1st EJP RD Joint Transnational Call for Rare Diseases Research Project (JTC 2019)
Basic Information
The ERA-Net E-Rare has successfully implemented ten Joint Transnational Calls for rare disease research projects since 2006. This effort continues in the framework of the European Joint Programme on Rare Diseases (EJP RD) that has been established to further help in coordinating the research efforts of European, Associated and non-European countries in the field of rare diseases and implement the objectives of the International Rare Disease Research Consortium (IRDiRC).
| Network | EJP RD | ||||||||
| Website | https://www.ejprarediseases.org/index.php/jtc2019-closed/ | ||||||||
| Aim of the joint call | The aim of the call is to enable scientists in different countries to build an effective collaboration on a common interdisciplinary research project based on complementarities and sharing of expertise, with a clear benefit for patients. Topic: Research projects to accelerate diagnosis and/or explore disease progression and mechanisms of rare diseases. | ||||||||
| Type of joint call | Two Stages - Call with pre-proposals and full proposals submissions | ||||||||
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| Is call co-funded? | Yes | ||||||||
| Call follow up funding | n/a | ||||||||
| Call reasons | n/a | ||||||||
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| Type of research |
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| Participating networks | n/a |
Organisations Participating
Funded Projects
| Acronym | Title | Start | End | No. partners |
|---|---|---|---|---|
| ALEXANDER | The astrocyte nanofilament system in Alexander disease – fro... | 6 | ||
| AspecT-NMO | Measuring autoantigen-specific T cells as new diagnostic sen... | 6 | ||
| DevDBA | Ontogeny as a critical determinant of DBA sensitivity in red... | 6 | ||
| ENISNIP | European Network on Inherited Sensory Neuropathies and Insen... | 7 | ||
| EurDyscover | Pathophysiology of dystonia - role of gene-environment inter... | 6 | ||
| FAIRVASC | FAIRVASC - building registry interoperability to inform clin... | 8 | ||
| FIGHT-CNNM2 | For Improving diagnostics and Grasping the disease mechanism... | 6 | ||
| GENOMIT | Title: Mitochondrial Disorders: from a global registry to me... | 8 | ||
| IDOLS-G | Improved diagnostic output in large sarcomeric genes | 8 | ||
| LQTS-NEXT | To the NEXT level of risk prediction in patients with Long Q... | 5 | ||
| MYOCITY | A multidimensional single-cell approach to understand muscle... | 5 | ||
| NG4Leuko | Exploring neuron-glia interactions in leukodystrophies using... | 5 | ||
| NSEuroNet | European network on Noonan syndrome and related disorders | 8 | ||
| PROGERIA | The rarest of the rare – exploring non-coding RNA in the dis... | 5 | ||
| PROSPAX | PROSPAX: an integrated multimodal progression chart in spast... | 8 | ||
| PhysPath-KS | Understanding the pathophysiology of Keutel Syndrome: A path... | 4 | ||
| PredACTINg | Predicting the clinical outcome of non-muscle actinopathies | 5 | ||
| RARE-ILD | RAISING DIAGNOSTIC ACCURACY AND THERAPEUTIC PERSPECTIVES IN ... | 7 | ||
| RiboEurope | The European Ribosomopathy Consortium | 8 | ||
| Solve-RET | Solving missing heritability in inherited retinal diseases u... | 8 | ||
| TARID | Thymic Abnormalities in Rare Immunological Diseases | 6 | ||
| URGENT | Unveiling the Role of Glutamate in dopaminE traNspoTer defic... | 5 |