Stefania Lenarduzzi

11PUBLICATIONS
95CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Innate immunityGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsWomen's studies (incl. girls' studies)
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Publications (11)

|Jul 08, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter Registry.

|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".

|Nov 25, 2025
Lactobacillus iners dominates the vaginal microbiota of healthy Italian women of reproductive age.

E Vinerbi, F Chillotti, A Maschio

|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
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

|Mar 27, 2024
The Women4Health cohort: a unique cohort to study women-specific mechanisms of cardio-metabolic regulation.

Fabio Busonero, Stefania Lenarduzzi, Francesca Crobu

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Frequent Collaborators

11 joint publications

Giorgia Girotto

7 joint publications

Beatrice Spedicati

7 joint publications

Anna Morgan

5 joint publications

Aurora Santin