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), S. e20913 (2011)

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, S. 925362 (2011)

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

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

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), S. 721 - 4 (2011)

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), S. 407 - 14 (2011)

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), S. 224 - 9 (2011)

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), S. 1383 - 94 (2011)

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, S. 158 (2011)

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), S. 652 - 5 (2011)

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), S. 717 - 20 (2011)

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), S. 301 - 5 (2011)

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

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), S. 115 - 7 (2011)

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), S. 2917 - 8 (2011)

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), S. D712 - D717 (2011)

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), S. 1427 - 35 (2011)

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), S. e21498 (2011)

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

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, S. 68 (2011)