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

Herrmann, F.; Garriga-Canut, M.; Baumstark, R.; Fajardo-Sanchez, E.; Cotterell, J.; Minoche, A.; Himmelbauer, H.; Isalan, M.: p53 Gene repair with zinc finger nucleases optimised by yeast 1-hybrid and validated by Solexa sequencing. PLoS ONE 6 (6), p. e20913 (2011)

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Hiltunen, M.; Bertram, L.; Saunders, A. J.: Genetic risk factors: their function and comorbidities in Alzheimer's disease. International Journal of Alzheimer's Disease 2011, p. 925362 (2011)

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Höhe, M. R.: Die zwei Versionen des menschlichen Genoms. GenomXPress 4 (11), pp. 4 - 7 (2011)

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Homilius, M.; Wiedenhoeft, J.; Thieme, S.; Standfuss, C.; Kel, I.; Krause, R.: Cocos: Constructing multi-domain protein phylogenies. PLoS Curr 3, p. RRN1240 (2011)

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Horn, D.; Robinson, P. N.: Progeroid facial features and lipodystrophy associated with a novel splice site mutation in the final intron of the FBN1 gene. Am J Med Genet A 155A (4), pp. 721 - 4 (2011)

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Hu, H.; Eggers, K.; Chen, W.; Garshasbi, M.; Motazacker, M. M.; Wrogemann, K.; Kahrizi, K.; Tzschach, A.; Hosseini, M.; Bahman, I. et al.; Hucho, T.; Muhlenhoff, M.; Gerardy-Schahn, R.; Najmabadi, H.; Ropers, H. H.; Kuss, A. W.: ST3GAL3 mutations impair the development of higher cognitive functions. Am J Hum Genet 89 (3), pp. 407 - 14 (2011)

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Huang, J.; Mirel, D.; Pugh, E.; Xing, C.; Robinson, P. N.; Pertsemlidis, A.; Ding, L.; Kozlitina, J.; Maher, J.; Rios, J. et al.; Story, M.; Marthandan, N.; Scheuermann, R. H.: Minimum Information about a Genotyping Experiment (MIGEN). Stand Genomic Sci 5 (2), pp. 224 - 9 (2011)

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Iwaniuk, K. M.; Schira, J.; Weinhold, S.; Jung, M.; Adjaye, J.; Muller, H. W.; Wernet, P.; Trompeter, H. I.: Network-like impact of MicroRNAs on neuronal lineage differentiation of unrestricted somatic stem cells from human cord blood. Stem Cells and Development 20 (8), pp. 1383 - 94 (2011)

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Jager, M.; Ott, C. E.; Grunhagen, J.; Hecht, J.; Schell, H.; Mundlos, S.; Duda, G. N.; Robinson, P. N.; Lienau, J.: Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing. BMC Genomics 12, p. 158 (2011)

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Jakobsen, L. P.; Bugge, M.; Ullmann, R.; Schjerling, C. K.; Borup, R.; Hansen, L.; Eiberg, H.; Tommerup, N.: 500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip. Am J Med Genet A 155A (3), pp. 652 - 5 (2011)

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Jensen, L. R.; Chen, W.; Moser, B.; Lipkowitz, B.; Schroeder, C.; Musante, L.; Tzschach, A.; Kalscheuer, V. M.; Meloni, I.; Raynaud, M. et al.; van Esch, H.; Chelly, J.; de Brouwer, A. P.; Hackett, A.; van der Haar, S.; Henn, W.; Gecz, J.; Riess, O.; Bonin, M.; Reinhardt, R.; Ropers, H. H.; Kuss, A. W.: Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1. Eur J Hum Genet 19 (6), pp. 717 - 20 (2011)

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Joss, S.; Kini, U.; Fisher, R.; Mundlos, S.; Prescott, K.; Newbury-Ecob, R.; Tolmie, J.: The face of Ulnar Mammary syndrome? Eur J Med Genet 54 (3), pp. 301 - 5 (2011)

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Jozefczuk, J.; Adjaye, J.: Quantitative real-time PCR-based analysis of gene expression. Methods in Enzymology 500, pp. 99 - 109 (2011)

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Kahrizi, K.; Hu, C. H.; Garshasbi, M.; Abedini, S. S.; Ghadami, S.; Kariminejad, R.; Ullmann, R.; Chen, W.; Ropers, H. H.; Kuss, A. W. et al.; Najmabadi, H.; Tzschach, A.: Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3. Eur J Hum Genet 19 (1), pp. 115 - 7 (2011)

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Kamburov, A.; Cavill, R.; Ebbels, T. M.; Herwig, R.; Keun, H. C.: Integrated pathway-level analysis of transcriptomics and metabolomics data with IMPaLA. Bioinformatics 27 (20), pp. 2917 - 8 (2011)

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Kamburov, A.; Pentchev, K.; Galicka, H.; Wierling, C.; Lehrach, H.; Herwig, R.: ConsensusPathDB: toward a more complete picture of cell biology. Nucleic Acids Research (London) 39 (Database issue), pp. D712 - D717 (2011)

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publisher-version

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Kariminejad, R.; Lind-Thomsen, A.; Tumer, Z.; Erdogan, F.; Ropers, H. H.; Tommerup, N.; Ullmann, R.; Moller, R. S.: High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations. Hum Mutat 32 (12), pp. 1427 - 35 (2011)

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Kenyon, E. J.; McEwen, G. K.; Callaway, H.; Elgar, G.: Functional analysis of conserved non-coding regions around the short stature hox gene (shox) in whole zebrafish embryos. PLoS ONE 6 (6), p. e21498 (2011)

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Kerick, M.: Technical Challenges of targeted DNA Enrichment to identify Geneic Variations in Cancer Patiens. BMC Medical Genomics 4 (68) (2011)

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Kerick, M.; Isau, M.; Timmermann, B.; Sultmann, H.; Herwig, R.; Krobitsch, S.; Schaefer, G.; Verdorfer, I.; Bartsch, G.; Klocker, H. et al.; Lehrach, H.; Schweiger, M. R.: Targeted high throughput sequencing in clinical cancer settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity. BMC Med Genomics 4, p. 68 (2011)

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