Tableau de bord de la cohorte

La mission du GP2 est de mieux comprendre l’architecture génétique de la maladie de Parkinson (MP) par le génotypage de groupes de patients différents et l’étude des formes soulevant une forte suspicion de cause monogénique de la MP. En soutien à cette mission, nous constituons des cohortes différentes dans le monde en collaborant et en partageant ouvertement les données, les processus et les résultats. Le tableau de bord ci-dessous présente les étapes que nous avons franchies jusqu’à présent. Consultez régulièrement cette page car les données sont mises à jour sur une base trimestrielle.

Total des données mondiales

0
Emplacements uniques
0
Cohortes
0
Echantillons prévus
0
Echantillons terminés

Last Updated: August 10, 2022 | Original design by GP2 Hackathon 2021 Team: Mary Makarious, Kajsa Brolin, Yeajin Song, and Anastasia Illarionova.

Showing 10 of 238 cohort studies.

Genetic Study for Pakinson's Disease in Mongolia

Mongolian National University of Medical Sciences | Ulaanbaatar, Mongolia
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

Genetic study of PD and related movement disorders

Stellenbosch University | Cape Town, South Africa
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

632 Completed out of 730 Expected
Non-PD Samples
Non-PD Samples

729 Completed out of 0 Expected
Total Samples
Total Samples

1,361 Completed out of 730 Expected
Ancestry Breakdown for Samples Completed
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Genetic study of PD and related movement disorders - M

Stellenbosch University | Cape Town, South Africa
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

45 Completed out of 50 Expected
Non-PD Samples
Non-PD Samples

13 Completed out of 0 Expected
Total Samples
Total Samples

58 Completed out of 50 Expected
Ancestry Breakdown for Samples Completed
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Genetic Testing in Patients with Movement Disorders and PD

Chulalongkorn University | Bangkok, Thailand
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

Genetics of Neurological Pathologies: New Variations, New Phenotypes

IRCCS Neuromed | Piozzilli, Italy
Number of Samples Completed and Expected
Case Samples
Case Samples

0 Completed out of 37 Expected
Non-PD Samples
Non-PD Samples

0 Completed out of 0 Expected
Total Samples
Total Samples

0 Completed out of 37 Expected

Genetics of Parkinson's Disease - TUMPD

Technical University of Munich (TUM), Klinikum rechts der Isar | Munich, Germany
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

Genomes Project

University College London | London, United Kingdom
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

Genomewide Association Study in PD among East Asians - NTUH

National Taiwan University Hospital | Taipei City, Taiwan
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

253 Completed out of 250 Expected
Non-PD Samples
Non-PD Samples

0 Completed out of 0 Expected
Total Samples
Total Samples

253 Completed out of 250 Expected
Ancestry Breakdown for Samples Completed
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Genotype-Phenotype Correlations in Nepalese PD Population - MMCTU

Tribhuvan University | Kathmandu, Nepal
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

27 Completed out of 50 Expected
Non-PD Samples
Non-PD Samples

11 Completed out of 50 Expected
Total Samples
Total Samples

38 Completed out of 100 Expected
Ancestry Breakdown for Samples Completed
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Genotype-Phenotype Correlations in PD and Related Movement Disorders - KUL

University of Malaysia | Kuala Lumpur, Malaysia
Access Data on AMP® PD
Number of Samples Completed and Expected
Case Samples
Case Samples

943 Completed out of 1,000 Expected
Non-PD Samples
Non-PD Samples

35 Completed out of 0 Expected
Total Samples
Total Samples

978 Completed out of 1,000 Expected
Ancestry Breakdown for Samples Completed
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Demande d’ensemble de données auprès de l’AMP-PD

Une fois que le GP2 a terminé le génotypage d’une cohorte, l’intégralité des données est partagée par le biais de la plateforme sécurisée AMP® PD. Il est obligatoire de s’inscrire pour demander l’accès aux données.

Soumettre une cohorte

Si vous souhaitez collaborer avec l’équipe du GP2, veuillez nous contacter pour soumettre une cohorte ou obtenir de plus amples renseignements sur la procédure à suivre pour devenir membre.

Rencontrez les membres du GP2 du monde entier

Découvrez les membres de notre organisation dont la contribution, notamment en termes d’échantillons et de données, nous permet de poursuivre nos travaux de recherche.