Maria Francesca Di Feo

5PUBLICATIONS
13CO-AUTHORS
Neurology and neuromuscular diseasesCancer diagnosisGene expression (incl. microarray and other genome-wide approaches)Molecular targetsNeurogenetics
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Publications (5)

|Feb 17, 2026
Over-Representation of TTN Truncating Variants in a Finnish Cohort of Patients With Axial Myopathy.

Maria Francesca Di Feo, Giuliana Capece, Marco Savarese

|Mar 05, 2025
Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohort.

Victoria Lillback, Gaber Bergant, Maria Francesca Di Feo

|Aug 29, 2024
Inferring disease course from differential exon usage in the wide titinopathy spectrum.

Maria Francesca Di Feo, Ali Oghabian, Ella Nippala

|Mar 28, 2023
The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum.

Maria Francesca Di Feo, Victoria Lillback, Manu Jokela

|May 05, 2022
Counseling and prenatal diagnosis in facioscapulohumeral muscular dystrophy: A retrospective study on a 13-year multidisciplinary approach.

Maria Francesca Di Feo, Cinzia Bettio, Valentina Salsi

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Frequent Collaborators

3 joint publications

Marco Savarese

3 joint publications

Bjarne Udd

1 joint publications

Rossella Tupler

1 joint publications

Elisa Giorgio