Author

Teodora Ribarska

Oslo University Hospital

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1

Frequent Co-Authors

Adam R. SmithiD· 1 shared Beatrice Pflüger‐Müller· 1 shared Can CaoiD· 1 shared Chanil ValasarajaniD· 1 shared Chao‐Chung KuoiD· 1 shared Christian Paolo RichteriD· 1 shared Claire TroakesiD· 1 shared Dominik Christian FuhrmanniD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

Adam R. SmithORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

HIF1α-AS1 is a DNA:DNA:RNA triplex-forming lncRNA interacting with the HUSH complex

Matthias S. Leisegang, Jasleen Kaur Bains, Sandra Seredinski, James A. Oo, Nina M. Krause, Chao‐Chung Kuo, Stefan Günther, Nevcin Sentürk Cetin, Timothy Warwick, Can Cao, Frederike Boos, Judit Izquierdo Ponce, Shaza Haydar, Rebecca Bednarz, Chanil Valasarajan, , Ralf Peter Brandes

The paper identifies HIF1α-AS1 as a DNA:DNA:RNA triplex-forming lncRNA that interacts with the HUSH complex to repress gene expression and modulates angiogenesis in pulmonary hypertension.

Nature Communications · Nov 2, 2022Peer-reviewedMolecular Biology

A histone acetylome-wide association study of Alzheimer’s disease: neuropathology-associated regulatory variation in the human entorhinal cortex

Sarah J. Marzi, Szi Kay Leung, Teodora Ribarska, Eilis J. Hannon, Adam R. Smith, Ehsan Pishva, Jérémie Poschmann, Karen Moore, Claire Troakes, Safa Al‐Sarraj, Stephan Beck, Stuart Newman, Katie Lunnon, Leonard C. Schalkwyk, Jonathan S. Mill

This study identifies widespread H3K27ac acetylomic variation in AD cases compared to controls, linking it to disease-related pathways and AD-associated genetic variants.

Nature Neuroscience · Oct 11, 2018Peer-reviewedGenomics