Love, M. I.: Statistical analysis of high-throughput sequencing count data. Dissertation (2014)

Schöfisch, K.: Untersuchungen zur Haploidspezifizität des t-Komplex Responders bei der nicht-Mendelschen Vererbung in der Maus. Dissertation, Mensch und Buch Verlag, Berlin (2013)

Köhler, S.: Phenotype informatics: network approaches towards understanding the diseasome. Dissertation, Berlin, Freie Universität (2013)

Emde, A.-K.: Next-generation sequencing algorithms: from read mapping to variant detection. Dissertation, Berlin, Freie Universität (2013)

Haupt, A.: Characterisation of mutation-specific interaction networks and their functional analysis in cancer cells. Dissertation, Berlin, Freie Universität (2013)

Klatt, S.: Evaluation of the protozoan parasite L. tarentolae as a eukaryotic expression host in biomedical research. Dissertation (2013)

Rubelt, F.: Investigations into the human immunoglobulin repertoire utilizing high-throughput sequencing. Dissertation (2012)

Boerno, S.: Analyses of DNA methylation patterns in prostate cancer. Dissertation (2012)

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)

Drews, K.: Viral and non-viral generation and characterization of induced pluripotent stem cells from human amniotic fluid cells. Dissertation (2012)

Grunert, M.: Computional Analysis of Next-Generation Sequencing Data in Cardiac Function and Disease. Dissertation (2012)

Kamburov, A.: More complete and more accurate interactomes for elucidating the mechanisms of complex diseases. Dissertation (2012)

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

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

Budach, S.: Technical artefacts and batch effects in RNA-Seq data. Habilitation (2013)

Schweiger, M.-R.: Translationale molekulare Medizin: Die Entschlüsselung der Genetik und Epigenetik von monogenetischen sowie komplexgenetischen Erkrankungen durch moderne Hochdurchsatz-Sequenziertechnologien. Habilitation (2012)

Dartsch, J.: Identifizierung eines neuen Gens für autosomal rezessive Mikrozaphalie in einer konsanguinen, kurdischen Familie. Diploma (2016)

Salaheddine, .: The role of the genomic architecture on Sox9 regulation during neuronal differentiation and embryogenesis. Diploma (2016)