Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
Times Cited: 10
Times Cited: 10
Times Cited
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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
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Recommendations for returning genomic incidental findings? We need to talk!
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Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
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The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience.
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Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing.
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Towards a European consensus for reporting incidental findings during clinical NGS testing.
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Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
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Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling.
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Return of individual genomic research results: are laws and policies keeping step?
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.