{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,8]],"date-time":"2026-10-08T02:55:38Z","timestamp":1791428138896,"version":"4.3.3"},"reference-count":22,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2020,7,23]],"date-time":"2020-07-23T00:00:00Z","timestamp":1595462400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"NHGRI\/ELSI","award":["R01HG008045-04S"],"award-info":[{"award-number":["R01HG008045-04S"]}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Journal of Genetic Counseling"],"published-print":{"date-parts":[[2021,2]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Genetic test results are often relevant not only to persons tested, but also to their children. Questions of whether, when, and how to disclose parental test results to children, particularly minors, can be difficult for parents to navigate. Currently, limited data are available on these questions from the perspective of minors. In this qualitative study, semi\u2010structured interviews were conducted with parents affected by or at risk for hereditary cancer (<jats:italic>N<\/jats:italic>\u00a0=\u00a017) or Huntington's disease (<jats:italic>N<\/jats:italic>\u00a0=\u00a014) and their mature minor children aged 15\u201317 (<jats:italic>N<\/jats:italic>\u00a0=\u00a034). Parents and mature minors were interviewed separately. Genetic counselors (GCs; <jats:italic>N<\/jats:italic>\u00a0=\u00a019) were also interviewed. Most parents interviewed wanted to protect minors from genetic risk information (GRI) and feared minors would not be able to handle GRI. However, most mature minors reported they did not receive enough information and wished their parent was more forthcoming. Parents recommended taking time to process one's own test results before communicating with minors, and mature minors recommended parents communicate GRI in an honest, hopeful way. Most parents and GCs felt additional resources on communicating with minors about GRI and various genetic conditions are needed. This study includes the experiences and perspectives of a well\u2010informed cohort, and results should be taken into careful consideration by parents, GCs, and others who are faced with communicating GRI to minors.<\/jats:p>","DOI":"10.1002\/jgc4.1314","type":"journal-article","created":{"date-parts":[[2020,7,23]],"date-time":"2020-07-23T11:27:45Z","timestamp":1595503665000},"page":"237-245","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":15,"title":["Whether, when, and how to communicate genetic risk to minors: \u2018I wanted more information but I think they were scared I couldn\u2019t handle it\u2019"],"prefix":"10.1002","volume":"30","author":[{"given":"Kelsey","family":"Stuttgen","sequence":"first","affiliation":[{"name":"Berman Institute of Bioethics Johns Hopkins University Baltimore MD USA"},{"name":"Institute of Genetic Medicine Johns Hopkins University School of Medicine Baltimore MD 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