欧洲遗传肿瘤风险综合征参考网络（ERN GENTURIS）：对患者、家庭和卫生保健提供者的益处。

IF 1.8 4区医学 Q3 GENETICS & HEREDITY

Familial Cancer Pub Date : 2025-03-30 DOI:10.1007/s10689-025-00457-9

Manon Engels, Katarzyna Urbanczyk, Jurriaan Hölzenspies, Claas Röhl, Nicoline Geverink, Nicoline Hoogerbrugge

引用次数: 0

摘要

欧洲遗传肿瘤风险综合征参考网络（ERN GENTURIS）成立于2017年，连接了50多个欧洲专家中心，改善了罕见遗传肿瘤风险综合征（遗传性癌症）患者的诊断、治疗和高质量医疗保健服务，无论他们生活在欧洲的哪个地方。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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The European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS): benefits for patients, families, and health care providers.

The European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS) established in 2017 and connecting more than 50 European expert centres improves access to diagnosis, treatment, and the provision of high-quality healthcare for patients with rare genetic tumour risk syndromes (hereditary cancer), no matter where they live in Europe.

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来源期刊

Familial Cancer 医学-遗传学

CiteScore

4.10

自引率

4.50%

发文量

审稿时长

6-12 weeks

期刊介绍： In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.