Author
Susanne Theiß
Heidelberg University
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
Biology Disciplines
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2022-2026 · peak 3/yrCo-Author Collaboration Network
10 top collaborators · 19 mutual co-author links5 papers
Recent·Most cited
- GeneticsbioRxivPreprint
SMCHD1 is a novel target for gene-activation therapy to treat Prader-Willi Syndrome
Megan Iminitoff, Anna K. Le Fevre, Tamara Cameron…·Marnie E. Blewitt
This study identifies SMCHD1 as a target for gene-activation therapy in Prader-Willi Syndrome by showing its role in repressing the PWS gene cluster and demonstrating gene activation in mouse models.
DOI 10.64898/2026.05.13.725051 - 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 BiologyCommunications BiologyPeer-reviewed
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.
- NeurosciencebioRxivPreprint
A truncating mutation of Magel2 in the rat modelled for the study of Schaaf-Yang and Prader-Willi syndromes alters select behavioral and physiological outcomes
Derek L. Reznik, Mingxiao V. Yang, Pedro Albelda de la Haza…·Rodney C. Samaco
This study generates and characterizes a rat model with a truncating Magel2 mutation, revealing altered behavioral and physiological traits consistent with human neurodevelopmental disorders.
DOI 10.1101/2022.08.09.503377