Publications

Journal Article

Freiwald, A.; Mao, L.; Kodelja, V.; Kliem, M.; Schuldt, D.; Schreiber, S.; Franke, A.; Sauer, S.: Differential analysis of Crohn's disease and ulcerative colitis by mass spectrometry. Inflamm Bowel Dis 17 (4), pp. 1051 - 2 (2011)

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Fullston, T.; Gabb, B.; Callen, D.; Ullmann, R.; Woollatt, E.; Bain, S.; Ropers, H. H.; Cooper, M.; Chandler, D.; Carter, K. et al.; Jablensky, A.; Kalaydjieva, L.; Gecz, J.: Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia. Am J Med Genet B Neuropsychiatr Genet 156 (2), pp. 204 - 14 (2011)

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Garshasbi, M.; Kahrizi, K.; Hosseini, M.; Nouri Vahid, L.; Falah, M.; Hemmati, S.; Hu, H.; Tzschach, A.; Ropers, H. H.; Najmabadi, H. et al.; Kuss, A. W.: A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian family. Am J Med Genet A 155A (8), pp. 1976 - 80 (2011)

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Georgieva, Y.; Konthur, Z.: Design and Screening of M13 Phage Display cDNA Libraries. Molecules 16 (2), pp. 1667 - 1681 (2011)

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Gilling, M.; Lind-Thomsen, A.; Mang, Y.; Bak, M.; Moller, M.; Ullmann, R.; Kristoffersson, U.; Kalscheuer, V. M.; Henriksen, K. F.; Bugge, M. et al.; Tumer, Z.; Tommerup, N.: Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation. Eur J Med Genet 54 (4), pp. e383 - 8 (2011)

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Goke, J.; Jung, M.; Behrens, S.; Chavez, L.; O'Keeffe, S.; Timmermann, B.; Lehrach, H.; Adjaye, J.; Vingron, M.: Combinatorial binding in human and mouse embryonic stem cells identifies conserved enhancers active in early embryonic development. PLoS Comput Biol 7 (12), e1002304 (2011)

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Gostner, J. M.; Fong, D.; Wrulich, O. A.; Lehne, F.; Zitt, M.; Hermann, M.; Krobitsch, S.; Martowicz, A.; Gastl, G.; Spizzo, G.: Effects of EpCAM overexpression on human breast cancer cell lines. BMC Cancer 11, p. 45 (2011)

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Goswami, C.; Kuhn, J.; Dina, O. A.; Fernandez-Ballester, G.; Levine, J. D.; Ferrer-Montiel, A.; Hucho, T.: Estrogen destabilizes microtubules through an ion-conductivity-independent TRPV1 pathway. J Neurochem 117 (6), pp. 995 - 1008 (2011)

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Gregor, A.; Albrecht, B.; Bader, I.; Bijlsma, E. K.; Ekici, A. B.; Engels, H.; Hackmann, K.; Horn, D.; Hoyer, J.; Klapecki, J. et al.; Kohlhase, J.; Maystadt, I.; Nagl, S.; Prott, E.; Tinschert, S.; Ullmann, R.; Wohlleber, E.; Woods, G.; Reis, A.; Rauch, A.; Zweier, C.: Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1. BMC Med Genet 12, p. 106 (2011)

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Gruning, N. M.; Ralser, M.: Cancer: Sacrifice for survival. Nature 480 (7376), pp. 190 - 1 (2011)

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Gruning, N. M.; Rinnerthaler, M.; Bluemlein, K.; Mulleder, M.; Wamelink, M. M.; Lehrach, H.; Jakobs, C.; Breitenbach, M.; Ralser, M.: Pyruvate kinase triggers a metabolic feedback loop that controls redox metabolism in respiring cells. Cell Metabolism 14 (3), pp. 415 - 27 (2011)

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Journal Article

Guo, G.; Gehle, P.; Doelken, S.; Martin-Ventura, J. L.; von Kodolitsch, Y.; Hetzer, R.; Robinson, P. N.: Induction of macrophage chemotaxis by aortic extracts from patients with Marfan syndrome is related to elastin binding protein. PLoS ONE 6 (5), p. e20138 (2011)

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Haapasalo, A.; Viswanathan, J.; Kurkinen, K. M.; Bertram, L.; Soininen, H.; Dantuma, N. P.; Tanzi, R. E.; Hiltunen, M.: Involvement of ubiquilin-1 transcript variants in protein degradation and accumulation. Communicative & Integrative Biology 4 (4), pp. 428 - 32 (2011)

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Hafemeister, C.; Krause, R.; Schliep, A.: Selecting oligonucleotide probes for whole-genome tiling arrays with a cross-hybridization potential. IEEE/ACM Trans Comput Biol Bioinform 8 (6), pp. 1642 - 52 (2011)

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Hagen, A.; Bigl, A.; Wand, D.; Klopocki, E.; Heller, R.; Siekmeyer, M.; Siekmeyer, W.; Kiess, W.; Merkenschlager, A.: Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findings. Am J Med Genet A 155A (12), pp. 3075 - 81 (2011)

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Hampel, H.; Prvulovic, D.; Teipel, S.; Jessen, F.; Luckhaus, C.; Frolich, L.; Riepe, M. W.; Dodel, R.; Leyhe, T.; Bertram, L. et al.; Hoffmann, W.; Faltraco, F.: The future of Alzheimer's disease: the next 10 years. Progress in Neurobiology 95 (4), pp. 718 - 28 (2011)

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Hasler, R.; Kerick, M.; Mah, N.; Hultschig, C.; Richter, G.; Bretz, F.; Sina, C.; Lehrach, H.; Nietfeld, W.; Schreiber, S. et al.; Rosenstiel, P.: Alterations of pre-mRNA splicing in human inflammatory bowel disease. European Journal of Cell Biology 90 (6-7), pp. 603 - 11 (2011)

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Haworth, A.; Bertram, L.; Carrera, P.; Elson, J. L.; Braastad, C. D.; Cox, D. W.; Cruts, M.; den Dunnen, J. T.; Farrer, M. J.; Fink, J. K. et al.; Hamed, S. A.; Houlden, H.; Johnson, D. R.; Nuytemans, K.; Palau, F.; Rayan, D. L.; Robinson, P. N.; Salas, A.; Schule, B.; Sweeney, M. G.; Woods, M. O.; Amigo, J.; Cotton, R. G.; Sobrido, M. J.: Call for participation in the neurogenetics consortium within the Human Variome Project. Neurogenetics 12 (3), pp. 169 - 73 (2011)

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Journal Article

Haworth, A.; Bertram, L.; Carrera, P.; Elson, J. L.; Braastad, C. D.; Cox, D. W.; Cruts, M.; den Dunnen, J. T.; Farrer, M. J.; Fink, J. K. et al.; Hamed, S. A.; Houlden, H.; Johnson, D. R.; Nuytemans, K.; Palau, F.; Rayan, D. L.; Robinson, P. N.; Salas, A.; Schule, B.; Sweeney, M. G.; Woods, M. O.; Amigo, J.; Cotton, R. G.; Sobrido, M. J.: Call for participation in the neurogenetics consortium within the Human Variome Project. Neurogenetics 12 (3), pp. 169 - 73 (2011)

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Heinrich, V.; Stange, J.; Dickhaus, T.; Imkeller, P.; Kruger, U.; Bauer, S.; Mundlos, S.; Robinson, P. N.; Hecht, J.; Krawitz, P. M.: The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process. Nucleic Acids Res (2011)

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Journal Article (247)