Acute and persistent symptoms in non-hospitalized PCR-confirmed COVID-19 patients von Bliddal, Sofie, Banasik, Karina, Pedersen, Ole Birger, Nissen, Janna, Cantwell, Lisa, Schwinn, Michael, Tulstrup, Morten, Westergaard, David, Ullum, Henrik, Brunak, Søren, Tommerup, Niels, Feenstra, Bjarke, Geller, Frank, Ostrowski, Sisse Rye, Grønbæk, Kirsten, Nielsen, Claus Henrik, Nielsen, Susanne Dam, Feldt-Rasmussen, Ulla

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RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis von Farooq, Muhammad, Lindbæk, Louise, Krogh, Nicolai, Doganli, Canan, Keller, Cecilie, Mönnich, Maren, Gonçalves, André Brás, Sakthivel, Srinivasan, Mang, Yuan, Fatima, Ambrin, Andersen, Vivi Søgaard, Hussain, Muhammad S., Eiberg, Hans, Hansen, Lars, Kjaer, Klaus Wilbrandt, Gopalakrishnan, Jay, Pedersen, Lotte Bang, Møllgård, Kjeld, Nielsen, Henrik, Baig, Shahid. M., Tommerup, Niels, Christensen, Søren Tvorup, Larsen, Lars Allan

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MicroRNA expression in the adult mouse central nervous system von Bak, Mads, Silahtaroglu, Asli, Møller, Morten, Christensen, Mette, Rath, Martin F, Skryabin, Boris, Tommerup, Niels, Kauppinen, Sakari

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Single-molecule denaturation mapping of DNA in nanofluidic channels von Reisner, Walter, Larsen, Niels B., Silahtaroglu, Asli, Kristensen, Anders, Tommerup, Niels, Tegenfeldt, Jonas O., Flyvbjerg, Henrik, Austin, Robert H.

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JARID2 regulates binding of the Polycomb repressive complex 2 to target genes in ES cells von Rappsilber, Juri, Cloos, Paul A. C, Johansen, Jens V, Pasini, Diego, Bukowski, John-Paul, Bak, Mads, Helin, Kristian, Olsson, Linda, Tommerup, Niels, Walfridsson, Julian

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Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation von Gardella, Elena, Becker, Felicitas, Møller, Rikke S., Schubert, Julian, Lemke, Johannes R., Larsen, Line H. G., Eiberg, Hans, Nothnagel, Michael, Thiele, Holger, Altmüller, Janine, Syrbe, Steffen, Merkenschlager, Andreas, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Mang, Yuan, Bakke Møller, Louise, Gellert, Pia, Heron, Sarah E., Dibbens, Leanne M., Weckhuysen, Sarah, Dahl, Hans Atli, Biskup, Saskia, Tommerup, Niels, Hjalgrim, Helle, Lerche, Holger, Beniczky, Sándor, Weber, Yvonne G.

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REST-mediated recruitment of polycomb repressor complexes in mammalian cells von Dietrich, Nikolaj, Lerdrup, Mads, Landt, Eskild, Agrawal-Singh, Shuchi, Bak, Mads, Tommerup, Niels, Rappsilber, Juri, Södersten, Erik, Hansen, Klaus

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The identification and functional annotation of RNA structures conserved in vertebrates von Seemann, Stefan E, Mirza, Aashiq H, Hansen, Claus, Bang-Berthelsen, Claus H, Garde, Christian, Christensen-Dalsgaard, Mikkel, Torarinsson, Elfar, Yao, Zizhen, Workman, Christopher T, Pociot, Flemming, Nielsen, Henrik, Tommerup, Niels, Ruzzo, Walter L, Gorodkin, Jan

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A human phenome-interactome network of protein complexes implicated in genetic disorders von Brunak, Søren, Lage, Kasper, Karlberg, E Olof, Størling, Zenia M, Ólason, Páll Í, Pedersen, Anders G, Rigina, Olga, Hinsby, Anders M, Tümer, Zeynep, Pociot, Flemming, Tommerup, Niels, Moreau, Yves

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A Functional Link between the Histone Demethylase PHF8 and the Transcription Factor ZNF711 in X-Linked Mental Retardation von Kleine-Kohlbrecher, Daniela, Christensen, Jesper, Vandamme, Julien, Abarrategui, Iratxe, Bak, Mads, Tommerup, Niels, Shi, Xiaobing, Gozani, Or, Rappsilber, Juri, Salcini, Anna Elisabetta, Helin, Kristian

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Genome-wide detection of chromosomal rearrangements, indels, and mutations in circular chromosomes by short read sequencing von Skovgaard, Ole, Bak, Mads, Løbner-Olesen, Anders, Tommerup, Niels

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Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes von Schöpflin, Robert, Melo, Uirá Souto, Moeinzadeh, Hossein, Heller, David, Laupert, Verena, Hertzberg, Jakob, Holtgrewe, Manuel, Alavi, Nico, Klever, Marius-Konstantin, Jungnitsch, Julius, Comak, Emel, Türkmen, Seval, Horn, Denise, Duffourd, Yannis, Faivre, Laurence, Callier, Patrick, Sanlaville, Damien, Zuffardi, Orsetta, Tenconi, Romano, Kurtas, Nehir Edibe, Giglio, Sabrina, Prager, Bettina, Latos-Bielenska, Anna, Vogel, Ida, Bugge, Merete, Tommerup, Niels, Spielmann, Malte, Vitobello, Antonio, Kalscheuer, Vera M., Vingron, Martin, Mundlos, Stefan

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Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination von Nazaryan-Petersen, Lusine, Bertelsen, Birgitte, Bak, Mads, Jønson, Lars, Tommerup, Niels, Hancks, Dustin C, Tümer, Zeynep

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Detection of microRNAs in frozen tissue sections by fluorescence in situ hybridization using locked nucleic acid probes and tyramide signal amplification von Silahtaroglu, Asli N, Nolting, Dorrit, Dyrskjøt, Lars, Berezikov, Eugene, Møller, Morten, Tommerup, Niels, Kauppinen, Sakari

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Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients von Rendtorff, Nanna Dahl, Karstensen, Helena Gásdal, Lodahl, Marianne, Tolmie, John, McWilliam, Catherine, Bak, Mads, Tommerup, Niels, Nazaryan-Petersen, Lusine, Kunst, Henricus, Wong, Melanie, Joss, Shelagh, Carelli, Valerio, Tranebjærg, Lisbeth

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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome von Larsen, Jan, Johannesen, Katrine Marie, Ek, Jakob, Tang, Shan, Marini, Carla, Blichfeldt, Susanne, Kibæk, Maria, Spiczak, Sarah, Weckhuysen, Sarah, Frangu, Mimoza, Neubauer, Bernd Axel, Uldall, Peter, Striano, Pasquale, Zara, Federico, Kleiss, Rebecca, Simpson, Michael, Muhle, Hiltrud, Nikanorova, Marina, Jepsen, Birgit, Tommerup, Niels, Stephani, Ulrich, Guerrini, Renzo, Duno, Morten, Hjalgrim, Helle, Pal, Deb, Helbig, Ingo, Møller, Rikke Steensbjerre, Craiu, DC, Caglayan, HS, Talvik, T, Weber, YG, Barisic, N

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Haploinsufficiency of ARHGAP42 is associated with hypertension von Fjorder, Amanda S, Rasmussen, Malene B, Mehrjouy, Mana M, Nazaryan-Petersen, Lusine, Hansen, Claus, Bak, Mads, Grarup, Niels, Nørremølle, Anne, Larsen, Lars A, Vestergaard, Henrik, Hansen, Torben, Tommerup, Niels, Bache, Iben

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Position effect, cryptic complexity, and direct gene disruption as disease mechanisms in de novo apparently balanced translocation cases von Aristidou, Constantia, Theodosiou, Athina, Bak, Mads, Mehrjouy, Mana M, Constantinou, Efthymia, Alexandrou, Angelos, Papaevripidou, Ioannis, Christophidou-Anastasiadou, Violetta, Skordis, Nicos, Kitsiou-Tzeli, Sophia, Tommerup, Niels, Sismani, Carolina

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Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization von Nazaryan-Petersen, Lusine, Eisfeldt, Jesper, Pettersson, Maria, Lundin, Johanna, Nilsson, Daniel, Wincent, Josephine, Lieden, Agne, Lovmar, Lovisa, Ottosson, Jesper, Gacic, Jelena, Mäkitie, Outi, Nordgren, Ann, Vezzi, Francesco, Wirta, Valtteri, Käller, Max, Hjortshøj, Tina Duelund, Jespersgaard, Cathrine, Houssari, Rayan, Pignata, Laura, Bak, Mads, Tommerup, Niels, Lundberg, Elisabeth Syk, Tümer, Zeynep, Lindstrand, Anna

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Hypomorphic Mutations in PGAP2, Encoding a GPI-Anchor-Remodeling Protein, Cause Autosomal-Recessive Intellectual Disability von Hansen, Lars, Tawamie, Hasan, Murakami, Yoshiko, Mang, Yuan, ur Rehman, Shoaib, Buchert, Rebecca, Schaffer, Stefanie, Muhammad, Safia, Bak, Mads, Nöthen, Markus M., Bennett, Eric P., Maeda, Yusuke, Aigner, Michael, Reis, André, Kinoshita, Taroh, Tommerup, Niels, Baig, Shahid Mahmood, Abou Jamra, Rami

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