Anna Morgan

29PUBLICATIONS

234CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Pacific Peoples and disabilityGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsComputational physiology

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Publications (29)

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|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

|May 07, 2025

Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant.

Valeria Capaci, Luisa Zupin, Martina Magistrati

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Frequent Collaborators

24 joint publications

Giorgia Girotto

10 joint publications

Beatrice Spedicati

Maria Pina Concas

Aurora Santin

Paola Tesolin

Stefania Lenarduzzi

Giuseppe Giovanni Nardone

4 joint publications

Anubha Mahajan

4 joint publications

Massimiliano Cocca

4 joint publications

Alexander Teumer

Frequent Collaborators

24 joint publications

Giorgia Girotto

10 joint publications

Beatrice Spedicati

8 joint publications

Maria Pina Concas

8 joint publications

Aurora Santin