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Research projects
CANADA
Québec
MONTRÉAL
Function of Parkinson Disease Genes in Mitochondrial Quality Control
Montreal Neurological Institute and Hospital
Fon Lab
CANADA
Québec
MONTRÉAL
Function of Parkinson Disease Role of PINK1 Processing in Mitochondrial Function and Parkinson's Disease
Montreal Neurological Institute and Hospital
Fon Lab
FRANCE
ILE-DE-FRANCE
PARIS
Selection and multicenter longitudinal prospective study of a cohort in non-idiopathic parkinson syndrome
AP-HP.Sorbonne Université - Hôpital de la Pitié-Salpêtrière
Service de pharmacologie médicale - Unité Pharmacologie Clinique
FRANCE
ILE-DE-FRANCE
PARIS
Development of therapeutic strategies for human degenerative diseases
Centre Paul Broca
Biologie et pathologie du neurone
GERMANY
Baden-Württemberg
TÜBINGEN
LRRK2 as a target for the treatment of Parkinson's disease
Hertie-Institut für klinische Hirnforschung (HIH)
Abteilung Neurologie mit Schwerpunkt neurodegenerative Erkrankungen
GERMANY
Baden-Württemberg
TÜBINGEN
Regulation of leucine-rich repeat kinase 2 a in macrophages
Hertie-Institut für klinische Hirnforschung (HIH)
Abteilung für Neurodegeneration - Funktionelle Neurogenetik
GERMANY
Berlin
BERLIN
EOPS-THS: Early-Onset-Parkinson-THS-Register
Charité - Universitätsmedizin Berlin (CCM)
Klinik für Neurologie (CCM)
ITALY
TRENTINO ALTO ADIGE
TRENTO
Parkinson's disease at the synaptic site: short and long term impact of pathological LRRK2 kinase activity
Università di Trento
Laboratory of Biology of Synapses
PORTUGAL
NORTE
PORTO
Clinical implications of genetic factors causing neurodegenerative diseases characterized by movement or cognitive dysfunction.
Instituto de Biologia Molecular e Celular
Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas
SPAIN
Cataluña
BARCELONA
OMICS analyses of cultured fibroblasts from LRRK2-associated Parkinson' s disease
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Institut d'Investigacions Biomèdiques August Pi i Sunyer
BELGIUM
VLAAMS BRABANT
LEUVEN
Longitudinal Measurement of Synaptic Density to Monitor Progression of Parkinson's Disease
UZ Leuven - Campus Gasthuisberg
Parkinson Plus Clinic
SWITZERLAND
Suisse Romande
LAUSANNE
Structural Studies of Human Brain in Neurodegeneration
EPFL
Laboratoire de microscopie électronique biologique EPFL - SB - IPHYS - LBEM
FINLAND
Finland
OULU
Novel Diagnostics and Treatment Strategies for Developmental Disorders, Childhood Epilepsies and Movement Disorders
University of Oulu
Biocenter Oulu
FRANCE
ILE-DE-FRANCE
PARIS
Neuroglobin gene overexpression: a promising tool for treating a large spectrum of neurological disorders thanks to its ability to safely and sustainably preserve mitochondrial integrity
Institut National de la Santé et de la Recherche Médicale
ITALY
LAZIO
ROMA
Diverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare
SPAIN
Cataluña
BARCELONA
Igenco: In-Depth genomics and cross-omics analysis for undiagnosed rare diseases on a user-friendly collaborative platform
Centro de Regulación Genómica
Centro Nacional de Análisis Genómico
SPAIN
Cataluña
BARCELONA
Igenco: In-Depth genomics and cross-omics analysis for undiagnosed rare diseases on a user-friendly collaborative platform
ISGlobal - Instituto de Salud Global de Barcelona
Programa de investigación en Enfermedades no transmisibles y medio ambiente
SPAIN
Comunidad Valenciana
VALENCIA
Clinical studies, genetic basis and prognosis biomarkers in rare neurodegenerative diseases
Centro de Investigación Príncipe Felipe (CIPF)
CIPF: Centro de Investigación Príncipe Felipe
CANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
SPAIN
Andalucía
SEVILLA
Development of bioinformatic tools for the automatic handling of secondary findings and their use in genetic and pharmacogenetic counseling
Fundación Progreso y Salud
Área de bioinformática clínica
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Centro de Regulación Genómica
Archivo europeo de genomas y fenomas del CRG
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Clínic de Barcelona
Servicio de Inmunologia
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari Vall d'Hebron
Laboratorio de Genética
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital de la Santa Creu i Sant Pau
Servicio de Genética
SPAIN
Cataluña
ESPLUGUES DE LLOBREGAT
Federated network for functional genomics of undiagnosed and rare diseases, RareFunction
Fundació Sant Joan de Déu - Institut de Recerca Sant Joan de Déu
Grupo de investigación en Neurogenética y Medicina Molecular
SPAIN
Cataluña
ESPLUGUES DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Sant Joan de Déu Barcelona
Servicio de Laboratorio
SPAIN
Cataluña
L'HOSPITALET DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari de Bellvitge
Unidad de Genética Molecular
SPAIN
Madrid
MADRID
Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
Multicentric Research projects
- Hertie-Institut für klinische Hirnforschung (HIH)
- Abteilung Neurologie mit Schwerpunkt neurodegenerative Erkrankungen
- Institut für Medizinische Genetik und angewandte Genomik Tübingen
- Institut für Medizinische Genetik und angewandte Genomik
- Institut für Medizinische Genetik und angewandte Genomik Tübingen
- Institut für Medizinische Genetik und angewandte Genomik
- Azienda Ospedaliera di Padova
- Clinica Pediatrica
GERMANY
Baden-Württemberg
TÜBINGEN
MEFOPA: European project on mendelian forms of Parkinson's disease (Terminated)
GERMANY
Baden-Württemberg
TÜBINGEN
RATSTREAM: European project on the characterisation of transgenic rat models for neurodegenerative and psychiatric diseases: Automated home cage analyses, live imaging and treatment (FINISHED)
GERMANY
Baden-Württemberg
TÜBINGEN
NEURASYNC: Academic-Industrial Training Network on Alpha-Synuclein-related Brain Diseases
ITALY
VENETO
PADOVA