Author
Magdalena Laugsch
Heidelberg UniversityORCID 0009-0006-6079-7017Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2021-2026 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 21 mutual co-author links4 papers
Recent·Most cited
- NeurosciencebioRxivPreprint
Multi-omics profiling reveals MAGEL2-driven defects in human corticogenesis shared across Prader-Willi and Schaaf-Yang syndromes.
Jannis Buecking, Baran E. Güler, Michael Eibl…·Magdalena Laugsch
This study identifies MAGEL2-driven defects in human corticogenesis shared between Prader-Willi and Schaaf-Yang syndromes using multi-omics profiling of induced neurons.
1 citation - Cell BiologybioRxivPreprint
Unravelling the conundrum of nucleolar NR2F1 localization: A comparative analysis of NR2F1 antibody-based approaches in vitro and in vivo.
Michele Bertacchi, Susanne Theiß, Ayat Ahmed…·Magdalena Laugsch
The paper investigates NR2F1 nucleolar localization using multiple antibodies in vitro and in vivo, finding it artificial and non-functional, and recommends optimal antibody use.
- GenomicsNature CommunicationsPeer-reviewed
Enhancer-associated H3K4 methylation safeguards in vitro germlinecompetence
Tore Bleckwehl, Giuliano Crispatzu, Kaitlin Schaaf…·Álvaro Rada-Iglesias
The paper shows that H3K4me1 retention in enhancers supports germline competence by maintaining enhancer accessibility and responsiveness during in vitro differentiation.