Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
Times Cited: 6
Times Cited: 6
Times Cited
Times Co-cited
Similarity
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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33
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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Jayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, Conny van Ravenswaaij-Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon-Thomsen, Philippos Patsalis, Joris Vermeesch,[...]. Eur J Hum Genet 2015
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Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
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Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice.
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Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
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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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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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Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.
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"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
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The incidentalome: a threat to genomic medicine.
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The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing.
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Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
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Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation.
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Parental origin of the extra chromosomes in polysomy X.
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Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
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Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
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Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations.
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Estimates of the live births, natural losses, and elective terminations with Down syndrome in the United States.
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Cost analysis of whole genome sequencing in German clinical practice.
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Estimates of live birth prevalence of children with Down syndrome in the period 1991-2015 in the Netherlands.
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Intragenic Enhancers Attenuate Host Gene Expression.
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Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.
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Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
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The ring 14 syndrome.
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16
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.