Valerio Marino

10PUBLICATIONS
24CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)PhotochemistryGeospatial information systems and geospatial data modellingGlycoconjugatesAnthropological genetics
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Publications (10)

|Feb 11, 2023
Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal Dystrophy.

Jan-Philipp Bodenbender, Valerio Marino, Leon Bethge

|Mar 25, 2022
Molecular Properties of Human Guanylate Cyclase-Activating Protein 3 (GCAP3) and Its Possible Association with Retinitis Pigmentosa.

Anna Avesani, Laura Bielefeld, Nicole Weisschuh

|Oct 13, 2021
A Novel GUCA1A Variant Associated with Cone Dystrophy Alters cGMP Signaling in Photoreceptors by Strongly Interacting with and Hyperactivating Retinal Guanylate Cyclase.

Amedeo Biasi, Valerio Marino, Giuditta Dal Cortivo

|Apr 30, 2021
Impaired Ca2+ Sensitivity of a Novel GCAP1 Variant Causes Cone Dystrophy and Leads to Abnormal Synaptic Transmission Between Photoreceptors and Bipolar Cells.

Valerio Marino, Giuditta Dal Cortivo, Paolo Enrico Maltese

|Mar 06, 2021
Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant.

Ulrich Kellner, Nicole Weisschuh, Silke Weinitz

|Jan 05, 2021
Expanding the Clinical and Genetic Spectrum of RAB28-Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian Families.

Giancarlo Iarossi, Valerio Marino, Paolo Enrico Maltese

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Frequent Collaborators

10 joint publications

Daniele Dell'Orco

4 joint publications

Paolo Enrico Maltese

3 joint publications

Matteo Bertelli

2 joint publications

Alberto Borsatto