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
0
Unique Locations
0
Cohorts
0
Samples Expected
0
Samples Completed
Last Updated: January 15, 2023 | 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
353 Completed out of 353 Expected
Non-pd Samples
84 Completed out of 84 Expected
Total Samples
437 Completed out of 437 Expected
Ancestry Breakdown for Samples Completed
ShowAncestry | Completed Case Samples | Completed Non-PD Samples |
---|---|---|
aac - african admixed | 12 | 0 |
afr - african ancestry | 3 | 0 |
fin - finnish population isolate | 0 | 0 |
aj - ashkenazi jewish | 38 | 10 |
amr - latino and indigenous people of the americas | 4 | 0 |
eur - general european ancestry | 285 | 73 |
eas - east asian ancestry | 3 | 1 |
sas - south asian ancestry | 3 | 0 |
cas - central asian ancestry | 3 | 0 |
mde - middle eastern ancestry | 2 | 0 |
other | 0 | 0 |
total | 353 | 84 |
Total Completed Samples for Cases and Non-PD | 437 |
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.