Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank
2019 · Genome Medicine · 112 citations
https://doi.org/10.1186/s13073-019-0691-1
S
Sabrina A. Suckiel
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Sabrina A. Suckiel is an academic researcher from Genomic Health (United States). 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 18, co-authored 57 publications.
ORCID: 0000-0003-3333-7526Papers by this author
worksImplementing genomic screening in diverse populations
2021 · Genome Medicine · 69 citations
https://doi.org/10.1186/s13073-021-00832-y
Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public
2015 · Genetics in Medicine · 68 citations
https://doi.org/10.1038/gim.2015.118
Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project
2017 · European Journal of Human Genetics · 64 citations
https://doi.org/10.1038/ejhg.2016.178
The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children
2021 · Trials · 34 citations
https://doi.org/10.1186/s13063-020-04953-4
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study
2025 · Public Health Genomics · 1 citations
https://doi.org/10.1159/000542444
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