Diagnostic and prognostic signatures from the small non-coding RNA transcriptome in prostate cancer von Martens-Uzunova, E S, Jalava, S E, Dits, N F, van Leenders, G J L H, Møller, S, Trapman, J, Bangma, C H, Litman, T, Visakorpi, T, Jenster, G

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Electron–Hole Crossover in Gate-Controlled Bilayer Graphene Quantum Dots von Banszerus, L, Rothstein, A, Fabian, T, Möller, S, Icking, E, Trellenkamp, S, Lentz, F, Neumaier, D, Watanabe, K, Taniguchi, T, Libisch, F, Volk, C, Stampfer, C

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Shoot Na⁺ Exclusion and Increased Salinity Tolerance Engineered by Cell Type-Specific Alteration of Na⁺ Transport in Arabidopsis von Møller, Inge S, Gilliham, Matthew, Jha, Deepa, Mayo, Gwenda M, Roy, Stuart J, Coates, Juliet C, Haseloff, Jim, Tester, Mark

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Low cardiac output predicts development of hepatorenal syndrome and survival in patients with cirrhosis and ascites von Krag, A, Bendtsen, F, Henriksen, J H, Møller, S

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Cardiovascular complications of cirrhosis von Møller, S, Henriksen, J H

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Prenatal and early postnatal exposure to perfluoroalkyl substances and bone mineral content and density in the Odense child cohort von F.D. Højsager, M. Andersen, A. Juul, F. Nielsen, S. Möller, H.T. Christensen, A. Grøntved, P. Grandjean, T.K. Jensen

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Influence of the illumination spectrum and observation angle on temperature measurements using thermochromic liquid crystals von Moller, S, König, J, Resagk, C, Cierpka, C

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Cost‐effectiveness of incisional negative pressure wound therapy compared with standard care after caesarean section in obese women: a trial‐based economic evaluation von Hyldig, N, Joergensen, JS, Wu, C, Bille, C, Vinter, CA, Sorensen, JA, Mogensen, O, Lamont, RF, Möller, S, Kruse, M

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GABRA1 and STXBP1: Novel genetic causes of Dravet syndrome von Carvill, Gemma L, Weckhuysen, Sarah, McMahon, Jacinta M, Hartmann, Corinna, Møller, Rikke S, Hjalgrim, Helle, Cook, Joseph, Geraghty, Eileen, O’Roak, Brian J, Petrou, Steve, Clarke, Alison, Gill, Deepak, Sadleir, Lynette G, Muhle, Hiltrud, von Spiczak, Sarah, Nikanorova, Marina, Hodgson, Bree L, Gazina, Elena V, Suls, Arvid, Shendure, Jay, Dibbens, Leanne M, De Jonghe, Peter, Helbig, Ingo, Berkovic, Samuel F, Scheffer, Ingrid E, Mefford, Heather C

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Effectiveness of a two-step population-based osteoporosis screening program using FRAX: the randomized Risk-stratified Osteoporosis Strategy Evaluation (ROSE) study von Rubin, K. H., Rothmann, M. J., Holmberg, T., Høiberg, M., Möller, S., Barkmann, R., Glüer, C. C., Hermann, A. P., Bech, M., Gram, J., Brixen, K.

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Two cytosolic glutamine synthetase isoforms play specific roles for seed germination and seed yield structure in Arabidopsis von Guan, M., Møller, I. S., Schjoerring, J. K.

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Adjuvant bisphosphonate treatment in early breast cancer: meta-analyses of individual patient data from randomised trials von Coleman, R, Powles, T, Paterson, A, Gnant, M, Anderson, S, Diel, I, Gralow, J, von Minckwitz, G, Moebus, V, Bergh, J, Pritchard, KI, Bliss, J, Cameron, D, Evans, V, Pan, H, Peto, R, Bradley, R, Gray, R, Bartsch, R, Dubsky, P, Fesl, C, Fohler, H, Greil, R, Jakesz, R, Lang, A, Luschin-Ebengreuth, G, Marth, C, Mlineritsch, B, Samonigg, H, Singer, CF, Steger, GG, Stoger, H, Olivotto, I, Ragaz, J, Christiansen, P, Ejlertsen, B, Ewertz, M, Jensen, MB, Moller, S, Mouridsen, HT, Eiermann, W, Hilfrich, J, Jonat, W, Kaufmann, M, Kreienberg, R, Schumacher, M, Blohmer, JU, Costa, SD, Eidtmann, H, Gerber, B, Jackisch, C, Loibl, S, Dafni, U, Markopoulos, C, Blomqvist, C, Saarto, T, Ahn, JH, Jung, KH, Perrone, F, Bass, G, Brown, A, Bryant, J, Costantino, J, Dignam, J, Fisher, B, Geyer, C, Mamounas, EP, Paik, S, Redmond, C, Swain, S, Wickerham, L, Wolmark, N, Perez, E, Ingle, JN, Suman, VJ, Hadji, P, A'Hern, R, Dowsett, M, Makris, A, Parton, M, Pennert, K, Powles, TJ, Smith, IE, Yarnold, JR, Clack, G, Van Poznak, C, Safra, T, Bell, R, Coleman, RE, Dodwell, D, Hinsley, S, Marshall, HC, Solomayer, E, Fehm, T, Lester, J, Winter, MC, Horsman, JM, Aft, R, Brufsky, AM, Llombart, HA

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Effects of insufficient sleep on circadian rhythmicity and expression amplitude of the human blood transcriptome von Möller-Levet, Carla S, Archer, Simon N, Bucca, Giselda, Laing, Emma E, Slak, Ana, Kabiljo, Renata, Lo, June C Y, Santhi, Nayantara, von Schantz, Malcolm, Smith, Colin P, Dijk, Derk-Jan

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Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic atonic seizures von Carvill, Gemma L., McMahon, Jacinta M., Schneider, Amy, Zemel, Matthew, Myers, Candace T., Saykally, Julia, Nguyen, John, Robbiano, Angela, Zara, Federico, Specchio, Nicola, Mecarelli, Oriano, Smith, Robert L., Leventer, Richard J., Møller, Rikke S., Nikanorova, Marina, Dimova, Petia, Jordanova, Albena, Petrou, Steven, Helbig, Ingo, Striano, Pasquale, Weckhuysen, Sarah, Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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Chronic pain and other sequelae in long-term breast cancer survivors: Nationwide survey in Denmark von Peuckmann, V, Ekholm, O, Rasmussen, N.K, Groenvold, M, Christiansen, P, Møller, S, Eriksen, J, Sjøgren, P

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Relation between tetR and tetA expression in tetracycline resistant Escherichia coli von Møller, Thea S B, Overgaard, Martin, Nielsen, Søren S, Bortolaia, Valeria, Sommer, Morten O A, Guardabassi, Luca, Olsen, John E

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A smartphone application supporting patients with psoriasis improves adherence to topical treatment: a randomized controlled trial von Svendsen, M.T., Andersen, F., Andersen, K.H., Pottegård, A., Johannessen, H., Möller, S., August, B., Feldman, S.R., Andersen, K.E.

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Identifying and validating blood mRNA biomarkers for acute and chronic insufficient sleep in humans: a machine learning approach von Laing, Emma E, Möller-Levet, Carla S, Dijk, Derk-Jan, Archer, Simon N

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Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability von Liu, Yuanyuan, Schubert, Julian, Sonnenberg, Lukas, Helbig, Katherine L, Hoei-Hansen, Christina E, Koko, Mahmoud, Rannap, Maert, Lauxmann, Stephan, Huq, Mahbubul, Schneider, Michael C, Johannesen, Katrine M, Kurlemann, Gerhard, Gardella, Elena, Becker, Felicitas, Weber, Yvonne G, Benda, Jan, Møller, Rikke S, Lerche, Holger

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Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency von Berryer, Martin H., Hamdan, Fadi F., Klitten, Laura L., Møller, Rikke S., Carmant, Lionel, Schwartzentruber, Jeremy, Patry, Lysanne, Dobrzeniecka, Sylvia, Rochefort, Daniel, Neugnot-Cerioli, Mathilde, Lacaille, Jean-Claude, Niu, Zhiyv, Eng, Christine M., Yang, Yaping, Palardy, Sylvain, Belhumeur, Céline, Rouleau, Guy A., Tommerup, Niels, Immken, LaDonna, Beauchamp, Miriam H., Patel, Gayle Simpson, Majewski, Jacek, Tarnopolsky, Mark A., Scheffzek, Klaus, Hjalgrim, Helle, Michaud, Jacques L., Di Cristo, Graziella

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