- Grants since 2016
- 611
- Awarded, last 5 years (where amounts are published)
- €94.6M
- Funded works, last 5 years
- 5 837
- Funded works, all time
- 8 569
Grants
2025–2027 · grant
nano-GLU: a glutamate-based retinal prosthesis to recover visual functions in Retinitis pigmentosa
Elisabetta Colombo · Italian Institute of Technology
2025–2027 · grant
Assigning incentive emotional valence to sensory and social stimuli: neuronal and behavioral substrates in the SHANK3 mutant mouse model of autism spectrum disorder
Benedetto Sacchetti · University of Turin
2025–2027 · grant
Omics analyses combined with neurodevelopmental assessment in Pitt-Hopkins syndrome patients to search for indicators of efficacy of new therapeutics
Marcella Zollino · Università Cattolica del Sacro Cuore
2025–2026 · grant
Clear-cut integration of Large payloads into Essential Alleles with spontaneous counterselection of NHEJ outcomes (CLEAN) for the treatment of Anderson-Fabry disease
Daniele Canarutto · Vita-Salute San Raffaele University
2025–2027 · grant
Exploring the therapeutic potential of cortical ADAM10 inhibition in Huntington’s Disease
Chiara Zuccato · University of Milan
2025–2026 · grant
A novel SHANK3 minigene for gene therapy approaches
Luca Colnaghi · Vita-Salute San Raffaele University
2025–2027 · grant
Fear of Falling in muscular dystrophy. Investigation of the phenomenon and a multidisciplinary rehabilitation approach to treat it.
Valentina Varalta · University of Verona
2025–2026 · grant
miRNAs expression and gut microbiota composition as potential biomarkers for Dravet Syndrome
Roberta Roberti · Magna Graecia University
2025–2027 · grant
Basic research on cognitive impairments in Noonan Syndrome: the NMDA-D1 receptor complex as a novel pharmacological target for the management of these disabilities
Chiara Fiorentini · University of Brescia
2025–2027 · grant
ARCADIA: Human mini-hearts to decipher and correct RRAGD cardiomyopathy
Milena Bellin · University of Padua
2025–2027 · grant
Impact of the WFS1-related mutations on immune system dysregulation in Wolfram Syndrome 1
Raniero Chimienti · Vita-Salute San Raffaele University
2025–2028 · grant
Respiratory progression in adult Duchenne muscular dystrophy. Natural history, identification of new biomarkers and design of a predictive algorithm
Federica Trucco · University of Genoa
2025–2026 · grant
Multiomics Analysis of Mitochondrial, autophagic, and lysosomal Balance in cblC methylmalonic Acidemia (MAMBA)
Marianna Caterino · University of Naples Federico II
2025–2030 · grant
RNA-BASED COMBINATORIAL MULTI TARGET THERAPY FOR THE TREATMENT OF INHERITED NEUROMUSCULAR DISEASES
Marco Sandri · Veneto Institute of Molecular Medicine
2025–2026 · grant
Exploring the Neuropsychological Profile of Sturge-Weber Syndrome for Developing Tailored Rehabilitation.
Laura Piccardi · Sapienza University of Rome
2025–2027 · grant
Tackling DNA damage and senescence pathways to identify new therapeutic targets for SBMA
Maria Pennuto · Veneto Institute of Molecular Medicine
2025–2026 · grant
Preventing PMS Regressions Through Non-Invasive Neuromodulation
Anna Letizia Allegra Mascaro · National Research Council
2025–2027 · grant
Molecular evolution of an hyperfunctional β-galactosidase for the HSC Gene Therapy of GM1 Gangliosidosis
Valentina Poletti · University of Padua
2024–2027 · grant
STandardizing Operating Procedures and end-Points in Myotonic Dystrophy type 1 (STOPP-DM1) – getting ready for clinical trials
Valeria Sansone · Centro Clinico Nemo
2024–2026 · grant
Cortical Astrocytes-Inhibitory Neurons Communication Define Opposite Social Profiles in 22q11.2 and 7q11.23 Deletion Syndromes
Francesco Papaleo · Italian Institute of Technology
2024–2025 · grant
Structural Bases of ACTG2-dependent smooth muscle Myopathies
Matteo De Rosa · National Research Council
2024–2026 · grant
Characterization of FRG2 gene family in the framework of FSHD
Rossella Ginevra Tupler · Università Degli Studi Di Modena E Reggio Emilia Unimore
2024–2027 · grant
PortoSinusoidal Vascular Disease: Risk stratification & Therapeutic Approaches
Alberto Zanetto · University of Padua
2024–2026 · grant
STABILITY AND PLASMID
Luigi Naldini · San Raffaele Telethon Institute For Gene Therapy - Sr-tiget
2024–2027 · grant
Reversing vessel instability: characterization of new molecular targets to struggle Hereditary Haemorrhagic Telangiectasia
Montserrat Climent Salarich · Humanitas University
2024–2025 · grant
Exploring extracellular matrix, proteostasis, and autophagy defects in vascular Ehlers-Danlos Syndrome: a proteomic and targeted functional approach
Marco Ritelli · University of Brescia
2024–2026 · grant
New therapeutic strategies for treating blindness in Wolfram syndrome
Vania Broccoli · National Research Council
2024–2025 · grant
Investigating the role of TFEB in Tuberous Sclerosis associated-kidney pathology using novel kidney organoid models.
Leopoldo Staiano · Fondazione Telethon
2024–2026 · grant
Deciphering the role of SOWAHC in Langerhans cell histiocytosis
Metello Innocenti · University of Milano-Bicocca
2024–2026 · grant
Utrophin Overexpression by Precise Base Editing of miRNA Binding Sites as a Universal Therapeutic Strategy for Duchenne Muscular Dystrophy
Francesco Chemello · University of Bologna
2024–2026 · grant
ZErareBRAL: ZEbrafish in vivo investigation of the fundamental role of Golgi dysfunction in the pathogenesis of a new class of rare cereBRAL malformations
Antonella Lauri · Ospedale Pediatrico Bambino Gesù - Irccs
2024–2025 · grant
Targeting the gut to improve seizure control in CDD
Aglaia Vignoli · University of Milan
2024–2026 · grant
DALRD3 and Translation: Lightning a Tdark?
Stefano Biffo · Istituto Nazionale Genetica Molecolare
2024–2026 · grant
Dietary interventions as therapeutic strategies in an ER-storage disease of the kidney
Luca Rampoldi · Vita-Salute San Raffaele University
2024–2026 · grant
Investigation of intertwined relationships between healthy and mutated GLUT1 using FDA approved compounds to identify a therapeutic approach
Paolo Grumati · Fondazione Telethon
2024–2027 · grant
Unveiling the molecular functions of CCDC32: a tDARK associated with non-specific syndromic intellectual disability and congenital abnormalities
Eugenio Fornasiero · University of Trieste
2024–2026 · grant
Deconstructing the involvement of abnormally protracted corticogenesis in the etiology of cortical defects in a postnatal mouse model of Tuberous Sclerosis Complex
Rossella Galli · Vita-Salute San Raffaele University
2024–2026 · grant
Astrocyte Calcium Rescue to Overcome Familial Alzheimer’s vascular Dysfunction (ACROFAD)
Micaela Zonta · National Research Council
2024–2026 · grant
SP5 as novel mediator of CAH multi-organ pathogenesis: from functional elucidation to therapeutic repurposing
Nicolò Caporale · University of Milan
2024–2026 · grant
Investigating the role of neuroinflammation as a central node to drive novel retinal phenotype observed in ARSACS zebrafish model
Valentina Naef · Fondazione Stella Maris - Irccs