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    • Molecular genetic investigation of apparently balanced translocations in patients with mental retardation and multiple congenital malformations.
    • Ghent University Hospital - UZGent
    • Center for Medical Genetics Ghent
    • More details
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • AcademicsIndustrialsFinancial investitors
    • Clinical exome sequencing for molecular diagnosis of polymalformative syndromes
    • CHU Sherbrooke - Hôpital Fleurimont
    • Service de génétique médicale
    • More details
    • CANADA
    • Québec
    • SHERBROOKE
    • Chromosomic errors and syndromic mental retardations
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Laboratoire de Génétique Moléculaire
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • SPATAX: autosomal recessive spastic paraplegia : identification of new genes and of mechanisms of degeneration
    • Université Saint-Joseph
    • Unité de génétique médicale
    • More details
    • LEBANON
    • Beyrouth
    • BEIRUT
    • Development of novel DNA diagnostic technologies for the detection of structural chromosomal abnormalities in case of mental retardation (EFT 5467).
    • University of Tartu
    • The Institute of Molecular and Cell Biology
    • More details
    • ESTONIA
    • Tartu
    • TARTU
    • Cryptic anomalies by CGH array in children with mental retardation and ophtalmologic anomalies
    • CHU Paris Seine-Saint-Denis - Hôpital Jean Verdier
    • Laboratoire de cytogénétique et biologie de la reproduction
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • BONDY
    • Identification of the molecular basis for unexplained mental retardation
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Laboratoire de Génétique Moléculaire
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • NGFN plus : IG German Mental Retardation Network - MR Centre Heidelberg (Project 9): Mutation screenings and functional characterisation on candidate genes
    • Universitätsklinikum Heidelberg
    • Abteilung Molekulare Humangenetik
    • More details
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • NGFN plus : IG German Mental Retardation Network - MR Zentrum Tübingen (project 3): High resolution SNP microarrays for identification of genome imbalances and segmental UPD's. Molecular (MLPA, qPCR) and molecular cytogenetic (FISH) techniques for validation of Copy Number Variants.
    • Universitätsklinikum Tübingen
    • Medizinische Genetik Tübingen
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • NGFN plus : IG German Mental Retardation Network (coordination)
    • Universitätsklinikum Erlangen
    • Humangenetisches Institut
    • More details
    • GERMANY
    • Bayern
    • ERLANGEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Munich (project4): Genome-wide hybridization of genomic DNA with oligonucleotide-based arrays
    • Technische Universität München
    • Institut für Humangenetik
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • NGFN plus : IG German Mental Retardation Network -MR Centre Berlin (Teilprojekt 2): Array CGH for detection of submicroscopic genome imbalances, homozygosity mapping using SNP arrays
    • Max-Planck-Institut für molekulare Genetik
    • Abteilung Human Molecular Genetics
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Bonn (Project 5): identification of candidate genes for mental retardation by the detection and analysis of submicroscopic CNCs
    • Universitätsklinikum Bonn
    • Institut für Humangenetik
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Essen (Project 8): genotype phenotype correlations in patients with mental retardation
    • Universitätsklinikum Essen
    • Institut für Humangenetik
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Münster (Project 6): Identification of diseases causing genes in mental retardation
    • Universitätsklinikum Münster
    • Institut für Humangenetik
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • NGFN plus : IG German Mental Retardation Network - MR Centre Dresden (Project 7): Clinical characterization, molecular karyotyping and gentype phenotype correlations
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • Institut für Klinische Genetik
    • More details
    • GERMANY
    • Sachsen
    • DRESDEN
    • Genetics basis of Mental Retardation
    • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • Struttura Semplice di Genetica
    • More details
    • ITALY
    • PIEMONTE
    • TORINO
    • Usefulness of 244K array-cgh in the ascertainment of cryptic chromosomal rearrangements in Mental Retardation and Autism
    • IRCCS OASI Maria Santissima
    • U.O.C.di Pediatria e Genetica Medica
    • More details
    • ITALY
    • SICILIA
    • TROINA
    • Usefulness of 244K array-cgh in the ascertainment of cryptic chromosomal rearrangements in Mental Retardation and Autism
    • IRCCS OASI Maria Santissima
    • Laboratorio di Diagnosi Genetica
    • More details
    • ITALY
    • SICILIA
    • TROINA
    • Emerging Team to identify and characterize novel and existing Hereditary Spastic Paraplegia (HSP) disease genes
    • CHUM Research Centre
    • Centre d'excellence en neuroscience de l'Université de Montréal
    • More details
    • CANADA
    • Québec
    • MONTRÉAL
    • Epidemiology and life quality issues of hereditary spastic paraplegia in Estonia and introducing genetic analysis
    • Tartu University Hospital
    • Department of Neurology
    • More details
    • ESTONIA
    • Tartu
    • TARTU
    • SPATAX: molecular basis of autosomic recessive and dominant spastic paraplegia
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • Maladies neurodégénératives
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • SPATAX-QUEST: Identification of new causative genes in spinocerebellar degenerations by combination of whole genome scan, next-generation sequencing and biological validation in vitro and in vivo
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • Maladies neurodégénératives
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Spastic paraplegia genetics
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • UF de Neurogénétique Moléculaire et Cellulaire
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • MITOTARGET: mitochondrial apoptotic pathways in neurodegenerative diseases and assessment of the effects of new small molecules (WP4)
    • Parc scientifique et technologiques de Luminy
    • Institut de Biologie du Développement de Marseille-Luminy
    • More details
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • MITOTARGET: dysfonction mitochondriale dans les maladies neurodégénératives: vers de nouvelles thérapies (coordination)
    • Parc scientifique et technologiques de Luminy
    • TROPHOS SA
    • More details
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • EUROSPA: European & Mediterranean network on spastic paraplegias (partner No. 2)
    • Universitätsklinikum Tübingen
    • Abteilung für Neurodegeneration
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • MITOTARGET: Mitochondriale Membran-Eigenschaften im Prozess der Neurodegeneration und Untersuchung der Effekte von neuen kleinen Molekülen (WP2)
    • Johann Wolfgang Goethe-Universität Frankfurt
    • Pharmakologisches Institut für Naturwissenschaftler
    • More details
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Dissecting the axonal transport pathway in hereditary spastic paraplegia
    • Universitätsmedizin Göttingen
    • Institut für Humangenetik
    • More details
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • NEUROLIPID: Lipid metabolism in the pathogenesis of hereditary spastic paraplegia: genes, biomarkers, and models for therapy (coordinator)
    • Universität zu Köln
    • Rugarli Lab
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • EUROSPA: European & Mediterranean network on spastic paraplegias (partner No. 4)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • Department of neurology
    • More details
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Genetic analysis in families with hereditary spastic paraplegia
    • CNR
    • Laboratorio di Genetica Molecolare 3
    • More details
    • ITALY
    • CALABRIA
    • MANGONE
    • Identification of novel disease genes in the disease hereditary spastic
    • Fondazione EBRI
    • Istituto di Neurobiologia e Medicina Molecolare
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • Search for new disease genes in the spastic paraplegia erediatria
    • Fondazione EBRI
    • Istituto di Neurobiologia e Medicina Molecolare
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • A national network for the study of spinocerebellars ataxia and spastic paraparesis in Italy
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • U.O. Biochimica e Genetica
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Hereditary spastic paraplegia due to mitochondrial defects. development of animal and cellular models of pathogenesis
    • IRCCS Ospedale San Raffaele - DIBIT
    • Unità di Genetica Umana e Molecolare
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • A mitochondrial connection between faulty development and neurodegeneration of cerebellum and spinal cord: the role of Afg3l2 in mitochondrial dynamics and metabolism
    • IRCCS Ospedale San Raffaele - DIBIT
    • Unità di Genetica Umana e Molecolare
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias
    • Instituto de Biologia Molecular e Celular
    • Centro de Genética Preditiva e Preventiva
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias
    • Instituto de Biologia Molecular e Celular
    • Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias
    • Hospital São Sebastião
    • Serviço de Neurologia
    • More details
    • PORTUGAL
    • NORTE
    • SANTA MARIA DA FEIRA
    • Modeling spastic paraplegia gene molecular function and pathology in Drosophila
    • Department of Genetics - University of Cambridge
    • Department of Genetics
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Genetic disorders of human brain development
    • Western General Hospital
    • MRC Human Genetics Unit
    • More details
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • MITOTARGET: mitochondrial metabolic function and oxidative stress in neurodegenerative diseases and assessment of the effects of new small molecules (WP3)
    • The Medical School - University of Sheffield
    • Academic Neurology Unit
    • More details
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • MITOTARGET: mitochondrial dynamics in neurodegenerative diseases and assessment of the effects of new small molecules (WP1)
    • The University of Sheffield
    • Department of Neuroscience
    • More details
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • The etiology of inherited neurological diseases
    • Sanford Research
    • Kruer Lab
    • More details
    • UNITED STATES
    • South Dakota
    • SIOUX FALLS
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM