Julianne O’Daniel - Concepedia

Author

Julianne O’Daniel

University of North Carolina at Chapel Hill ORCID

Also Known As

Berg, J.S., Berg, Jonathan S., Burke, Wylie, Canter, Courtney, Comer, Lydia H., Conway, C., Das, Soma, Giovanni, Monica A., Henderson, Gail E., J. O’Daniel

189

Publications

5.7K

Citations

H-Index

Concepts

All Affiliations

University of North Carolina at Chapel Hill Duke University Baylor College of Medicine National Human Genome Research Institute Stanford University

About

Julianne O’Daniel is an author at University of North Carolina at Chapel Hill specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	23	4.4K
2	Education	3	3	50
3	Arts	1	1	24
4	Health Sciences	1	1	44
5	Humanities	1	1	24

Julianne O’Daniel

Publications

5.5K

Citations

H-Index

Page 1

	Year	Citations
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing Robert C. Green, Jonathan S. Berg, Wayne W. Grody, Genetics in Medicine Next-generation SequencingAcmg RecommendationsDiagnosisPathologyPersonal Genomics	2013	2.5K
Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource Natasha T. Strande, Erin Rooney Riggs, Adam H. Buchanan, The American Journal of Human Genetics Clinical Genome ResourceGene-disease AssociationsGenome-wide Association StudyClinical ValidityMedicine	2017	536
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
A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation Jessica Ezzell Hunter, Stephanie A. Irving, Leslie G. Biesecker, Genetics in Medicine	2016	146
Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG) Catherine Rehder, Lora Jh Bean, David Bick, Genetics in Medicine Genetic TestingSequencingMedicineGeneticsNext-generation Sequencing	2021	126
Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project Tamara S. Roman, Stephanie B. Crowley, Myra I. Roche, The American Journal of Human Genetics Newborn ScreeningNeonatal GenomicsNext-generation SequencingGeneticsNc Nexus Project	2020	117
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing Jonathan S. Berg, Ann Katherine M. Foreman, Julianne O’Daniel, Genetics in Medicine	2015	98
Germline Analysis from Tumor–Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings Bryce A. Seifert, Julianne O’Daniel, Krunal Amin, Clinical Cancer Research	2016	97
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories Julianne O’Daniel, Heather M. McLaughlin, Laura M. Amendola, Genetics in Medicine Genetic TestingSequencingReporting ProcessesMedicineGenetics	2016	84
Public Perspectives on Returning Genetics and Genomics Research Results Julianne O’Daniel, Susanne B. Haga Public Health Genomics	2011	81

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