ArticleScientific data2025
Extended Lombardy's Neonatal Screening Dataset.
Article in Scientific data, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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Abstract
Neonatal Screening (NS) is a mandatory secondary prevention program established in the 1960s to detect rare genetic disorders in newborns. Early diagnosis through NS enables timely interventions, helping to prevent severe health complications. Despite its long-standing implementation, there remains a scarcity of publicly available datasets to support medical research and academic analysis. In this work, we present a comprehensive dataset containing blood samples and associated information from nearly a decade of Neonatal Screening in Lombardy. This dataset offers valuable insights for medical studies on genetic disorders, early diagnostics, and treatment efficacy. Additionally, it can support academic research in data-driven healthcare analysis and policy development. By making this dataset publicly available, we aim to enhance research opportunities in neonatal health and contribute to the improvement of early intervention strategies.
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Registered trials
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