Patient-partnered research
Patients partner with our scientists to accelerate the pace of discovery and find better treatments.
Count Me In enables anyone in the US and Canada ever diagnosed with cancer to accelerate research by sharing their samples, their clinical information, and their voices.
The Eating Disorders Genetics study is recruiting people in the U.S. ever diagnosed with an eating disorder to explore these disorders' genetic risk factors.
Our study collects health and genetic information from patients diagnosed with spontaneous coronary artery dissection to improve prevention and treatment.
OurHealth studies health and genetic information of South Asians living in the United States to better prevent and manage cardiovascular disease risk.
The PBN clinical research study aims to identify measurable, robust, and replicable biological markers to support clinical trials for schizophrenia and bipolar spectrum disorders.
The Rare Genomes Project is a patient-driven research study making the latest advances in genomic sequencing accessible to families with rare and undiagnosed conditions.
