Publications

Journal Article

Musante, L.; Püttmann, L.; Kahrizi, K.; Garshasbi, M.; Hu, H.; Stehr, H.; Lipkowitz, B.; Otto, S.; Jensen, L. R.; Tzschach, A. et al.; Jamali, P.; Wienker, T. F.; Najmabadi, H.; Ropers, H. H.; Kuss, A. W.: Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability. Human Mutations 38 (6), pp. 621 - 636 (2017)

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Journal Article

Cauchy, P.; Koch, F.; Andrau, J.-C.: Two possible modes of pioneering associated with combinations of H2A.Z and p300/CBP at nucleosome-occupied enhancers. Transcription 8 (3), pp. 179 - 184 (2017)

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Journal Article

Alber, M.; Kalscheuer, V. M.; Marco, E.; Sherr, E.; Lesca, G.; Till, M.; Gradek, G.; Wiesener, A.; Korenke, C.; Mercier, S. et al.; Becker, F.; Yamamoto, T.; Scherer, S. W.; Marshall, C. R.; Walker, S.; Dutta, U. R.; Dalal, A. B.; Suckow, V.; Jamali, P.; Kahrizi, K.; Najmabadi, H.; Minassian, B. A.: ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation. Neurology Genetics 3 (3), e148 (2017)

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Journal Article

Choi, J.; Clement, K.; Huebner, A. J.; Webster, J.; Etchegaray, J.-P.; Gu, H.; Boyle, P.; Elling, U.; Mostoslavsky, R.; Sadreyev, R. et al.; Park, P. J.; Gygi, S. P.; Meissner, A.; Hochedlinger, K.: DUSP9 Modulates DNA Hypomethylation in Female Mouse Pluripotent Stem Cells. Cell Stem Cell 20 (5), pp. 706 - 719 (2017)

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Journal Article

Lorenz, C.; Lesimple, P.; Bukowiecki, R.; Zink, A.; Inak, G.; Mlody, B.; Singh, M.; Semtner, M.; Mah, N.; Auré, K. et al.; Leong, M.; Zabiegalov, O.; Lyras, E.-M.; Pfiffer, V.; Fauler, B.; Eichhorst, J.; Wiesner, B.; Huebner, N.; Priller, J.; Mielke, T.; Meierhofer, D.; Izsvák, Z.; Meier, J. C.; Bouillaud, F.; Adjaye, J.; Schuelke, M.; Wanker, E. E.; Lombès, A.; Prigione, A.: Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders. Cell Stem Cell 20 (5), e9, pp. 659 - 674 (2017)

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Journal Article

Wolkenstein, L.; Kanske, P.; Bailer, J.; Wessa, M.; Hautzinger, M.; Joormann, J.: Impaired cognitive control over emotional material in euthymic bipolar disorder. Journal of Affective Disorders 214, pp. 108 - 114 (2017)

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Journal Article

Ravindran, E.; Hu, H.; Yuzwa, S. A.; Hernandez-Miranda, L. R.; Kraemer, N.; Ninnemann, O.; Musante, L.; Boltshauser, E.; Schindler, D.; Hübner, A. et al.; Reinecker, H. C.; Ropers, H. H.; Birchmeier, C.; Miller, F. D.; Wienker, T. F.; Hübner, C.; Kaindl, A. M.: Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation. PLoS Genetics 13 (4), e1006746 (2017)

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Journal Article

Said, N.; Krupp, F.; Anedchenko, E.; Santos, K. F.; Dybkov, O.; Huang, Y. H.; Lee, C. T.; Loll, B.; Behrmann, E.; Buerger, J. et al.; Mielke, T.; Loerke, J.; Urlaub, H.; Spahn, C. M. T.; Weber, G.; Wahl, M. C.: Structural basis for λN-dependent processive transcription antitermination. Nature Microbiology 2, 2:17062 (2017)

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Journal Article

Twardziok, M.; Meierhofer, D.; Börno, S. T.; Timmermann, B.; Jäger, S.; Boral, S.; Eggert, A.; Delebinski, C. I.; Seifeert, G.: Transcriptomic and proteomic insight into the effects of a defined European mistletoe extract in Ewing sarcoma cells reveals cellular stress responses. BMC Complementary and Alternative Medicine 2017, 17:237 (2017)

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Journal Article

Kuruoglu, E. E.; Arndt, P. F.: The information capacity of the genetic code: Is the natural code optimal? Journal of Theoretical Biology 419, pp. 227 - 237 (2017)

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Journal Article

Medina, A. B.; Banaszczak, M.; Ni, Y.; Aretz, I.; Meierhofer, D.: ρ⁰ Cells Feature De-Ubiquitination of SLC Transporters and Increased Levels and Fluxes of Amino Acids. International Journal of Molecular Sciences 18, E879 (2017)

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Journal Article

Lienhard, M.; Grasse, S.; Rolff, J.; Frese, S.; Schirmer, U.; Becker, M.; Börno, S. T.; Timmermann, B.; Chavez, L.; Sültmann, H. et al.; Leschber, G.; Fichtner, I.; Schweiger, M. R.; Herwig, R.: QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments. Nucleic Acids Research (London) 45 (6), e44 (2017)

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Mutukula, N.; Elkabetz, Y.: "Neural Killer" Cells: Autologous Cytotoxic Neural Stem Cells for Fighting Glioma. Cell Stem Cell 20 (4), pp. 426 - 428 (2017)

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Warren, C. R.; O’Sullivan, J. F.; Friesen, M.; Becker, C. E.; Zhang, X.; Liu, P.; Wakabayashi, Y.; Morningstar, J. E.; Shi, X.; Choi, J. et al.; Xia, F.; Peters, D. T.; Florido, M. H. C.; Tsankov, A. M.; Duberow, E.; Comisar, L.; Shay, J.; Jiang, X.; Meissner, A.; Musunuro, K.; Kathiresan, S.; Daheron, L.; Zhu, J.; Gerszten, R. E.; Deo, R. C.; Vasan, R. S.; O’Donnell, C. J.; Cowan, C. A.: Induced Pluripotent Stem Cell Differentiation Enables Functional Validation of GWAS Variants in Metabolic Disease. Cell Stem Cell 20 (4), pp. 547 - 557 (2017)

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Journal Article

Winter, K.; Spengler, S.; Bermpohl, F.; Singer, T.; Kanske, P.: Social cognition in aggressive offenders: Impaired empathy, but intact theory of mind. Scientific Reports 7, 670 (2017)

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Journal Article

Skopkova, M.; Hennig, F.; Shin, B. S.; Turner, C. E.; Stanikova, D.; Brennerova, K.; Stanik, J.; Fischer, U.; Henden, L.; Müller, U. et al.; Steinberger, D.; Leshinsky-Silver, E.; Bottani, A.; Kurdiova, T.; Ukropec, J.; Nyitrayova, O.; Kolnikova, M.; Klimes, I.; Borck, G.; Bahlo, M.; Haas, S. A.; Kim, J. R.; Lotspeich-Cole, L. E.; Gasperikova, D.; Dever, T. E.; Kalscheuer, V. M.: EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO. Human Mutation 38 (4), pp. 409 - 425 (2017)

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Journal Article

Grosse Wiesmann, C.; Schreiber, J.; Singer, T.; Steinbeis, N.; Friederici, A. D.: White matter maturation is associated with the emergence of Theory of Mind in early childhood. Nature Communications 8, 14692 (2017)

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Journal Article

van der Werf, I. M.; Van Dijck, A.; Reyniers, E.; Helsmoortel, C.; Kumar, A. A.; Kalscheuer, V. M.; de Brouwer, A. P.; Kleefstra, T.; van Bokhoven, H.; Mortier, G. et al.; Janssens, S.; Vandeweyer, G.; Kooy, R. F.: Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. Gene 605, pp. 92 - 98 (2017)

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Journal Article

Zapata, J.; Moretto, E.; Hannan, S.; Murru, L.; Longatti, A.; Mazza, D.; Benedetti, L.; Fossati, M.; Heise, C.; Ponzoni, L. et al.; Valnegri, P.; Braida, D.; Sala, M.; Francolini, M.; Hildebrand, J.; Kalscheuer, V.; Fanelli, F.; Sala, C.; Bettler, B.; Bassani, S.; Smart, T. G.; Passafaro, M.: Epilepsy and intellectual disability linked protein Shrm4 interaction with GABABRs shapes inhibitory neurotransmission. Nature Communications 8, 8:14536 (2017)

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