FinnGen

A look at how genetics influence Raynaud’s syndrome symptoms and treatment.

New research highlights genetic factors in epilepsy diagnosis and risk assessment.

Bronchiolitis is a viral lung infection affecting infants, potentially leading to asthma.

New insights into recessive genetic contributions to common diseases are revealed through extensive research.

Examining the genetic links between Type 1 diabetes and autoimmune diseases.

Researchers identify genetic connections to migraines and potential treatment pathways.

Study reveals how genetics may influence sedentary lifestyles and cardiovascular risks.

Study compares EHR models and genetic scores for predicting disease risks.

Study reveals genetic links and implications for OSA diagnosis and treatment.