https://doi.org/10.1038/s41436-021-01171-4
L
Laura M. Amendola
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Laura M. Amendola is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Genomics and Rare Diseases & BRCA gene mutations in cancer & Cancer Genomics and Diagnostics. The author has an h-index of 37, co-authored 122 publications.
ORCID: 0000-0002-5506-6168Papers by this author
worksRecommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
2021 · Genetics in Medicine · 244 citations
Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
2024 · JAMA · 84 citations
https://doi.org/10.1001/jama.2024.19662
Refining the structure and content of clinical genomic reports
2014 · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 46 citations
https://doi.org/10.1002/ajmg.c.31395
Human genome meeting 2016
2016 · Human Genomics · 41 citations
https://doi.org/10.1186/s40246-016-0063-5
Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases
2021 · Genetics in Medicine · 32 citations
https://doi.org/10.1038/s41436-020-01084-8
Clinicopathologic characteristics of breast cancer in BRCA-carriers and non-carriers in women 35 years of age or less
2014 · The Breast · 26 citations
https://doi.org/10.1016/j.breast.2014.08.010
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