Publications

Abo-Dalo, B.; Kim, H.-G.; Roes, M.; Stefanova, M.; Higgins, A.; Shen, Y.; Mundlos, S.; Quade, B. J.; Gusella, J. F.; Kutsche, K.: Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome. American Journal of Medical Genetics / Part A 143 (22), pp. 2668 - 2674 (2007)

Seitz, V.; Stiege, A. C.; Mundlos, S.; Lenze, D.; Lammert, H.; Clermont, A.; Hirsch, B.; Von Der Wall, E.; Müller, H.; Kirsch, A. et al.; Diaz-Espada, F.; Uharek, L.; Anagnostopoulos, I.; Stein, H.; Hummel, M.: Immunoglobulin receptor evolution in follicular lymphoma and a review of literature. Leukemia & Lymphoma 48 (10), pp. 2063 - 2067 (2007)

Uhrig, S.; Schlembach, D.; Waldispuehl-Geigl, J.; Schaffer, W.; Geigl, J.; Klopcki, E.; Mundlos, S.; Speicher, M. R.: Impact of array comparative genomic hybridization-derived information on genetic counseling demonstrated by prenatal diagnosis of the TAR (thrombocytopenia-absent-radius) syndrome-associated microdeletion 1q21.1. American Journal of Human Genetics: AJHG 81 (4), pp. 866 - 868 (2007)

Grossmann, S.; Bauer, S.; Robinson, P. N.; Vingron, M.: Improved detection of overrepresentation of Gene-Ontology annotations with parent child analysis. Bioinformatics 23 (22), pp. 3024 - 3031 (2007)

Lehmann, K.; Seemann, P.; Silan, F.; Goecke, T. O.; Irgang, M.; Kjaer, K. W.; Kjaergaard, S.; Mahoney, M. J.; Morlot, S.; Reissner, C. et al.; Kerr, B.; Wilkie, A. O. M.; Mundlos, S.: A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN. The American Journal of Human Genetics: AJHG 81 (12), pp. 388 - 396 (2007)

Reijntjes, S.; Stricker, S.; Mankoo, B. S.: A comparative analysis of Meox1 and Meox2 in the developing somites and limbs of the chick embryo. International Journal of Developmental Biology (Ijdb) 51 (8), pp. 753 - 759 (2007)

Meyer, S.; Fergusson, W. D.; Whetton, A. D.; Moreira-Leite, F.; Pepper, S. D.; Miller, C.; Saunders, E. K.; White, D. J.; Will, A. M.; Eden, T. et al.; Ikeda, H.; Ullmann, R.; Tuerkmen, S.; Gerlach, A.; Klopocki, E.; Tönnies, H.: Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption. Genes, Chromosomes and Cancer 46 (4), pp. 359 - 372 (2007)

Trepczi, B.; Lienau, J.; Schell, H.; Epari, D. R.; Thompson, M. S.; Hoffmann, J.-E.; Kadow-Romacker, A.; Mundlos, S.; Duda, G. N.: Endochondral ossification in vitro is influenced by mechanical bending. Bone 40 (3), pp. 597 - 603 (2007)

Kolanczyk, M.; Kossler, N.; Kühnisch, J.; Lavitas, L.; Stricker, S.; Wilkening, U.; Manjubala, I.; Fratzl, P.; Spörle, R.; Herrmann, B. G. et al.; Parada, L. F.; Kornak, U.; Mundlos, S.: Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics 16 (8), pp. 232 - 240 (2007)

Castori, M.; Brancati, F.; Mingarelli, R.; Mundlos, S.; Dallapiccola, B.: A novel patient with Cooks syndrome supports splitting from "classic" brachydactyly type B. American Journal of Medical Genetics/ Part A 143 (2), pp. 195 - 199 (2007)

Klopocki, E.; Schulze, H.; Strauß, G.; Ott, C.-E.; Hall, J.; Trotier, F.; Fleischhauer, S.; Greenhalgh, L.; Newbury-Ecob, R. A.; Neumann, L. M. et al.; Habenicht, R.; König, R.; Seemanova, E.; Megarbane, A.; Ropers, H.-H.; Ullmann, R.; Mundlos, S.: Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), pp. 232 - 240 (2007)

Klopocki, E.; Schulze, H.; Strauß, G.; Ott, C.-E.; Hall, J.; Trotier, F.; Fleischhauer, S.; Greenhalgh, L.; Newbury-Ecob, R. A.; Neumann, L. M. et al.; Habenicht, R.; König, R.; Seemanova, E.; Megarbane, A.; Ropers, H.-H.; Ullmann, R.; Mundlos, S.: Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), pp. 232 - 240 (2007)

Lichtenauer, U. D.; Duchniewicz, M.; Kolanczyk, M.; Hoeflich, A.; Hahner, S.; Else, T.; Bicknell, A. B.; Zemojtel, T.; Stallings, N. R.; Schulte, D. M. et al.; Kamps, M. P.; Hammer, G. D.; Scheele, J. S.; Beuschlein, F.: Pre-B-cell transcription factor 1 and steroidogenic factor 1 synergistically regulate adrenocortical growth and steroidogenesis. Endocrinology: Official Journal of the Endocrine Society 148 (2), pp. 693 - 704 (2007)

Lichtenauer, U. D.; Duchniewicz, M.; Kolanczyk, M.; Hoeflich, A.; Hahner, S.; Else, T.; Bicknell, A. B.; Zemojtel, T.; Stallings, N. R.; Schulte, D. M. et al.; Kamps, M. P.; Hammer, G. D.; Scheele, J. S.; Beuschlein, F.: Pre-B-cell transcription factor 1 and steroidogenic factor 1 synergistically regulate adrenocortical growth and steroidogenesis. Endocrinology: Official Journal of the Endocrine Society 148 (2), pp. 693 - 704 (2007)

Zenker, M.; Lehmann, K.; Schulz, A. L.; Barth, H.; Hansmann, D.; Koenig, R.; Korinthenberg, R.; Kreiss-Nachtsheim, M.; Meinecke, P.; Morlot, S. et al.; Mundlos, S.; Quante, A. S.; Raskin, S.; Schnabel, D.; Wehner, L.-E.; Kratz, C. P.; Horn, D.; Kutsche, K.: Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. Journal of Medical Genetics 44 (2), pp. 131 - 135 (2007)

Gurok, U.; Bork, K.; Nuber, U.; Spörle, R.; Nöhring, S.; Horstkorte, R.: Expression of Ndufb11 encoding the neuronal protein 15.6 during neurite outgrowth and development. Mechanisms of Development: Gene Expression Patterns: Gep ; A Section of Mechanisms of Development 7 (3), pp. 370 - 374 (2007)

Hecht, J.; Seitz, V.; Urban, M.; Wagner, F.; Robinson, P. N.; Stiege, A.; Dieterich, C.; Kornak, U.; Wilkening, U.; Brieske, N. et al.; Zwingman, C.; Kidess, A.; Stricker, S.; Mundlos, S.: Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2−/− mouse model. Gene Expression Patterns: A Section of Brain Research Devoted to Patterns of Expression of Genes during the Development, Maturity and Aging of the Central Nervous System 7 (1 - 2), pp. 102 - 112 (2007)

Hecht, J.: Gene-Expression analysis in bone development and fracture healing Genexpressionsanalysen zum besseren Verständnis von Knochenheilung und -entwicklung. Dissertation, Freie Universität Berlin, Berlin (2007)