Studying the Genetic Origins of Disease
At Sanford Research, we study how all the genes in your body – the genome – work in concert to promote healthy cellular function. We focus on studying origins of disease at the level of people, organs, or even one individual cell at a time.
Harnessing the power of bioinformatics and big data, we work to generate more personalized medicines and individualized treatments.
The Genetics and Genomics Group focuses on:
- Understanding cellular identity and what leads to disease progression
- Using genomic sequencing and bioinformatics to understand cell development
- Developing personalized therapies and treatments
We use this information to integrate clinical genetics into everyday primary care. Providers can then make better decisions on prescribing medications and screening for risk of chronic disorders.
The Genetics and Genomics Group supports:
Primary Faculty
Secondary Faculty
Sanford Health News
-
background-image
Sanford Research earns NIH grant to study rare bone cancer
Research focuses on skeletal genetic pathways affecting tumors in teens and young adults
-
background-image
Sanford Health joins Undiagnosed Diseases Network
Sanford plans to enroll at least five patients each year who meet criteria
Classes & Events
-
background-image
PROMISE Summer Programs
Wed 06/04/25 8:30 AM - Wed 06/04/25 3:00 PM
Sanford Research Center -
background-image
PROMISE Summer Programs
Tue 06/10/25 8:30 AM - Tue 06/10/25 3:00 PM
NDSU Campus