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RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases

Although individually uncommon, rare diseases (RDs) collectively affect 6–8% of the population. The unmet need of the rare disease community was recognized by the European Commission which in 2012 funded three flagship projects, RD-Connect, NeurOmics, and EURenOmics, to help move the field forward w...

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Autores principales: Lochmüller, Hanns, Badowska, Dorota M., Thompson, Rachel, Knoers, Nine V., Aartsma-Rus, Annemieke, Gut, Ivo, Wood, Libby, Harmuth, Tina, Durudas, Andre, Graessner, Holm, Schaefer, Franz, Riess, Olaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974013/
https://www.ncbi.nlm.nih.gov/pubmed/29487416
http://dx.doi.org/10.1038/s41431-018-0115-5
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author Lochmüller, Hanns
Badowska, Dorota M.
Thompson, Rachel
Knoers, Nine V.
Aartsma-Rus, Annemieke
Gut, Ivo
Wood, Libby
Harmuth, Tina
Durudas, Andre
Graessner, Holm
Schaefer, Franz
Riess, Olaf
author_facet Lochmüller, Hanns
Badowska, Dorota M.
Thompson, Rachel
Knoers, Nine V.
Aartsma-Rus, Annemieke
Gut, Ivo
Wood, Libby
Harmuth, Tina
Durudas, Andre
Graessner, Holm
Schaefer, Franz
Riess, Olaf
author_sort Lochmüller, Hanns
collection PubMed
description Although individually uncommon, rare diseases (RDs) collectively affect 6–8% of the population. The unmet need of the rare disease community was recognized by the European Commission which in 2012 funded three flagship projects, RD-Connect, NeurOmics, and EURenOmics, to help move the field forward with the ambition of advancing -omics research and data sharing at their core in line with the goals of IRDiRC (International Rare Disease Research Consortium). NeurOmics and EURenOmics generate -omics data and improve diagnosis and therapy in rare renal and neurological diseases, with RD-Connect developing an infrastructure to facilitate the sharing, systematic integration and analysis of these data. Here, we summarize the achievements of these three projects, their impact on the RD community and their vision for the future. We also report from the Joint Outreach Day organized by the three projects on the 3rd of May 2017 in Berlin. The workshop stimulated an open, multi-stakeholder discussion on the challenges of the rare diseases, and highlighted the cross-project cooperation and the common goal: the use of innovative genomic technologies in rare disease research.
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spelling pubmed-59740132018-06-20 RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases Lochmüller, Hanns Badowska, Dorota M. Thompson, Rachel Knoers, Nine V. Aartsma-Rus, Annemieke Gut, Ivo Wood, Libby Harmuth, Tina Durudas, Andre Graessner, Holm Schaefer, Franz Riess, Olaf Eur J Hum Genet Review Article Although individually uncommon, rare diseases (RDs) collectively affect 6–8% of the population. The unmet need of the rare disease community was recognized by the European Commission which in 2012 funded three flagship projects, RD-Connect, NeurOmics, and EURenOmics, to help move the field forward with the ambition of advancing -omics research and data sharing at their core in line with the goals of IRDiRC (International Rare Disease Research Consortium). NeurOmics and EURenOmics generate -omics data and improve diagnosis and therapy in rare renal and neurological diseases, with RD-Connect developing an infrastructure to facilitate the sharing, systematic integration and analysis of these data. Here, we summarize the achievements of these three projects, their impact on the RD community and their vision for the future. We also report from the Joint Outreach Day organized by the three projects on the 3rd of May 2017 in Berlin. The workshop stimulated an open, multi-stakeholder discussion on the challenges of the rare diseases, and highlighted the cross-project cooperation and the common goal: the use of innovative genomic technologies in rare disease research. Springer International Publishing 2018-02-27 2018-06 /pmc/articles/PMC5974013/ /pubmed/29487416 http://dx.doi.org/10.1038/s41431-018-0115-5 Text en © European Society of Human Genetics 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Lochmüller, Hanns
Badowska, Dorota M.
Thompson, Rachel
Knoers, Nine V.
Aartsma-Rus, Annemieke
Gut, Ivo
Wood, Libby
Harmuth, Tina
Durudas, Andre
Graessner, Holm
Schaefer, Franz
Riess, Olaf
RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases
title RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases
title_full RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases
title_fullStr RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases
title_full_unstemmed RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases
title_short RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases
title_sort rd-connect, neuromics and eurenomics: collaborative european initiative for rare diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974013/
https://www.ncbi.nlm.nih.gov/pubmed/29487416
http://dx.doi.org/10.1038/s41431-018-0115-5
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