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 (247)

Journal Article

Mertes, F.; Elsharawy, A.; Sauer, S.; van Helvoort, J. M.; van der Zaag, P. J.; Franke, A.; Nilsson, M.; Lehrach, H.; Brookes, A. J.: Targeted enrichment of genomic DNA regions for next-generation sequencing. Brief Funct Genomics 10 (6), pp. 374 - 86 (2011)

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Meunier, D.; Patra, K.; Smits, R.; Hagebarth, A.; Luttges, A.; Jaussi, R.; Wieduwilt, M. J.; Quintanilla-Fend, L.; Himmelbauer, H.; Fodde, R. et al.; Fundele, R. H.: Expression analysis of proline rich 15 (Prr15) in mouse and human gastrointestinal tumors. Molecular Carcinogenesis 50 (1), pp. 8 - 15 (2011)

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Mills, R. E.; Walter, K.; Stewart, C.; Handsaker, R. E.; Chen, K.; Alkan, C.; Abyzov, A.; Yoon, S. C.; Ye, K.; Cheetham, R. K. et al.; Chinwalla, A.; Conrad, D. F.; Fu, Y.; Grubert, F.; Hajirasouliha, I.; Hormozdiari, F.; Iakoucheva, L. M.; Iqbal, Z.; Kang, S.; Kidd, J. M.; Konkel, M. K.; Korn, J.; Khurana, E.; Kural, D.; Lam, H. Y.; Leng, J.; Li, R.; Li, Y.; Lin, C. Y.; Luo, R.; Mu, X. J.; Nemesh, J.; Peckham, H. E.; Rausch, T.; Scally, A.; Shi, X.; Stromberg, M. P.; Stutz, A. M.; Urban, A. E.; Walker, J. A.; Wu, J.; Zhang, Y.; Zhang, Z. D.; Batzer, M. A.; Ding, L.; Marth, G. T.; McVean, G.; Sebat, J.; Snyder, M.; Wang, J.; Eichler, E. E.; Gerstein, M. B.; Hurles, M. E.; Lee, C.; McCarroll, S. A.; Korbel, J. O.: Mapping copy number variation by population-scale genome sequencing. Nature 470 (7332), pp. 59 - 65 (2011)

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Minoche, A. E.; Dohm, J. C.; Himmelbauer, H.: Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and Genome Analyzer systems. Genome Biology 12 (11), p. R112 (2011)

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Mitter, D.; Ullmann, R.; Muradyan, A.; Klein-Hitpass, L.; Kanber, D.; Ounap, K.; Kaulisch, M.; Lohmann, D.: Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions. Eur J Hum Genet 19 (9), pp. 947 - 58 (2011)

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Mohamed, M.; Kouwenberg, D.; Gardeitchik, T.; Kornak, U.; Wevers, R. A.; Morava, E.: Metabolic cutis laxa syndromes. J Inherit Metab Dis 34 (4), pp. 907 - 16 (2011)

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Morava, E.; Kuhnisch, J.; Drijvers, J. M.; Robben, J. H.; Cremers, C.; van Setten, P.; Branten, A.; Stumpp, S.; de Jong, A.; Voesenek, K. et al.; Vermeer, S.; Heister, A.; Claahsen-van der Grinten, H. L.; O'Neill, C. W.; Willemsen, M. A.; Lefeber, D.; Deen, P. M.; Kornak, U.; Kremer, H.; Wevers, R. A.: Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family. J Clin Endocrinol Metab 96 (1), pp. E189 - 98 (2011)

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Muhs, M.; Yamamoto, H.; Ismer, J.; Takaku, H.; Nashimoto, M.; Uchiumi, T.; Nakashima, N.; Mielke, T.; Hildebrand, P. W.; Nierhaus, K. H. et al.; Spahn, C. M.: Structural basis for the binding of IRES RNAs to the head of the ribosomal 40S subunit. Nucleic Acids Res 39 (12), pp. 5264 - 75 (2011)

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Muhs, M.; Yamamoto, H.; Ismer, J.; Takaku, H.; Nashimoto, M.; Uchiumi, T.; Nakashima, N.; Mielke, T.; Hildebrand, P. W.; Nierhaus, K. H. et al.; Spahn, C. M.: Structural basis for the binding of IRES RNAs to the head of the ribosomal 40S subunit. Nucleic Acids Research 39 (12), pp. 5264 - 75 (2011)

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Muller, H.; Schmidt, D.; Dreher, F.; Herwig, R.; Ploubidou, A.; Lange, B. M.: Gene ontology analysis of the centrosome proteomes of Drosophila and human. Communicative & Integrative Biology 4 (3), pp. 308 - 11 (2011)

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Muradyan, A.; Gilbertz, K.; Stabentheiner, S.; Klause, S.; Madle, H.; Meineke, V.; Ullmann, R.; Scherthan, H.: Acute high-dose X-radiation-induced genomic changes in A549 cells. Radiat Res 175 (6), pp. 700 - 7 (2011)

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Najmabadi, H.; Hu, H.; Garshasbi, M.; Zemojtel, T.; Abedini, S. S.; Chen, W.; Hosseini, M.; Behjati, F.; Haas, S.; Jamali, P. et al.; Zecha, A.; Mohseni, M.; Puttmann, L.; Vahid, L. N.; Jensen, C.; Moheb, L. A.; Bienek, M.; Larti, F.; Mueller, I.; Weissmann, R.; Darvish, H.; Wrogemann, K.; Hadavi, V.; Lipkowitz, B.; Esmaeeli-Nieh, S.; Wieczorek, D.; Kariminejad, R.; Firouzabadi, S. G.; Cohen, M.; Fattahi, Z.; Rost, I.; Mojahedi, F.; Hertzberg, C.; Dehghan, A.; Rajab, A.; Banavandi, M. J.; Hoffer, J.; Falah, M.; Musante, L.; Kalscheuer, V.; Ullmann, R.; Kuss, A. W.; Tzschach, A.; Kahrizi, K.; Ropers, H. H.: Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature 478 (7367), pp. 57 - 63 (2011)

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Norton, L. J.; Zhang, Q.; Saqib, K. M.; Schrewe, H.; Macura, K.; Anderson, K. E.; Lindsley, C. W.; Brown, H. A.; Rudge, S. A.; Wakelam, M. J.: PLD1 rather than PLD2 regulates phorbol-ester-, adhesion-dependent and Fc{gamma}-receptor-stimulated ROS production in neutrophils. J Cell Sci 124 (Pt 12), pp. 1973 - 1983 (2011)

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Ott, C. E.; Grunhagen, J.; Jager, M.; Horbelt, D.; Schwill, S.; Kallenbach, K.; Guo, G.; Manke, T.; Knaus, P.; Mundlos, S. et al.; Robinson, P. N.: MicroRNAs differentially expressed in postnatal aortic development downregulate elastin via 3' UTR and coding-sequence binding sites. PLoS ONE 6 (1), p. e16250 (2011)

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Pabst, S.; Golebiewski, M.; Herms, S.; Karpushova, A.; Diaz-Lacava, A.; Walier, M.; Zimmer, S.; Cichon, S.; Wienker, T. F.; Nothen, M. M. et al.; Nickenig, G.; Meyer, R.; Skowasch, D.; Grohe, C.: Caspase recruitment domain 15 gene haplotypes in sarcoidosis. Tissue Antigens 77 (4), pp. 333 - 337 (2011)

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Pagan, C.; Botros, H. G.; Poirier, K.; Dumaine, A.; Jamain, S.; Moreno, S.; de Brouwer, A.; Van Esch, H.; Delorme, R.; Launay, J. M. et al.; Tzschach, A.; Kalscheuer, V.; Lacombe, D.; Briault, S.; Laumonnier, F.; Raynaud, M.; van Bon, B. W.; Willemsen, M. H.; Leboyer, M.; Chelly, J.; Bourgeron, T.: Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability. BMC Med Genet 12, p. 17 (2011)

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Pak, C.; Garshasbi, M.; Kahrizi, K.; Gross, C.; Apponi, L. H.; Noto, J. J.; Kelly, S. M.; Leung, S. W.; Tzschach, A.; Behjati, F. et al.; Abedini, S. S.; Mohseni, M.; Jensen, L. R.; Hu, H.; Huang, B.; Stahley, S. N.; Liu, G.; Williams, K. R.; Burdick, S.; Feng, Y.; Sanyal, S.; Bassell, G. J.; Ropers, H. H.; Najmabadi, H.; Corbett, A. H.; Moberg, K. H.; Kuss, A. W.: Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans. Proc Natl Acad Sci U S A 108 (30), pp. 12390 - 5 (2011)

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Pangrazio, A.; Cassani, B.; Guerrini, M. M.; Crockett, J. C.; Marrella, V.; Zammataro, L.; Strina, D.; Schulz, A.; Schlack, C.; Kornak, U. et al.; Mellis, D. J.; Duthie, A.; Helfrich, M. H.; Durandy, A.; Moshous, D.; Vellodi, A.; Chiesa, R.; Veys, P.; Iacono, N. L.; Vezzoni, P.; Fischer, A.; Villa, A.; Sobacchi, C.: RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. J Bone Miner Res (2011)

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Pech, M.; Karim, Z.; Yamamoto, H.; Kitakawa, M.; Qin, Y.; Nierhaus, K. H.: Elongation factor 4 (EF4/LepA) accelerates protein synthesis at increased Mg2+ concentrations. Proc Natl Acad Sci U S A 108 (8), pp. 3199 - 203 (2011)

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Pfeiffer, T.; Bertram, L.; Ioannidis, J. P.: Quantifying selective reporting and the Proteus phenomenon for multiple datasets with similar bias. PLoS ONE 6 (3), p. e18362 (2011)

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