Cohort Dashboard

GP2’s mission is to further understand the genetic architecture of Parkinson’s disease (PD) through genotyping diverse participant groups and studying highly suspected monogenic forms of PD. In support of this mission, we continue to collect diverse cohorts from around the world through collaboration and openly sharing data, processes, and results. Explore the dashboard below to understand our milestones achieved so far, and continue to visit this page as data will be updated monthly.

Total Global Data

Unique Locations

Cohorts

Samples Expected

Samples Completed

Last Updated: September 15, 2022 | Original design by GP2 Hackathon 2021 Team: Mary Makarious, Kajsa Brolin, Yeajin Song, and Anastasia Illarionova

Showing 1 cohort study at Baylor College of Medicine.

BCM-UMD

University of Maryland | College Park, United States

Access Data on AMP® PD

Number of Samples Completed and Expected

Case Samples

358 Completed out of 358 Expected

Control Samples

83 Completed out of 83 Expected

Total Samples

441 Completed out of 441 Expected

Ancestry Breakdown for Samples Completed

Show

Ancestry	Completed Case Samples	Completed Control Samples
AAC - African Admixed	14	0
AFR - African Ancestry	2	0
AJ - Ashkenazi Jewish	45	10
AMR - Latino and Indigenous People of the Americas	4	1
EUR - General European Ancestry	284	71
EAS - East Asian Ancestry	3	1
SAS - South Asian Ancestry	6	0
FIN - Finnish Population Isolate	0	0
Other	0	0
Total	358	83
Total Completed Samples for Cases and Controls		441

Request AMP® PD Data Set

As GP2 completes cohort genotyping, all data is shared through the secured AMP® PD platform. Register to request access to this data.

Submit a Cohort

If you would like to collaborate with GP2, reach out to submit a cohort or get more information on how to become a member.

Discover GP2 Members from Around the Globe

Explore the organizational members that make our research possible through their collaboration and contribution of samples and data.