09:00 Registration Panel I – Introduction to the topic Moderator: Andres Metspalu, EGC, University of Tartu   09:25-09:30 Introduction of ePerMed project, Merike Leego 09:30-10:30 Health political situation and attitudes in Estonia, Finland and Switzerland 9.30 Estonia – Margus Lember, Tartu University Hospital 9.50 Finland – Elisabeth Widen, FIMM, University of Helsinki 10.10 Switzerland – Alexandre Reymond, CIG, University of Lausanne 10:30-11:10 Lili Milani, EGCUT, Estonia - Introduction to human genetics and pharmacogenomics 11:10-11:25 Coffee break Panel II - Rare and developmental diseases Moderator: Sander Pajusalu, Tartu University Hospital   11:25-11:50 Stylianos Antonarakis, University of Geneva Medical School - TBA 11:50-12:15 Alexandre Reymond/Katrin Männik, CIG, University of Lausanne – Rare CNVs and genomic disorders in general population 12:15-12:40 Thomas Meitinger, Klinikum rechts der Isar, Technische Universität München - Monogenic variation outside of the coding region 12:40-13:05 Bogdan Draganski, LREN, Lausanne University Hospital – The link between human brain and genes – how can we solve the mystery? 13:05-14:05 Lunch Panel III - Common diseases Moderator: Elin Org, EGC, University of Tartu   14:05-14:30 Taru Tukiainen, FIMM, University of Helsinki - Insights into obesity through transcriptome sequencing 14:30-14:55 Jacques Fellay, École polytechnique fédérale de Lausanne – Human genetics of infectious disease 14:55-15:20 Elisabeth Widen, FIMM, University of Helsinki - Utilizing genome information to predict cardiovascular disease 15:20-16:00 Apero (snacks and drinks) To provide an opportunity to clinical community to express their opinion and to ask questions from speakers in informal atmosphere.