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
Pfenninger, C. V.; Steinhoff, C.; Hertwig, F.; Nuber, U. A.: Prospectively isolated CD133/CD24-positive ependymal cells from the adult spinal cord and lateral ventricle wall differ in their long-term in vitro self-renewal and in vivo gene expression. GLIA 59 (1), pp. 68 - 81 (2011)
Journal Article
Prigione, A.; Hossini, A. M.; Lichtner, B.; Serin, A.; Fauler, B.; Megges, M.; Lurz, R.; Lehrach, H.; Makrantonaki, E.; Zouboulis, C. C. et al.; Adjaye, J.: Mitochondrial-associated cell death mechanisms are reset to an embryonic-like state in aged donor-derived iPS cells harboring chromosomal aberrations. PLoS ONE 6 (11), p. e27352 (2011)
Journal Article
Prigione, A.; Lichtner, B.; Kuhl, H.; Struys, E. A.; Wamelink, M.; Lehrach, H.; Ralser, M.; Timmermann, B.; Adjaye, J.: Human induced pluripotent stem cells harbor homoplasmic and heteroplasmic mitochondrial DNA mutations while maintaining human embryonic stem cell-like metabolic reprogramming. Stem Cells 29 (9), pp. 1338 - 48 (2011)
Journal Article
Puente, X. S.; Pinyol, M.; Quesada, V.; Conde, L.; Ordonez, G. R.; Villamor, N.; Escaramis, G.; Jares, P.; Bea, S.; Gonzalez-Diaz, M. et al.; Bassaganyas, L.; Baumann, T.; Juan, M.; Lopez-Guerra, M.; Colomer, D.; Tubio, J. M.; Lopez, C.; Navarro, A.; Tornador, C.; Aymerich, M.; Rozman, M.; Hernandez, J. M.; Puente, D. A.; Freije, J. M.; Velasco, G.; Gutierrez-Fernandez, A.; Costa, D.; Carrio, A.; Guijarro, S.; Enjuanes, A.; Hernandez, L.; Yague, J.; Nicolas, P.; Romeo-Casabona, C. M.; Himmelbauer, H.; Castillo, E.; Dohm, J. C.; de Sanjose, S.; Piris, M. A.; de Alava, E.; San Miguel, J.; Royo, R.; Gelpi, J. L.; Torrents, D.; Orozco, M.; Pisano, D. G.; Valencia, A.; Guigo, R.; Bayes, M.; Heath, S.; Gut, M.; Klatt, P.; Marshall, J.; Raine, K.; Stebbings, L. A.; Futreal, P. A.; Stratton, M. R.; Campbell, P. J.; Gut, I.; Lopez-Guillermo, A.; Estivill, X.; Montserrat, E.; Lopez-Otin, C.; Campo, E.: Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature 475 (7354), pp. 101 - 5 (2011)
Journal Article
Rademacher, N.; Hambrock, M.; Fischer, U.; Moser, B.; Ceulemans, B.; Lieb, W.; Boor, R.; Stefanova, I.; Gillessen-Kaesbach, G.; Runge, C. et al.; Korenke, G. C.; Spranger, S.; Laccone, F.; Tzschach, A.; Kalscheuer, V. M.: Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features. Neurogenetics 12 (2), pp. 165 - 7 (2011)
Journal Article
Rafiq, M. A.; Kuss, A. W.; Puettmann, L.; Noor, A.; Ramiah, A.; Ali, G.; Hu, H.; Kerio, N. A.; Xiang, Y.; Garshasbi, M. et al.; Khan, M. A.; Ishak, G. E.; Weksberg, R.; Ullmann, R.; Tzschach, A.; Kahrizi, K.; Mahmood, K.; Naeem, F.; Ayub, M.; Moremen, K. W.; Vincent, J. B.; Ropers, H. H.; Ansar, M.; Najmabadi, H.: Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability. Am J Hum Genet 89 (1), pp. 176 - 82 (2011)
Journal Article
Rietschel, M.; Mattheisen, M.; Degenhardt, F.; Kahn, R. S.; Linszen, D. H.; Os, J. V.; Wiersma, D.; Bruggeman, R.; Cahn, W.; de Haan, L. et al.; Krabbendam, L.; Myin-Germeys, I.; Muhleisen, T. W.; Kirsch, P.; Esslinger, C.; Herms, S.; Demontis, D.; Steffens, M.; Strohmaier, J.; Haenisch, B.; Breuer, R.; Czerski, P. M.; Giegling, I.; Strengman, E.; Schmael, C.; Mors, O.; Mortensen, P. B.; Hougaard, D. M.; Orntoft, T.; Kapelski, P.; Priebe, L.; Basmanav, F. B.; Forstner, A. J.; Hoffmann, P.; Meier, S.; Nikitopoulos, J.; Moebus, S.; Alexander, M.; Mossner, R.; Wichmann, H. E.; Schreiber, S.; Rivandeneira, F.; Hofman, A.; Uitterlinden, A. G.; Wienker, T. F.; Schumacher, J.; Hauser, J.; Maier, W.; Cantor, R. M.; Erk, S.; Schulze, T. G.; Stefansson, H.; Steinberg, S.; Gustafsson, O.; Sigurdsson, E.; Petursson, H.; Kong, A.; Stefansson, K.; Pietilainen, O. P.; Tuulio-Henriksson, A.; Paunio, T.; Lonnqvist, J.; Suvisaari, J.; Peltonen, L.; Ruggeri, M.; Tosato, S.; Walshe, M.; Murray, R.; Collier, D. A.; Clair, D. S.; Hansen, T.; Ingason, A.; Jakobsen, K. D.; Duong, L.; Werge, T.; Melle, I.; Andreassen, O. A.; Djurovic, S.; Bitter, I.; Rethelyi, J. M.; Abramova, L.; Kaleda, V.; Golimbet, V.; Jonsson, E. G.; Terenius, L.; Agartz, I.; Winkel, R. V.; Kenis, G.; Hert, M. D.; Veldink, J.; Wiuf, C.; Didriksen, M.; Craddock, N.; Owen, M. J.; O'Donovan, M. C.; Borglum, A. D.; Rujescu, D.; Walter, H.; Meyer-Lindenberg, A.; Nothen, M. M.: Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol Psychiatry (2011)
Journal Article
Rivera-Brugues, N.; Albrecht, B.; Wieczorek, D.; Schmidt, H.; Keller, T.; Gohring, I.; Ekici, A. B.; Tzschach, A.; Garshasbi, M.; Franke, K. et al.; Klopp, N.; Wichmann, H. E.; Meitinger, T.; Strom, T. M.; Hempel, M.: Cohen syndrome diagnosis using whole genome arrays. J Med Genet 48 (2), pp. 136 - 40 (2011)
Journal Article
Robinson, P. N.; Krawitz, P.; Mundlos, S.: Strategies for exome and genome sequence data analysis in disease-gene discovery projects. Clin Genet 80 (2), pp. 127 - 32 (2011)
Journal Article
Rodelsperger, C.; Guo, G.; Kolanczyk, M.; Pletschacher, A.; Kohler, S.; Bauer, S.; Schulz, M. H.; Robinson, P. N.: Integrative analysis of genomic, functional and protein interaction data predicts long-range enhancer-target gene interactions. Nucleic Acids Res 39 (7), pp. 2492 - 502 (2011)
Journal Article
Rodelsperger, C.; Krawitz, P.; Bauer, S.; Hecht, J.; Bigham, A. W.; Bamshad, M.; de Condor, B. J.; Schweiger, M. R.; Robinson, P. N.: Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics 27 (6), pp. 829 - 36 (2011)
Journal Article
Rodelsperger, C.; Krawitz, P.; Bauer, S.; Hecht, J.; Bigham, A. W.; Bamshad, M.; de Condor, B. J.; Schweiger, M. R.; Robinson, P. N.: Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics 27 (6), pp. 829 - 36 (2011)
Journal Article
Roepcke, S.; Stahlberg, S.; Klein, H.; Schulz, M. H.; Theobald, L.; Gohlke, S.; Vingron, M.; Walther, D. J.: A tandem sequence motif acts as a distance-dependent enhancer in a set of genes involved in translation by binding the proteins NonO and SFPQ. BMC Genomics 12, p. 624 (2011)
Journal Article
Ropers, F.; Derivery, E.; Hu, H.; Garshasbi, M.; Karbasiyan, M.; Herold, M.; Nurnberg, G.; Ullmann, R.; Gautreau, A.; Sperling, K. et al.; Varon, R.; Rajab, A.: Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP. Hum Mol Genet 20 (13), pp. 2585 - 90 (2011)
Journal Article
Rump, P.; Jongbloed, J. D.; Sikkema-Raddatz, B.; Mundlos, S.; Klopocki, E.; van der Luijt, R. B.: Madelung deformity in a girl with a novel and de novo mutation in the GNAS gene. Am J Med Genet A 155A (10), pp. 2566 - 70 (2011)
Journal Article
Rybczynski, M.; Treede, H.; Sheikhzadeh, S.; Groene, E. F.; Bernhardt, A. M.; Hillebrand, M.; Mir, T. S.; Kuhne, K.; Koschyk, D.; Robinson, P. N. et al.; Berger, J.; Reichenspurner, H.; Meinertz, T.; von Kodolitsch, Y.: Predictors of outcome of mitral valve prolapse in patients with the Marfan syndrome. Am J Cardiol 107 (2), pp. 268 - 74 (2011)
Journal Article
Salton, M.; Elkon, R.; Borodina, T.; Davydov, A.; Yaspo, M. L.; Halperin, E.; Shiloh, Y.: Matrin 3 binds and stabilizes mRNA. PLoS ONE 6 (8), p. e23882 (2011)
Journal Article
Santos-Reboucas, C. B.; Fintelman-Rodrigues, N.; Jensen, L. R.; Kuss, A. W.; Ribeiro, M. G.; Campos, M.; Santos, J. M.; Pimentel, M. M.: A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay. Neurosci Lett 498 (1), pp. 67 - 71 (2011)
Journal Article
Sarajarvi, T.; Tuusa, J. T.; Haapasalo, A.; Lackman, J. J.; Sormunen, R.; Helisalmi, S.; Roehr, J. T.; Parrado, A. R.; Makinen, P.; Bertram, L. et al.; Soininen, H.; Tanzi, R. E.; Petaja-Repo, U. E.; Hiltunen, M.: Cysteine 27 variant of the delta-opioid receptor affects amyloid precursor protein processing through altered endocytic trafficking. Molecular and Cellular Biology 31 (11), pp. 2326 - 40 (2011)
Journal Article
Scherthan, H.; Adelfalk, C.: Live cell imaging of meiotic chromosome dynamics in yeast. Methods Mol Biol 745, pp. 537 - 48 (2011)
Go to Editor View