SOLVE-RD - Solving the unsolved rare diseases


The main ambitions of the Solve-RD proposal are (i) to solve large numbers of RD, for which a molecular cause is not known yet, by sophisticated combined Omics approaches, and (ii) to improve diagnostics of RD patients through a “genetic knowledge web”. Solve-RD will pursue a clear visionary and integrated “beyond the exome” approach. The entire Solve-RD proposal has been motivated, designed and put together by a core group of four ERNs, but also reaches out to all 24 ERNs.
To tackle diseases which are unsolved by applying cutting edge strategies, Solve-RD has thus formed a consortium that comprises (i) leading clinicians, geneticists and translational researchers of these ERNs, (ii) RD research and diagnostic infrastructures, (iii) patient organisations, as well as (iv) leading experts in the field of -omics technologies, bioinformatics and knowledge management. Solve-RD will deliver 7 main implementation steps: (i) Collect Phenotypes, (ii) New phenotype patterns, (iii) Re-analyse exomes / genomes, (iv) Novel molecular strategies, (v) Functional analysis, (iv) Clinical utility and (vii) Towards therapy. For analysis Solve-RD will apply data driven and expert driven approaches. We anticipate to increase diagnostic yield from 19.000 unsolved exomes/genomes by about 3-5%. Cohort specific innovative -omis strategies will be
pursued, also addressing cost-effective issues. Analysis of more than 800 patients with highly peculiar (ultra-rare) phenotypes will highly increase the chance to find novel disease genes and novel disease mechanisms. We anticipate to solve more than 2.000 cases. Finding further matching patients will be secured by newly developed matchmaking approaches and by screening using MIPs technology in the more than 20.000 unclassified patients of the ERNs. For the first time in Europe we will also implement a novel brokerage structure connecting clinicians, gene discoverer and basic researcher to quickly verify novel genes and disease mechanisms.

eu_flag.jpgThis project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 779257

Project details

Scientific responsability: Alessandra Ferlini

Funding source: HORIZON 2020

Call: H2020-HEALTH - SC1-2017-RTD
Start date 1/01/2018 - end date 31/12/2022
Eu contribution: 15.361.621 €
Eu contribution to UniFe: 56.250 €


  • Eberhard Karls Universitaet Tuebingen (Germany), Coordinator
  • Stichting Katholieke Universiteit (Netherlands)
  • University of Leicester (United Kingdom)
  • University of Newcastle upon Tyne (United Kingdom)
  • Central Manchester University Hospitals NHS Foundation Trust (United Kingdom)
  • Centre Hospitalier Reg Universitaire Dijon (France)
  • Fundacio Centre de Regulacio Genomica (Spain)
  • EURORDIS – European Organisation for Rare Diseases Association (France)
  • Institut National de la Sante et de la Recherche Medicale (France)
  • Univerzita Karlova (Czech Republic)
  • European Molecular Biology Laboratory (United Kingdom)
  • The Jackson Laboratory Non Profit Corporation (USA)
  • King’s College London (United Kingdom)
  • University College London (United Kingdom)
  • Universiteit Antwerpen (Belgium)
  • Universita degli Studi della Campania Luigi Vanvitelli (Italy)
  • Universita degli Studi di Ferrara (Italy)
  • Universitaetsklinikum Bonn (Germany)
  • Instituto de Patologia Eimunologia Molecular da Universidade do Porto (Portugal)
  • Academisch Ziekenhuis Groningen (Netherlands)
  • Charite – Universitaetsmedizin Berlin, Charité (Germany);