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32 Result(s)

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    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • 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
    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of British Columbia
    • Faculty of Medicine
    • More details
    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of Ottawa
    • Faculty of Medicine -
    • More details
    • CANADA
    • Québec
    • MONTREAL
    • FORGE - Finding of Rare Disease Genes in Canada
    • Centre hospitalier universitaire Sainte-Justine
    • Pédiatrie
    • More details
    • ESTONIA
    • Tartu
    • TARTU
    • 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
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • KAREP : Kainate receptors in acute and chronic mouse models of epilepsy
    • Institut François Magendie
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • BONDY
    • 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
    • PARIS
    • Identification of the molecular basis for unexplained mental retardation
    • CHU Paris - Hôpital Necker - Enfants Malades
    • Département de génétique
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Chromosomic errors and syndromic mental retardations
    • CHU Paris - Hôpital Necker - Enfants Malades
    • Département de génétique
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • RoME : Role of Microglia in Epilepsy
    • Neurophysiology & New Microscopies Laboratory
    • More details
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Study of genetic diseases affecting normal cortical development
    • Faculté de Médecine de La Timone
    • Génétique Médicale et Génomique Fonctionnelle
    • More details
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • METANEX: metabolic management of neuronal hyperexcitability: a new approach to treat epilepsy
    • Parc scientifique et technologiques de Luminy
    • Institut de Neurobiologie de la Méditerranée
    • More details
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • 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
    • TÜBINGEN
    • EPICURE: Functional genomics and neurobiology of epilepsy: a basis for new therapeutic strategies (coordination)
    • Hertie-Institut für klinische Hirnforschung
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • 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
    • Bayern
    • ERLANGEN
    • NGFN plus : IG German Mental Retardation Network (coordination)
    • Friedrich-Alexander-Universität Erlangen-Nürnberg
    • Humangenetisches Institut
    • More details
    • GERMANY
    • Bayern
    • ERLANGEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Erlangen (Project 1): Identification, validation and functional characterization of disease causing genes and proteines in patients with mental retardation of unkown cause
    • Friedrich-Alexander-Universität Erlangen-Nürnberg
    • Humangenetisches Institut
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • BNE: BrainNet Europe II: European brain tissue bank - Network for clinical neuroscience and basic research (coordination)
    • Ludwig-Maximilians-Universität München
    • Zentrum für Neuropathologie und Prionforschung
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • 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
    • Berlin
    • BERLIN
    • 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
    • Nordrhein-Westfalen
    • BONN
    • 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
    • Universität Bonn
    • Institut für Humangenetik
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • 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
    • MÜNSTER
    • 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
    • Sachsen
    • DRESDEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Dresden (Project 7): Clinical characterization, molecular karyotyping and gentype phenotype correlations
    • Medizinische Fakultät Carl Gustav Carus der TU Dresden
    • Institut für Klinische Genetik
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene.
    • Istituto CSS-Mendel
    • Laboratorio di Biologia Molecolare e Citogenetica
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Functional study of epileptogenic na+ channel mutations in transfected neurons and animal models
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • Dipartimento di Neurofisiopatologia ed Epilettologia Diagnostica
    • More details
    • ITALY
    • PIEMONTE
    • TORINO
    • 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
    • SICILIA
    • TROINA
    • 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
    • PORTUGAL
    • SUL
    • LISBOA
    • Noninvasive dynamic neuroimaging in epilepsy
    • Instituto Superior Técnico
    • LaSEEB-Evolutionary Systems and Biomedical Engineering Lab
    • More details
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Industrials
    • High definition genomic screening of candidate genes for neurodevelopmental disorders
    • Hospital Universitario La Fe (Campanar)
    • Unidad de Genética y Diagnóstico Prenatal
    • More details
    • SWITZERLAND
    • Suisse Alémanique
    • SCHWERZENBACH
    • NGFN plus : IG German Mental Retardation Network - MR Centre Erlangen (Project 1): Identification, validation and functional characterization of disease causing genes and proteines in patients with mental retardation of unkown cause
    • Universität Zürich
    • IMG - Institut für Medizinische Genetik
    • More details