Katzke, S.; Booms, P.; Tiecke, F.; Palz, M.; Pletschacher, A.; Türkmen, S.; Neumann, L. M.; Pregla, R.; Leitner, C.; Schramm, C. et al.; Lorenz, P.; Hagemeier, C.; Fuchs, J.; Skovby, F.; Rosenberg, T.; Robinson, P. N.: TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies. Human Mutation 20 (3), pp. 197 - 208 (2002)

Robinson, P. N.; Booms, P.; Katzke, S.; Ladewig, M.; Neumann, L. M.; Palz, M.; Pregla, R.; Tiecke, F.; Rosenberg, T.: Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies. Human Mutation 20 (3), pp. 153 - 161 (2002)

Rinke-Appel, J.; Osswald, M.; von Knoblauch, K.; Mueller, F.; Brimacombe, R.; Sergiev, P.; Avdeeva, O.; Bogdanov, A.; Dontsova, O.: Crosslinking of 4.5S RNA to the Escherichia coli ribosome in the presence or absence of the protein Ffh. RNA 8 (5), pp. 612 - 625 (2002)

Stricker, S.; Fundele, R.; Vortkamp, A.; Mundlos, S.: Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 245 (1), pp. 95 - 108 (2002)

Stricker, S.; Fundele, R.; Vortkamp, A.; Mundlos, S.: Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 245 (1), pp. 95 - 108 (2002)

Stricker, S.; Fundele, R.; Vortkamp, A.; Mundlos, S.: Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 245 (1), pp. 95 - 108 (2002)

Kalache, K. D.; Lehmann, K.; Chaoui, R.; Kivelitz, D. E.; Mundlos, S.; Bollmann, R.: Prenatal diagnosis of partial agenesis of the corpus callosum in a fetus with thanatophoric dysplasia type 2. Prenatal Diagnosis 22 (5), pp. 404 - 407 (2002)

Schultz, E. S.; Kaufmann, D.; Tinschert, S.; Schell, H.; von den Driesch, P.; Schuler, G.: Segmental Neurofibromatosis. Dermatology 204 (4), pp. 296 - 297 (2002)

Otto, F.; Kanegane, H.; Mundlos, S.: Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. Human Mutation 19 (3), pp. 209 - 216 (2002)

Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), pp. 53 - 67 (2002)

Albrecht, A. N.; Schwabe, G. C.; Stricker, S.; Böddrich, A.; Wanker, E. E.; Mundlos, S.: The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 112 (1-2), pp. 53 - 67 (2002)

Mundlos, S.; Horn, D.: Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 pp.

Schulz, M. H.; Köhler, S.; Bauer, S.; Vingron, M.; Robinson, P. N.: Exact Score Distribution Computation for Similarity Searches in Ontologies. In: Algorithms in Bioinformatics, pp. 298 - 309 (Eds. Salzberg, S. L.; Warnow, T.). Springer, New York [et al] (2009)

Klever, M.-K.; Sträng, E.; Jungnitsch, J.; Melo, U. S.; Hetzel, S.; Dolnik, A.; Schöpflin, R.; Schrezenmeier, J. F.; Blau, O.; Westermann, J. et al.; Döhner, K.; Schrezenmeier, H.; Spielmann, M.; Meissner, A.; Mundlos, S.; Bullinger, L.: Integration of Hi-C and Nanopore Sequencing for Structural Variant Analysis in AML with a Complex Karyotype: (Chromothripsis)². 62nd Annual Meeting and Exposition of the American Society of Hematology (ASH) (Virtual meeting), December 05, 2020 - December 08, 2020. Blood 136, S28, (2020)

Schöpflin, R.; Andrey, G.; Heinrich, V.; Franke, M.; Ibrahim, D.; Paliou, C.; Mundlos, S.; Vingron, M.: Identification of potential regulatory elements in Capture-C interaction profiles. In: Genome Regulation in 3D. Genome Regulation in 3D, Rehovot, Israel, June 28, 2015 - June 30, 2015. Weizmann Institute, Rehovot, Israel (2015)

Ibrahim, D.; Lupiáñez, D. G.: LilBUBome - Why would you crowdfund a cute cat? Open Science Days 2016, Berlin (2016)

Viebig, J.: Sequenzierung des LoxP flankierten Exon 6 des Gens Piga im Mausmodell. Humboldt Universität zu Berlin, (2015)

Wiegmann Rollet, R.: Analyse von Mutationen monogener Erkrankungen bezüglich evolutionärer Konservierung und Transkriptionsfaktorbindungsstellen. Freie Universität Berlin (2015)

Henck, J.: Single cell sequencing as a phenotyping strategy to decipher the molecular mechanisms of developmental disorder. Dissertation (2023)

Grünhagen, J.: Nicht kodierende RNAs in der Knochenentwicklung. Dissertation, Medizinische Fakultät Charité - Universitätsmedizin Berlin (2015)