Join Roundtables

Please contact us to join our

Open science monthly roundtables

kaiti@project8p.org

The NDD-CNV Portal

For our July 2022 Research Roundtable, Dennis Lal, PhD presented the NDD-CNV Portal. If you’re interested in exploring the 8p data portal more, click here.

Play Video
Play Video

Artificial Intelligence (AI)-driven Drug Repurposing for Rare Disease

For our June 2022 Research Roundtable, Aleksandra Foksinska from Hugh Kaul Precision Medicine Institute at the University of Alabama at Birmingham presented “Artificial Intelligence (AI)-driven Drug Repurposing for Rare Disease”

Phenotyping of mitochondrial dysfunction and DNA damage/repair in Chromosome 8p disorder

For our May 2022 Research Roundtable, we had Dr. Nicoleta Moisoi from De Montfort University, Leicester, UK discuss “Phenotyping of mitochondrial dysfunction and DNA damage/repair in Chromosome 8p disorder.”

Play Video

The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.
  • Lead with knowledge from patients. Currently, there is no cure for 8p disorders, nor is there a standard course of treatment.

The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Raise transformative funding for pioneering scientific research into treatments for a complex, rare disease involving 250+ affected genes on the short arm of the 8 th chromosome (8p). Rearrangements of these genes causes significant abnormalities to the entire neurological system, thus all organs and functions of the body– with variance in cognitive functions, gross motor skills, social development and other challenges during infancy, and throughout life;
  • Empower a unified community of 8p patients and their families so they can have meaningful lives today; and
  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.