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Newborn Genomic Screening (gNBS): A public health necessity in the 21st century

  • When: Thursday, 19 February 2026, 14:00–21:00 

  • Where: Hellenic American Union Amphitheater, Massalias 22, Athens

Newborn Genomic Screening (gNBS)

 

A future where genomic sequencing (gNBS) is seamlessly integrated into newborn care, providing families and healthcare professionals with the necessary tools to make informed decisions about a child's health is not a distant reality. gNBS integrated in public health could be the tool for life-long personalized medicine. 

 

The conference will focus on public health ethics, data governance, handling of personal data, data storage and data utilization for innovation and drug development. 

 

The conference is organized by FirstSteps, the genomic screening initiative of Greece. 

Program

14:00-14:45: Registration

 

14:45-15:00: Welcome and Introduction

                       Petros Tsipouras

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15:00-16:30: Session I: Precision Medicine

                       Chairs: Paul R. Billings, Dimitrios Thanos

15:00-15:15: Building Greece’s Genomic Future: From Newborn Screening to Precision Medicine for all

                       Dimitris Thanos

15:15-15:30: Setting the Stage for gNBS with public health ethics

                       Bartha Maria Knoppers

15:30-16:30: Panel: Newborn genomic screening as a gateway to life-long precision medicine.

                       Moderator: Paul R. Billings

                       Panelists: David Bick*, Ali Gharavi*, Manolis Papasavas, Martin Reese, Kyriakos Souliotis

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16:30-17:30: Session II: Data Governance

                       Chairs: Silvia Salardi, Takis Vidalis

16:30-16:40: Ethical principles for data governance

                       Silvia Salardi

16:40-16:50: Emerging EU data governance

                       Fruzsina Molnar-Gabor

16:50-17:30: Panel: Data governance

                       Moderator: Takis Vidalis

                       Panelists: David Bick*, Eftychia Oikonomou, Fruzsina Molnar-Gabor, Silvia Salardi

 

 

17:30-18:00: Coffee Break

18:00-18:30: Official Opening

18:30-19:30: Session III: Innovation

                       Chairs: Maria Chatzou*, Mimi Lee

18:30-18:40: Breaking borders in Biomedical Research: How Datα Federation is accelerating cures 

                       Maria Chatzou​*

18:40-19:30: Panel: How innovation can drive population screening programs 

                       Moderator: Mimi Lee

                       Panelists: Maria Chatzou*, Kevin Hall, John Bouros, Terry Pirovolakis*, Winston Yan* 

18:30-19:30: Session III: Innovation

                       Chairs: Maria Chatzou*, Mimi Lee

18:30-18:40: Breaking borders in Biomedical Research: How Datα Federation is accelerating cures 

                       Maria Chatzou​*

18:40-19:30: Panel: How innovation can drive population screening programs 

                       Moderator: Mimi Lee

                       Panelists: Maria Chatzou*, Kevin Hall, John Bouros, Terry Pirovolakis*, Winston Yan* 

19:30-20:50: Session IV: Ethics and Public health Screening Programs

                       Chairs: Metropolitan Konstantinos, Bartha Maria Knoppers 

19:30-19:45: Genomic sequencing in Newborn Screening: What it is-and is Not  

                       Mei Baker*

19:45-19:55: Demographic changes in Greece: Are there any solutions? 

                       Aristeidis Antsaklis

19:55-20:50: Panel: Ethics and Public Health Screening Programs 

                       Moderator: Metropolitan Konstantinos 

                       Panelists: Dimitris Athanasiou, Mei Baker, Bartha Maria Knoppers 

 

 

20:50-21:00: Concluding Remarks

                       Petros Tsipouras

FirstSteps is the first Greek initiative dedicated to the implementation of newborn genomic screening, aiming to integrate responsible genomic medicine into public health through scientific rigor, ethical governance, and institutional collaboration.

Innovation in genomic medicine requires more than technology.
It requires collaboration, governance, and trust.

©2026 by Beginnings - Newborn Sequencing Initiative

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