Disputationer i Dumanskis grupp

Hamid Reza Razzaghian, Post-zygotic Genetic Variation in Health and Disease, Uppsala University, 2013. (http://uu.diva-portal.org/smash/record.jsf?searchId=1&pid=diva2:609581)

Johanna Sandgren, Array-based Genomic and Epigenomic Studies in Healthy Individuals and Endocrine Tumours. Uppsala University, 2010. (http://uu.diva-portal.org/smash/record.jsf?searchId=1&pid=diva2:344247)

Helena Nord, Application of Genomic and Expression Arrays for Identification of new Cancer Genes. Uppsala University, 2010. (http://uu.diva-portal.org/smash/record.jsf?searchId=1&pid=diva2:306953)

Robin Andersson, Decoding the Structural Layer of Transcriptional Regulation: Computational Analyses of Chromatin and Chromosomal Aberrations. Uppsala University, 2010. (http://uu.diva-portal.org/smash/record.jsf?searchId=1&pid=diva2:352369)

Cecilia De Bustos, Genetic and Epigenetic Variation in the Human Genome: Analysis of Phenotypically Normal Individuals and Patients Affected with Brain Tumors. Uppsala University, 2006. (http://publications.uu.se/theses/abstract.xsql?dbid=6629)

Caisa Marie Hansson, Analysis of Genetic Alterations in Patients Affected with Neurofibromatosis Type 2 and its Associated Tumors. Uppsala University, 2006. (http://publications.uu.se/theses/abstract.xsql?dbid=6511)

Magdalena Benetkiewicz, Development and Application of Human Chromosome 22 Genomic Microarray: Chromosome 22-Associated Disorders Analyzed by Array-Based Comparative Genomic Hybridization. Uppsala University, 2006. (http://publications.uu.se/theses/abstract.xsql?dbid=6272)

Kiran K. Mantripragada, Microarray-Based Comparative Genomic Hybridization in Neurofibromatoses and DiGeorge Syndrome. Uppsala University, 2005. (http://publications.uu.se/theses/abstract.xsql?dbid=5743)

Patrick Buckley, Development and Application of Microarray-Based Comparative Genomic Hybridization: Analysis of Neurofibromatosis Type-2, Schwannomatosis and Related Tumors. Uppsala University, 2005. (http://publications.uu.se/theses/abstract.xsql?dbid=4786)

Hajnalka Kiss, Characterization of a putative tumor suppressor region identified by the elimination test on human 3p21.3. Karolinska Institutet, 2003. (http://diss.kib.ki.se/2003/91-7349-558-1/)

Isabel Tapia Páez, Characterization of human chromosome 22: cloning of breakpoints of the constitutional translocation t(11;22)(q23;q11) and detection of small constitutional deletions by microarray-CGH. Karolinska Institutet, 2003. (http://diss.kib.ki.se/2003/91-7349-505-0/)

Giedre Grigelioniene, Clinical and genetic investigation of hypochondroplasia and dyschondrosteosis. Karolinska Institutet, 2001. (http://diss.kib.ki.se/2001/91-7349-014-8/)

Carl E.G. Bruder, Genetic analysis of neurofibromatosis type 2 (NF2) patients and NF2-associated tumors with emphasis on chromosome 22 deletions. Karolinska Institutet, 2000. (http://diss.kib.ki.se/2000/91-628-4370-2/)

Kevin O´Brien, The role of PDGFB in dermatofibrosarcoma protuberans and giant cell fibroblastoma. Karolinska Institutet, 2000. (http://diss.kib.ki.se/2000/91-628-4017-7/)

Darek Kedra, Characterization of candidate disease genes from human chromosomes 11q13 and 22q. Karolinska Institutet, 1999. (http://diss.kib.ki.se/1999/91-628-3792-3/)

Myriam Peyrard, From a candidate region to gene characterizations: Analysis of the three new genes with respect to meningioma tumorigenesis. Karolinska Institutet, 1998. (http://diss.kib.ki.se/1998/91-628-2926-2/)