Shortening the path to rare disease diagnosis by using newborn genetic screening and digital technologies

Informazioni relative al progetto

SCREEN4CARE

ID dell’accordo di sovvenzione: 101034427

DOI

10.3030/101034427

Data della firma CE 13 Ottobre 2021

Data di avvio 1 Ottobre 2021

Data di completamento 30 Settembre 2026

Finanziato da

• SOCIETAL CHALLENGES - Health, demographic change and well-being

Costo totale

€ 26 247 174,00

Contributo UE

€ 11 938 568,75

Coordinato da

UNIVERSITA DEGLI STUDI DI FERRARA
Italy

CORDIS fornisce collegamenti ai risultati finali pubblici e alle pubblicazioni dei progetti ORIZZONTE.

I link ai risultati e alle pubblicazioni dei progetti del 7° PQ, così come i link ad alcuni tipi di risultati specifici come dataset e software, sono recuperati dinamicamente da .OpenAIRE .

Risultati finali

Websites, patent fillings, videos etc. (2)

Project Website
Audio-visual material 1

Demonstrators, pilots, prototypes (1)

Viable implementation of the metadata repository incl. report on data access right management

Documents, reports (1)

Initial Definition of the CDM

Pubblicazioni

Peer reviewed articles (12)

Are the European reference networks for rare diseases ready to embrace machine learning? A mixed-methods study

Autori: Georgi Iskrov, Ralitsa Raycheva, Kostadin Kostadinov, Sandra Gillner, Carl Rudolf Blankart, Edith Sky Gross, Gulcin Gumus, Elena Mitova, Stefan Stefanov, Georgi Stefanov, Rumen Stefanov
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 19, 2024, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-024-03047-7

We're implementing AI now, so why not ask us what to do? – How AI providers perceive and navigate the spread of diagnostic AI in complex healthcare systems

Autori: Sandra Gillner
Pubblicato in: Social Science & Medicine, Numero 340, 2024, Pagina/e 116442, ISSN 0277-9536
Editore: Pergamon Press Ltd.
DOI: 10.1016/j.socscimed.2023.116442

The modernisation of newborn screening as a pan-European challenge – An international delphi study

Autori: Sandra Gillner, Gulcin Gumus, Edith Gross, Georgi Iskrov, Ralitsa Raycheva, Georgi Stefanov, Rumen Stefanov, Anne-Sophie Chalandon, Alicia Granados, Julian Nam, Andreas Clemens, Carl Rudolf Blankart
Pubblicato in: Health Policy, Numero 149, 2024, Pagina/e 105162, ISSN 0168-8510
Editore: Elsevier BV
DOI: 10.1016/j.healthpol.2024.105162

Effect of tissue fixation on the optical properties of structural components assessed by non-linear microscopy imaging

Autori: Markus, M. Andrea; Ferrari, Daniele P.; Alves, Frauke; Ramos-Gomes, Fernanda
Pubblicato in: Optica Publishing Group, Numero Vol. 14, Numero 8, 2023, Pagina/e 3988-4002, ISSN 2156-7085
Editore: The Optical Society
DOI: 10.1364/boe.488453

Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project

Autori: Alessandra Ferlini, Edith Sky Gross, Nicolas Garnier, null null, Joanne Berghout, Aldona Zygmunt, Deependra Singh, Kui A. Huang, Waltraud Kantz, Carl Rudolf Blankart, Sandra Gillner, Jiawei Zhao, Richard Roettger, Christina Saier, Jan Kirschner, Joern Schenk, Leon Atkins, Nuala Ryan, Kaja Zarakowska, Jana Zschüntzsch, Michela Zuccolo, Matthias Müllenborn, Yuen-Sum Man, Liz Goodman, Marie Trad Ly
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 18, 2023, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.1186/s13023-023-02916-x

Challenges in mapping European rare disease databases, relevant for ML-based screening technologies in terms of organizational, FAIR and legal principles: scoping review

Autori: Ralitsa Raycheva, Kostadin Kostadinov, Elena Mitova, Nataliya Bogoeva, Georgi Iskrov, Georgi Stefanov, Rumen Stefanov
Pubblicato in: Frontiers in Public Health, 2023, Pagina/e 11, ISSN 2296-2565
Editore: Frontiers in Public Health
DOI: 10.3389/fpubh.2023.1214766

Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy

Autori: Oliver Schwartz, Katharina Vill, Michelle Pfaffenlehner, Max Behrens, Claudia Weiß, Jessika Johannsen, Johannes Friese, Andreas Hahn, Andreas Ziegler, Sabine Illsinger, Martin Smitka, Arpad von Moers, Heike Kölbel, Gudrun Schreiber, Nadja Kaiser, Ekkehard Wilichowski, Marina Flotats-Bastardas, Ralf A. Husain, Matthias Baumann, Cornelia Köhler, Regina Trollmann, Annette Schwerin-Nagel, Astrid Ei
Pubblicato in: JAMA Pediatrics, Numero 178, 2024, Pagina/e 540, ISSN 2168-6203
Editore: American Medical Association
DOI: 10.1001/jamapediatrics.2024.0492

Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe

Autori: Nicolas Garnier, Joanne Berghout, Aldona Zygmunt, Deependra Singh, Kui A. Huang, Waltraud Kantz, Carl Rudolf Blankart, Sandra Gillner, Jiawei Zhao, Richard Roettger, Christina Saier, Jan Kirschner, Joern Schenk, Leon Atkins, Nuala Ryan, Kaja Zarakowska, Jana Zschüntzsch, Michela Zuccolo, Matthias Müllenborn, Yuen-Sum Man, Liz Goodman, Marie Trad, Anne Sophie Chalandon, Stefaan Sansen, Maria Mart
Pubblicato in: PLOS ONE, Numero 18, 2023, Pagina/e e0293503, ISSN 1932-6203
Editore: Public Library of Science
DOI: 10.1371/journal.pone.0293503

Landscape analysis of available European data sources amenable for machine learning and recommendations on usability for rare diseases screening

Autori: Ralitsa Raycheva, Kostadin Kostadinov, Elena Mitova, Georgi Iskrov, Georgi Stefanov, Merja Vakevainen, Kaisa Elomaa, Yuen-Sum Man, Edith Gross, Jana Zschüntzsch, Richard Röttger, Rumen Stefanov
Pubblicato in: Orphanet Journal of Rare Diseases, Numero 147 (2024), 2024, ISSN 1750-1172
Editore: BioMed Central
DOI: 10.21203/rs.3.rs-3448625/v1

Non-invasive optoacoustic imaging of glycogen-storage and muscle degeneration in Late-onset Pompe disease

Autori: Ferdinand Knieling, Lina Tan, Jana Zschüntzsch, Stefanie Meyer, Alica Stobbe, Hannah Bruex, Adrian Regensburger, Frauke Alves, Jörg Jüngert, Ulrich Rother, Yi Li, Vera Danko, Werner Lang, Matthias Türk, Sandy Schmidt, Matthias Vorgerd, Lara Schlaffke, Joachim Wölfle, Andreas Hahn, Alexander Mensch, Martin Winterholler, Regina Trollmann, Rafael Heiß, Alexandra Wagner, Roman Raming
Pubblicato in: Nature Communications, Numero 15(1):7843, 2024, ISSN 2041-1723
Editore: Nature Publishing Group
DOI: 10.21203/rs.3.rs-3731485/v1

Patient preferences in genetic newborn screening for rare diseases: study protocol

Autori: Sylvia MARTIN, Emanuele Angolini, Jennifer Audi, Enrico Bertini, Lucia Pia Bruno, Joshua Coulter, Alessandra Ferlini, Fernanda Fortunato, Vera Frankova, Nicolas Garnier, Åsa Grauman, Edith Gross, Brett Hauber, Mats Hansson, Janbernd Kirschner, Ferdinand Knieling, Gergana Kyosovksa, Silvia Ottombrino, Antonio Novelli, Roman Raming, Stefaan Sansen, Christina Saier, Jorien Veldwijk
Pubblicato in: BMJ Open, Numero 14, 2024, Pagina/e e081835, ISSN 2044-6055
Editore: BMJ Publishing Group
DOI: 10.1136/bmjopen-2023-081835

Genomic newborn screening: Are we entering a new era of screening?

Autori: Ute Spiekerkoetter, David Bick, Richard Scott, Henrietta Hopkins, Tanja Krones, Edith Sky Gross, James R. Bonham
Pubblicato in: Journal of Inherited Metabolic Disease, 2023, Pagina/e 759-1003, ISSN 1573-2665
Editore: John Wiley & Sons Ltd
DOI: 10.1002/jimd.12650

Other (2)

Data-driven prioritization of genetic disorders for global genomic newborn screening programs

Autori: Minten T, Gold NB, Bick S, Adelson S, Gehlenborg N, Amendola LM, Boemer F, Coffey AJ, Encina N, Ferlini A, Kirschner J, Russell BE, Servais L, Sund KL, Taft RJ, Tsipouras P, Zouk H; ICoNS Gene List Contributors; Bick D, Green RC; International Consortium on Newborn Sequencing (ICoNS)
Pubblicato in: medRxiv [Preprint], Numero 2024 Sep 16:2024.03.24.24304797, 2024, ISSN 2692-8205
Editore: Cold Spring Harbor Laboratory

Newborn Screening by Genomic Sequencing: Opportunities and Challenges

Autori: Avid Bick, Arzoo Ahmed, Dasha Deen, Alessandra Ferlini, Nicolas Garnier, Dalia Kasperaviciute, Mathilde Leblond, Amanda Pichini, Augusto Rendon, Aditi Satija, Alice Tuff-Lacey and Richard H. Scott
Pubblicato in: Int. J. Neonatal Screening, 2022
Editore: Int. J. Neonatal Screening
DOI: 10.3390/ijns8030040

Book chapters (1)

Improving Clinical Documentation of Rare Neuromuscular Diseases: Development of a Standardised Information Model

Autori: Miriam Hübner, Elisabeth Nyoungui, Elisabetta Gazzero, Lina Hassoun, Jana Zschüntzsch, Dagmar Krefting, Josef Schepers, Richard Röttgerd
Pubblicato in: Studies in Health Technology and Informatics, Digital Health and Informatics Innovations for Sustainable Health Care Systems, 2024, ISSN 0926-9630
Editore: IOS Press
DOI: 10.3233/shti240677