Personlig profil
Primære forskningsområder
I have a mechanistic interest into genome-wide and locus specific regulation and fine-tuning of tissue-specific gene expression. We are interested in the 3D-organization of genome within the nuclear space, non-coding RNAs and epigenetic modifications especially methylation and hydroxymethylation. The interaction of these linear and 3-dimentional mechanisms in gene regulation within the healthy brain and the neurodegenerative diseases is the primary interest.
For a very long time we have been working on a specific familial balanced translocation t(8;20) segregating with early onset cerebellar ataxi and use this translocation in learning about the organization and the function of the genome around the breakpoints. The synapse associated DLGAP4 gene which spans one of the breakpoints became my favorite gene over the years.
I do not like being limited by the technical short-comings when I need to find answers to biological questions. Therefore, I have a great interest in developing novel methods based on in situ hybridization both at RNA and DNA level, and I try novel probe technologies and develop new nuclear preparation methods in order to study the genome organization by pushing the resolution limits from different sides . We think multidiciplinary projects are always exciting. Over the years, we have been collaborating with DTU Nanotech in developing lab-on-a-chip devices for genetic analyses.
Aktuel forskning
- Is distrupted genomic architecture the cause or the effect in the neurodegenerative diseases? The organization of the genome in territories, domains and loops is essential for normal development and function. This non-random organization provides a new layer of fine transcriptional regulation especially in the brain. The role of spatial genome organization in normal and diseased brain cells is being investigated and it is suggested as a potential tool for presymptomatic diagnosis in neurodegenerative diseases.
- Using a balanced translocation t(8;20) segregating with Early Onset Cerebellar ataxia, we have found DLGAP4 gene at one breakpoint as the candidate for the ataxia phenotype. We are characterizing the function of DLGAP4 and some of the novel non-coding RNAs found in the vicinity of the breakpoints.
- Developing tools for high resolution visual analysis of the genome has always been a great interest. We are working on chromatin spreading techniques in collaboration with Niels Tommerup as well as collaborating with Jesper Wengel, SDU on locked nucleic acid based new probe technologies for possibilities of hybridization without the need for denaturation which is suggested to change the genomic architecture.
- In collaboration with DTU Nanotech, we are developing a work flow for sequencing of long DNA molecules as a supplementary method for next generation sequencing. The method is based on obtaining megabase-sized single DNA Molecules from a specific region of the genome for optical mapping in a nanofluidic device.
Sprogkundskaber
Engelsk
Dansk
Trykisk
Tysk (Lidt)
CV
Employment
Associate Professor, Department of Cellular and Molecular Medicine, Faculty of Health Sciences, University of Copenhagen (2009- )
Various posts as senior scientist, postdoc, assistant Professor or research associate Professor at the;
University of Copenhagen, Healthsciences Faculty, Wilhelm Johannsen Centre for Functional Genome Research (1999-2009)
Istanbul University, Cerrahpasa Medical Faculty, Division of Biomedical Sciences (1990-1999)
Education
Ph.D in Medical Biology (major in genetics), Istanbul University, “Assessment and application of fluorescence in situ hybridization on meiotic and mitotic chromosomes” Research performed at the J.F. Kennedy Institute, Denmark (1995)
MSc (Med.Sci.) in Medical Genetics, Glasgow University,“Assessment of non-isotopic method of in situ hybridization in detection of trisomy 21 in interphase nuclei” (1989)
BSc in Biomedical Sciences, Istanbul University, Cerrahpasa Medical Faculty, Division of Biomedical Sciences,(1988)
Memberships
- Danish Association of Reproduction and Fetal Development (Board Member/Chairman 2004-2010)
- Danish & Turkish Associations of Medical Genetics
- American & European Societies of Human Genetics
Emneord
- Det Sundhedsvidenskabelige Fakultet
- In situ hybridization
- Epigenetics
- 5’-Hydroxymethycytosine
- Non-coding RNAs
- Cytogenetics
Samarbejde og topforskningsområder i de sidste fem år
Publikation
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ROGDI-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense Variant
Gverdtsiteli, S., Hammer, T. B., Hermann, X., Andersen, N. B., Ros-Pardo, D., Marcos-Alcalde, I., Gomez-Puertas, P., Brook, A. H., Silahtaroglu, A. & Tumer, Z., 2025, I: Genes. 16, 10, 12 s., 1207.Publikation: Bidrag til tidsskrift › Review › peer review
Åben adgangFil1 Downloads (Pure) -
Targeted Genetic Education in Dentistry in the Era of Genomics
Asa’ad, F., Nørremølle, A., Khan, Q., Larsson, L., Tommerup, N., Hermann, N. V. & Silahtaroglu, A., 2024, I: Genes. 15, 12, 12 s., 1499.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
Åben adgangFil1 Citationer (Scopus)18 Downloads (Pure) -
PRRT2 benign familial infantile seizures (BFIS) with atypical evolution to encephalopathy related to status epilepticus during sleep (ESES)
Cossu, A., Santos, J. L., Galati, G., Nikanorova, M., Costa, P., Mang, Y., Silahtaroglu, A., Rubboli, G., Tommerup, N., Dalla Bernardina, B., Møller, R. S., Cantalupo, G. & Gardella, E., 2023, I: Neurological Sciences. 44, 6, s. 2173-2176 4 s.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
3 Citationer (Scopus) -
3D genome organization
Silahtaroglu, A., Bridger, J. M. & Lei, E. P., 2022, I: Scientific Reports. 12, 22106.Publikation: Bidrag til tidsskrift › Leder › Forskning › peer review
Åben adgangFil33 Downloads (Pure) -
The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratio
Holm, A., Possovre, M. L., Bandarabadi, M., Moseholm, K. F., Justinussen, J. L., Bozic, I., Lemcke, R., Arribat, Y., Amati, F., Silahtaroglu, A., Juventin, M., Adamantidis, A., Tafti, M. & Kornum, B. R., 2022, I: Proceedings of the National Academy of Sciences of the United States of America. 119, 17, 10 s.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
Åben adgangFil23 Citationer (Scopus)60 Downloads (Pure) -
The Interchromatin Compartment Participates in the Structural and Functional Organization of the Cell Nucleus
Cremer, T., Cremer, M., Hübner, B., Silahtaroglu, A., Hendzel, M., Lanctôt, C., Strickfaden, H. & Cremer, C., 2020, I: BioEssays. 42, 2, 18 s., 1900132.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
Åben adgangFil75 Citationer (Scopus)101 Downloads (Pure) -
Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease model
Reynolds, R. H., Petersen, M. H., Willert, C. W., Heinrich, M., Nymann, N., Dall, M., Treebak, J. T., Björkqvist, M., Silahtaroglu, A., Hasholt, L. & Nørremølle, A., apr. 2018, I: Molecular and Cellular Neuroscience. 88, s. 118-129Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
42 Citationer (Scopus) -
Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes
Halgren, C., Nielsen, N. M., Nazaryan-Petersen, L., Silahtaroglu, A., Collins, R. L., Lowther, C., Kjaergaard, S., Frisch, M., Kirchhoff, M., Brøndum-Nielsen, K., Lind-Thomsen, A., Mang, Y., El-Schich, Z., Boring, C. A., Mehrjouy, M. M., Jensen, P. K. A., Fagerberg, C., Krogh, L. N., Hansen, J. & Bryndorf, T. & 5 flere, , 2018, I: American Journal of Human Genetics. 102, 6, s. 1090-1103 14 s.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
40 Citationer (Scopus)
Aktiviteter
- 1 Medlemskab af styrelse i virksomhed eller organisation
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Dansk Foregning for Reproduktion og Fosterudvikling (Ekstern organisation)
Silahtaroglu, A. (Medlem)
13 apr. 2008 → …Aktivitet: Medlemskab - typer › Medlemskab af bestyrelse i virksomhed eller organisation