Genetic Counseling (GC)
遗传咨询(GC)
基本信息
- 批准号:10611311
- 负责人:
- 金额:$ 14.37万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1997
- 资助国家:美国
- 起止时间:1997-05-09 至 2025-04-30
- 项目状态:未结题
- 来源:
- 关键词:AddressAdherenceApplications GrantsAreaBasic ScienceBehavioral ResearchCancer BiologyCancer CenterCancer Center Support GrantCatchment AreaChemopreventionClinicClinicalClinical InvestigatorClinical ResearchClinical TrialsCollaborationsCollectionCommunicationConsultationsDataEffectivenessElectronic Health RecordEnsureEthicsFamilial Adenomatous Polyposis SyndromeFundingGenesGeneticGenetic AnticipationGenetic CounselingGenetic ResearchGenetic ServicesGoalsGrantGuidelinesHereditary Malignant NeoplasmHereditary Neoplastic SyndromesImageIndividualInheritedInterventionMalignant NeoplasmsMedical GeneticsMethodsMissionNational Cancer InstituteOncologyOutcomeParticipantPatient-Focused OutcomesPatientsPeer ReviewPopulationPopulation PoliciesPrincipal InvestigatorProgram Research Project GrantsProtocols documentationPublicationsQualifyingRecording of previous eventsResearchResearch DesignResearch InstituteResearch PersonnelResource SharingResourcesRiskRisk ManagementRural PopulationSamplingScienceScientific Advances and AccomplishmentsServicesSyndromeTranslatingTranslationsUtahWorkanticancer researchcancer carecancer geneticscancer predispositioncancer riskclinical careclinical implementationclinical phenotypeclinically significantcohortdesignethical, legal, and social implicationgene discoverygenetic analysisgenetic counselorgenetic informationgenetic testinginnovationmembernovelnovel strategiesprimary care patientprogramsrecruitscreeningtooltranslational genetics
项目摘要
GENETIC COUNSELING SHARED RESOURCE
ABSTRACT
The Genetic Counseling Shared Resource (GC) facilitates basic science, clinical, and behavioral research
necessary to translate genetic discoveries into clinical care. GC has provided clinical genetics services and
supported genetic research at Huntsman Cancer Institute (HCI) since 2003 (supported by the Cancer Center
Support Grant since 2009) and has been directed by Wendy Kohlmann, MS, CGC, since 2006. GC is
quintessential to HCI’s mission and builds on HCI’s long history of gene discovery by leading practice-changing
research endeavors to determine the clinical utility of genetic testing, optimal methods for risk communication
and delivery of genetic counseling, and strategies to manage risk conveyed by inherited cancer
predispositions. GC is integral to a major goal of the Cancer Center, bringing scientific discoveries to the clinic
and into applications for the population. GC provides several key services necessary for translational genetic
research, including identifying cohorts of patients for gene research or studies of syndromes; helping
investigators design studies to optimally incorporate genetic information and to anticipate and address ethical,
legal, and social issues related to genetic analysis; providing genetic counseling interventions; and collecting
clinical phenotypes and longitudinal outcomes data. The aims of GC are 1) to provide cancer genetics
expertise, genetic counseling services, and interventions, and 2) to support the scientific research objectives of
the Cancer Center, especially in the context of translation of genetics to the clinic and population.
Access to research genetic counseling services has allowed Cancer Center members to study novel
approaches for providing genetic information and to include participants across our catchment area, the State
of Utah. GC adds value to the Cancer Center by ensuring genetics expertise is available to all Cancer Center
members and clinical investigators. The broad impact of GC across HCI is indicated by its contribution to 61
publications since 2014. Cancer Center members with peer-reviewed funding comprise 53% of the users, and
100% of GC’s work is cancer-related.
HCI’s establishment of a top-quality, research-oriented Genetic Counseling Shared Resource is highly
innovative and unique among National Cancer Institute cancer centers. The Director and staff of the Shared
Resource participate in national committees, and they extend the impact of HCI research by incorporating
findings into guidelines for genetic testing and management of hereditary cancer. GC allows HCI to excel in all
areas of hereditary cancer research and to be a leader in genetic discoveries and translation of findings into
clinical implementation and population policy.
遗传咨询共享资源
摘要
遗传咨询共享资源(GC)促进基础科学、临床和行为研究
将基因发现转化为临床护理所必需的。GC提供临床遗传学服务和
自2003年起支持亨斯迈癌症研究所(HCI)的基因研究(由癌症中心提供支持
支持赠款),自2006年以来一直由CGC硕士温迪·科尔曼指导。GC是
HCI使命的精髓,并通过领先的实践变革建立在HCI悠久的基因发现历史基础上
研究致力于确定基因检测的临床效用,即风险沟通的最佳方法
和提供遗传咨询,以及管理遗传性癌症风险的策略
先天倾向。GC是癌症中心的一个主要目标,为临床带来科学发现
并转化为面向大众的应用程序。GC提供翻译基因所需的几项关键服务
研究,包括确定用于基因研究或症状研究的患者队列;帮助
研究人员设计研究,以最佳方式整合遗传信息,并预测和解决伦理问题,
与基因分析有关的法律和社会问题;提供遗传咨询干预;收集
临床表型和纵向结果数据。GC的目标是:1)提供癌症遗传学
专业知识、遗传咨询服务和干预,以及2)支持科学研究目标
癌症中心,特别是在将遗传学转化为临床和人口的背景下。
获得研究遗传咨询服务使癌症中心的成员能够学习新的
提供遗传信息并将参与者包括在我们的集水区、州
犹他州。GC通过确保所有癌症中心都可以获得遗传学专业知识来增加癌症中心的价值
成员和临床研究人员。GC对整个人机界面的广泛影响体现在它对61
自2014年以来的出版物。拥有同行评审资金的癌症中心成员占用户的53%,以及
GC的工作100%都与癌症有关。
HCI建立高质量、研究型遗传咨询共享资源
在国家癌症研究所癌症中心中具有创新性和独特性。共享的董事和工作人员
资源参与国家委员会,他们通过将
遗传性癌症基因检测和治疗指南的研究结果。GC使HCI在所有方面都出类拔萃
在遗传性癌症研究领域,并在基因发现和将发现转化为
临床实施和人口政策。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Wendy K Kohlmann其他文献
NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2024.
NCCN 指南®见解:遗传/家族高风险评估:乳腺、卵巢和胰腺,版本 2.2024。
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
M. B. Daly;Tuya Pal;K. Maxwell;Jane Churpek;Wendy K Kohlmann;Zahraa AlHilli;Banu K Arun;S. Buys;Heather H Cheng;S. Domchek;Susan Friedman;V. Giri;M. Goggins;Andrea Hagemann;Ashley Hendrix;M. Hutton;B. Karlan;Nawal Kassem;Seema Khan;Katia Khoury;Allison W. Kurian;Christine Laronga;Julie S. Mak;John Mansour;K. McDonnell;Carolyn S. Menendez;S. Merajver;B. Norquist;K. Offit;Dominique Rash;Gwen Reiser;Leigha Senter;Kristen Mahoney Shannon;K. Visvanathan;Jeanna Welborn;Myra J. Wick;Marie Wood;M. Yurgelun;M. Dwyer;S. Darlow - 通讯作者:
S. Darlow
Wendy K Kohlmann的其他文献
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{{ truncateString('Wendy K Kohlmann', 18)}}的其他基金
Analysis of BRCA Testing Patterns Using the Utah Population Database
使用犹他州人口数据库分析 BRCA 检测模式
- 批准号:
9233674 - 财政年份:2017
- 资助金额:
$ 14.37万 - 项目类别:
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