Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future Sequencing is a research paper published in International Journal of Neonatal Screening (2020). On theSindex it has a DataRank of 0. It has been cited 19 times.
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National Institutes of Health
Grant: U19HD077627
National Institutes of Health
Grant: 3U19HD077627-04S1
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
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Keywords
Sustainable Development Goals
Additional file 3 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 3 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 4 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 4 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 6 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 6 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 1 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 7 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 8 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 9 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 7 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 8 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 9 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 5 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 5 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 2 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 2 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
Additional file 1 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden