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Farrall, A.; Lienhard, M.; Grimm, C.; Kuhl, H.; Sluka, S. H. M.; Caparros Rodriguez, M.; Forejt, J.; Timmermann, B.; Herwig, R.; Herrmann, B. G. et al.; Morkel, M.: PWD/Ph-encoded genetic variants modulate the cellular Wnt/β-Catenin response to suppress ApcMin-triggered intestinal tumor formation. Cancer research: an official organ of the American Association for Cancer Research 81 (1), pp. 38 - 49 (2021)

Veenvliet, J. V.; Bolondi, A.; Kretzmer, H.; Haut, L.; Scholze-Wittler, M.; Schifferl, D.; Koch, F.; Guignard, L.; Sampath Kumar, A.; Pustet, M. et al.; Heimann, S.; Buschow, R.; Wittler, L.; Timmermann, B.; Meissner, A.; Herrmann, B. G.: Mouse embryonic stem cells self-organize into trunk-like structures with neural tube and somites. Science 370 (6522), eaba4937 (2020)

Brandt, R.; Sell, T.; Lüthen, M.; Uhlitz, F.; Klinger, B.; Riemer, P.; Giesecke-Thiel, C.; Schulze, S.; El-Shimy, I. A.; Kunkel, D. et al.; Fauler, B.; Mielke, T.; Mages, N.; Herrmann, B. G.; Sers, C.; Blüthgen, N.; Morkel, M.: Cell type-dependent differential activation of ERK by oncogenic KRAS in colon cancer and intestinal epithelium. Nature Communications 10 (1), 2919 (2019)

Weitensteiner, V.; Zhang, R.; Bungenberg, J.; Marks, M.; Gehlen, J.; Ralser, D. J.; Hilger, A. C.; Sharma, A.; Schumacher , J.; Gembruch, U. et al.; Merz, W. M.; Becker, A.; Altmüller, J.; Thiele, H.; Herrmann, B. G.; Odermatt , B.; Ludwig, M.; Reutter, H.: Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth Defects Research 110 (7), pp. 587 - 597 (2018)

Beisaw, A.; Tsaytler, P.; Koch, F.; Schmitz, S. U.; Melissari, M.-T.; Senf, A. D.; Wittler, L.; Pennimpede, T.; Macura, K.; Herrmann, B. G. et al.; Grote, P.: BRACHYURY directs histone acetylation to target loci during mesoderm development. EMBO Reports 19 (1), pp. 118 - 134 (2018)

Koch, F.; Scholze, M.; Wittler, L.; Schifferl, D.; Sudheer, S.; Grote, P.; Timmermann, B.; Macura, K.; Herrmann, B. G.: Antagonistic Activities of Sox2 and Brachyury Control the Fate Choice of Neuro-Mesodermal Progenitors. Developmental Cell 42, pp. 514 - 526 (2017)

Lange, L.; Marks, M.; Liu, J.; Wittler, L.; Bauer, H.; Piehl, S.; Bläß, G.; Timmermann, B.; Herrmann, B. G.: Pattering and gastrulation deffects caused by the tw18 lethal are due to loss of Ppp2r1a. Biology Open 6 (6), pp. 752 - 764 (2017)

Riemer, P.; Rydenfelt, M.; Marks, M.; van Eunen, K.; Thedieck, K.; Herrmann, B. G.; Blüthgen, N.; Sers, C.; Morkel, M.: Oncogenic ß-catenin and PIK3CA instruct network states and cancer phenotypes in intestinal organoids. The Journal of Cell Biology: JCB 216 (6), pp. 1567 - 1577 (2017)

Schmitz, S. U.; Grote, P.; Herrmann, B. G.: Mechanisms of long noncoding RNA function in development and disease. Cellular and Molecular Life Sciences 73 (13), pp. 2491 - 2509 (2016)

Sudheer, S.; Liu, J.; Marks, M.; Koch, F.; Anurin, A.; Scholze, M.; Senft, A. D.; Wittler, L.; Macura, K.; Grote, P. et al.; Herrmann, B. G.: Different Concentrations of FGF Ligands, FGF2 or FGF8 Determine Distinct States of WNT-Induced Presomitic Mesoderm. Stem Cells 34 (7), pp. 1790 - 800 (2016)

Marks, M.; Pennimpede, T.; Lange, L.; Grote, P.; Herrmann, B. G.; Wittler, L.: Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene 575 (2 Pt 2), pp. 438 - 451 (2016)

Grote, P.; Herrmann, B. G.: Long noncoding RNAs in organogenesis: Making the difference. Trends in Genetics 31 (6), pp. 329 - 335 (2015)

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)

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)

Liao, J.; Jijon, H. B.; Kim, I. R.; Goel, G.; Doan, A.; Sokol, H.; Bauer, H.; Herrmann, B. G.; Lassen, K. G.; Xavier, R. J.: An Image-Based Genetic Assay Identifies Genes in T1D Susceptibility Loci Controlling Cellular Antiviral Immunity in Mouse. PLoS One 9 (9), e108777 (2014)

Kumar, V.; Cheng, S.-C.; Johnson, M. D.; Smeekens, S.; Wojtowicz, A.; Giamarellos-Bourboulis, E.; Karjalainen, J.; Franke, L.; Withoff, S.; Plantinga, T. S. et al.; van de Veerdonk, F.; van der Meer, J.; Joosten, L. A. B.; Sokol, H.; Bauer, H.; Herrmann, B. G.; Bochud, P.-Y.; Marchetti, O.; Perfect, J. R.; Xavier, R.; Kullberg, B. J.; Wijmenga, C.; Netea, M.: Immunochip SNP array identifies novel genetic variants conferring susceptibility to candidaemia. Nature Communications 5, 5:4675 (2014)

Riemer, P.; Sreekumar, A.; Reinke, S.; Rad, R.; Schäfer, R.; Sers, C.; Bläker, H.; Herrmann, B. G.; Morkel, M.: Transgenic expression of oncogenic BRAF induces loss of stem cells in the mouse intestine, which is antagonized by β-Catenin activity. Oncogene 2014, pp. 1 - 12 (2014)

Schwartz, B.; Marks, M.; Wittler, L.; Werber, M.; Währisch, S.; Nordheim, A.; Herrmann, B. G.; Grote, P.: SRF is essential for mesodermal cell migration during elongation of the embryonic body axis. Mechanisms of Development 133, pp. 23 - 35 (2014)

Draaken, M.; Baudisch, F.; Timmermann, B.; Kuhl, H.; Kerick, M.; Proske, J.; Wittler, L.; Pennimpede, T.; Ebert, A. K.; Rösch, W. et al.; Stein, R.; Bartels, E.; von Lowtzow, C.; Boemers, T. M.; Herms, S.; Gearhart, J. P.; Lakshmanan, Y.; Kockum, C. C.; Holmdahl, G.; Läckgren, G.; Nordenskjöld, A.; Boyadjiev, S. A.; Herrmann, B. G.; Nöthen, M. M.; Ludwig, M.; Reutter, H.: Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Research Part A: Clinical and Molecular Teratology 100 (6), pp. 512 - 517 (2014)

Saisawat, P.; Kohl, S.; Hilger, A. C.; Hwang, D.-Y.; Gee, H. Y.; Dworschak, G. C.; Tasic, V.; Pennimpede, T.; Natarajan, S.; Sperry, E. et al.; Matassa, D. S.; Stajic, N.; Bogdanovic, R.; de Blaauw, I.; Marcelis, C. L. M.; Wijers, C. H. W.; Bartels, E.; Schmiedeke, E.; Schmidt, D.; Märzheuser, S.; Grasshoff-Derr, S.; Holland-Cunz, S.; Ludwig, M.; Nöthen, M. M.; Draaken, M.; Brosens, E.; Heij, H.; Tibboel, D.; Hermann, B. G.; Solomon, B. D.; de Klein, A.; van Rooij, I. A. L. M.; Esposito, F.; Reutter, H. M.; Hildebrandt, F.: Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association. Kidney International 85 (6), pp. 1310 - 1317 (2014)