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For: Wain KE, Palen E, Savatt JM, Shuman D, Finucane B, Seeley A, Challman TD, Myers SM, Martin CL. The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variants. Hum Mutat 2018;39:1660-7. [PMID: 30311381 DOI: 10.1002/humu.23607] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
Number Citing Articles
1 Kaushik V, Plazzer JP, Winship I, Macrae F. Genetic variant interpretation: a primer for clinicians. Intern Med J 2021;51:1401-6. [PMID: 34541770 DOI: 10.1111/imj.15485] [Reference Citation Analysis]
2 Wain KE, Azzariti DR, Goldstein JL, Johnson AK, Krautscheid P, Lepore B, O'Daniel JM, Ritter D, Savatt JM, Riggs ER, Martin CL. Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties. Genet Med 2020;22:785-92. [PMID: 31754268 DOI: 10.1038/s41436-019-0705-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
3 Chaudhari BP, Manickam K, McBride KL. A pediatric perspective on genomics and prevention in the twenty-first century. Pediatr Res 2020;87:338-44. [PMID: 31578042 DOI: 10.1038/s41390-019-0597-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
4 Ji J, Leung ML, Baker S, Deignan JL, Santani A. Clinical Exome Reanalysis: Current Practice and Beyond. Mol Diagn Ther 2021;25:529-36. [PMID: 34283395 DOI: 10.1007/s40291-021-00541-7] [Reference Citation Analysis]
5 Berrios C, Hurley EA, Willig L, Thiffault I, Saunders C, Pastinen T, Goggin K, Farrow E. Challenges in genetic testing: clinician variant interpretation processes and the impact on clinical care. Genet Med 2021. [PMID: 34257423 DOI: 10.1038/s41436-021-01267-x] [Reference Citation Analysis]
6 Rehm HL, Berg JS, Plon SE. ClinGen and ClinVar – Enabling Genomics in Precision Medicine. Human Mutation 2018;39:1473-5. [DOI: 10.1002/humu.23654] [Cited by in Crossref: 9] [Article Influence: 2.3] [Reference Citation Analysis]
7 Morales A, Ing A, Antolik C, Austin-Tse C, Baudhuin LM, Bronicki L, Cirino A, Hawley MH, Fietz M, Garcia J, Ho C, Ingles J, Jarinova O, Johnston T, Kelly MA, Kurtz CL, Lebo M, Macaya D, Mahanta L, Maleszewski J, Manrai AK, Murray M, Richard G, Semsarian C, Thomson KL, Winder T, Ware JS, Hershberger RE, Funke BH, Vatta M; ClinGen Cardiovascular Clinical Domain Working Group., Cardiomyopathy Variant Curation Expert Panel. Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert Panel. J Mol Diagn 2021;23:589-98. [PMID: 33631351 DOI: 10.1016/j.jmoldx.2021.01.014] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]