PD GENEration is a large international observational study (not a treatment trial) run by the Parkinson's Foundation in partnership with the Global Parkinson's Genetics Program (GP2). This preprint reports on its expansion beyond North America to Latin American countries (Colombia, Chile, Mexico, Peru, Ecuador) and Israel, and on a major upgrade from a 7-gene targeted test to whole-genome sequencing (WGS). WGS reads the entire genetic blueprint rather than just pre-selected gene sections, which means it can also flag unrelated but medically actionable findings — such as hereditary breast cancer genes (BRCA1/BRCA2) and a familial cholesterol condition. Every participant receives their results plus genetic counselling, at no cost.
The earlier North American phase (10,500+ participants, published 2024) found that 13% of people with Parkinson's carry a reportable genetic variant linked to the disease — meaningfully higher than the long-assumed 5–10%. The most common was a GBA1 variant (7.7%), followed by LRRK2 (2.4%) and PRKN (2.1%). Crucially, 9% of people with none of the classic warning signs — no early onset, no family history, no high-risk ancestry — still carried a variant. This international paper extends those findings across more diverse populations where variant frequencies differ, providing the first large-scale genetic picture of Parkinson's across Latin American and Middle Eastern communities. The study has now enrolled more than 20,000 participants.
For someone living with Parkinson's today, the most actionable implication is that knowing your genetic status is no longer just for those with a strong family history or early onset — the data increasingly support offering testing universally. A positive result (especially GBA1 or LRRK2) does not change current standard medication but does open doors to precision-medicine clinical trials targeted at those specific gene variants, and trials for both are actively enrolling. This is an observational registry study — it describes genetics in the population, it does not test a treatment — so it does not change day-to-day clinical care directly. Asking your neurologist about genetic testing remains the practical next step; in many countries PD GENEration offers it free of charge.