Genome-wide detection of chromosomal rearrangements, indels, and mutations in circular chromosomes by short read sequencing

Por Skovgaard, Ole, Bak, Mads, Løbner-Olesen, Anders, Tommerup, Niels
Publicado em 2011

Dysregulation of FOXG1 by ring chromosome 14

Por Alosi, Daniela, Klitten, Laura Line, Bak, Mads, Hjalgrim, Helle, Møller, Rikke Steensbjerre, Tommerup, Niels
Publicado no Mol Cytogenet (2015)

The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes

Por Pantano, Lorena, Jodar, Meritxell, Bak, Mads, Ballescà, Josep Lluís, Tommerup, Niels, Oliva, Rafael, Vavouri, Tanya
Publicado no RNA (2015)

MicroRNA expression in the adult mouse central nervous system

Por Bak, Mads, Silahtaroglu, Asli, Møller, Morten, Christensen, Mette, Rath, Martin F., Skryabin, Boris, Tommerup, Niels, Kauppinen, Sakari
Publicado em 2008

Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity

Por Halgren, Christina, Bache, Iben, Bak, Mads, Myatt, Mikkel Wanting, Anderson, Claire Marie, Brøndum-Nielsen, Karen, Tommerup, Niels
Publicado em 2012

REST–Mediated Recruitment of Polycomb Repressor Complexes in Mammalian Cells

Por Dietrich, Nikolaj, Lerdrup, Mads, Landt, Eskild, Agrawal-Singh, Shuchi, Bak, Mads, Tommerup, Niels, Rappsilber, Juri, Södersten, Erik, Hansen, Klaus
Publicado em 2012

Profiling microRNAs in lung tissue from pigs infected with Actinobacillus pleuropneumoniae

Por Podolska, Agnieszka, Anthon, Christian, Bak, Mads, Tommerup, Niels, Skovgaard, Kerstin, Heegaard, Peter MH, Gorodkin, Jan, Cirera, Susanna, Fredholm, Merete
Publicado em 2012

MicroRNA-138 regulates osteogenic differentiation of human stromal (mesenchymal) stem cells in vivo

Por Eskildsen, Tilde, Taipaleenmäki, Hanna, Stenvang, Jan, Abdallah, Basem M., Ditzel, Nicholas, Nossent, Anne Yael, Bak, Mads, Kauppinen, Sakari, Kassem, Moustapha
Publicado em 2011

Jarid1b targets genes regulating development and is involved in neural differentiation

Por Schmitz, Sandra U, Albert, Mareike, Malatesta, Martina, Morey, Lluis, Johansen, Jens V, Bak, Mads, Tommerup, Niels, Abarrategui, Iratxe, Helin, Kristian
Publicado em 2011

YKL-40 Is Differentially Expressed in Human Embryonic Stem Cells and in Cell Progeny of the Three Germ Layers

Por Brøchner, Christian B., Johansen, Julia S., Larsen, Lars A., Bak, Mads, Mikkelsen, Hanne B., Byskov, Anne Grete, Andersen, Claus Yding, Møllgård, Kjeld
Publicado em 2012

The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation

Por Fonseca, Ana Carolina S., Bonaldi, Adriano, Fonseca, Simone A. S., Otto, Paulo A., Kok, Fernando, Bak, Mads, Tommerup, Niels, Vianna-Morgante, Angela M.
Publicado no Mol Cytogenet (2015)

Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing

Por Aristidou, Constantia, Koufaris, Costas, Theodosiou, Athina, Bak, Mads, Mehrjouy, Mana M., Behjati, Farkhondeh, Tanteles, George, Christophidou-Anastasiadou, Violetta, Tommerup, Niels, Sismani, Carolina
Publicado no PLoS One (2017)

A Functional Link between the Histone Demethylase PHF8 and the Transcription Factor ZNF711 in X-Linked Mental Retardation

Por Kleine-Kohlbrecher, Daniela, Christensen, Jesper, Vandamme, Julien, Abarrategui, Iratxe, Bak, Mads, Tommerup, Niels, Shi, Xiaobing, Gozani, Or, Rappsilber, Juri, Salcini, Anna Elisabetta, Helin, Kristian
Publicado em 2010

Genome-wide Analysis of CDX2 Binding in Intestinal Epithelial Cells (Caco-2)

Por Boyd, Mette, Hansen, Morten, Jensen, Tine G. K., Perearnau, Anna, Olsen, Anders K., Bram, Lotte L., Bak, Mads, Tommerup, Niels, Olsen, Jørgen, Troelsen, Jesper T.
Publicado em 2010

Validation of Genome-Wide Intervertebral Disk Calcification Associations in Dachshund and Further Investigation of the Chromosome 12 Susceptibility Locus

Por Mogensen, Mette Sloth, Scheibye-Alsing, Karsten, Karlskov-Mortensen, Peter, Proschowsky, Helle Friis, Jensen, Vibeke Frøkjær, Bak, Mads, Tommerup, Niels, Kadarmideen, Haja N., Fredholm, Merete
Publicado em 2012

Sequence and expression analysis of gaps in human chromosome 20

Por Minocherhomji, Sheroy, Seemann, Stefan, Mang, Yuan, El-schich, Zahra, Bak, Mads, Hansen, Claus, Papadopoulos, Nickolas, Josefsen, Knud, Nielsen, Henrik, Gorodkin, Jan, Tommerup, Niels, Silahtaroglu, Asli
Publicado em 2012

Partial USH2A deletions contribute to Usher syndrome in Denmark

Por Dad, Shzeena, Rendtorff, Nanna D, Kann, Erik, Albrechtsen, Anders, Mehrjouy, Mana M, Bak, Mads, Tommerup, Niels, Tranebjærg, Lisbeth, Rosenberg, Thomas, Jensen, Hanne, Møller, Lisbeth B
Publicado no Eur J Hum Genet (2015)

Partial USH2A deletions contribute to Usher syndrome in Denmark

Por Dad, Shzeena, Rendtorff, Nanna D, Kann, Erik, Albrechtsen, Anders, Mehrjouy, Mana M, Bak, Mads, Tommerup, Niels, Tranebjærg, Lisbeth, Rosenberg, Thomas, Jensen, Hanne, Møller, Lisbeth B
Publicado no Eur J Hum Genet (2015)

The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2

Por Nazaryan, Lusine, Stefanou, Eunice G, Hansen, Claus, Kosyakova, Nadezda, Bak, Mads, Sharkey, Freddie H, Mantziou, Theodora, Papanastasiou, Anastasios D, Velissariou, Voula, Liehr, Thomas, Syrrou, Maria, Tommerup, Niels
Publicado em 2014

Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57

Por Bak, Mads, Boonen, Susanne E., Dahl, Christina, Hahnemann, Johanne M. D., Mackay, Deborah J. D. G., Tümer, Zeynep, Grønskov, Karen, Temple, I. Karen, Guldberg, Per, Tommerup, Niels
Publicado no BMC Med Genet (2016)