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Communication in genomic and precision medicine: Editorial - .

作者信息

Campbell-Salome Gemme

机构信息

Department of Genomic Health, Department of Population Health Sciences, Geisinger, 100 N Academy Ave., Danville, PA 17822, United States of America.

出版信息

PEC Innov. 2023 Jan 25;2:100126. doi: 10.1016/j.pecinn.2023.100126. eCollection 2023 Dec.

DOI:10.1016/j.pecinn.2023.100126
PMID:37214511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10194269/
Abstract
摘要

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Development of a novel measure of advanced cancer patients' perceived utility of secondary germline findings from tumor genomic profiling.一种针对晚期癌症患者对肿瘤基因组分析中二级胚系结果的感知效用的新型测量方法的开发。
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Investigation of interest in and timing preference for cancer predisposition testing and expanded carrier screening among women of reproductive age.对育龄女性进行癌症易感性检测及扩大携带者筛查的兴趣和时间偏好调查。
PEC Innov. 2023 Jan 24;2:100128. doi: 10.1016/j.pecinn.2023.100128. eCollection 2023 Dec.
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Do people with hereditary cancer syndromes inform their at-risk relatives? A systematic review and meta-analysis.患有遗传性癌症综合征的人会告知他们有患病风险的亲属吗？一项系统评价和荟萃分析。
PEC Innov. 2023 Feb 17;2:100138. doi: 10.1016/j.pecinn.2023.100138. eCollection 2023 Dec.
4
Navigating the uncertainty of precision cancer screening: The role of shared decision-making.应对精准癌症筛查的不确定性：共同决策的作用。
PEC Innov. 2023 Jan 24;2:100127. doi: 10.1016/j.pecinn.2023.100127. eCollection 2023 Dec.
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"How is it going to help?": Exploring Black breast cancer patients' questions about biomarker testing to predict chemotherapy-induced peripheral neuropathy.“这将如何提供帮助？”：探究黑人乳腺癌患者关于预测化疗引起的周围神经病变的生物标志物检测的问题。
PEC Innov. 2022 Dec 13;2:100118. doi: 10.1016/j.pecinn.2022.100118. eCollection 2023 Dec.
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Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model condition.开发一种故事讲述沟通促进工具（SCFT）以促进父母与子女之间关于复杂基因诊断的讨论：一项以22q11.2缺失综合征为模型疾病的试点研究。
PEC Innov. 2022 Dec 6;2:100115. doi: 10.1016/j.pecinn.2022.100115. eCollection 2023 Dec.
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Evaluation of an educational conference for persons affected by hereditary frontotemporal degeneration and amyotrophic lateral sclerosis.针对遗传性额颞叶变性和肌萎缩侧索硬化症患者的教育会议评估
PEC Innov. 2022 Nov 24;2:100108. doi: 10.1016/j.pecinn.2022.100108. eCollection 2023 Dec.
8
Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study.促进家族性高胆固醇血症遗传风险的家庭沟通：评估IMPACT-FH研究中对创新聊天机器人技术的参与度。
PEC Innov. 2023 Feb 4;2:100134. doi: 10.1016/j.pecinn.2023.100134. eCollection 2023 Dec.
9
A randomized controlled trial of analogue pharmacogenomic testing feedback for psychotropic medications.一项关于精神药物类似物药物基因组学检测反馈的随机对照试验。
PEC Innov. 2022 Dec 16;2:100119. doi: 10.1016/j.pecinn.2022.100119. eCollection 2023 Dec.
10
Results of a randomized controlled trial of a decision support intervention for disclosing maternal genetic test results to children and adolescents.一项关于向儿童和青少年披露母亲基因检测结果的决策支持干预随机对照试验的结果。
PEC Innov. 2023 Jan 26;2:100129. doi: 10.1016/j.pecinn.2023.100129. eCollection 2023 Dec.