Rare kidney diseases present significant challenges due to small patient populations and gaps in understanding of their biology. Advances in large-scale genomic and clinical data integration provide opportunities to uncover disease mechanisms and generate new insights into conditions such as NPHS2-related disorders. In this webinar, Moin Saleem, Bryce Powerman, and Dinah Clark will present a case study illustrating how longitudinal clinicogenomic datasets can illuminate disease pathways and inform the development of new therapeutic strategies.
Topics to be covered:
- How genomic data reveals mechanisms of rare kidney diseases
- Methods for extracting and analyzing insights from longitudinal clinicogenomic datasets
- The impact of collaboration on advancing precision medicine and targeted therapies
- How data-driven partnerships accelerate research and healthcare innovation.
Thursday, October 9th, 2025 | 11:00 AM - 1:00 PM Eastern Time
This webinar will be available to view live and on demand.
Speakers
Moin Saleem, PhD
Co-founder & Chief Scientific Advisor, Professor & Pediatric Nephrologist
Purespring Therapeutics and Bristol Children's Hospital
Bryce Powerman
Director of Business Development
Natera
.jpeg "Dinah Clark")
Dinah Clark
Director of Medical Education
Natera
