Agnese Feresin

8PUBLICATIONS
48CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Genetic immunologyGene mapping
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Publications (8)

|Jul 28, 2026
Exploring the Clinical and Psychosocial Impact of Genetic Diagnosis in Congenital Hearing Loss: A Comparative Study Between Syndromic and Non-Syndromic Conditions.

|Dec 13, 2025
Uncovering the Genetic Landscape of Spinal Dysraphism: A Retrospective Analysis of 150 Fetal Cases.

I Bedei, A Feresin, R Zemet

|Oct 29, 2025
Beyond the Curtains: Identification of the Genetic Cause of Foetal Developmental Abnormalities Through the Application of Molecular Autopsy.

Beatrice Spedicati, Giulia Pianigiani, Aurora Santin

|Jan 08, 2025
In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder.

Agnese Feresin, Mathilde Lefebvre, Emilie Sjøstrøm

|Jun 27, 2024
Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature Review.

Maria Teresa Bonati, Agnese Feresin, Paolo Prontera

|Jun 07, 2022
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition.

Luciana Musante, Flavio Faletra, Kolja Meier

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Frequent Collaborators

4 joint publications

Giorgia Girotto

3 joint publications

Maria Teresa Bonati

2 joint publications

Caterina Zanus

2 joint publications

Eva Orzan