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Article

Incidental medical information in whole-exome sequencing.

Pediatrics - 1 Jun 2012

Solomon Benjamin D, Hadley Donald W, Pineda-Alvarez Daniel E, Kamat Aparna, Teer Jamie K, Cherukuri Praveen F, Hansen Nancy F, Cruz Pedro, Young Alice C, Berkman Benjamin E, Chandrasekharappa Settara C, Mullikin James C

Abstract excerpt

Genomic technologies, such as whole-exome sequencing, are a powerful tool in genetic research. Such testing yields a great deal of incidental medical information, or medical information not related to the primary research target. We describe the management of incidental medical information derived from whole-exome sequencing in the research context. We performed whole-exome sequencing on a monozygotic twin pair...

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Share to Congenital Abnormalities
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Infant, Newborn

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Share to Twins, Monozygotic

Source

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Identifiers

PMID: 22585771
DOI: 10.1542/peds.2011-0080
PMCID: PMC3362899

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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