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What We Fund. What We've Found. Where We're Going.

The Grant Program

Violehealth makes investigator-initiated grants to academic and clinical researchers advancing the science of KCNQ2 loss-of-function disorders. We prioritize work with a clear path from mechanism toward therapy.

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Priority Research Areas

1.

Functional characterization of p.R325M via patch-clamp electrophysiology.

2.

AAV-based KCNQ2 supplementation in iPSC-derived neurons.

3.

Suppression–replacement (SupRep) gene therapy models.

4.

PIP₂ pathway pharmacology.

Current Projects

Functional Characterization of p.R325M (Patch-Clamp Electrophysiology)

Planned

To be awarded · To be determined

Patch-clamp electrophysiology to characterize how the R325M substitution disrupts PIP2 binding and the M-current, establishing the first functional data for this variant.

AAV-Based KCNQ2 Supplementation in iPSC-Derived Neurons

Planned

To be awarded · To be determined

Testing AAV delivery of healthy KCNQ2 copies in patient-derived iPSC neurons as a gene-supplementation strategy for dominant-negative loss-of-function variants.

Research Partners

Baylor College of Medicine
Columbia University
Children's Hospital of Philadelphia (CHOP)

Progress Timeline

2025

Foundation Founded

Violehealth is established in honor of Violetta.

2026

First Grant Cycle Opens

Investigator-initiated grants for KCNQ2 loss-of-function research.

Next

First Research Published

Functional data for the R325M variant.

?

Toward Therapy

Bridging mechanism to clinical translation.