Bryce A. Seifert - Concepedia

Author

Bryce A. Seifert

University of North Carolina at Chapel Hill ORCID

Also Known As

B Seifert, Bryce A Seifert, Bryce A. Seifert, Bryce Seifert, Bryce A. Seifert, Earp, H. Shelton, Garrett, Jeremy R., M. Pfyffer, Plon, Sharon E., U. Hehr

Publications

Citations

H-Index

Concepts

All Affiliations

University of North Carolina at Chapel Hill Baylor College of Medicine Harvard University Brigham and Women's Hospital Broad Institute

About

Bryce A. Seifert is an author at University of North Carolina at Chapel Hill specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	1.2K
2	Public Health	5	5	872
3	Biostatistics	2	2	211
4	Engineering	1	1	38
5	Cell Biology	1	1	16

Bryce A. Seifert

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
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
Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes Jodie Ingles, Jennifer Goldstein, Courtney Thaxton, Circulation Genomic and Precision Medicine	2019	438
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
Specifications of the ACMG/AMP variant interpretation guidelines for germline <i>TP53</i> variants Cristina Fortuño, Kristy Lee, Magali Olivier, Human Mutation OncologyClingen Tp53 VcepGeneticsIntense Cancer SurveillanceGenetic Epidemiology	2020	159
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
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
Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels Kristy Lee, Bryce A. Seifert, Hermela Shimelis, Genetics in Medicine Genetic TestingBreast OncologyMedicineGeneticsHereditary Breast	2018	69
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, Clinical Genome ResourceGeneticsGenetic EpidemiologyDisease Gene IdentificationGenomics	2017	56
Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG) Lina Shao, Yassmine Akkari, Linda D. Cooley, Genetics in Medicine Genetic TestingGeneticsDna MicroarraysDiagnosisPathology	2021	52
Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease Gloria Haskell, Brian C. Jensen, Leigh Ann Samsa, Circulation Cardiovascular Genetics	2017	41

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