Summary

Inclusion of individual's genetic variation data (e.g. specific genetic test results, SNPs, whole genome sequencing) in the EHR is becoming increasingly important for Personalised/Precision Medicine.

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• Amnon Shabo (Shvo) (Philips)

• Gianluigi Zanetti (CRS4 - Italy)

• Patrik Georgii-Hemming (Karolinska)

• Navin Ramachandran (UCL/NHS - OpenCancer)
  

• Wai Keong Wong (UCL/NHS - OpenCancer)
  

• Ian McNicoll (openEHR co-chair)

• Koray Atalag (openEHR, Univ. of Auckland)

• Thomas Beale (openEHR)
  

• Diego Bosca (VeraTech)

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Clinical modelling group

• Cecilia Mascia (CRS4)
• Paolo Uva (CRS4)
• Francesca Frexia (CRS4)
• Gideon Giacomelli (HiGHmed)
• Christina Jaeger-Schmidt (HiGHmed)
• Simon Schumacher (HiGHmed)
• Florian Kärcher (HiGHmed)
• Priscila Maranhão (CINTESIS)
• Gustavo Bacelar-Silva (CINTESIS)
• Duarte Gonçalves-Ferreira (CINTESIS)
• Ricardo Correia (CINTESIS)
• Sjur Gjerald (BigMed)
• Bjørn Næss (BigMed/DIPS)
• Anca Heyd (DIPS)
• Heather Leslie (openEHR clinical program)
• Vebjørn Arntzen (openEHR clinical program)
• John Tore Valand (openEHR clinical program)
• Silje Ljosland Bakke (openEHR clinical program)

 Related Work / Resources

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