2017 October 11 dr. Violeta Mikštienė at the "Latest News of Genome Editing Research" conference gave “Editing a Human Genome in Medicine - Where We are and Which Way We Going?“ oral presentation.
2017 December 05 scientific-practical conference "Laboratory Diagnostics of 2017. New Laboratory Diagnostic Opportunities and Clinical Interpretations of Research." organized by Evidence-Based Medicine and Lithuanian Laboratory Medical Society”, in which dr. Eglė Preikšaitienė read " New Technologies and Genetics" presentation.
2018 May 10-12 During the 14th Baltic Congress of Medical Medicine, PhD student Evelina Siavrienė delivered a report entitled "Functional Genome Analysis in Patients with Intellectual Disability", which included the data of the InGenes project.
2018 May 25-26 PhD student Evelina Siavrienė at the "56th Polish and 14th International Juvenes Pro Medicina“ conference in Poland, presented a report "Functional genome analysis aiming to define the genetic cause of intellectual disability", in which InGenes project was introduced.
2018 June 5-8 4th international conference "Evolutionary Medicine: Health and Diseases in Changing Environment" was organized by Vilnius University Faculty of Medicine. During the conference, the oral presentation "Genome editing in medicine: state of the art and perspectives" was presented by dr. Violeta Mikštienė.
2018 June 16-20 The annual conference organized by the European Society of Human Genetics (ESHG) took place in Milan (Italy). Two poster presentations ralated with InGenes project were presented:
1) “Microduplication of the 13q31.3 miR17 ~ 92 cluster results in the syndrome with Feingold syndrome 2” This poster provides studies of 13q31.3 miR17 ~ 92 microduplication in UNIGENE and Ingenes projects. Authors of the report: Evelina Siavrienė, dr. Eglė Preikšaitienė, dr. Živilė Maldžienė, dr. Laima Ambrozaitytė, dr. Lucie Gueneau, prof. Alexandre Reymond, prof. Vaidutis Kučinskas.
2) "De de novo 8q22.2q22.3 interstitial microdeletion in a girl with developmental delay and congenital defects" The identification of de novo 8q22.2q22.3 microdelection in a patient with congenital developmental defects. Authors of the report: Rūta Marcinkutė, Deimantė Braždžiūnaitė, dr. Neringa Burokienė, Vaidas Dirsė, dr. Eglė Preikšaitienė, prof. Algirdas Utkus