Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project
2020 · The American Journal of Human Genetics · 117 citations
https://doi.org/10.1016/j.ajhg.2020.08.001
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Julianne O’Daniel
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Julianne O’Daniel is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Genomics and Rare Diseases & BRCA gene mutations in cancer & Ethics in Clinical Research. The author has an h-index of 31, co-authored 161 publications.
ORCID: 0000-0001-5843-4432Papers by this author
worksA semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing
2015 · Genetics in Medicine · 98 citations
https://doi.org/10.1038/gim.2015.104
Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making
2021 · Genome Medicine · 34 citations
https://doi.org/10.1186/s13073-021-00867-1
Application of a framework to guide genetic testing communication across clinical indications
2021 · Genome Medicine · 29 citations
https://doi.org/10.1186/s13073-021-00887-x
P530: Point-of-care genetic testing with paired E-consult: An effective alternative service delivery model for patients with breast cancer
2024 · Genetics in Medicine Open · 0 citations
https://doi.org/10.1016/j.gimo.2024.101429
Additional file 2 of Application of a framework to guide genetic testing communication across clinical indications
2021 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.14516336
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