Share4Rare, in collaboration with the World Duchenne Organization and the John Walton Muscular Dystrophy Research Centre, is hosting a webinar for families who want to join the Share4Rare research pilot. This research project focuses on how being or caring for a person with neuromuscular diseases (NMD) affects learning & work opportunities. The event will take […]
Read MoreAs part of Solve-RD, Solving the unsolved rare diseases, a European project H2020 on genetic research, the Health Economics Team of the Economics Laboratory of Dijon (University of Burgundy) organises the “European Conference on the Diffusion of Genomic Medicine: Health Economics & Policy” from May 26th to 28th, 2021. You will find the programme here. Registration is open here. More information: https://ecogenomics.sciencesconf.org/
Read MoreRegistration are open until 30 April 2021 (deadline for Early Bird registration) Abstract Submission are open until 31 March 2021 The Virtual Scientific CDG Symposium 2021 will cover all aspects of Congenital Disorders of Glycosylation and related disorders, including the discovery of novel types, the study of fundamental aspects of glycosylation, better understanding of the […]
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Heritable human genome editing has been proposed as a means of helping parents avoid passing genetic diseases to future generations. But can heritable human genome editing be used safely? On February 26, 2021 at 9:00 am EST (2 pm GMT / 3pm CET / 10 pm CST), join members of the International Commission on the […]
Read More1- 2 March 2021 ONLINE The 1st International Conference on Rare Diseases “Building a Pathway from Diagnosis to Access” recognises that the next decade holds great potential for improvement and that while we cannot predict the future, we all have a role in preparing for it. As the EU shapes its future regulations, strategies and […]
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Pr. Gert Matthijs, partner of EJP RD, is part of the Scientific Programme Committee of this year’s Curating the Clinical Genome Conference (12-14 May 2021). The conference will provide an ideal opportunity for the clinical genomics and biodata community to share best practices for the clinical use of genomic data and the consensus generation of […]
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