Posters
Please note that poster authors are not exempt from paying the full registration fees to attend ECRD 2020.
Poster authors will be able to interact with the audience via the platform chat and messaging feature. No oral presentation will be required by poster authors.
Posters will be published in a dedicated posters section reachable from the main Lobby. They will be divided into themes and they will be listed including the name of the presenting authors, so that participants can contact them at any time. Push notifications will encourage all participants to visit the posters area at dedicated times (see our programme at a glace). All posters will also be included, together with the names of the authors, in the final full conference programme.
We encourage all posters authors to attend this virtual tour to familiarize yourself with the online platform.
Poster themes
Theme 1:
Diagnosis of RD patients: from research to care
Session 0101
Olaf Riess – State of the art: Diagnosing Genetic Diseases
Isabelle Bros – Video presentation
Alessandra Renieri – Exome Diagnostic rates
Lauren Roberts – Keeping patients at the heart of diagnostic advancements
Session 0102
Diego Ardigo – Overview of the major bottlenecks in translating research
Daniel Lewi – How to get research done on your rare disease
Alison Metcalfe – How to develop and adapt a co-design model to design interventions for communicating genetic diagnoses
Lucia Monaco – How to make exploitable research?
Jon Timmis – Crack-IT Challenges from an Industry Perspective
Session 0103
Dimitrios Athanasiou – Megafunds: The concept
Heather Etchevers – The challenges and opportunities of crowdfunding rare disease research
Majid Jafar – How can a non-profit advance research into a specific rare disease?
Daria Julkowska – Innovative funding partnerships: challenges & opportunities
Session 0104
Virginie Bros-Facer – Why and how can patients be trained in scientific research to become stronger partners?
Orion Buske – Building tools to empower patient experts
Sean Kelly – “Together we are stronger” Patient associations joining forces to fund rare disease research
Session 0105
Heidi Howard – Genome Editing Brief Overview
Theme 2:
Rights to Health & Inclusion in Society
Session 0101
Olaf Riess – State of the art: Diagnosing Genetic Diseases
Isabelle Bros – Video presentation
Alessandra Renieri – Exome Diagnostic rates
Lauren Roberts – Keeping patients at the heart of diagnostic advancements
Session 0102
Diego Ardigo – Overview of the major bottlenecks in translating research
Daniel Lewi – How to get research done on your rare disease
Alison Metcalfe – How to develop and adapt a co-design model to design interventions for communicating genetic diagnoses
Lucia Monaco – How to make exploitable research?
Jon Timmis – Crack-IT Challenges from an Industry Perspective
Session 0103
Dimitrios Athanasiou – Megafunds: The concept
Heather Etchevers – The challenges and opportunities of crowdfunding rare disease research
Majid Jafar – How can a non-profit advance research into a specific rare disease?
Daria Julkowska – Innovative funding partnerships: challenges & opportunities
Session 0104
Virginie Bros-Facer – Why and how can patients be trained in scientific research to become stronger partners?
Orion Buske – Building tools to empower patient experts
Sean Kelly – “Together we are stronger” Patient associations joining forces to fund rare disease research
Session 0105
Heidi Howard – Genome Editing Brief Overview
Theme 3:
Share, Care Rare 2030
Session 0101
Olaf Riess – State of the art: Diagnosing Genetic Diseases
Isabelle Bros – Video presentation
Alessandra Renieri – Exome Diagnostic rates
Lauren Roberts – Keeping patients at the heart of diagnostic advancements
Session 0102
Diego Ardigo – Overview of the major bottlenecks in translating research
Daniel Lewi – How to get research done on your rare disease
Alison Metcalfe – How to develop and adapt a co-design model to design interventions for communicating genetic diagnoses
Lucia Monaco – How to make exploitable research?
Jon Timmis – Crack-IT Challenges from an Industry Perspective
Session 0103
Dimitrios Athanasiou – Megafunds: The concept
Heather Etchevers – The challenges and opportunities of crowdfunding rare disease research
Majid Jafar – How can a non-profit advance research into a specific rare disease?
Daria Julkowska – Innovative funding partnerships: challenges & opportunities
Session 0104
Virginie Bros-Facer – Why and how can patients be trained in scientific research to become stronger partners?
Orion Buske – Building tools to empower patient experts
Sean Kelly – “Together we are stronger” Patient associations joining forces to fund rare disease research
Session 0105
Heidi Howard – Genome Editing Brief Overview
Theme 4:
When therapies meet the needs – enabling a patient-centric approach to therapeutic development
Session 0101
Olaf Riess – State of the art: Diagnosing Genetic Diseases
Isabelle Bros – Video presentation
Alessandra Renieri – Exome Diagnostic rates
Lauren Roberts – Keeping patients at the heart of diagnostic advancements
Session 0102
Diego Ardigo – Overview of the major bottlenecks in translating research
Daniel Lewi – How to get research done on your rare disease
Alison Metcalfe – How to develop and adapt a co-design model to design interventions for communicating genetic diagnoses
Lucia Monaco – How to make exploitable research?
Jon Timmis – Crack-IT Challenges from an Industry Perspective
Session 0103
Dimitrios Athanasiou – Megafunds: The concept
Heather Etchevers – The challenges and opportunities of crowdfunding rare disease research
Majid Jafar – How can a non-profit advance research into a specific rare disease?
Daria Julkowska – Innovative funding partnerships: challenges & opportunities
Session 0104
Virginie Bros-Facer – Why and how can patients be trained in scientific research to become stronger partners?
Orion Buske – Building tools to empower patient experts
Sean Kelly – “Together we are stronger” Patient associations joining forces to fund rare disease research
Session 0105
Heidi Howard – Genome Editing Brief Overview
Theme 5:
Assessment & Appraisal
Session 0101
Olaf Riess – State of the art: Diagnosing Genetic Diseases
Isabelle Bros – Video presentation
Alessandra Renieri – Exome Diagnostic rates
Lauren Roberts – Keeping patients at the heart of diagnostic advancements
Session 0102
Diego Ardigo – Overview of the major bottlenecks in translating research
Daniel Lewi – How to get research done on your rare disease
Alison Metcalfe – How to develop and adapt a co-design model to design interventions for communicating genetic diagnoses
Lucia Monaco – How to make exploitable research?
Jon Timmis – Crack-IT Challenges from an Industry Perspective
Session 0103
Dimitrios Athanasiou – Megafunds: The concept
Heather Etchevers – The challenges and opportunities of crowdfunding rare disease research
Majid Jafar – How can a non-profit advance research into a specific rare disease?
Daria Julkowska – Innovative funding partnerships: challenges & opportunities
Session 0104
Virginie Bros-Facer – Why and how can patients be trained in scientific research to become stronger partners?
Orion Buske – Building tools to empower patient experts
Sean Kelly – “Together we are stronger” Patient associations joining forces to fund rare disease research
Session 0105
Heidi Howard – Genome Editing Brief Overview
Theme 6:
Innovation & Technology
Session 0101
Olaf Riess – State of the art: Diagnosing Genetic Diseases
Isabelle Bros – Video presentation
Alessandra Renieri – Exome Diagnostic rates
Lauren Roberts – Keeping patients at the heart of diagnostic advancements
Session 0102
Diego Ardigo – Overview of the major bottlenecks in translating research
Daniel Lewi – How to get research done on your rare disease
Alison Metcalfe – How to develop and adapt a co-design model to design interventions for communicating genetic diagnoses
Lucia Monaco – How to make exploitable research?
Jon Timmis – Crack-IT Challenges from an Industry Perspective
Session 0103
Dimitrios Athanasiou – Megafunds: The concept
Heather Etchevers – The challenges and opportunities of crowdfunding rare disease research
Majid Jafar – How can a non-profit advance research into a specific rare disease?
Daria Julkowska – Innovative funding partnerships: challenges & opportunities
Session 0104
Virginie Bros-Facer – Why and how can patients be trained in scientific research to become stronger partners?
Orion Buske – Building tools to empower patient experts
Sean Kelly – “Together we are stronger” Patient associations joining forces to fund rare disease research
Session 0105
Heidi Howard – Genome Editing Brief Overview
Theme 7:
Rare Disease Patient Groups Innovations
Session 0101
Olaf Riess – State of the art: Diagnosing Genetic Diseases
Isabelle Bros – Video presentation
Alessandra Renieri – Exome Diagnostic rates
Lauren Roberts – Keeping patients at the heart of diagnostic advancements
Session 0102
Diego Ardigo – Overview of the major bottlenecks in translating research
Daniel Lewi – How to get research done on your rare disease
Alison Metcalfe – How to develop and adapt a co-design model to design interventions for communicating genetic diagnoses
Lucia Monaco – How to make exploitable research?
Jon Timmis – Crack-IT Challenges from an Industry Perspective
Session 0103
Dimitrios Athanasiou – Megafunds: The concept
Heather Etchevers – The challenges and opportunities of crowdfunding rare disease research
Majid Jafar – How can a non-profit advance research into a specific rare disease?
Daria Julkowska – Innovative funding partnerships: challenges & opportunities
Session 0104
Virginie Bros-Facer – Why and how can patients be trained in scientific research to become stronger partners?
Orion Buske – Building tools to empower patient experts
Sean Kelly – “Together we are stronger” Patient associations joining forces to fund rare disease research
Session 0105
Heidi Howard – Genome Editing Brief Overview
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