Laura M. Amendola - Concepedia

Author

Laura M. Amendola

University of Washington Medical Center ORCID

Also Known As

Amendola, Laura M., Angelo, F., Brian H. Shirts, Carlos A. Bacino, Conlin, Laura K., Cooper, Greg M., Eva Baker, François Boemer, Garraway, Levi, Ghazani, Arezou A.

143

Publications

6.5K

Citations

H-Index

Concepts

All Affiliations

University of Washington Medical Center University of Washington Baylor College of Medicine University of North Carolina at Chapel Hill Harvard University

About

Laura M. Amendola is an author at University of Washington Medical Center specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	29	4K
2	Public Health	14	14	2.1K
3	Engineering	2	2	57
4	Education	1	1	21
5	Nursing	1	1	21

Laura M. Amendola

Publications

5.3K

Citations

H-Index

Page 1

	Year	Citations
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium Laura M. Amendola, Gail P. Jarvik, Michael C. Leo, The American Journal of Human Genetics SequencingMedicineGeneticsNext-generation SequencingGenetic Epidemiology	2016	564
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) David T. Miller, Kristy Lee, Wendy K. Chung, Genetics in Medicine Secondary FindingsAcmg SfNext-generation SequencingGeneticsGenetic Epidemiology	2021	541
Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes Michael O. Dorschner, Laura M. Amendola, Emily H. Turner, The American Journal of Human Genetics Pathogenic Incidental FindingsGenetic EpidemiologyMendelian DisorderPathology	2013	381
Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between Gail P. Jarvik, Laura M. Amendola, Jonathan S. Berg, The American Journal of Human Genetics Genomic ResultsGenetic TestingResearch ParticipantsGeneticsStatistical Genetics	2014	368
ACMG SF v3.2 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) David T. Miller, Kristy Lee, Noura S. Abul‐Husn, Genetics in Medicine Secondary FindingsSequencingAcmg SfNext-generation SequencingGenetics	2023	364
Actionable exomic incidental findings in 6503 participants: challenges of variant classification Laura M. Amendola, Michael O. Dorschner, Peggy D. Robertson, Genome Research Genome-wide Association StudyEpidemiologySequencingExome SequencingGenetics	2015	356
Recommendations 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) David T. Miller, Kristy Lee, Laura M. Amendola, Genetics in Medicine American CollegeClinical ExomeDiagnosisPathologyGynecology	2021	244
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik, The American Journal of Human Genetics EpidemiologySequencingMedicineNext-generation SequencingGenomics	2016	161
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations Laura M. Amendola, Jonathan S. Berg, Carol R. Horowitz, The American Journal of Human Genetics BioinformaticsMedicineGeneticsNext-generation SequencingGenomic Medicine	2018	158
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study Ragan Hart, Barbara B. Biesecker, Carrie L. Blout Zawatsky, Genetics in Medicine Genetic TestingClinical Genomic SequencingNext-generation SequencingGenetic EpidemiologyGenomics	2018	154

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