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Research projects

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberDeveloping classification criteria for the uveitides
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberDiagnosis and treatment of ocular inflammatory disease (uveitis)
Institution: Information not provided - US

FRANCE

GRAND-EST
ILLKIRCH-GRAFFENSTADEN

Funded by an IRDiRC memberPREDACTING: Predicting the clinical outcome of non-muscle actinopathies - FR
Institut de génétique et de biologie moléculaire et cellulaire - IGBMC
Département Biologie du développement et cellules souches

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

Research for one gene involved in Goldenhar syndrome
CHU de Bordeaux-GH Pellegrin
Laboratoire Maladies Rares : Génétique et Métabolisme (MRGM)

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

Funded by an IRDiRC memberFurther delineation of molecular bases of Oculo-Auriculo-Vertebral Spectrum
CHU de Bordeaux-GH Pellegrin
Laboratoire Maladies Rares : Génétique et Métabolisme (MRGM)

HUNGARY

Közép-Magyarország
BUDAPEST

Funded by an IRDiRC memberPREDACTING: Predicting the clinical outcome of non-muscle actinopathies - HU
Semmelweis University
Department of Biophysics and Radiation Biology

IRELAND

County Dublin
DUBLIN

Exploration of theraputic strategies for ocular disorders
Trinity College Dublin
Smurfit Institute of Genetics

ITALY

LOMBARDIA
MILANO

ITALY

TOSCANA
SESTO FIORENTINO (FIRENZE)

Funded by an IRDiRC memberPREDACTING: Predicting the clinical outcome of non-muscle actinopathies - IT
Università degli Studi di Firenze
Dipartimento di Biologia

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

FRANCE

GRAND-EST
STRASBOURG

Retinis Pigmentosa: validation of the molecular diagnostic using next generation sequencing
CHU de Strasbourg - Hôpital Civil
Laboratoire de diagnostic génétique

FRANCE

GRAND-EST
STRASBOURG

Funded by an IRDiRC memberSolving missing heritability in inherited retinal diseases using integrated omics and gene editing in human cellular and animal models
Faculté de médecine de Strasbourg - Louis Pasteur
Laboratoire de génétique médicale - Unité Inserm U1112

FRANCE

ILE-DE-FRANCE
PARIS

Epidemiological study in hereditary dystrophies of retina
Institut de la Vision
Centre d'Investigation Clinique (CIC) de l'hôpital des Quinze-Vingts

FRANCE

ILE-DE-FRANCE
PARIS

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

Molecular analysis of patients affected by oculo-cutaneous albinism
CHU de Bordeaux-GH Pellegrin
Laboratoire Maladies Rares : Génétique et Métabolisme (MRGM)

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

Funded by an IRDiRC memberSearch for new albinism genes
Université de Bordeaux

FRANCE

OCCITANIE
MONTPELLIER

Gene therapy of retinal dystrophy on human models: differentiation of patients iPS cells to retinal cells
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

GERMANY

Niedersachsen
GÖTTINGEN

KFO 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Institut für Humangenetik der Universität Göttingen
Institut für Humangenetik

GERMANY

Nordrhein-Westfalen
BONN

GERMANY

Saarland
HOMBURG

Description of clinical variability of ocular and cutaneous phenotypes in albinism
Universitätsklinikum des Saarlandes
Klinik für Augenheilkunde

GERMANY

Schleswig-Holstein
LÜBECK

KFO 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Dermatologie, Allergologie und Venerologie

GERMANY

Schleswig-Holstein
LÜBECK

KFO 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Lübecker Institut für Experimentelle Dermatologie

IRELAND

County Dublin
DUBLIN

Target 5000: A Study of Inherited Retinal Degeneration
Mater Misericordiae Hospital
Department of Ophthalmology

IRELAND

County Dublin
DUBLIN

Target 5000: A Study of Inherited Retinal Degeneration
Royal Victoria Eye and Ear Hospital
Ophthalmology Research Department

IRELAND

County Dublin
DUBLIN

Target 5000: A Study of Inherited Retinal Degeneration
Trinity College Dublin
Smurfit Institute of Genetics

ITALY

CAMPANIA
NAPOLI

Funded by an IRDiRC memberCRISPR/Cas9 microRNAs Editing as gene-independent therapeutic approach in Inherited Retinal Dystrophies (IRDs)
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

SPAIN

Castilla - La Mancha
ALBACETE

Funded by an IRDiRC memberAnalysis of the genetic and molecular bases of congenital and juvenile glaucoma: Diagnostic and therapeutic implications
Universidad de Castilla-La Mancha. Campus de Albacete. Facultad de Medicina
Departamento de Genética

SPAIN

Cataluña
BARCELONA

Funded by an IRDiRC memberInduced pluripotent cells and cell reprogramming in cell-based therapy approaches for corneal regeneration
IIB Sant Pau - Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Grupo de investigación en medicina regenerativa y bioingeniería de tejidos

SPAIN

Comunidad Valenciana
VALENCIA

Funded by an IRDiRC memberThe cell therapeutic strategy for hereditary retinal dystrophies in small and large animals: MERTK associated Retinitis pigmentosa
Fundación de la Comunidad Valenciana Centro de Investigación Príncipe Felipe
Fundación de la Comunidad Valenciana Centro de Investigación Príncipe Felipe (CIPF)

SPAIN

Madrid
MADRID

Funded by an IRDiRC memberAnalysis of the genetic and molecular bases of congenital and juvenile glaucoma: Diagnostic and therapeutic implications
Universidad Complutense de Madrid. Facultad de Óptica y Optometría
Facultad de Óptica y Optometría

SWITZERLAND

Suisse Alémanique
BASEL

Non-Mendelian inheritance in retinal degenerations
Institute of Molecular and Clinical Ophthalmology Basel (IOB)

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberAnimal models of ocular disease
Institution: Information not provided - US

AUSTRIA

WIEN
ADDRESS: NOT PROVIDED - AT

CANADA

Alberta
EDMONTON

FINLAND

Finland
HELSINKI

CRMCC (cerebroretinal microangiopathy with calcifications and cysts)
HUS - Helsinki University Hospital
New Children's Hospital

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

GRAND-EST
ILLKIRCH-GRAFFENSTADEN

Funded by an IRDiRC memberRAinRARE: Integrated analyses of retinoic acid signaling to understand and treat rare form of progressive motor impairment - FR (Parner 1)
Institut de génétique et de biologie moléculaire et cellulaire - IGBMC
Département Biologie du développement et cellules souches

FRANCE

ILE-DE-FRANCE
PARIS

Funded by an IRDiRC memberAAK-INSIGHT: Aniridia - Novel therapeutic tools to treat or prevent progressive cornea opacification - FR
Hôpital Necker-Enfants Malades
Service d'Ophtalmologie enfants et adultes

FRANCE

ILE-DE-FRANCE
PARIS

Funded by an IRDiRC memberTRansdifferentiation for Autologous Corneal Cell ThERapy (TRACER)
Institut National de la Santé et de la Recherche Médicale

FRANCE

PAYS DE LA LOIRE
ANGERS

GERMANY

Baden-Württemberg
TÜBINGEN

Funded by an IRDiRC memberTargetRD: PKG and CNGC as targets for mutation-independent therapy for inherited retinal degeneration.
Department für Augenheilkunde Tübingen
Forschungsinstitut für Augenheilkunde

GERMANY

Bayern
MÜNCHEN

Funded by an IRDiRC memberENISNIP: European Network on Inherited Sensory Neuropathies and Insensitivity to Pain (partner DE)
Friedrich-Baur-Institut
Friedrich-Baur-Institut an der Neurologischen Klinik und Poliklinik

GERMANY

Bremen
BREMEN

Funded by an IRDiRC memberTargetRD: PKG and CNGC as targets for mutation-independent therapy for inherited retinal degeneration.
Biolog Life Science Institute GmbH & Co. KG
Biolog Life Science Institute

GERMANY

Hamburg
HAMBURG

Molecular and functional investigation on microphthalmia with linear skin defects (MLS) - syndrome
UKE - Universitätsklinikum Hamburg-Eppendorf
Institut für Humangenetik

GERMANY

Nordrhein-Westfalen
AACHEN

GERMANY

Rheinland-Pfalz
MAINZ

TIC-PEA: Telemedical Interdisciplinary Care for Patients with Esophageal Atresia
Universitätsmedizin Mainz
Klinik und Poliklinik für Kinderchirurgie

GERMANY

Schleswig-Holstein
LÜBECK

The role of complement in mucous membrane pemphigoid
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Dermatologie, Allergologie und Venerologie

GERMANY

Schleswig-Holstein
LÜBECK

The role of complement in mucous membrane pemphigoid
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Lübecker Institut für Experimentelle Dermatologie

ITALY

FRIULI VENEZIA GIULIA
TRIESTE

Funded by an IRDiRC memberDevelopment of Exon Specific U1 snRNA-based therapy for Familial Dysautonomia
International Centre For Genetic Engineering And Biotechnology - ICGEB
Human Molecular Genetics Laboratory

ITALY

FRIULI VENEZIA GIULIA
TRIESTE

Funded by an IRDiRC memberA novel exon-specific U1 snRNA strategy to correct splicing in Familial Dysautonomia
International Centre For Genetic Engineering And Biotechnology - ICGEB
Human Molecular Genetics Laboratory

SPAIN

Andalucía
SEVILLA

Funded by an IRDiRC memberBiomedical research and clinical innovation in hereditary retinal dystrophies: towards personalized medicine in rare diseases
Hospital Universitario Virgen del Rocío
Unidad de Medicina Maternofetal, Genética y Reproducción

SPAIN

Cataluña
BARCELONA

SPAIN

Madrid
MADRID

Genetic bases of bilateral congenital cataract
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Oftalmogenética Molecular

SPAIN

Navarra
PAMPLONA

Funded by an IRDiRC memberCorrelation between tau protein burden, neuronal dysfunction and clinical phenotype in patients with PSP: neuroimaging and histological studies
IdiSNA - Instituto de Investigación Sanitaria de Navarra
Instituto de Investigación Sanitaria de Navarra

SWEDEN

Region Stockholm
STOCKHOLM

Genetic and molecular mechanisms in familial visual impairment
Karolinska Institutet - Solna
Department of molecular medicine and surgery

SWEDEN

Region Västra Götaland
GÖTEBORG

Molecular defence against retinopathy of prematurity: screening, prevention and treatment
The Queen Silvia Children's Hospital - Sahlgrenska
Department of clinical neurosciences

UNITED STATES

California
BERKELEY

Funded by an IRDiRC memberRole of nrf2 in retinal vascularization and rop
University Of California Berkeley
Ophthalmology

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberClinical and molecular studies of malformations
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberGenetic modifiers of retinal disease
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberPathogenic role of epac1 signaling in retinopathy of prematurity
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberRetinal neurovascular patterning in preterm infants
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberInherited ocular diseases
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberPre-clinical studies of ntbc as a potential treatment for albinism
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberNeuro-ophthalmic mechanisms of disease
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberNeonatal translational
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberOcular nsaids/caffeine potentiation in oxygen-induced retinopathy
Institution: Information not provided - US

AUSTRIA

TIROL
INNSBRUCK

Epitope specificity of MOG antibodies
Medizinische Universität Innsbruck
Universitätsklinik für Neurologie

BELGIUM

OOST-VLAANDEREN
GENT

Characterisation of genes and molecular mechanisms involved in hereditary connective tissue diseases by studying transgenic animal models and human tissues
Centrum Medische Genetica Gent - Universitair Ziekenhuis Gent
Centrum Medische Genetica Gent / Centre for Medical Genetics Ghent

FRANCE

AUVERGNE-RHONE-ALPES
AUBIÈRE

Funded by an IRDiRC memberDisease-causing mutations in human mitochondrial DNA replication factors: A single-molecule study
Laboratoire de Physique de Clermont
Health, Environment and Energy

FRANCE

AUVERGNE-RHONE-ALPES
BRON

Funded by an IRDiRC memberASPECT-NMO: Measuring autoantigen-specific T cells as new diagnostic sensors and therapeutic targets in neuromyelitis optica - FR
CHU de Lyon HCL - GH Est
Service de neurologie - sclérose en plaques, pathologies de la myéline et neuro-inflammation

GERMANY

Baden-Württemberg
TÜBINGEN

Funded by an IRDiRC memberTreatOPON : Preclinical Development of Treatments for OPA1-linked Optic Neuropathies (coordinator)
Department für Augenheilkunde Tübingen
Molekulargenetisches Labor

GERMANY

Niedersachsen
OLDENBURG

Funded by an IRDiRC memberTreatOPON : Preclinical Development of Treatments for OPA1-linked Optic Neuropathies (partner no 2 )
Carl von Ossietzky Universität Oldenburg
Abteilung für Humangenetik

ITALY

CAMPANIA
NAPOLI

Funded by an IRDiRC memberModulation of miR181a/b as a new therapeutic approach for Leber hereditary optic neuropathy (LHON)
TIGEM - Telethon Institute of Genetics and Medicine
Laboratorio di Ricerca

ITALY

EMILIA ROMAGNA
PARMA

Funded by an IRDiRC memberPre-clinical identification of drugs targeting POLG disorders by using a Zebrafish/Yeast trans-species approach (ZIPPY)
Università degli Studi di Parma
Dipartimento di Scienze Chimiche, della Vita e della Sostenibilità Ambientale

ITALY

VENETO
PADOVA

Funded by an IRDiRC memberA therapeutic approach for rare genodermatoses caused by aberrant connexin hemichannels
Venetian Institute of Molecular Medicine
Centro Interdipartimentale per lo Studio dei Segnali Cellulari

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

SPAIN

Galicia
VIGO

Funded by an IRDiRC memberMolecular mechanisms in ciliopathies
Universidade de Vigo
Grupo de Enfermedades raras

SPAIN

Madrid
MADRID

Funded by an IRDiRC memberDeciphering the genetic complexity of congenital hypopituitarism
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Endocrinología Molecular

SWEDEN

Region Stockholm
STOCKHOLM

Understanding Genetic Mechanisms in Disorders and Development of Diagostic Methods
Karolinska Institutet - Solna
Department of Molecular Medicine and Surgery

UNITED KINGDOM

West Midlands
BIRMINGHAM

EURO-WABB: EURO-Rare Diabetes Project (coordination)
Birmingham Children's Hospital NHS Foundation Trust
Diabetes Unit

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberWnt signaling-mediated control of blood-retinal barrier
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberColor vision in inherited retinal degenerations
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberOcular gene therapy
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

AUSTRIA

TIROL
INNSBRUCK

Mobility_APP - Mobility in Atypical Parkinsonism: a Randomized Trial of Physiotherapy - AT
Medizinische Universität Innsbruck
Universitätsklinik für Neurologie

AUSTRIA

TIROL
INNSBRUCK

Pharmacotherapeutic potential Cav1.4 calcium channels
Universität Innsbruck
Institut für Pharmazie

BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

ODAK - Orphan Drug for Acanthamoeba Keratitis
European Commission
DG Research - Directorate General for Research

CANADA

Ontario
TORONTO

FINLAND

Finland
JYVÄSKYLÄ

Psychological well-being in families having a child with a Usher syndrome
University of Jyväskylä
Department of Psychology

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

GRAND-EST
STRASBOURG

Bardet-Biedl syndrome: new genes identification and biological characterization of a new gene BBS10
Faculté de médecine de Strasbourg - Louis Pasteur
Laboratoire de génétique médicale - Unité Inserm U1112

FRANCE

ILE-DE-FRANCE
EVRY

Funded by an IRDiRC memberRetinal tissue engineering from human pluripotent stem cells for the treatment of retinal dystrophies
GENOPOLE - Campus 1
I-Stem - Institut des cellules Souches pour le Traitement et l'Etude des maladies Monogéniques

FRANCE

ILE-DE-FRANCE
PARIS

Animal model creation of Stargardt disease by interfering RNA
Hôpital Necker-Enfants Malades
Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement

FRANCE

ILE-DE-FRANCE
PARIS

Decoding the genetic of Leber congenital amaurosis and progression of the therapeutic approach by exon skipping of the major mutation of the CEP290 gene
Hôpital Necker-Enfants Malades
Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement

FRANCE

ILE-DE-FRANCE
PARIS

Funded by an IRDiRC memberGenetic deciphering of new syndrome associating early and severe retinal dystrophy and sensorineural hearing loss
Hôpital Necker-Enfants Malades
Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement

FRANCE

ILE-DE-FRANCE
PARIS

Hereditary dystrophies of retina: physiopathologic and clinic research
Institut de la Vision
Centre d'Investigation Clinique (CIC) de l'hôpital des Quinze-Vingts

FRANCE

ILE-DE-FRANCE
PARIS

Hereditary dystrophies of retina: pharmacological research and new therapeutics development (cell and gene therapies)
Institut de la Vision
Centre d'Investigation Clinique (CIC) de l'hôpital des Quinze-Vingts

FRANCE

ILE-DE-FRANCE
PARIS

FRANCE

ILE-DE-FRANCE
PARIS

Funded by an IRDiRC memberNon viral gene editing for autosomal dominant retinitis pigmentosa
Institut de la Vision
Centre de Recherche Institut de la Vision

FRANCE

OCCITANIE
MONTPELLIER

Genetics of autosomal recessive retinitis pigmentosa and of macular dystrophies
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

FRANCE

OCCITANIE
MONTPELLIER

Dominant autosomic retinitis pigmentosa: prevalence of known genes and identification of new ones
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

FRANCE

OCCITANIE
MONTPELLIER

Funded by an IRDiRC memberGET-READY: Genetic therapy for EYS- and USH2A-associated retinal disease - FR
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

FRANCE

PAYS DE LA LOIRE
NANTES

FRANCE

PAYS DE LA LOIRE
NANTES

Evaluation of the immune response in Briards dogs RPE65 -/- treated with gene therapy
CHU de Nantes - Hôtel Dieu
Vecteurs viraux et transfert de genes in vivo

GERMANY

Baden-Württemberg
TÜBINGEN

Genetics and pathophysiology of autosomal recessive achromatopsia
Department für Augenheilkunde Tübingen
Molekulargenetisches Labor

GERMANY

Baden-Württemberg
TÜBINGEN

GERMANY

Baden-Württemberg
TÜBINGEN

GERMANY

Baden-Württemberg
TÜBINGEN

GERMANY

Baden-Württemberg
TÜBINGEN

Rate of Progression in USH2A Related Retinal Degeneration
Department für Augenheilkunde Tübingen
Universitäts-Augenklinik

GERMANY

Berlin
BERLIN

Identification of molecular mechanisms acting at the jObes1 locus in the Berlin Fat Mouse with effect on juvenile fat deposition
Humboldt-Universität zu Berlin
Fachbereich Züchtungsbiologie und molekulare Genetik

GERMANY

Hessen
GIEßEN

Natural History Study of CEP290-Related Retinal Degeneration
Augenklinik des UKGM am Standort Gießen
Klinik und Poliklinik für Augenheilkunde

GERMANY

Rheinland-Pfalz
MAINZ

Characterization of the retinal phenotype and pre-clinical evaluation of AAV mediated gene augmentation in the transgenic USH1C pig
Institut für Zoologie der Universität Mainz
Institut für Zoologie - Abt. I - AG Wolfrum

GERMANY

Rheinland-Pfalz
MAINZ

IRELAND

County Dublin
DUBLIN

Inherited childhood sight loss: understanding visual cycle biology to develop treatments
University College Dublin
UCD Conway Institute of Biomolecular and Biomedical Research

ITALY

CAMPANIA
NAPOLI

Funded by an IRDiRC memberDesigning therapeutic strategies to rescue epidermal defects in AEC syndrome
Biotecnologie Avanzate Srl
Ceinge Biotecnologie Avanzate SCarl

ITALY

CAMPANIA
NAPOLI

Funded by an IRDiRC memberA mutation-independent genome editing approach for ABCA4 gene correction in photoreceptors
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

ITALY

EMILIA ROMAGNA
MODENA

Funded by an IRDiRC memberPigment Epithelium-derived Factor (PEDF) peptides as therapeutic agents for inherited retinal degeneration
Università degli Studi di Modena e Reggio Emilia
Laboratorio Eye Diseases

ITALY

LAZIO
ROMA

Funded by an IRDiRC memberUnderstanding molecular basis for Inherited Retinal Diseases (IRDs)
ISS - Istituto Superiore di Sanità
Centro Nazionale per la Ricerca e la Valutazione preclinica e clinica dei Farmaci

ITALY

LIGURIA
GENOVA

Funded by an IRDiRC memberDevelopment and application of optoneural prosthetic devices as a therapeutic approach for Retinitis pigmentosa
IRCCS Ospedale Policlinico San Martino - IST - DIMI
Dipartimento di Medicina Sperimentale

ITALY

SICILIA
ACI S. ANTONIO

ODAK - Orphan Drug for Acanthamoeba Keratitis
Società Industria Farmaceutica Italiana S.p.A.(S.I.F.I.)

ITALY

TOSCANA
PISA

ITALY

VENETO
VERONA

Funded by an IRDiRC memberCone dystrophies and retinal degeneration from protein structures to biological networks. Toward the design of therapeutic molecules
Università degli Studi di Verona
Dipartimento di Neuroscienze, Biomedicina e Movimento

KOREA, REPUBLIC OF

KOREA, REPUBLIC OF
KOREA

KOREA, REPUBLIC OF

KOREA, REPUBLIC OF
SEOUL

NETHERLANDS

Gelderland
NIJMEGEN

Identification of the genetic causes of inherited retinal dystrophies
Radboudumc - Radboud universitair medisch centrum
Afdeling Genetica

NETHERLANDS

Gelderland
NIJMEGEN

TREATCilia: Novel Therapeutic Avenues for dynein-related Ciliopathies
Radboudumc - Radboud universitair medisch centrum
Afdeling Genetica

NETHERLANDS

Gelderland
NIJMEGEN

Identification of the genetic causes of inherited retinal dystrophies
Radboudumc - Radboud universitair medisch centrum
Afdeling Oogheelkunde

NETHERLANDS

Noord-Holland
AMSTERDAM

Funded by an IRDiRC memberA retinal origin of congenital nystagmus
Nederlands Herseninstituut

SPAIN

Cataluña
BARCELONA

Mitochondrial and metabolic dynamics in a retinitis pigmentosa model. A new therapeutic approach?
Universitat de Barcelona. Facultat de Biologia
Departamento de Genética, Biología y Estadística

SPAIN

Comunidad Valenciana
VALENCIA

Funded by an IRDiRC memberDevelopment of anti-inflammatory nanotherapies for retinitis pigmentosa
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en biomedicina molecular, celular y genómica

SPAIN

Comunidad Valenciana
VALENCIA

Funded by an IRDiRC memberRetinal Dystrophies. Usher syndrome: genomic, cellular, functional and bioinformatic approaches to accelerate their diagnosis and treatment and to measure their impact
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en biomedicina molecular, celular y genómica

SPAIN

Madrid
MADRID

Lost heritability in sRP and LCA cases. Search for CNVs and new variants
Fundación Jiménez Díaz
Área de Genética y Genómica

SPAIN

Madrid
MADRID

SWITZERLAND

Suisse Alémanique
BASEL

Therapeutic RNA base editing for Stargardt disease
Institute of Molecular and Clinical Ophthalmology Basel (IOB)

SWITZERLAND

Suisse Alémanique
BASEL

Single-cell genomic reconstruction of retina developmental disorders
Institute of Molecular and Clinical Ophthalmology Basel (IOB)

SWITZERLAND

Suisse Alémanique
ZÜRICH

UNITED KINGDOM

Tayside
DUNDEE

UNITED STATES

California
BERKELEY

UNITED STATES

California
SAN FRANCISCO

Funded by an IRDiRC memberCortical structure and function in blindness and following restored vision
University Of California, San Francisco
Neurology

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberPreclinical innovation
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberDrug repurposing screening for rare and neglected diseases
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberGenetic epidemiology of complex diseases
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberThe role of complement in recessive stargardt disease
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberLarge animal therapy studies
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberCilium-associated structures in rod cells
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberCone rescue in retinitis pigmentosa
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberHeparanase in herpetic keratitis
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberMechanism of death of bystander retinal cells during mcmv infection
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberFunction of c8orf37 in photoreceptors
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberImaging the functional biomarker of photoreceptors
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberModulation of lipid bisretinoids clearance with beta-cyclodextrins
Institution: Information not provided - US

UNITED STATES

Washington
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Funded by an IRDiRC memberNoninvasive assessment of pathophysiology in retinitis pigmentosa
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberRole of microglia in retinitis pigementosa
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberThe role of arap1 in retinal photoreceptor homeostasis
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
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Funded by an IRDiRC memberDisease mechanism and therapies for retinal degeneration
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberHuman rhodopsin-adrp studies
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberInterventional approaches for restoring vision
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberLarge animal (dog) experimental support module
Institution: Information not provided - US

UNITED STATES

Washington
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Funded by an IRDiRC memberMechanisms of retinal degeneration in inherited diseases
Institution: Information not provided - US

UNITED STATES

Washington
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Funded by an IRDiRC memberMolecular genetics of early eye development
Institution: Information not provided - US

UNITED STATES

Washington
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Funded by an IRDiRC memberThe focal electro-oculogram in macular disease
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberRetinal gene therapy
Institution: Information not provided - US

UNITED STATES

Washington
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Funded by an IRDiRC memberPreclinical safety studies
Institution: Information not provided - US

UNITED STATES

Washington
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Funded by an IRDiRC memberRetinal aging and inherited neurodegenerative diseases
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberNeuroendocrine regulation of metabolism and neurocognition
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberPhysiology; psychology; and genetics of obesity
Institution: Information not provided - US

UNITED STATES

Washington
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Funded by an IRDiRC memberReciprocal signaling in synaptogenesis
Institution: Information not provided - US

GERMANY

Bayern
REGENSBURG

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberTherapeutic genome editing to treat best disease
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberNatural history and genetic studies of usher syndrome
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Multicentric Research projects