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Year | Number of Results |
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2023 | 1 |
2024 | 2 |
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Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.
Orphanet J Rare Dis. 2023 Oct 4;18(1):310. doi: 10.1186/s13023-023-02916-x.
Orphanet J Rare Dis. 2023.
PMID: 37794437
Free PMC article.
Are the European reference networks for rare diseases ready to embrace machine learning? A mixed-methods study.
Iskrov G, Raycheva R, Kostadinov K, Gillner S, Blankart CR, Gross ES, Gumus G, Mitova E, Stefanov S, Stefanov G, Stefanov R.
Iskrov G, et al.
Orphanet J Rare Dis. 2024 Jan 25;19(1):25. doi: 10.1186/s13023-024-03047-7.
Orphanet J Rare Dis. 2024.
PMID: 38273306
Free PMC article.
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Landscape analysis of available European data sources amenable for machine learning and recommendations on usability for rare diseases screening.
Raycheva R, Kostadinov K, Mitova E, Iskrov G, Stefanov G, Vakevainen M, Elomaa K, Man YS, Gross E, Zschüntzsch J, Röttger R, Stefanov R.
Raycheva R, et al.
Orphanet J Rare Dis. 2024 Apr 6;19(1):147. doi: 10.1186/s13023-024-03162-5.
Orphanet J Rare Dis. 2024.
PMID: 38582900
Free PMC article.
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