Recent Stories


Family faces multiple diagnoses for genetic condition NF1

Family faces multiple diagnoses for genetic condition NF1

A baby’s unique birthmarks lead to genetic testing and specialty care for whole family
Courtney Collen 8 min read
Sanford partners with Helix to improve preventive care

Sanford partners with Helix to improve preventive care

Screening will identify individuals and communities at higher risk for disease
Jon Berg 6 min read
Genetic test alerts Army veteran to possible side effects

Genetic test alerts Army veteran to possible side effects

Simple blood test can show how the body responds to certain medications
Jason Anschutz 5 min read
Seeing your options through eye disease

Seeing your options through eye disease

Visual impairment is common worldwide, and some runs in families
SHN Staff 6 min read
Sanford Imagenetics featured at world conference

Sanford Imagenetics featured at world conference

Precision Medicine World Conference focuses on genomics and medical research
Jon Berg 3 min read
Lynch syndrome: The genetics of colon cancer

Lynch syndrome: The genetics of colon cancer

This inherited condition can cause several types of cancer
SHN Staff 9 min read
Pharmacogenomics: Your genes hold valuable information

Pharmacogenomics: Your genes hold valuable information

DNA test can help doctors decide which medications may work best for you
Jennifer Morgan, APRN-CNP, DNP 5 min read
Veterans get free genetic testing at Sanford Health

Veterans get free genetic testing at Sanford Health

Pharmacogenomics test improves medication accuracy for Air Force veteran
Matt Holsen 6 min read
Researcher earns $1.9M grant to study kidney disease genes

Researcher earns $1.9M grant to study kidney disease genes

Chandrasekar Lab team looks for what goes wrong in human kidney cells when genes mutate
Jon Berg 2 min read
Sanford researcher receives $2M grant to study rare disease

Sanford researcher receives $2M grant to study rare disease

Deadly brain condition known as MoCD impacts 1 in 100,000 people
Jon Berg 2 min read