<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>32(7)</volume><submitter>Hammer-Hansen S</submitter><funding>Børnecancerfonden</funding><funding>The European Union’s Interregional Øresund–Kattegat–Skagerrak grant</funding><funding>Kræftens Bekæmpelse</funding><pubmed_abstract>The care for patients with serious conditions is increasingly guided by genomic medicine, and genomic medicine may equally transform care for healthy individual if genomic population screening is implemented. This study examines the medical impact of opportunistic genomic screening (OGS) in a cohort of patients undergoing comprehensive genomic germline DNA testing for childhood cancer, including the impact on their relatives. Medical actionability and uptake after cascade testing in the period following disclosure of OGS results was quantified. A secondary finding was reported to 19/595 (3.2%) probands primarily in genes related to cardiovascular and lipid disorders. After a mean follow up time of 1.6 years (Interquartile range (IQR): 0.57-1.92 yrs.) only 12 (63%) of these variants were fo</pubmed_abstract><journal>European journal of human genetics : EJHG</journal><pagination>846-857</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11220050</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort.</pubmed_title><pmcid>PMC11220050</pmcid><pubmed_authors>Bundgaard H</pubmed_authors><pubmed_authors>Bartels E</pubmed_authors><pubmed_authors>Juul K</pubmed_authors><pubmed_authors>Stoltze U</pubmed_authors><pubmed_authors>Schmiegelow K</pubmed_authors><pubmed_authors>Hammer-Hansen S</pubmed_authors><pubmed_authors>Byrjalsen A</pubmed_authors><pubmed_authors>Tybjærg-Hansen A</pubmed_authors><pubmed_authors>Diness BR</pubmed_authors><pubmed_authors>Tfelt J</pubmed_authors><pubmed_authors>Wadt K</pubmed_authors><pubmed_authors>Hansen TVO</pubmed_authors></additional><is_claimable>false</is_claimable><name>Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort.</name><description>The care for patients with serious conditions is increasingly guided by genomic medicine, and genomic medicine may equally transform care for healthy individual if genomic population screening is implemented. This study examines the medical impact of opportunistic genomic screening (OGS) in a cohort of patients undergoing comprehensive genomic germline DNA testing for childhood cancer, including the impact on their relatives. Medical actionability and uptake after cascade testing in the period following disclosure of OGS results was quantified. A secondary finding was reported to 19/595 (3.2%) probands primarily in genes related to cardiovascular and lipid disorders. After a mean follow up time of 1.6 years (Interquartile range (IQR): 0.57-1.92 yrs.) only 12 (63%) of these variants were fo</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-07-15T08:23:17.137Z</modification><creation>2025-04-04T12:21:31.876Z</creation></dates><accession>S-EPMC11220050</accession><cross_references><pubmed>38740897</pubmed><doi>10.1038/s41431-024-01618-7</doi></cross_references></HashMap>