Federico Zara

33PUBLICATIONS
254CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Infant and child healthNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (33)

|Oct 07, 2026
Skipping of Exon 38 in Neurofibromatosis Type 1 Gene Is Not a Pathogenic Variant.

|Feb 13, 2026
Isolated absence epilepsy associated with a de novo FBXW7 missense variant in the F-box domain.

Anees Muhammad, Mohammad Sadegh Shams Nosrati, Alireza Dostmohammadi

|Feb 13, 2026
Potential Link Between a Disruptive CAPN6 Variant and Neurodevelopmental Disorders.

Francesco Calì, Simone Treccarichi, Mirella Vinci

|Feb 03, 2026
Functional Characterization of a De Novo SCN2A Mixed Variant Linked to Early Infantile Developmental and Epileptic Encephalopathy.

Anna Corradi, Antonella Riva, Bruno Sterlini

|Dec 31, 2025
The Emerging TNNT3 Spectrum: From Distal Arthrogryposis to Congenital Myopathy.

Nami Altin, Kamel Mamchaoui, Jessica Ohana

|Dec 11, 2025
SLC35A2-Related Brain Disorders: Genetics, Pathophysiology, and Therapeutic Insights.

Beatrice Risso, Antonella Riva, Greta Volpedo

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Frequent Collaborators

14 joint publications

Marcello Scala

12 joint publications

Pasquale Striano

10 joint publications

Marzia Ognibene

7 joint publications

Valeria Capra