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Almuth Caliebe

5PUBLICATIONS

161CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesPredictive and prognostic markersStructural properties of condensed matterGene expression (incl. microarray and other genome-wide approaches)

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Publications (5)

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|Jan 08, 2026

DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects.

Gregor Dombrowsky, Liselot van der Laan, Ananília Silva

|May 16, 2025

Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.

Caroline Nava, Benjamin Cogne, Amandine Santini

|Mar 27, 2023

Formin-mediated nuclear actin at androgen receptors promotes transcription.

Julian Knerr, Ralf Werner, Carsten Schwan

|Feb 09, 2023

Aberrant phase separation and nucleolar dysfunction in rare genetic diseases.

Martin A Mensah, Henri Niskanen, Alexandre P Magalhaes

|Jul 29, 2021

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.

Enrique Audain, Anna Wilsdon, Jeroen Breckpot

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Frequent Collaborators

3 joint publications

Malte Spielmann

3 joint publications

Marc-Phillip Hitz

2 joint publications

Enrique Audain

2 joint publications

Brigitte Stiller

2 joint publications

Felix Berger

2 joint publications

Gregor Dombrowsky

2 joint publications

Sven Dittrich

1 joint publications

Anna Wilsdon

1 joint publications

Florian Wünnemann

1 joint publications

Yasset Perez-Riverol

Frequent Collaborators

3 joint publications

Malte Spielmann

3 joint publications

Marc-Phillip Hitz

2 joint publications

Enrique Audain

2 joint publications

Brigitte Stiller

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