Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liver von Elmén, Joacim, Lindow, Morten, Silahtaroglu, Asli, Bak, Mads, Christensen, Mette, Lind-Thomsen, Allan, Hedtjärn, Maj, Hansen, Jens Bo, Hansen, Henrik Frydenlund, Straarup, Ellen Marie, McCullagh, Keith, Kearney, Phil, Kauppinen, Sakari

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The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases von Ahsan, Muhammad, Ek, Weronica E, Rask-Andersen, Mathias, Karlsson, Torgny, Lind-Thomsen, Allan, Enroth, Stefan, Gyllensten, Ulf, Johansson, Åsa

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Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes von Halgren, Christina, Nielsen, Nete M., Nazaryan-Petersen, Lusine, Silahtaroglu, Asli, Collins, Ryan L., Lowther, Chelsea, Kjaergaard, Susanne, Frisch, Morten, Kirchhoff, Maria, Brøndum-Nielsen, Karen, Lind-Thomsen, Allan, Mang, Yuan, El-Schich, Zahra, Boring, Claire A., Mehrjouy, Mana M., Jensen, Peter K.A., Fagerberg, Christina, Krogh, Lotte N., Hansen, Jan, Bryndorf, Thue, Hansen, Claus, Talkowski, Michael E., Bak, Mads, Tommerup, Niels, Bache, Iben

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Genetic association studies in lumbar disc degeneration: a systematic review von Eskola, Pasi J, Lemmelä, Susanna, Kjaer, Per, Solovieva, Svetlana, Männikkö, Minna, Tommerup, Niels, Lind-Thomsen, Allan, Husgafvel-Pursiainen, Kirsti, Cheung, Kenneth M C, Chan, Danny, Samartzis, Dino, Karppinen, Jaro

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A glycogene mutation map for discovery of diseases of glycosylation von Hansen, Lars, Lind-Thomsen, Allan, Joshi, Hiren J, Pedersen, Nis Borbye, Have, Christian Theil, Kong, Yun, Wang, Shengjun, Sparso, Thomas, Grarup, Niels, Vester-Christensen, Malene Bech, Schjoldager, Katrine, Freeze, Hudson H, Hansen, Torben, Pedersen, Oluf, Henrissat, Bernard, Mandel, Ulla, Clausen, Henrik, Wandall, Hans H, Bennett, Eric P

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High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations von Kariminejad, Roxana, Lind-Thomsen, Allan, Tümer, Zeynep, Erdogan, Fikret, Ropers, Hans H., Tommerup, Niels, Ullmann, Reinhard, Møller, Rikke S.

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Semiautomated improvement of RNA alignments von Andersen, Ebbe S, Lind-Thomsen, Allan, Knudsen, Bjarne, Kristensen, Susie E, Havgaard, Jakob H, Torarinsson, Elfar, Larsen, Niels, Zwieb, Christian, Sestoft, Peter, Kjems, Jørgen, Gorodkin, Jan

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Fast and sensitive detection of indels induced by precise gene targeting von Yang, Zhang, Steentoft, Catharina, Hauge, Camilla, Hansen, Lars, Thomsen, Allan Lind, Niola, Francesco, Vester-Christensen, Malene B, Frödin, Morten, Clausen, Henrik, Wandall, Hans H, Bennett, Eric P

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DNA Origami Design of Dolphin-Shaped Structures with Flexible Tails von Andersen, Ebbe S, Dong, Mingdong, Nielsen, Morten M, Jahn, Kasper, Lind-Thomsen, Allan, Mamdouh, Wael, Gothelf, Kurt V, Besenbacher, Flemming, Kjems, Jørgen

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The myosin chaperone UNC45B is involved in lens development and autosomal dominant juvenile cataract von Hansen, Lars, Comyn, Sophie, Mang, Yuan, Lind-Thomsen, Allan, Myhre, Layne, Jean, Francesca, Eiberg, Hans, Tommerup, Niels, Rosenberg, Thomas, Pilgrim, David

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Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes von Rasmussen, Malene B, Nielsen, Jakob V, Lourenço, Charles M, Melo, Joana B, Halgren, Christina, Geraldi, Camila V L, Marques, Wilson, Rodrigues, Guilherme R, Thomassen, Mads, Bak, Mads, Hansen, Claus, Ferreira, Susana I, Venâncio, Margarida, Henriksen, Karen F, Lind-Thomsen, Allan, Carreira, Isabel M, Jensen, Niels A, Tommerup, Niels

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Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 von Ebert, Grit, Steininger, Anne, Weißmann, Robert, Boldt, Vivien, Lind-Thomsen, Allan, Grune, Jana, Badelt, Stefan, Heßler, Melanie, Peiser, Matthias, Hitzler, Manuel, Jensen, Lars R, Müller, Ines, Hu, Hao, Arndt, Peter F, Kuss, Andreas W, Tebel, Katrin, Ullmann, Reinhard

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50 - Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization von Tommerup, Niels, Rasmussen, Malene B., Mehrjouy, Mana M., Bache, Iben, Lind-Thomsen, Allan, dos Santos Fonseca, Ana Carolina, Halgren, Christina, Bak, Mads, Jacky, Peter

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Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization von Tommerup, Niels, Rasmussen, Malene B, Mehrjouy, Mana M, Bache, Iben, Lind-Thomsen, Allan, dos Santos Fonseca, Ana Carolina, Halgren, Christina, Bak, Mads, Jacky, Peter

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International Breakpoint Mapping Consortium (IBMC). Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization von Tommerup, Niels, Rasmussen, Malene B, Mehrjouy, Mana M, Bache, Iben, Lind-Thomsen, Allan, dos Santos Fonseca, Ana Carolina, Halgren, Christina, Bak, Mads, Jacky, Peter

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Meta-analysis of exome array data identifies six novel genetic loci for lung function von Jackson, Victoria E., Latourelle, Jeanne C., Wain, Louise V., Smith, Albert V., Grove, Megan L., Bartz, Traci M., Obeidat, Ma'en, Province, Michael A., Gao, Wei, Qaiser, Beenish, Porteous, David J., Cassano, Patricia A., Ahluwalia, Tarunveer S., Grarup, Niels, Li, Jin, Altmaier, Elisabeth, Marten, Jonathan, Harris, Sarah E., Manichaikul, Ani, Pottinger, Tess D., Li-Gao, Ruifang, Lind-Thomsen, Allan, Mahajan, Anubha, Lahousse, Lies, Imboden, Medea, Teumer, Alexander, Prins, Bram, Lyytikäinen, Leo-Pekka, Eiriksdottir, Gudny, Franceschini, Nora, Sitlani, Colleen M., Brody, Jennifer A., Bossé, Yohan, Timens, Wim, Kraja, Aldi, Loukola, Anu, Tang, Wenbo, Liu, Yongmei, Bork-Jensen, Jette, Justesen, Johanne M., Linneberg, Allan, Lange, Leslie A., Rawal, Rajesh, Karrasch, Stefan, Huffman, Jennifer E., Smith, Blair H., Davies, Gail, Burkart, Kristin M., Mychaleckyj, Josyf C., Bonten, Tobias N., Enroth, Stefan, Lind, Lars, Brusselle, Guy G., Kumar, Ashish, Stubbe, Beate, Kähönen, Mika, Wyss, Annah B., Psaty, Bruce M., Heckbert, Susan R., Hao, Ke, Rantanen, Taina, Kritchevsky, Stephen B., Lohman, Kurt, Skaaby, Tea, Pisinger, Charlotta, Hansen, Torben, Schulz, Holger, Polasek, Ozren, Campbell, Archie I., Starr, John M., Rich, Stephen S., Mook-Kanamori, Dennis O., Johansson, Åsa, Ingelsson, Erik, Uitterlinden, André G., Weiss, Stefan, Raitakari, Olli T., Gudnason, Vilmundur, North, Kari E., Gharib, Sina A., Sin, Don D., Taylor, Kent D., O'Connor, George T., Kaprio, Jaakko, Harris, Tamara B., Pederson, Oluf, Vestergaard, Henrik, Wilson, James G., Strauch, Konstantin, Hayward, Caroline, Kerr, Shona M., Deary, Ian J., Barr, R. Graham, de Mutsert, Renée, Gyllensten, Ulf, Morris, Andrew P., Ikram, M. Arfan, Probst-Hensch, Nicole, Gläser, Sven, Zeggini, Eleftheria

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Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation von Gilling, Mette, Lind-Thomsen, Allan, Mang, Yuan, Bak, Mads, Møller, Morten, Ullmann, Reinhard, Kristoffersson, Ulf, Kalscheuer, Vera M, Henriksen, Karen Friis, Bugge, Merete, Tümer, Zeynep, Tommerup, Niels

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GLI1 is involved in cell cycle regulation and proliferation of NT2 embryonal carcinoma stem cells von Vestergaard, Janni, Lind-Thomsen, Allan, Pedersen, Mikkel W, Jarmer, Hanne Ostergaard, Bak, Mads, Hasholt, Lis, Tommerup, Niels, Tümer, Zeynep, Larsen, Lars Allan

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The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases von Ahsan, Muhammad, Ek, Weronica E, Rask-Andersen, Mathias, Karlsson, Torgny, Lind-Thomsen, Allan, Enroth, Stefan, Gyllensten, Ulf B, Johansson, Åsa

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Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders von Lowther, Chelsea, Mehrjouy, Mana M, Collins, Ryan L, Bak, Mads C, Dudchenko, Olga, Brand, Harrison, Dong, Zirui, Rasmussen, Malene B, Gu, Huiya, Weisz, David, Nazaryan-Petersen, Lusine, Fjorder, Amanda S, Mang, Yuan, Lind-Thomsen, Allan, Mendez, Juan M M, Calle, Xabier, Chopra, Anuja, Hansen, Claus, Bugge, Merete, Broekema, Roeland V, Varilo, Teppo, Luukkonen, Tiia, Engelen, John, Vianna-Morgante, Angela M, Fonseca, Ana Carolina S, Mazzeu, Juliana F, Dornelles-Wawruk, Halinna, Abe, Kikue T, Vermeesch, Joris R, Van Den Bogaert, Kris, Schinzel, Albert

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