Federica Baldan
Udine, 33100, Italy
Last Updated: 09/26/2026
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Found 48 publications
SINEUP-Mediated Overexpression of Endogenous α-Amylase as a Therapeutic Approach in Lafora Disease.
Journal: Genes
Published: February 06, 2026
The molecular landscape of hereditary ataxia: a single-center study.
Journal: Human genetics
Published: October 23, 2024
Longitudinal detection of somatic mutations in the saliva of head and neck squamous cell carcinoma-affected patients: a pilot study.
Journal: Frontiers in oncology
Published: August 13, 2024
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance.
Journal: Gene
Published: July 31, 2024
The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases.
Journal: Clinical genetics
Published: March 20, 2024
A bird's eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases.
Journal: Journal of human genetics
Published: November 20, 2023
GSK2801 Reverses Paclitaxel Resistance in Anaplastic Thyroid Cancer Cell Lines through MYCN Downregulation.
Journal: International journal of molecular sciences
Published: December 21, 2022
Role of m6A RNA Methylation in Thyroid Cancer Cell Lines.
Journal: International journal of molecular sciences
Published: August 02, 2022
NK2 homeobox gene cluster: Functions and roles in human diseases.
Journal: Genes & diseases
Published: June 08, 2022
Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structure.
Journal: Endocrine
Published: May 24, 2022
Somatic genomic imbalances in 'tumour-free' surgical margins of oral cancer.
Journal: International journal of oral and maxillofacial surgery
Published: February 24, 2022
Last Updated: 09/26/2026