Cohort Dashboard

GP2の使命は、多様な患者グループの遺伝子型を特定し、PDのモノジェニック型が疑われる事例を研究して、パーキンソン病(PD)の遺伝的構造をさら深く理解することです。 私たちはこの使命をサポートするために、コラボレーション、そしてデータ、プロセス、結果の公開・共有を通して、世界中から多様なコホートを集めています。 私たちのこれまでのマイルストーンと活動実績は以下のダッシュボードから見ることができます。このページのデータは各四半期ごとに更新されます。

全グローバルデータ

0
地域
0
コホート
0
予想サンプル
0
完成サンプル

最終更新日:2022年 8月 10日 | GP2ハッカソン2021チームによるオリジナルデザイン:Mary Makarious、Kajsa Brolin、Yeajin Song、Anastasia Illarionova

Showing 10 of 238 cohort studies.

Central Asian and Transcaucasian PD (CAT-PD) - South Kazakhstan Medical Academy

South Kazakhstan Medical Academy | Shymkent, Kazakhstan
Number of Samples Completed and Expected
Case Samples
Case Samples

Pending
Non-PD Samples
Non-PD Samples

Pending
Total Samples
Total Samples

0 Completed out of 0 Expected

Central Asian and Transcaucasian PD (CAT-PD) - Tbilisi State Medical University

Tbilisi State Medical University | Tbilisi, Georgia
Number of Samples Completed and Expected
Case Samples
Case Samples

Pending
Non-PD Samples
Non-PD Samples

Pending
Total Samples
Total Samples

0 Completed out of 0 Expected

Christchurch Longitudinal Parkinson's Study

Southern Health and Disability Ethics Committee | Christchurch, New Zealand
Number of Samples Completed and Expected
Case Samples
Case Samples

0 Completed out of 350 Expected
Non-PD Samples
Non-PD Samples

0 Completed out of 80 Expected
Total Samples
Total Samples

0 Completed out of 430 Expected

Clinical and genetic study of Unusual/Familial Movement Disorders

University of Cincinnati | Cincinnati, United States
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

63 Completed out of 500 Expected
Non-PD Samples
Non-PD Samples

0 Completed out of 180 Expected
Total Samples
Total Samples

63 Completed out of 680 Expected
Ancestry Breakdown for Samples Completed
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Clinical and genetic study of Unusual/Familial Movement Disorders - M

University of Cincinnati | Cincinnati, United States
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

6 Completed out of 10 Expected
Non-PD Samples
Non-PD Samples

0 Completed out of 0 Expected
Total Samples
Total Samples

6 Completed out of 10 Expected
Ancestry Breakdown for Samples Completed
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Clinicogenetic Study of PD in Tunisia

National Institute of Neurology Mongi-Ben Hamida | Tunis, Tunisia
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

43 Completed out of 150 Expected
Non-PD Samples
Non-PD Samples

0 Completed out of 150 Expected
Total Samples
Total Samples

43 Completed out of 300 Expected
Ancestry Breakdown for Samples Completed
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CORIELL

CORIELL | Camden, United States
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

4,329 Completed out of 4,478 Expected
Non-PD Samples
Non-PD Samples

4,389 Completed out of 4,111 Expected
Total Samples
Total Samples

8,718 Completed out of 8,589 Expected
Ancestry Breakdown for Samples Completed
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CSF Biomarkers

University of Perugia | Perugia, Italy
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

93 Completed out of 60 Expected
Non-PD Samples
Non-PD Samples

0 Completed out of 0 Expected
Total Samples
Total Samples

93 Completed out of 60 Expected
Ancestry Breakdown for Samples Completed
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DATATOP

Michael J. Fox Foundation | Rochester, United States
Number of Samples Completed and Expected
Case Samples
Case Samples

Pending
Non-PD Samples
Non-PD Samples

Pending
Total Samples
Total Samples

0 Completed out of 0 Expected

DeNoPa

University of Göttingen | Goettingen, Germany
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

131 Completed out of 140 Expected
Non-PD Samples
Non-PD Samples

136 Completed out of 100 Expected
Total Samples
Total Samples

267 Completed out of 240 Expected
Ancestry Breakdown for Samples Completed
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AMP-PDデータセットのリクエスト

GP2がコホートの遺伝子型同定を完了すると、すべてのデータは安全なAMP® PDプラットフォームを介して共有されます。登録してこのデータへのアクセスをリクエストする。

コホートを提出する

GP2とコラボレーションをご希望または、コホートを提出したり、メンバーになるための詳細情報を入手したい場合はご連絡ください。

世界のGP2メンバーを探す

サンプルとデータのコラボレーションと貢献を通し、私たちの研究を可能にしてくれる機関メンバーを探す