Maria Eriksson

11PUBLICATIONS
25CO-AUTHORS
Respiratory diseasesMolecular targetsPredictive and prognostic markersGenome structure and regulationComputational physiology
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Publications (11)

|Aug 14, 2026
Dysregulated lncRNAs are associated with the progressive arterial phenotype in Hutchinson-Gilford Progeria Syndrome.

|Aug 20, 2025
Induced somatic mutation accumulation during skeletal muscle regeneration reduces muscle strength.

Peter Vrtačnik, Lara G Merino, Santhilal Subhash

|Jun 10, 2025
Recurrent somatic mutation and progerin expression in early vascular aging of chronic kidney disease.

Gwladys Revêchon, Anna Witasp, Nikenza Viceconte

|Nov 18, 2022
The Heterochromatin protein 1 is a regulator in RNA splicing precision deficient in ulcerative colitis.

Jorge Mata-Garrido, Yao Xiang, Yunhua Chang-Marchand

|Jun 02, 2022
Transient expression of an adenine base editor corrects the Hutchinson-Gilford progeria syndrome mutation and improves the skin phenotype in mice.

Daniel Whisenant, Kayeong Lim, Gwladys Revêchon

|Apr 18, 2022
Challenges of proving a causal role of somatic mutations in the aging process.

Irene Franco, Gwladys Revêchon, Maria Eriksson

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Frequent Collaborators

7 joint publications

Gwladys Revêchon

3 joint publications

Irene Franco

2 joint publications

Hafdis T Helgadottir

2 joint publications

Lara Garcia Merino