Henriette Skovgaard Andersen

Henriette Skovgaard Andersen is a researcher at the Department of Biochemistry and Molecular Biology, University of Southern Denmark. Her work focuses on molecular biology, genetics, and RNA splicing mechanisms, particularly in neurodegenerative diseases like spinal muscular atrophy and Costello syndrome. She utilizes advanced sequencing technologies and oligonucleotide-based therapies to explore gene regulation and splicing defects.

Her research spans translational medicine, with a focus on:

• RNA splicing regulation in genetic disorders
• Development of splicing-correcting therapeutics
• Neurodegenerative disease mechanisms

Recent publications highlight her expertise in SMN2/SMN1 gene interactions, HRAS mutations, and resveratrol's role in metabolic disorders. Collaborations include international conferences and workshops on sequencing technologies and presentation techniques.

She contributes to peer-reviewed journals and is involved in academic workshops, demonstrating active participation in research networks and educational events.