Anna Morgan

30PUBLICATIONS
237CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Pacific Peoples and disabilityNeurogeneticsComputational physiology
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Publications (30)

|Aug 27, 2026
Phenotypic Expansion of PPP1R12A-Related Syndrome: A Novel Splicing Variant Associated with Hearing Loss and Inner Ear Malformations.

|Jun 26, 2026
Reply to Small, K.W. Comment on "Spedicati et al. Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication. Biomedicines 2025, 13, 1904".

|Jun 25, 2026
Presbycusis Across the Lifespan: Genetic, Molecular, and Multi-Omics Contributions.

|Sep 27, 2025
Unraveling the Functional Impact of Splicing Variants in Inherited Hearing Disorders Through Minigene Splicing Assays.

Lara Emily Rosso, Giulia Pianigiani, Anna Morgan

|Aug 28, 2025
A Hitchhiker Guide to Structural Variant Calling: A Comprehensive Benchmark Through Different Sequencing Technologies.

Giuseppe Giovanni Nardone, Valentina Andrioletti, Aurora Santin

|Aug 28, 2025
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel PRDM13 and CCNC Duplication.

Beatrice Spedicati, Domizia Pasquetti, Aurora Santin

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Frequent Collaborators

25 joint publications

Giorgia Girotto

11 joint publications

Beatrice Spedicati

8 joint publications

Maria Pina Concas

8 joint publications

Aurora Santin