- not yet recruitingNA
Initiative for Clinical Long-read Sequencing
This study aims to improve how we find genetic causes for rare diseases and cancer risks. Researchers are using advanced long-read genetic testing to get better diagnosis, especially for complex genetic changes.
Germany - recruitingNA
COsegregation of VARiants in Panel of Genes
This study, called COVAR, aims to better understand gene changes linked to cancer. It looks at changes in genes like BRCA1 and BRCA2, which are connected to inherited breast and ovarian cancer. By collecting information from many families, researchers hope to improve genetic counseling and patient care.
France · Guadeloupe · Martinique - recruiting
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH)
This study looks for early signs of heart muscle disease (cardiomyopathy) in people with a family history of specific genes. We're hoping to find simple tests, like blood or urine tests, that can show if someone is developing heart problems before they feel unwell. This could help doctors give treatment sooner.
United Kingdom - recruiting
Precision Medicine in the Prostate Cancer Care Pathway
This study looks at a special genetic test for prostate cancer. It helps men understand their personal risk and how this information can guide decisions about screening and treatment. The aim is to use genetic insights for more tailored prostate cancer care.
United Kingdom - recruiting
Pancreatic Cancer Early Detection Consortium
This study aims to find better ways to spot pancreatic cancer early, especially in people with a higher risk due to family history or specific genetic changes. Researchers will collect health information and samples over time to understand how the disease develops.
United States · Australia · Canada