Working Group – Registries

Date: Sunday 23 September 2018
Time: 16:00 – 18:30

Time Session
16:00 – 17:00 Population Based Registries

Chair: Mark Jenkins

16:00 – 16:10
  • Australian/New Zealand registries – Mark Jenkins
16:10 – 16:20
  • N60 – Lynch syndrome registries in South America – Mev D Valentin
16:20 – 16:30
  • N73 – The Danish HNPCC – Registry from 1991 – 2018 – Inge Bernstein
16:30 – 16:40
  • N01 – The German HNPCC Consortium: aims, structure, methods and data – Christoph Engel
16:40 – 16:50
  • The Finnish Registry – Toni Seppälä
16:50 – 17:00
  • Discussion
17:00 – 18:00 International Research Registries

Chair: Pål Møller

17:00 – 17:15
  • C4CMMRD (5 minutes structure, 10 minutes results) – Chrystelle Colas
17:15 – 17:30
  • CCFR (5 minutes structure, 10 minutes results) – Mark Jenkins
17:30 – 17:45
  • N09: Worldwide study of cancer risks for lynch syndrome: International Mismatch Repair Consortium (IMRC) (5 minutes structure, 10 minutes results) – Mark Jenkins
17:45 – 18:00
  • N39: The Prospective Lynch Syndrome Database – Pål Møller, Toni Seppälä, Julian Sampson, Mev D Valentin
18:00 – 18:15
  • Discussion
18:15 – 19:00 Gene-Specific Variant Databases

Chair: Finlay Macrae

18:15 – 18:30
  • MMR variant database – Finlay Macrae
18:30 – 18:40
  • APC – Stefan Aretz
18:40 – 18:50
  • SMAD4/BMPR1A – Karl Heinimann
18:50 – 19:00
  • Discussion

 

Submit a registries poster for your country!

We would like to know more about the situation for hereditary disease in your country!

Please share this information with us and it is our aim to receive this information from 50 countries. There will be a special poster exhibition and we invite you to use the abstract template provided here.

We will inform you of acceptance or get back to you with questions.

Deadline for registry posters is September 1, 2018.

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