Publications

Max Planck Institute for Molecular Genetics

The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (140)

Journal Article

Kariminejad, A.; Kariminejad, R.; Tzschach, A.; Ullmann, R.; Ahmed, A.; Asghari-Roodsari, A.; Salehpour, S.; Afroozan, F.; Ropers, H.-H.; Kariminejad, M. H.: Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis. American Journal of Medical Genetics Part A 149 (7), pp. 1544 - 1549 (2009)

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Ott, C.-E.; Bauer, S.; Manke, T.; Ahrens, S.; Rödelsperger, C.; Grünhagen, J.; Kornak, U.; Duda, G.; Mundlos, S.; Robinson, P. N.: Promiscuous and depolarization-induced immediate-early response genes are induced by mechanical strain of osteoblasts. Journal of Bone and Mineral Research 24 (7), pp. 1247 - 1262 (2009)

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Raile, K.; Klopocki, E.; Holder, M.; Wessel, T.; Galler, A.; Deiss, D.; Müller, D.; Riebel, T.; Horn, D.; Maringa, M. et al.; Weber, J.; Ullmann, R.; Grüters, A.: Expanded clinical spectrum in hepatocyte nuclear factor 1B-maturity-onset diabetes of the young. Journal of Clinical Endocrinology & Metabolism 94 (7), pp. 2658 - 2664 (2009)

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Ralser, M.; Wamelink, M. M. C.; Latkolik, S.; Jansen, E. E. W.; Lehrach, H.; Jakobs, C.: Correspondence: Metabolic reconfiguration precedes transcriptional regulation in the antioxidant response. Nature biotechnology 27 (7), pp. 604 - 605 (2009)

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Schimmelmann, B. G.; Friedel, S.; Nguyen, T. T.; Sauer, S.; Ganz Vogel, C. I.; Konrad, K.; Wilhelm, C.; Sinzig, J.; Renner, T. J.; Romanos, M. et al.; Palmason, H.; Dempfle, A.; Walitza, S.; Freitag, C.; Meyer, J.; Linder, M.; Schäfer, H.; Warnke, A.; Lesch, K. P.; Herpertz-Dahlman, B.; Hinney, A.; Hebebrand, J.: Exploring the genetic link between RLS and ADHD. Journal of Psychiatric Research 43 (10), pp. 941 - 945 (2009)

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Chung, H.-R.; Vingron, M.: Comparison of sequence-dependent tiling array normalization approaches. BMC Bioinformatics 10, p. 204 - 204 (2009)

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Milenković, T.; Filippis, I.; Lappe, M.; Pržulj, N.: Optimized null model for protein structure networks. PLoS ONE 4 (6), p. e5967 - e5967 (2009)

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Ye, K.; Schulz, M. H.; Long, Q.; Apweiler, R.; Ning, Z.: Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics 25 (21), pp. 2865 - 2871 (2009)

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Hucthagowder, V.; Morava, E.; Kornak, U.; Lefeber, D. J.; Fischer, B.; Dimopoulou, A.; Aldinger, A.; Choi, J.; Davis, E. C.; Abuelo, D. N. et al.; Adamowicz, M.; Al-Aama, J.; Basel-Vanagaite, L.; Fernandez, B.; Greally, M. T.; Gillessen-Kaesbach, G.; Kayserili, H.; Lemyre, E.; Tekin, M.; Türkmen, S.; Tuysuz, B.; Yüksel-Konuk, B.; Mundlos, S.; Van Maldergem, L.; Wevers, R. A.; Urban, Z.: Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival. Human Molecular Genetics 18 (12), pp. 2149 - 2165 (2009)

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Schinke, T.; Schilling, A. F.; Baranowsky, A.; Seitz, S.; Marshall, R. P.; Linn, T.; Blaeker, M.; Huebner, A. K.; Schulz, A.; Simon, R. et al.; Gebauer, M.; Priemel, M.; Kornak, U.; Perkovic, S.; Barvencik, F.; Beil, F. T.; Del Fattore, A.; Frattini, A.; Streichert, T.; Pueschel, K.; Villa, A.; Debatin, K.-M.; Rueger, J. M.; Teti, A.; Zustin, J.; Sauter, G.; Amling, M.: Impaired gastric acidification negatively affects calcium homeostasis and bone mass. Nature Medicine 15, pp. 674 - 681 (2009)

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Shoichet, S. A.; Waibel, S.; Endruhn, S.; Sperfeld, A. D.; Vorwerk, B.; Mümlller, I.; Erdogan, F.; Ludolph, A. C.; Ropers, H.-H.; Ullmann, R.: Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization. Amyotrophic Lateral Sclerosis 10 (3), pp. 162 - 169 (2009)

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Tzschach, A.: Genetik der nichtsyndromalen geistigen Behinderung. Medizinische Genetik 21 (2), pp. 231 - 236 (2009)

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Tzschach, A.; Ramel, C.; Kron, A.; Seipel, B.; Wüster, C.; Cordes, U.; Liehr, T.; Hoeltzenbein, M.; Menzel, C.; Ropers, H.-H. et al.; Ullmann, R.; Kalscheuer, V.; Decker, J.; Steinberger, D.: Hypergonadotropic hypogonadism in a patient with inv ins (2;4). International Journal of Andrology 32 (3), pp. 226 - 230 (2009)

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Zatkova, A.; Merk, S.; Wendehack, M.; Bilban, M.; Muzik, E. M.; Muradyan, A.; Haferlach, C.; Haferlach, T.; Wimmer, K.; Fonatsch, C. et al.; Ullmann, R.: AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes. Genes, Chromosomes and Cancer 48 (6), pp. 510 - 520 (2009)

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Zuccotti, M.; Merico, V.; Sacchi, L.; Bellone, M.; Brink, T. C.; Stefanelli, M.; Redi, C. A.; Bellazzi, R.; Adjaye, J.; Garagna, S.: Oct-4 regulates the expression of Stella and Foxj2 at the Nanog locus: implications for the developmental competence of mouse oocytes. Human Reproduction 24 (9), pp. 2225 - 2237 (2009)

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Türkmen, S.; Guo, G.; Garshasbi, M.; Hoffmann, K.; Alshalah, A. J.; Mischung, C.; Kuss, A.; Humphrey, N.; Mundlos, S.; Robinson, P. N.: CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait. PLoS Genetics 5, p. e1000487 - e1000487 (2009)

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Schweiger, M. R.; Kerick, M.; Timmermann, B.; Albrecht, M. W.; Borodina, T.; Parkhomchuk, D.; Zatloukal, K.; Lehrach, H.: Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. PLoS ONE 4 (5), p. e5548 - e5548 (2009)

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Geibela, S.; Banchenkoa, S.; Engela, M.; Lanka, E.; Saenger, W.: Structure and function of primase RepB' encoded by broad-host-range plasmid RSF1010: that replicates exclusively in leading-strand mode. Proceedings of the National Academy of Sciences 106 (19), pp. 7810 - 7815 (2009)

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Jürgens, A. S.; Kolanczyk, M.; Moebest, D. C. C.; Zemojtel, T.; Lichtenauer, U.; Duchniewicz, M.; Gantert, M. P.; Hecht, J.; Hattenhorst, U.; Burdach, S. et al.; Dorn, A.; Kamps, M. P.; Beuschlein, F.; Räpple, D.; Scheele, J. S.: PBX1 is dispensable for neural commitment of RA-treated murine ES cells. In Vitro Cellular & Developmental Biology - Animal 45 (5-6), pp. 252 - 263 (2009)

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Scheele, J. S.; Kolanczyk, M.; Gantert, M.; Zemojtel, T.; Dorn, A.; Sykes, D. B.; Möbest, D. C. C.; Kamps, M. P.; Räpple, D.: The Spt-Ada-Gcn5-acetyltransferase complex interaction motif of E2a is essential for a subset of transcriptional and oncogenic properties of E2a-Pbx1. Leukemia & Lymphoma 50 (5), pp. 816 - 828 (2009)

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