PhD Theses

Rossi, F.: Decoding the role of PHF13 in genome regulation and chromatin organization. Dissertation, 138 Seiten pp. (2025)

Khaveh, N.: From pig to cell: experimental investigation of transcriptional patterns promoting phenotypic expression in the pig. Dissertation, xi, 101 Seiten pp. (2025)

Phan, M. H. Q.: Uncovering Functionally Conserved Regulatory Elements in Divergent Genomes: A Case For The Heart. Dissertation, 178 Seiten pp. (2025)

Schindler, M.: Evolution of Morphological Novelty Through the Repurposing of Cell Programs. Dissertation, 139 pp. (2025)

Henck, J.: Single cell sequencing as a phenotyping strategy to decipher the molecular mechanisms of developmental disorders. Dissertation, 128 Seiten pp. (2024)

Hertzberg, J.: Identification and Prioritization of Putative Pathogenic Structural Variants based on Functional Annotation. Dissertation, 134 Seiten pp. (2024)

Ringel, A. R.: Mechanisms of Regulatory Adaptation in the Evolving Genome. Dissertation, 129 pp. (2023)

Ali, S.: The 3D gene regulatory landscape in human bone cells and its influence on cell differentiation and disease. Dissertation, 134 Seiten pp. (2023)

Despang, A.: The Role of Topologically Associating Domains for Developmental Gene Regulation - ⁠ A Systematic Functional Analysis at the Sox9 and Shh Loci. Dissertation, 107 Seiten pp. (2021)

Paliou, C.: The role of chromatin architecture in regulating Shh gene during mouse limb development. Dissertation, 120 pp. (2019)

Hennig, F.: CRISPR/Cas9 Gen-Editierung in der Maus und funktionelle Analysen zum besseren Verständnis von seltenen monogenen Entwicklungsstörungen. Dissertation, XVIII, 201 Blätter pp. (2019)

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

Ibrahim, D.: ChIP-seq Reveals Mutation-Specific Pathomechanismus of HOXD13 Missense Mutations. Dissertation, Humboldt University, FB Mathemathik, Berlin (2014)

Bosquillon de Jarcy, L.: Brachydaktylie Typ E und ZNF521. Dissertation, Charité Berlin, Berlin (2014)

Grohmann, J.: The role of the tumour suppressor Nf1 in growth and metabolism of skeletal muscle cells. Dissertation, TU Berlin, Fakultät III - Prozesswissenschaften, Berlin (2014)

Sprenger, S.: The role of Pycr1 in the Pathomechanism of Autosomal recessive Cutis Laxa. Dissertation, TU Berlin, FB Biotechnol., Berlin (2014)

Zimmer, J.: From Skeletal Diseases to Bone Regeneration: Analysis of Agonist-Antagonist Interactions for Design of tailored bone Morphogenetic Protein2 Variants with improved biological activity. Dissertation (2012)

Köhler, S.: Penotype informatics: Network approaches towards understanding the diseasome. Dissertation (2012)

Chan, W. L.: Molecular basis of Gerodermia Osteodysplastica, apremature ageing disorder. Dissertation (2012)

Forler, S.: Effekte von Polymorphysmen auf die geschlechtsspezifische Proteinexpression in gesunden und hüpertrophierten Herzen. Dissertation (2011)

Rödelsperger, C.: Computational Characterization of Genome-wide DNA-binding Pro les. Dissertation, Freie Universität Berlin, Berlin (2011)

Bauer, S.: Algorithms for Knoledge Integration in Biomedical Sciences. Dissertation (2011)

Schwarzer, W.: Phenotypic variability in monogenic disorders involving skeletal malformations. Dissertation, Freie Universität Berlin, Berlin (2010)

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)