Laura M. Amendola

National Institutes of Health — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

37h-index6.5kcitations143works7.42yr avg
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Research Topics

Genomics and Rare Diseases(88), BRCA gene mutations in cancer(44), Cancer Genomics and Diagnostics(26), Ethics in Clinical Research(22), Genetic factors in colorectal cancer(14)

Publications131 total

Development of a comprehensive cardiovascular disease genetic risk assessment test
Genetics in Medicine Open·2025Open Access
Abstract 4366327: Diagnostic Yield and Clinical Impact of Routine Genome Sequencing in Cardiovascular Patients
Circulation·2025
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
UNC Libraries·2025Open Access
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
UNC Libraries·2025Open Access
Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
Obstetrical & Gynecological Survey·2025· 1 cited
ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2025· 24 cited
Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
UNC Libraries·2025Open Access
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
UNC Libraries·2025Open Access
Data-driven consideration of genetic disorders for global genomic newborn screening programs
Genetics in Medicine·2025· 22 citedOpen Access
CLINICAL GENOME SEQUENCING IN ROUTINE CARDIOLOGY: INITIAL FINDINGS OF THE CARDIOSEQ STUDY
Journal of the American College of Cardiology·2025Open Access
Long‐Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia
Case Reports in Genetics·2025Open Access
When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research
Genetics in Medicine Open·2025Open Access
Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
JAMA·2024· 80 citedOpen Access
Satisfaction with mode of delivery of genomic sequencing results in a diverse national sample of research participants through the Clinical Sequencing Evidence-Generating Research Consortium
Genetics in Medicine·2024· 1 citedOpen Access
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2024· 10 citedOpen Access
Development of a comprehensive genome-wide cardiovascular disease genetic risk assessment test
2024Open Access
A framework for the evaluation and reporting of incidental findings in clinical genomic testing
European Journal of Human Genetics·2024· 4 citedOpen Access
Data-driven consideration of genetic disorders for global genomic newborn screening programs
2024· 20 citedOpen Access
LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants
BMC Genomics·2024Open Access
Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population
Translational Behavioral Medicine·2024· 1 citedOpen Access
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Frequent Co-authors

Gail P. Jarvik(26), Wendy K. Chung(15), Michael O. Dorschner(14), Jonathan S. Berg(13), Gregory M. Cooper(11), Heidi L. Rehm(11), Wylie Burke(11), Peter H. Byers(11), Benjamin S. Wilfond(11), Sawona Biswas(10), Leslie G. Biesecker(10), C. Sue Richards(10), Kevin M. Bowling(9), Robert C. Green(9), Sharon E. Plon(9), Brian H. Shirts(9), Kyle B. Brothers(9), Katrina A.B. Goddard(9), Laura K. Conlin(8), Ragan Hart(8)