List of publications

Lesca, G.; Moizard, M. P.; Bussy, G.; Boggio, D.; Hu, H.; Haas, S. A.; Ropers, H. H.; Kalscheuer, V. M.; Des Portes, V.; Labalme, A. et al.; Sanlaville, D.; Edery, P.; Raynaud, M.; Lespinasse, J.: Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. American Journal of Medical Genetics Part A 161A (12), pp. 3063 - 3071 (2013)

Szczurek, E.; Misra, N.; Vingron, M.: Synthetic sickness or lethality points at candidate combination therapy targets in glioblastoma. International Journal of Cancer 133 (9), pp. 2123 - 2132 (2013)

Van Maldergem, L.; Hou, Q.; Kalscheuer, V. M.; Rio, M.; Doco-Fenzy, M.; Medeira, A.; de Brouwer, A. P.; Cabrol, C.; Haas, S. A.; Cacciagli, P. et al.; Moutton, S.; Landais, E.; Motte, J.; Colleaux, L.; Bonnet, C.; Villard, L.; Dupont, J.; Man, H. Y.: Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth. Human Molecular Genetics 22 (16), pp. 3306 - 3314 (2013)

Hirata, H.; Nanda, I.; van Riesen, A.; McMichael, G.; Hu, H.; Hambrock, M.; Papon, M. A.; Fischer, U.; Marouillat, S.; Ding, C. et al.; Alirol, S.; Bienek, M.; Preisler-Adams, S.; Grimme, A.; Seelow, D.; Webster, R.; Haan, E.; MacLennan, A.; Stenzel, W.; Yap, T. Y.; Gardner, A.; Nguyen, L. S.; Shaw, M.; Lebrun, N.; Haas, S. A.; Kress, W.; Haaf, T.; Schellenberger, E.; Chelly, J.; Viot, G.; Shaffer, L. G.; Rosenfeld, J. A.; Kramer, N.; Falk, R.; El-Khechen, D.; Escobar, L. F.; Hennekam, R.; Wieacker, P.; Hubner, C.; Ropers, H. H.; Gecz, J.; Schuelke, M.; Laumonnier, F.; Kalscheuer, V. M.: ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity. The American Journal of Human Genetics 92 (5), pp. 681 - 695 (2013)

Feldmann, R.; Fischer, C.; Kodelja, V.; Behrens, S.; Haas, S.; Vingron, M.; Timmermann, B.; Geikowski, A.; Sauer, S.: Genome-wide analysis of LXRalpha activation reveals new transcriptional networks in human atherosclerotic foam cells. Nucleic Acids Research (London) 41 (6), pp. 3518 - 3531 (2013)

Feldmann, R.; Fischer, C.; Kodelja, V.; Behrens, S.; Haas, S.; Vingron, M.; Timmermann, B.; Geikowski, A.; Sauer, S.: Genome-wide analysis of LXRα activation reveals new transcriptional networks in human atherosclerotic foam cells. Nucleic Acids Research (London) 41 (6), pp. 3518 - 3531 (2013)

Emde, A.-K.: Next-generation sequencing algorithms: from read mapping to variant detection. Dissertation, Berlin, Freie Universität (2013)