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)

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|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

Beatrice Spedicati

Anna Morgan

Aurora Santin

Giuseppe Giovanni Nardone

Paola Tesolin

Serena Sanna

Andrea Maschio

Francesca Crobu

Daniela Mazzà

Frequent Collaborators

11 joint publications

Giorgia Girotto

7 joint publications

Beatrice Spedicati

7 joint publications

Anna Morgan

5 joint publications

Aurora Santin