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Page 1
Genomic newborn screening: Are we entering a new era of screening?
J Inherit Metab Dis. 2023 Sep;46(5):778-795. doi: 10.1002/jimd.12650. Epub 2023 Jul 17.
J Inherit Metab Dis. 2023.
PMID: 37403863
Review.
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. Among authors: gross es.
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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European Health Data Space-An Opportunity Now to Grasp the Future of Data-Driven Healthcare.
Horgan D, Hajduch M, Vrana M, Soderberg J, Hughes N, Omar MI, Lal JA, Kozaric M, Cascini F, Thaler V, Solà-Morales O, Romão M, Destrebecq F, Sky Gross E.
Horgan D, et al. Among authors: sky gross e.
Healthcare (Basel). 2022 Aug 26;10(9):1629. doi: 10.3390/healthcare10091629.
Healthcare (Basel). 2022.
PMID: 36141241
Free PMC article.
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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. Among authors: gross es.
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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