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
Scherthan, H.; Sfeir, A.; de Lange, T.: Rap1-independent telomere attachment and bouquet formation in mammalian meiosis. Chromosoma 120 (2), pp. 151 - 7 (2011)
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Schjeide, B. M.; Schnack, C.; Lambert, J. C.; Lill, C. M.; Kirchheiner, J.; Tumani, H.; Otto, M.; Tanzi, R. E.; Lehrach, H.; Amouyel, P. et al.; von Arnim, C. A.; Bertram, L.: The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels. Archives of General Psychiatry 68 (2), pp. 207 - 13 (2011)
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Schraders, M.; Haas, S. A.; Weegerink, N. J.; Oostrik, J.; Hu, H.; Hoefsloot, L. H.; Kannan, S.; Huygen, P. L.; Pennings, R. J.; Admiraal, R. J. et al.; Kalscheuer, V. M.; Kunst, H. P.; Kremer, H.: Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment. Am J Hum Genet 88 (5), pp. 628 - 34 (2011)
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Schraders, M.; Haas, S. A.; Weegerink, N. J.; Oostrik, J.; Hu, H.; Hoefsloot, L. H.; Kannan, S.; Huygen, P. L.; Pennings, R. J.; Admiraal, R. J. et al.; Kalscheuer, V. M.; Kunst, H. P.; Kremer, H.: Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment. Am J Hum Genet 88 (5), pp. 628 - 34 (2011)
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Schulz, M. H.; Kohler, S.; Bauer, S.; Robinson, P. N.: Exact score distribution computation for ontological similarity searches. BMC Bioinformatics 12, p. 441 (2011)
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Schulz, N.; Himmelbauer, H.; Rath, M.; van Weeghel, M.; Houten, S.; Kulik, W.; Suhre, K.; Scherneck, S.; Vogel, H.; Kluge, R. et al.; Wiedmer, P.; Joost, H. G.; Schurmann, A.: Role of medium- and short-chain L-3-hydroxyacyl-CoA dehydrogenase in the regulation of body weight and thermogenesis. Endocrinology 152 (12), pp. 4641 - 51 (2011)
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Schutze, T.; Rubelt, F.; Repkow, J.; Greiner, N.; Erdmann, V. A.; Lehrach, H.; Konthur, Z.; Glokler, J.: A streamlined protocol for emulsion polymerase chain reaction and subsequent purification. Analytical Biochemistry 410 (1), pp. 155 - 157 (2011)
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Schutze, T.; Wilhelm, B.; Greiner, N.; Braun, H.; Peter, F.; Morl, M.; Erdmann, V. A.; Lehrach, H.; Konthur, Z.; Menger, M. et al.; Arndt, P. F.; Glokler, J.: Probing the SELEX Process with Next-Generation Sequencing. PLoS ONE 6 (12), p. e29604 - e29604 (2011)
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Schweiger, M. R.; Kerick, M.; Timmermann, B.; Isau, M.: The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations. Cancer Metastasis Reviews 30 (2), pp. 199 - 210 (2011)
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Serin, A.; Vingron, M.: DeBi: Discovering Differentially Expressed Biclusters using a Frequent Itemset Approach. Algorithms Mol Biol 6 (1), p. 18 (2011)
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Sheikhzadeh, S.; Rybczynski, M.; Habermann, C. R.; Bernhardt, A. M.; Arslan-Kirchner, M.; Keyser, B.; Kaemmerer, H.; Mir, T. S.; Staebler, A.; Oezdal, N. et al.; Robinson, P. N.; Berger, J.; Meinertz, T.; von Kodolitsch, Y.: Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2. Clin Genet 79 (6), pp. 568 - 74 (2011)
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Skidmore, D. L.; Chitayat, D.; Morgan, T.; Hinek, A.; Fischer, B.; Dimopoulou, A.; Somers, G.; Halliday, W.; Blaser, S.; Diambomba, Y. et al.; Lemire, E. G.; Kornak, U.; Robertson, S. P.: Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Delta(1)-pyrroline-5-carboxylate synthase (P5CS). Am J Med Genet A 155A (8), pp. 1848 - 56 (2011)
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Sklar, P.; Ripke, S.; Scott, L. J.; Andreassen, O. A.; Cichon, S.; Craddock, N.; Edenberg, H. J.; Nurnberger, J. I.; Rietschel, M.; Blackwood, D. et al.; Corvin, A.; Flickinger, M.; Guan, W.; Mattingsdal, M.; McQuillin, A.; Kwan, P.; Wienker, T. F.; Daly, M.; Dudbridge, F.; Holmans, P. A.; Lin, D.; Burmeister, M.; Greenwood, T. A.; Hamshere, M. L.; Muglia, P.; Smith, E. N.; Zandi, P. P.; Nievergelt, C. M.; McKinney, R.; Shilling, P. D.; Schork, N. J.; Bloss, C. S.; Foroud, T.; Koller, D. L.; Gershon, E. S.; Liu, C.; Badner, J. A.; Scheftner, W. A.; Lawson, W. B.; Nwulia, E. A.; Hipolito, M.; Coryell, W.; Rice, J.; Byerley, W.; McMahon, F. J.; Schulze, T. G.; Berrettini, W.; Lohoff, F. W.; Potash, J. B.; Mahon, P. B.; McInnis, M. G.; Zollner, S.; Zhang, P.; Craig, D. W.; Szelinger, S.; Barrett, T. B.; Breuer, R.; Meier, S.; Strohmaier, J.; Witt, S. H.; Tozzi, F.; Farmer, A.; McGuffin, P.; Strauss, J.; Xu, W.; Kennedy, J. L.; Vincent, J. B.; Matthews, K.; Day, R.; Ferreira, M. A.; O'Dushlaine, C.; Perlis, R.; Raychaudhuri, S.; Ruderfer, D.; Hyoun, P. L.; Smoller, J. W.; Li, J.; Absher, D.; Thompson, R. C.; Meng, F. G.; Schatzberg, A. F.; Bunney, W. E.; Barchas, J. D.; Jones, E. G.; Watson, S. J.; Myers, R. M.; Akil, H.; Boehnke, M.; Chambert, K.; Moran, J.; Scolnick, E.; Djurovic, S.; Melle, I.; Morken, G.; Gill, M.; Morris, D.; Quinn, E.; Muhleisen, T. W.; Degenhardt, F. A.; Mattheisen, M.: Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nat Genet 43 (10), pp. 977 - 83 (2011)
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Smallwood, J.: Mind-wandering while reading: Attentional decoupling, mindless reading and the cascade model of inattention. Language and Linguistics Compass 5 (2), pp. 63 - 77 (2011)
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Smallwood, J.: Stimulus independence, social cognition and consciousness. Cognitive Neuroscience 2 (2), pp. 122 - 123 (2011)
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Soler-Lopez, M.; Zanzoni, A.; Lluis, R.; Stelzl, U.; Aloy, P.: Interactome mapping suggests new mechanistic details underlying Alzheimer's disease. Genome Res 21 (3), pp. 364 - 76 (2011)
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Spielmann, M.; Reichelt, G.; Hertzberg, C.; Trimborn, M.; Mundlos, S.; Horn, D.; Klopocki, E.: Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and congenital retinal dysfunction in siblings. Eur J Med Genet 54 (4), pp. e441 - 5 (2011)
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Stacher, E.; Boldt, V.; Leibl, S.; Halbwedl, I.; Popper, H. H.; Ullmann, R.; Tavassoli, F. A.; Moinfar, F.: Chromosomal aberrations as detected by array comparative genomic hybridization in early low-grade intraepithelial neoplasias of the breast. Histopathology 59 (3), pp. 549 - 55 (2011)
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Stanke, F.; Becker, T.; Kumar, V.; Hedtfeld, S.; Becker, C.; Cuppens, H.; Tamm, S.; Yarden, J.; Laabs, U.; Siebert, B. et al.; Fernandez, L.; Macek, M.; Radojkovic, D.; Ballmann, M.; Greipel, J.; Cassiman, J. J.; Wienker, T. F.; Tummler, B.: Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. J Med Genet 48 (1), pp. 24 - 31 (2011)
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Stehr, H.; Jang, S. H.; Duarte, J. M.; Wierling, C.; Lehrach, H.; Lappe, M.; Lange, B. M.: The structural impact of cancer-associated missense mutations in oncogenes and tumor suppressors. Molecular Cancer 10, p. 54 (2011)
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