Ipek Akol

Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective

T. Vogel, Fabian Gather, Ipek Akol, 2021, International journal of molecular sciences.

Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome

Stefanie Heidrich, T. Vogel, T. Manke, 2023, Proceedings of the National Academy of Sciences of the United States of America.

DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons

T. Vogel, A. Cheffer, H. Franz, 2023, bioRxiv.

MMP2 and MMP9 Activity Is Crucial for Adult Visual Cortex Plasticity in Healthy and Stroke-Affected Mice

S. Löwel, J. Pielecka-Fortuna, Evgenia Kalogeraki, 2021, The Journal of Neuroscience.

Integrative multi-omics analyses reveal multi-modal FOXG1 functions acting on epigenetic processes and in concert with NEUROD1 to regulate synaptogenesis in the mouse hippocampus

Stefanie Heidrich, T. Vogel, T. Manke, 2021, bioRxiv.

Nucleophosmin 1 cooperates with the methyltransferase DOT1L to preserve peri-nucleolar heterochromatin organization by regulating H3K27me3 levels and DNA repeats expression

Stefanie Heidrich, Ipek Akol, Patrick Bovio, 2023, Epigenetics & Chromatin.