Reiner, G.; Dreher, F.; Drungowski, M.; Hoeltig, D.; Bertsch, N.; Selke, M.; Willems, H.; Gerlach, G. F.; Probst, I.; Tuemmler, B. et al.; Waldmann, K.-H.; Herwig, R.: Pathway deregulation and expression QTLs in response to Actinobacillus pleuropneumoniae infection in swine. Mammalian Genome 25 (11-12), pp. 600 - 617 (2014)

Scherthan, H.; Schöfisch, K.; Dell, T.; Illner, D.: Contrasting behavior of heterochromatic and euchromatic chromosome portions and pericentric genome separation in pre-bouquet spermatocytes of hybrid mice. Chromosoma: Biology of the Nucleus 123 (6), pp. 609 - 624 (2014)

Weidner, C.; Fischer, C.; Sauer, S.: PHOXTRACK-a tool for interpreting comprehensive datasets of post-translational modifications of proteins. Bioinformatics 30 (23), pp. 3410 - 3411 (2014)

Hoehe, M. R.; Church, G. M.; Lehrach, H.; Kroslak, T.; Palczewski, S.; Nowick, K.; Schulz, S.; Suk, E.-K.; Huebsch, T.: Multiple haplotype-resolved genomes reveal population patterns of gene and protein diplotypes. Nature Communications 5, 5:5569 (2014)

Zhang, Z.; Liao, W.; Bernhardt, B. C.; Wang, Z.; Sun, K.; Yang, F.; Liu, Y.; Lu, G.: Brain iron redistribution in mesial temporal lobe epilepsy: A susceptibility-weighted magnetic resonance imaging study. BMC Neuroscience 15, 117 (2014)

Ahmed, I.; Lee, P.-C.; Lill, C. M.; Nielsen, S. S.; Artaud, F.; Gallagher, L. G.; Loriot, M.-A.; Mulot, C.; Nacfer, M.; Liu, T. et al.; Biernacka, J. M.; Armasu, S.; Anderson, K.; Farin, F. M.; Lassen, C. F.; Hansen, J.; Olsen, J. H.; Bertram, L.; Maraganore, D. M.; Checkoway, H.; Ritz, B.; Elbaz, A.: Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease. PLoS Genetics 10 (11), e1004788 (2014)

Ahmed, I.; Lee, P.-C.; Lill, C. M.; Searles Nielsen, S.; Artaud, F.; Gallagher, L. G.; Loriot, M.-A.; Mulot, C.; Nacfer, M.; Liu, T. et al.; Biernacka, J. M.; Armasu, S.; Anderson, K.; Farin, F. M.; Funch Lassen, C.; Hansen, J.; Olsen, J. H.; Bertram, L.; Maraganore, D. M.; Checkoway, H.; Ritz, B.; Elbaz, A.: Lack of Replication of the GRIN2A-by-Coffee Interaction in Parkinson Disease. PLoS Genetics 10 (11), e1004788 (2014)

Steinbeis, N.; Singer, T.: Projecting my envy onto you: Neurocognitive mechanisms of offline emotional egocentricity bias. NeuroImage 102 (2), pp. 370 - 380 (2014)

Rudat, C.; Grieskamp, T.; Röhr, C.; Airik, R.; Wrede, C.; Hegermann, J.; Herrmann, B. G.; Schuster-Gossler, K.; Kispert, A.: Upk3b is dispensable for development and integrity of urothelium and mesothelium. PLoS One 9 (11), e112112 (2014)

Athanasiadis, E. I.; Antonopoulou, K.; Chatzinasiou, F.; Lill, C. M.; Bourdakou, M. M.; Sakellariou, A.; Kypreou, K.; Stefanaki, I.; Evangelou, E.; Ioannidis, J. P.A. et al.; Bertram, L.; Stratigos, A. J.; Spyrou, G. M.: A Web-based database of genetic association studies in cutaneous melanoma enhanced with network-driven data exploration tools. Database: The Journal of Biological Databases and Curation 2014, bau101 (2014)

Hülsmann, H. J.; Rolff, J.; Bender, C.; Jarahian, M.; Korf, U.; Herwig, R.; Fröhlich, H.; Thomas, M.; Merk, J.; Fichtner, I. et al.; Sültmann, H.; Kuner, R.: Activation of AMP-activated protein kinase sensitizes lung cancer cells and H1299 xenografts to erlotinib. Lung Cancer 86 (2), pp. 151 - 157 (2014)

Reuter, M. S.; Musante, L.; Hu, H.; Diederich, S.; Sticht, H.; Ekici, A. B.; Uebe, S.; Wienker, T. F.; Bartsch, O.; Zechner, U. et al.; Oppitz, C.; Keleman, K.; Jamra, R. A.; Najmabadi, H.; Schweiger, S.; Reis, A.; Kahrizi, K.: NDST1 missense mutations in autosomal recessive intellectual disability. American Journal of Medical Genetics Part A 164A (11), pp. 2753 - 2763 (2014)

Rybkina, V. L.; Azizova, T. V.; Scherthan, H.; Meineke, V.; Doerr, H.; Adamova, G. V.; Teplyakova, O. V.; Osovets, S. V.; Bannikova, M. V.; Zurochka, A. V.: Expression of blood serum proteins and lymphocyte differentiation clusters after chronic occupational exposure to ionizing radiation. Radiation and Environmental Biophysics 53 (4), pp. 659 - 670 (2014)

Vaags, A. K.; Bowdin, S.; Smith, M. L.; Gilbert-Dussardier, B.; Brocke-Holmefjord, K. S.; Sinopoli, K.; Gilles, C.; Haaland, T. B.; Vincent-Delorme, C.; Lagrue, E. et al.; Harbuz, R.; Walker, S.; Marshall, C. R.; Houge, G.; Kalscheuer, V. M.; Scherer, S. W.; Minassian, B. A.: Absent CNKSR2 causes seizures and intellectual, attention, and language deficits. Annals of Neurology 76 (5), pp. 758 - 764 (2014)

Willems, T.; Gymrek, M.; Highnam, G.; The 1000 Genomes Project, C.; Herwig, R.; Lehrach, H.; Sudbrak, R.; Timmermann, B.; Mittelman, D.; Erlich, Y.: The landscape of human STR variation. Genome Research 24 (11), pp. 1894 - 1904 (2014)

Pandey, V.; Sultan, M.; Kashofer, K.; Ralser, M.; Amstislavskiy, V.; Starmann, J.; Osprian, I.; Grimm, C.; Hache, H.; Yaspo, M. L. et al.; Sultmann, H.; Trauner, M.; Denk, H.; Zatloukal, K.; Lehrach, H.; Wierling, C.: Comparative analysis and modeling of the severity of steatohepatitis in DDC-treated mouse strains. PLoS One 9 (10), e111006 (2014)

Conrad, T.; Marsico, A.; Gehre, M.; Ørom, U. A.: Microprocessor activity controls differential miRNA biogenesis In Vivo. Cell Reports 9 (2), pp. 542 - 554 (2014)

Reutter, H.; Draaken, M.; Pennimpede, T.; Wittler, L.; Brockschmidt, F. F.; Ebert, A. K.; Bartels, E.; Rösch, W.; Boemers, T. M.; Hirsch, K. et al.; Schmiedeke, E.; Meesters, C.; Becker, T.; Stein, R.; Utsch, B.; Mangold, E.; Nordenskjöld, A.; Barker, G.; Kockum, C. C.; Zwink, N.; Homdahl, G.; Läckgren, G.; Jenetzky, E.; Feitz, W. F.; Marcelis, C.; Wijers, C. H.; Van Rooij, I. A.; Gearhart, J. P.; Herrmann, B. G.; Ludwig, M.; Boyadjiev, S. A.; Nöthen, M. M.; Mattheisen, M.: Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Human Molecular Genetics 23 (20), pp. 5536 - 5544 (2014)

Liu, J.; Wang, X.; Li, J.; Wang, H.; Wei, G.; Yan, J.: Reconstruction of the Gene Regulatory Network Involved in the Sonic Hedgehog Pathway with a Potential Role in Early Development of the Mouse Brain. PLoS Computational Biology 10 (10), e1003884 (2014)

Hooli, B. V.; Parrado, A. R.; Mullin, K.; Yip, W. K.; Liu, T.; Roehr, J. T.; Qiao, D.; Jessen, F.; Peters, O.; Becker, T. et al.; Ramirez, A.; Lange, C.; Bertram, L.; Tanzi, R. E.: The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. Neurology 83 (15), pp. 1353 - 1358 (2014)