL1 confirms an Emery-Dreifuss plus phenotype with pulmonary artery hypoplasia and facial dysmorphology.
European Journal of Medical Genetics,
58(4), 222-229.
https://doi.org/10.1016/j.ejmg.2015.02.003
Arcanjo, D. D. R., Vasconcelos, A. G.
, Comerma-Steffensen, S. G., Jesus, J. R., Silva, L. P., Pires, O. R., Costa-Neto, C. M., Oliveira, E. B., Migliolo, L., Franco, O. L., Restini, C. B. A., Paulo, M., Bendhack, L. M., Bemquerer, M. P., Oliveira, A. P.
, Simonsen, U. & Leite, J. R. D. S. D. A. (2015).
A Novel Vasoactive Proline-Rich Oligopeptide from the Skin Secretion of the Frog Brachycephalus ephippium.
PLOS ONE,
10(12), e0145071.
https://doi.org/10.1371/journal.pone.0145071