News
Screen4Care Invited to Joint Conference of the 22nd Annual Meeting of Asian and Oceanian Myology Center and the 10th Annual Meeting of Japan Muscle Society
Alessandra Ferlini, Scientific Coordinator for Screen4Care, participated as an invited speaker at the Joint Conference of the 22nd Annual Meeting of the Asian and Oceanian Myology Center and the 10th...
Screen4Care features on CORDIS
CORDIS recently published an update about the main goals of the EU-funded Screen4Care project. The project aims to implement genetic newborn screening in Europe to detect a high number of rare disease...
UCB, Revvity, and CHU Dijon-Bourgogne Join Screen4Care as Project Partners
As of 13.06.2024, Screen4Care is pleased to announce that three esteemed partners have joined our consortium. These new partners bring unique expertise that will significantly contribute to our missio...
The Screen4Care Consortium Meets Again – Second Face-to-Face Consortium meeting in Copenhagen, Denmark
We are thrilled to share the highlights of our highly successful 2nd in-person meeting, held on April 25-26, 2024, in Copenhagen, Denmark. This meeting brought together an esteemed group of experts an...
Screen4Care Joins the 12th European Conference on Rare Diseases & Orphan Products (ECRD 2024) as an Associate Partner
The Screen4Care consortium is delighted to announce its participation as an associate partner in the 12th European Conference on Rare Diseases & Orphan Products (ECRD 2024).
ECRD is Europe's leadin...
How Do You Pursue a Medical Degree While Living with a Rare Disease? Exploring Unique Paths to Women's Empowerment in Conversation with Ina Baumann
Being a woman and working in STEM is no easy feat. Despite the changes observed over the past decades, the persistent gatekeeping in this field remains evident in the annual statistics, undoubtedl...
Screen4Care at the 2023 Annual ICoNS Conference in London, UK
The second Annual Conference of the International Consortium on Newborn Sequencing (ICoNS) brought together global experts from eight newborn sequencing research projects: BabySeq, Genomics England, G...
Screen4Care Co-Announces the Formation of the International Consortium on Newborn Sequencing (ICoNS)
Our project proudly joins the launch of the International Consortium on Newborn Sequencing (ICoNS), with the aim of aligning stakeholders and establishing guidelines based on empirical evidence for th...
Signalise Podcast: Screen4Care EFPIA Lead Nicolas Garnier in Conversation With Kimberly Thomas-Tague
In episode 22 of Signalise: a Dazzle4Rare Podcast, Dr. Nicolas Garnier, EFPIA Lead of Screen4Care, joins host Kimberly Thomas-Tague for an engaging discussion on newborn screening. The episode sheds...
Coming Together to Shorten the Path to Rare Disease Diagnosis – First Face-To-Face Meeting of the Screen4Care Partners Held in Ferrara, Italy
The location for the long-awaited first in-person Annual Meeting of Screen4Care could not have been more welcoming than the beautiful city of Ferrara, Italy. From March 6th to 7th, 36 project partners...
EU Knowledge Valorisation Week 2023: Learn More on Turning Research into Solutions
Join stakeholders and policymakers at the EU Knowledge Valorisation Week between 25 April and 28 April 2023. The annual event highlights best practices promoting the uptake of research results and sci...
New partner brings valuable expertise to the table: Biopharma company PTC Therapeutics joins Screen4Care
Accelerating rare disease diagnostics through genetic newborn screening and digital solutions.
Since launching in October 2021, Screen4Care is dedicated to shorten the diagnosis journey for people l...
Screen4Care workshop on legal, ethical and business-related issues in Bern
On 22 April, the members of Work Package 1 met in Bern to discuss legal, ethical and business-related issues. The workshop was held in hybrid form with online and offline groups in the new building...
EURORDIS' Rare Barometer Survey on the Journey to Diagnosis for People Living with a Rare Disease
Screen4Care’s key partner EURORDIS has launched the Rare Barometer survey – an international survey on the journey to diagnosis for people living with a rare disease. The survey is open to people...
New EU Research Project “Screen4Care”
Accelerating Diagnosis for Rare Disease Patients Through Genetic Newborn Screening and Artificial Intelligence
The international consortium aims to tackle the major hurdle for rare disease patients...