European training requirements for the specialty of medical genetics

IF 4.6 2区生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY

European Journal of Human Genetics Pub Date : 2025-07-02 DOI:10.1038/s41431-025-01899-6

Ute Moog, Jonathan Berg, Siobhan Kerr, Peter D. Turnpenny, Alain Verloes, Working Group ETR for Medical Genetics, Johannes Zschocke

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Abstract

The development of European training standards is a major contribution to the improvement of medical training at the European level and one of the core activities of the European Union of Medical Specialists (Union Européenne des Médecins Spécialistes, UEMS). European Training Requirements for the specialty of Medical Genetics (ETR-MG) were first developed and approved in 2017. Here we report the content and objectives of the 2023 revision, carried out by the ETR-MG Working Group and the officers of the UEMS Section of Medical Genetics in close cooperation with the ESHG and the European Board of Medical Genetics (EBMG). New aspects concern an update of the description of the specialty, the integration of the examination for the European Certificate in Medical Genetics and Genomics (ECMGG), a complete restructuring of the syllabus, and the adaption to novel concepts of medical education.

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医学遗传学专业的欧洲培训要求。

制定欧洲培训标准是对改进欧洲一级医疗培训的一项重大贡献，也是欧洲医学专家联盟的核心活动之一（欧洲医学专家联盟，UEMS）。欧洲医学遗传学专业培训要求（etrg - mg）于2017年首次制定并批准。在此，我们报告了2023年修订的内容和目标，该修订由etrg - mg工作组和UEMS医学遗传学科的官员与ESHG和欧洲医学遗传学委员会（EBMG）密切合作进行。新的方面涉及专业描述的更新，欧洲医学遗传学和基因组学证书（ECMGG）考试的整合，教学大纲的完全重组，以及适应医学教育的新概念。

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来源期刊

European Journal of Human Genetics 生物-生化与分子生物学

CiteScore

9.90

自引率

5.80%

发文量

216

审稿时长

2 months

期刊介绍： The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics