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Year | Number of Results |
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2023 | 1 |
2024 | 2 |
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Landscape analysis of available European data sources amenable for machine learning and recommendations on usability for rare diseases screening.
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.
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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Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI project.
Ferlini A, Gross ES, Garnier N; Screen4Care consortium.
Ferlini A, et al.
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.
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