At Pairnomix, we are committed to better understanding rare genetic conditions.
What We Do
Pairnomix offers personalized screening services that help physicians better understand their patients’ rare genetic mutations. Our services involve creating a laboratory model of the individual’s genetic mutation, performing experiments to understand the impact of that mutation on cellular function, and testing more than 1,300 approved drugs against the laboratory model to identify those that can reverse the mutation’s functional consequence. We provide our findings to the patient’s physician so together they can consider this information.
Opportunities for Collaboration
We actively seek partnerships with other organizations that share our goal of advancing knowledge of rare diseases. With our platform of rare genetic disease models, our networks of physicians and patient communities, and our extensive experience in genetic research and high throughput drug screening, we bring considerable expertise and resources to potential partners.
Pairnomix is already collaborating with a variety of companies and institutions in the rare CNS disorders space. To read about our partnership with StemoniX, please click here.
Please don’t hesitate to contact us with any inquiries into potential collaboration. We welcome the opportunity to discuss how Pairnomix may be able to work with your organization to achieve our mutual goals.